HuGE Literature Finder
Records 1-30
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The genetic variants in calcium signaling related genes influence anti-tuberculosis drug induced liver injury: A prospective study.
Medicine 2019 Nov 98 (44): e17821. Lyu Mengyuan, Zhou Jian, Chen Hao, Bai Hao, Song Jiajia, Liu Tangyuheng, Cheng Yuhui, Ying Bin |
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Interleukin-10 and Transforming Growth Factor Beta1 Gene Polymorphisms in Chronic Heart Failure.
Acta bio-medica : Atenei Parmensis 2019 May 90 (2): 221-227. Mahmoudi Mohammad Jafar, Hedayat Mona, Taghvaei Mohammad, Harsini Sara, Nematipour Ebrahim, Rezaei Nima, Farhadi Elham, Mahmoudi Maryam, Sadr Maryam, Esfahanian Nilufar, Nourijelyani Keramat, Amirzargar Ali Akb |
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An initial genetic analysis of gemcitabine-induced high-grade neutropenia in pancreatic cancer patients CALGB 80303 (Alliance).
Pharmacogenetics and genomics 2019 Mar . Innocenti Federico, Jiang Chen, Sibley Alexander B, Denning Stefanie, Etheridge Amy S, Watson Dorothy, Niedzwiecki Donna, Hatch Ace J, Hurwitz Herbert I, Nixon Andrew B, Furukawa Yoichi, Kubo Michiaki, Crona Daniel J, Kindler Hedy L, McLeod Howard L, Ratain Mark J, Owzar Kour |
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Genome-Wide Association Analysis of Single Breath Diffusing Capacity of Carbon Monoxide (DLCO).
American journal of respiratory cell and molecular biology 2019 Jan . Sakornsakolpat Phuwanat, McCormack Meredith, Bakke Per, Gulsvik Amund, Make Barry J, Crapo James D, Cho Michael H, Silverman Edwin |
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Significant Association and Increased Risk of Primary Open Angle Glaucoma with
Reports of biochemistry & molecular biology 2019 Jan 7 (2): 210-216. Derakhshan Akbar, Sadeghi Allah Abadi Javad, Tavakkol-Afshari Jalil, Nikpoor Amin Reza, Daneshvar Ramin, Shokoohi Rad Saeed, Ansari-Astaneh Mohammad-Reza, Ghafarian Sade |
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Nature communications 2018 May 9 (1): 1864. Iglesias Adriana I, Mishra Aniket, Vitart Veronique, Bykhovskaya Yelena, Höhn René, Springelkamp Henriët, Cuellar-Partida Gabriel, Gharahkhani Puya, Bailey Jessica N Cooke, Willoughby Colin E, Li Xiaohui, Yazar Seyhan, Nag Abhishek, Khawaja Anthony P, Polašek Ozren, Siscovick David, Mitchell Paul, Tham Yih Chung, Haines Jonathan L, Kearns Lisa S, Hayward Caroline, Shi Yuan, van Leeuwen Elisabeth M, Taylor Kent D, , Bonnemaijer Pieter, Rotter Jerome I, Martin Nicholas G, Zeller Tanja, Mills Richard A, Staffieri Sandra E, Jonas Jost B, Schmidtmann Irene, Boutin Thibaud, Kang Jae H, Lucas Sionne E M, Wong Tien Yin, Beutel Manfred E, Wilson James F, , , Uitterlinden André G, Vithana Eranga N, Foster Paul J, Hysi Pirro G, Hewitt Alex W, Khor Chiea Chuen, Pasquale Louis R, Montgomery Grant W, Klaver Caroline C W, Aung Tin, Pfeiffer Norbert, Mackey David A, Hammond Christopher J, Cheng Ching-Yu, Craig Jamie E, Rabinowitz Yaron S, Wiggs Janey L, Burdon Kathryn P, van Duijn Cornelia M, MacGregor Stua |
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Comparison of SNP Genotypes Related to Proliferative Vitreoretinopathy (PVR) across Slovenian and European Subpopulations.
Journal of ophthalmology 2018 2018 8761625. Lumi Xhevat, Jelen Mateja M, Jevšinek Skok Daša, Boštjan?i? Emanuela, Ravnik-Glava? Metka, Hawlina Marko, Glava? Damj |
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Transforming Growth Factor- ? Protects against Inflammation-Related Atherosclerosis in South African CKD Patients.
International journal of nephrology 2018 2018 8702372. Hassan Muzamil Olamide, Duarte Raquel, Dix-Peek Therese, Dickens Caroline, Naidoo Sagren, Vachiat Ahmed, Grinter Sacha, Manga Pravin, Naicker Saralade |
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Transforming growth factor-? signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population.
Scientific reports 2017 Oct 7 (1): 13589. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Tsai Shih-J |
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Matrix Metalloproteinase Polymorphisms in Patients with Floppy Mitral Valve/Mitral Valve Prolapse (FMV/MVP) and FMV/MVP Syndrome.
Cardiology 2017 Jul 138 (3): 179-185. Lima Sarah M, Pitsis Antonios A, Kelpis Timotheos G, Shahin Mohamed H, Langaee Taimour Y, Cavallari Larisa H, Theofilogiannakos Efstratios K, Boudoulas Harisios, Boudoulas Konstantinos De |
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Genetic variance of transforming growth factor ?2 gene in conotruncal heart defects.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2016 Aug 1-7. Chen Yu, Zhang Rui, Xie Jun, Li Yajiao, Shi Shaoqing, Qian Hong, Yan Zhiguo, Rao |
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Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing.
American journal of medical genetics. Part A 2016 Feb . Schubert Jeffrey A, Landis Benjamin J, Shikany Amy R, Hinton Robert B, Ware Stephanie |
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Genetic variants of ADAM17 are implicated in the pathological process of Kawasaki disease and secondary coronary artery lesions via the TGF-?/SMAD3 signaling pathway.
European journal of pediatrics 2016 Feb . Peng Qian, Deng Yan, Yang Xiling, Leng Xiangyou, Yang Yuan, Liu Hanm |
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Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
International journal of legal medicine 2016 Feb . Neubauer Jacqueline, Haas Cordula, Bartsch Christine, Domingo-Medeiros Argelia, Berger Wolfga |
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Correlation of Aqueous Humor Lysyl Oxidase Activity with TGF-ß Levels and LOXL1 Genotype in Pseudoexfoliation.
Current eye research 2016 10 41 (10): 1331-1338. Gayathri Ramakrishnan, Coral Karunakaran, Sharmila Ferdinamarie, Sripriya Sarangapani, Sripriya Krishnamoorthy, Manish Panday, Shantha B, Ronnie George, Vijaya Lingam, Narayanasamy Angayarkan |
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A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
BMC genetics 2015 Dec 16 138. Lutz Sharon M, Cho Michael H, Young Kendra, Hersh Craig P, Castaldi Peter J, McDonald Merry-Lynn, Regan Elizabeth, Mattheisen Manuel, DeMeo Dawn L, Parker Margaret, Foreman Marilyn, Make Barry J, Jensen Robert L, Casaburi Richard, Lomas David A, Bhatt Surya P, Bakke Per, Gulsvik Amund, Crapo James D, Beaty Terri H, Laird Nan M, Lange Christoph, Hokanson John E, Silverman Edwin K, , |
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The NR3C1 Glucocorticoid Receptor Gene Polymorphisms May Modulate the TGF-beta mRNA Expression in Asthma Patients.
Inflammation 2015 Aug 38 (4): 1479-92. Panek Micha?, Pietras Tadeusz, Fabijan Artur, Zio?o Jan, Wieteska ?ukasz, Ma?achowska Beata, Fendler Wojciech, Szemraj Janusz, Kuna Pio |
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[Association study between candidate genes on transforming growth factor-? signaling pathway and the risk of non-syndromic cleft lip with or without cleft palate in Chinese populations].
Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences 2015 Jun 47 (3): 384-9. Wang Zhu-qing, Wang Ping, Wu-Chou Yah-huei, Ye Xiao-qian, Huang Shang-zhi, Shi Bing, Wang Ke, Yuan Yuan, Liu Dong-jing, Wu Tao, Wang Hong, Beaty Terri |
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Transforming growth factor-? receptor 2 gene polymorphisms are associated with end-stage renal disease.
Kidney research and clinical practice 2015 Jun 34 (2): 93-7. Ki Hye-Jin, Kim Se Yun, Lee Sang Ho, Moon Ju-Young, Jeong Kyung Hwan, Lee Tae Won, Ihm Chun Gyoo, Kim Su Kang, Chung Joo-Ho, Kang Sun Woo, Kim Tae Hee, Kim Yeong-Hoon, Kim Yang Gy |
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Association analysis of TGFBR3 gene with Behçet's disease and idiopathic intermediate uveitis in a Caucasian population.
The British journal of ophthalmology 2015 May 99 (5): 696-9. Barry Robert J, Alsalem Jawaher A, Faassen Juliet, Murray Philip I, Curnow S John, Wallace Graham |
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Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.
American journal of respiratory and critical care medicine 2014 Aug 190 (4): 399-409. Castaldi Peter J, Cho Michael H, San José Estépar Raúl, McDonald Merry-Lynn N, Laird Nan, Beaty Terri H, Washko George, Crapo James D, Silverman Edwin K, |
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Large-scale evaluation of common variation in regulatory T cell-related genes and ovarian cancer outcome.
Cancer immunology research 2014 Apr 2 (4): 332-40. Charbonneau Bridget, Moysich Kirsten B, Kalli Kimberly R, Oberg Ann L, Vierkant Robert A, Fogarty Zachary C, Block Matthew S, Maurer Matthew J, Goergen Krista M, Fridley Brooke L, Cunningham Julie M, Rider David N, Preston Claudia, Hartmann Lynn C, Lawrenson Kate, Wang Chen, Tyrer Jonathan, Song Honglin, deFazio Anna, Johnatty Sharon E, Doherty Jennifer A, Phelan Catherine M, Sellers Thomas A, Ramirez Starr M, Vitonis Allison F, Terry Kathryn L, Van Den Berg David, Pike Malcolm C, Wu Anna H, Berchuck Andrew, Gentry-Maharaj Aleksandra, Ramus Susan J, Diergaarde Brenda, Shen Howard, Jensen Allan, Menkiszak Janusz, Cybulski Cezary, Lubi?ski Jan, Ziogas Argyrios, Rothstein Joseph H, McGuire Valerie, Sieh Weiva, Lester Jenny, Walsh Christine, Vergote Ignace, Lambrechts Sandrina, Despierre Evelyn, Garcia-Closas Montserrat, Yang Hannah, Brinton Louise A, Spiewankiewicz Beata, Rzepecka Iwona K, Dansonka-Mieszkowska Agnieszka, Seibold Petra, Rudolph Anja, Paddock Lisa E, Orlow Irene, Lundvall Lene, Olson Sara H, Hogdall Claus K, Schwaab Ira, du Bois Andreas, Harter Philipp, Flanagan James M, Brown Robert, Paul James, Ekici Arif B, Beckmann Matthias W, Hein Alexander, Eccles Diana, Lurie Galina, Hays Laura E, Bean Yukie T, Pejovic Tanja, Goodman Marc T, Campbell Ian, Fasching Peter A, Konecny Gottfried, Kaye Stanley B, Heitz Florian, Hogdall Estrid, Bandera Elisa V, Chang-Claude Jenny, Kupryjanczyk Jolanta, Wentzensen Nicolas, Lambrechts Diether, Karlan Beth Y, Whittemore Alice S, Culver Hoda Anton, Gronwald Jacek, Levine Douglas A, Kjaer Susanne K, Menon Usha, Schildkraut Joellen M, Pearce Celeste Leigh, Cramer Daniel W, Rossing Mary Anne, Chenevix-Trench Georgia, , , Pharoah Paul D P, Gayther Simon A, Ness Roberta B, Odunsi Kunle, Sucheston Lara E, Knutson Keith L, Goode Ellen |
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Thrombospondin-1 polymorphisms influence risk of corneal allograft rejection.
Investigative ophthalmology & visual science 2014 Apr 55 (4): 2115-20. Winton Helen L, Bidwell Jeffrey L, Armitage W Jo |
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Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.
The Lancet. Respiratory medicine 2014 Mar 2 (3): 214-25. Cho Michael H, McDonald Merry-Lynn N, Zhou Xiaobo, Mattheisen Manuel, Castaldi Peter J, Hersh Craig P, Demeo Dawn L, Sylvia Jody S, Ziniti John, Laird Nan M, Lange Christoph, Litonjua Augusto A, Sparrow David, Casaburi Richard, Barr R Graham, Regan Elizabeth A, Make Barry J, Hokanson John E, Lutz Sharon, Dudenkov Tanda Murray, Farzadegan Homayoon, Hetmanski Jacqueline B, Tal-Singer Ruth, Lomas David A, Bakke Per, Gulsvik Amund, Crapo James D, Silverman Edwin K, Beaty Terri H, |
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Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.
Nature communications 2014 5 4020. Navarini Alexander A, Simpson Michael A, Weale Michael, Knight Jo, Carlavan Isabelle, Reiniche Pascale, Burden David A, Layton Alison, Bataille Veronique, Allen Michael, Pleass Robert, Pink Andrew, Creamer Daniel, English John, Munn Stephanie, Walton Shernaz, , Willis Carolyn, Déret Sophie, Voegel Johannes J, Spector Tim, Smith Catherine H, Trembath Richard C, Barker Jonathan |
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Role of TGF-? pathway polymorphisms in sporadic thoracic aortic aneurysm: rs900 TGF-?2 is a marker of differential gender susceptibility.
Mediators of inflammation 2014 2014 165758. Scola Letizia, Di Maggio Federica M, Vaccarino Loredana, Bova Manuela, Forte Giusy I, Pisano Calogera, Candore Giuseppina, Colonna-Romano Giuseppina, Lio Domenico, Ruvolo Giovanni, Balistreri Carmela |
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Common DNA variants predict tall stature in Europeans.
Human genetics 2013 Nov . Liu F, Hendriks AE, Ralf A, Boot AM, Benyi E, Sävendahl L, Oostra BA, van Duijn C, Hofman A, Rivadeneira F, Uitterlinden AG, Drop SL, Kayser M |
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Associations between genetic variants in the TGF-? signaling pathway and breast cancer risk among Hispanic and non-Hispanic white women.
Breast cancer research and treatment 2013 Sep 141 (2): 287-97. Boone Stephanie D, Baumgartner Kathy B, Baumgartner Richard N, Connor Avonne E, Pinkston Christina M, John Esther M, Hines Lisa M, Stern Mariana C, Giuliano Anna R, Torres-Mejia Gabriela, Brock Guy N, Groves Frank D, Kerber Richard A, Wolff Roger K, Slattery Martha |
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AMD-associated genes encoding stress-activated MAPK pathway constituents are identified by interval-based enrichment analysis.
PloS one 2013 8 (8): e71239. SanGiovanni John Paul, Lee Phil |
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The genotype and expression of the TGF?2 gene in children with congenital conotruncal defects.
Pediatric cardiology 2013 34 (8): 1823-8. Meng Yingying, Ma Xiaojing, Zhang Jing, Wang Huijun, Ma Duan, Huang Guoyi |
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TGF?RIIb mutations trigger aortic aneurysm pathogenesis by altering transforming growth factor ?2 signal transduction.
Circulation. Cardiovascular genetics 2012 Dec 5 (6): 621-9. Bee Katharine J, Wilkes David C, Devereux Richard B, Basson Craig T, Hatcher Cathy |
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Cytokine gene polymorphisms affect reactivation of cytomegalovirus in patients with cancer.
Cytokine 2012 Nov 60 (2): 417-22. Cano Pedro, Han Faye S, Wang Huan-Ling, Fernandez-Vina Marcelo, Han Xiang |
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Multiple Single-Nucleotide Polymorphism-Based Risk Model for Clinical Outcomes After Allogeneic Stem-Cell Transplantation, Especially for Acute Graft-Versus-Host Disease.
Transplantation 2012 Nov . Kim DD, Yun J, Won HH, Cheng L, Su J, Xu W, Uhm J, Gupta V, Kuruvilla J, Messner HA, Lipton JH |
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DNA sequencing of TGF?2 in sporadic patients with tetralogy of Fallot.
Experimental and therapeutic medicine 2012 May 3 (5): 878-880. Gao Yan, Ma Xiao-Jing, Huang Guo-Ying, Zhang Jing, Wang Hui-Jun, Ma Duan, Wu Y |
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[Association between rs6658835 polymorphism of transforming growth factor beta 2 gene and congenital heart diseases in Chinese Han population].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2012 Apr 29 (2): 210-3. Xie Jun, Chen Yu, Li Hui, Zhou Bin, Rao |
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Common TGF?2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma.
Molecular vision 2012 18 1526-39. Park Soo, Jamshidi Yalda, Vaideanu Daniela, Fraser Scott, Sowden Jane |
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Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.
PLoS genetics 2011 Dec 7 (12): e1002439. Chan Yingleong, Holmen Oddgeir L, Dauber Andrew, Vatten Lars, Havulinna Aki S, Skorpen Frank, Kvaløy Kirsti, Silander Kaisa, Nguyen Thutrang T, Willer Cristen, Boehnke Michael, Perola Markus, Palotie Aarno, Salomaa Veikko, Hveem Kristian, Frayling Timothy M, Hirschhorn Joel N, Weedon Michael |
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Polymorphisms of transforming growth factor-? signaling pathway and Kawasaki disease in the Taiwanese population.
Journal of human genetics 2011 Dec 56 (12): 840-5. Kuo Ho-Chang, Onouchi Yoshihiro, Hsu Yu-Wen, Chen Wei-Chiao, Huang Jin-Ding, Huang Ying-Hsien, Yang Ya-Ling, Chao Mei-Chyn, Yu Hong-Ren, Juan Yung-Shun, Kuo Chiu-Ming, Yang Kuender D, Huang Jung-San, Chang Wei-Chi |
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Development of a multicomponent prediction model for acute esophagitis in lung cancer patients receiving chemoradiotherapy.
International journal of radiation oncology, biology, physics 2011 Oct 81 (2): 537-44. De Ruyck Kim, Sabbe Nick, Oberije Cary, Vandecasteele Katrien, Thas Olivier, De Ruysscher Dirk, Lambin Phillipe, Van Meerbeeck Jan, De Neve Wilfried, Thierens Hube |
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Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Nature genetics 2011 Sep 43 (11): 1082-90. Soler Artigas María, Loth Daan W, Wain Louise V, Gharib Sina A, Obeidat Ma'en, Tang Wenbo, Zhai Guangju, Zhao Jing Hua, Smith Albert Vernon, Huffman Jennifer E, Albrecht Eva, Jackson Catherine M, Evans David M, Cadby Gemma, Fornage Myriam, Manichaikul Ani, Lopez Lorna M, Johnson Toby, Aldrich Melinda C, Aspelund Thor, Barroso Inês, Campbell Harry, Cassano Patricia A, Couper David J, Eiriksdottir Gudny, Franceschini Nora, Garcia Melissa, Gieger Christian, Gislason Gauti Kjartan, Grkovic Ivica, Hammond Christopher J, Hancock Dana B, Harris Tamara B, Ramasamy Adaikalavan, Heckbert Susan R, Heliövaara Markku, Homuth Georg, Hysi Pirro G, James Alan L, Jankovic Stipan, Joubert Bonnie R, Karrasch Stefan, Klopp Norman, Koch Beate, Kritchevsky Stephen B, Launer Lenore J, Liu Yongmei, Loehr Laura R, Lohman Kurt, Loos Ruth J F, Lumley Thomas, Al Balushi Khalid A, Ang Wei Q, Barr R Graham, Beilby John, Blakey John D, Boban Mladen, Boraska Vesna, Brisman Jonas, Britton John R, Brusselle Guy G, Cooper Cyrus, Curjuric Ivan, Dahgam Santosh, Deary Ian J, Ebrahim Shah, Eijgelsheim Mark, Francks Clyde, Gaysina Darya, Granell Raquel, Gu Xiangjun, Hankinson John L, Hardy Rebecca, Harris Sarah E, Henderson John, Henry Amanda, Hingorani Aroon D, Hofman Albert, Holt Patrick G, Hui Jennie, Hunter Michael L, Imboden Medea, Jameson Karen A, Kerr Shona M, Kolcic Ivana, Kronenberg Florian, Liu Jason Z, Marchini Jonathan, McKeever Tricia, Morris Andrew D, Olin Anna-Carin, Porteous David J, Postma Dirkje S, Rich Stephen S, Ring Susan M, Rivadeneira Fernando, Rochat Thierry, Sayer Avan Aihie, Sayers Ian, Sly Peter D, Smith George Davey, Sood Akshay, Starr John M, Uitterlinden André G, Vonk Judith M, Wannamethee S Goya, Whincup Peter H, Wijmenga Cisca, Williams O Dale, Wong Andrew, Mangino Massimo, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, North Kari E, Omenaas Ernst, Palmer Lyle J, Pietiläinen Kirsi H, Pin Isabelle, Pola Sbreve Ek Ozren, Pouta Anneli, Psaty Bruce M, Hartikainen Anna-Liisa, Rantanen Taina, Ripatti Samuli, Rotter Jerome I, Rudan Igor, Rudnicka Alicja R, Schulz Holger, Shin So-Youn, Spector Tim D, Surakka Ida, Vitart Veronique, Völzke Henry, Wareham Nicholas J, Warrington Nicole M, Wichmann H-Erich, Wild Sarah H, Wilk Jemma B, Wjst Matthias, Wright Alan F, Zgaga Lina, Zemunik Tatijana, Pennell Craig E, Nyberg Fredrik, Kuh Diana, Holloway John W, Boezen H Marike, Lawlor Debbie A, Morris Richard W, Probst-Hensch Nicole, , , Kaprio Jaakko, Wilson James F, Hayward Caroline, Kähönen Mika, Heinrich Joachim, Musk Arthur W, Jarvis Deborah L, Gläser Sven, Järvelin Marjo-Riitta, Ch Stricker Bruno H, Elliott Paul, O'Connor George T, Strachan David P, London Stephanie J, Hall Ian P, Gudnason Vilmundur, Tobin Martin |
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Transforming growth factor-{beta} gene polymorphisms in different phenotypes of sarcoidosis.
The European respiratory journal 2011 Jul 38 (1): 169-75. Pabst S, Fränken T, Schönau J, Stier S, Nickenig G, Meyer R, Skowasch D, Grohé |
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TGF-? signaling pathway and breast cancer susceptibility.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2011 Jun 20 (6): 1112-9. Scollen Serena, Luccarini Craig, Baynes Caroline, Driver Kristy, Humphreys Manjeet K, Garcia-Closas Montserrat, Figueroa Jonine, Lissowska Jolanta, Pharoah Paul D, Easton Douglas F, Hesketh Robin, Metcalfe James C, Dunning Alison |
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Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2011 Apr 22 (4): 1079-90. Zmuda J M, Yerges-Armstrong L M, Moffett S P, Klei L, Kammerer C M, Roeder K, Cauley J A, Kuipers A, Ensrud K E, Nestlerode C S, Hoffman A R, Lewis C E, Lang T F, Barrett-Connor E, Ferrell R E, Orwoll E S, |
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Transforming growth factor-beta signaling pathway in patients with Kawasaki disease.
Circulation. Cardiovascular genetics 2011 Feb 4 (1): 16-25. Shimizu Chisato, Jain Sonia, Davila Sonia, Hibberd Martin L, Lin Kevin O, Molkara Delaram, Frazer Jeffrey R, Sun Shelly, Baker Annette L, Newburger Jane W, Rowley Anne H, Shulman Stanford T, Davila Sonia, Burgner David, Breunis Willemijn B, Kuijpers Taco W, Wright Victoria J, Levin Michael, Eleftherohorinou Hariklia, Coin Lachlan, Popper Stephen J, Relman David A, Fury Wen, Lin Calvin, Mellis Scott, Tremoulet Adriana H, Burns Jane |
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Large-scale candidate gene analysis of HDL particle features.
PloS one 2011 6 (1): e14529. Kaess Bernhard M, Tomaszewski Maciej, Braund Peter S, Stark Klaus, Rafelt Suzanne, Fischer Marcus, Hardwick Robert, Nelson Christopher P, Debiec Radoslaw, Huber Fritz, Kremer Werner, Kalbitzer Hans Robert, Rose Lynda M, Chasman Daniel I, Hopewell Jemma, Clarke Robert, Burton Paul R, Tobin Martin D, Hengstenberg Christian, Samani Nilesh |
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A variant in the fibrillin-3 gene is associated with TGF-? and inhibin B levels in women with polycystic ovary syndrome.
Fertility and sterility 2010 Dec 94 (7): 2916-9. Raja-Khan Nazia, Kunselman Allen R, Demers Laurence M, Ewens Kathryn G, Spielman Richard S, Legro Richard |
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A large-scale candidate gene association study of age at menarche and age at natural menopause.
Human genetics 2010 Nov 128 (5): 515-27. He Chunyan, Kraft Peter, Chasman Daniel I, Buring Julie E, Chen Constance, Hankinson Susan E, Paré Guillaume, Chanock Stephen, Ridker Paul M, Hunter David |
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Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.
Diabetes care 2010 Oct 33 (10): 2250-3. Bailey Swneke D, Xie Changchun, Do Ron, Montpetit Alexandre, Diaz Rafael, Mohan Viswanathan, Keavney Bernard, Yusuf Salim, Gerstein Hertzel C, Engert James C, Anand Sonia, |
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A multilocus candidate approach identifies ACE and HIF1A as susceptibility genes for cellulite.
Journal of the European Academy of Dermatology and Venereology : JEADV 2010 Aug 24 (8): 930-5. Emanuele E, Bertona M, Geroldi |
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Common polymorphisms in ITGA2, PON1 and THBS2 are associated with coronary atherosclerosis in a candidate gene association study of the Chinese Han population.
Journal of human genetics 2010 Aug 55 (8): 490-4. Wang Ying, Fu Wenqing, Xie Fang, Wang Yi, Chu Xun, Wang Haifeng, Shen Min, Wang Ying, Wang Yi, Sun Weiwei, Lei Rong, Yang Lin, Wu Hong, Foo Jianee, Liu Jianjun, Jin Li, Huang W |
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Interferon gamma receptor 2 gene variants are associated with liver fibrosis in patients with chronic hepatitis C infection.
Gut 2010 Aug 59 (8): 1120-6. Nalpas Bertrand, Lavialle-Meziani Roubila, Plancoulaine Sabine, Jouanguy Emmanuelle, Nalpas Antoine, Munteanu Mona, Charlotte Frederic, Ranque Brigitte, Patin Etienne, Heath Simon, Fontaine Hélène, Vallet-Pichard Anaïs, Pontoire Dominique, Bourlière Marc, Casanova Jean-Laurent, Lathrop Mark, Bréchot Christian, Poynard Thierry, Matsuda Fumihiko, Pol Stanislas, Abel Laure |
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Evaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot".
PLoS genetics 2010 Jul 6 (7): e1001016. Johnatty Sharon E, Beesley Jonathan, Chen Xiaoqing, Macgregor Stuart, Duffy David L, Spurdle Amanda B, deFazio Anna, Gava Natalie, Webb Penelope M, Rossing Mary Anne, Doherty Jennifer Anne, Goodman Marc T, Lurie Galina, Thompson Pamela J, Wilkens Lynne R, Ness Roberta B, Moysich Kirsten B, Chang-Claude Jenny, Wang-Gohrke Shan, Cramer Daniel W, Terry Kathryn L, Hankinson Susan E, Tworoger Shelley S, Garcia-Closas Montserrat, Yang Hannah, Lissowska Jolanta, Chanock Stephen J, Pharoah Paul D, Song Honglin, Whitemore Alice S, Pearce Celeste L, Stram Daniel O, Wu Anna H, Pike Malcolm C, Gayther Simon A, Ramus Susan J, Menon Usha, Gentry-Maharaj Aleksandra, Anton-Culver Hoda, Ziogas Argyrios, Hogdall Estrid, Kjaer Susanne K, Hogdall Claus, Berchuck Andrew, Schildkraut Joellen M, Iversen Edwin S, Moorman Patricia G, Phelan Catherine M, Sellers Thomas A, Cunningham Julie M, Vierkant Robert A, Rider David N, Goode Ellen L, Haviv Izhak, Chenevix-Trench Georgia, , , |
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Interleukin-9 polymorphism in infants with respiratory syncytial virus infection: an opposite effect in boys and girls.
Pediatric pulmonology 2010 Jun 45 (6): 608-13. Schuurhof Annemieke, Bont Louis, Siezen Christine L E, Hodemaekers Hennie, van Houwelingen Hans C, Kimman Tjeerd G, Hoebee Barbara, Kimpen Jan L L, Janssen Ri |
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Human variation in alcohol response is influenced by variation in neuronal signaling genes.
Alcoholism, clinical and experimental research 2010 May 34 (5): 800-12. Joslyn Geoff, Ravindranathan Ajay, Brush Gerry, Schuckit Marc, White Raymond |
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New genetic associations detected in a host response study to hepatitis B vaccine.
Genes and immunity 2010 Apr 11 (3): 232-8. Davila S, Froeling F E M, Tan A, Bonnard C, Boland G J, Snippe H, Hibberd M L, Seielstad |
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Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.
PloS one 2010 5 (7): e11493. Jugessur Astanand, Shi Min, Gjessing Håkon Kristian, Lie Rolv Terje, Wilcox Allen James, Weinberg Clarice Ring, Christensen Kaare, Boyles Abee Lowman, Daack-Hirsch Sandra, Nguyen Truc Trung, Christiansen Lene, Lidral Andrew Carl, Murray Jeffrey Cla |
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Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children.
PloS one 2010 5 (6): e11141. Sambo Maria Rosário, Trovoada Maria Jesus, Benchimol Carla, Quinhentos Vatúsia, Gonçalves Lígia, Velosa Rute, Marques Maria Isabel, Sepúlveda Nuno, Clark Taane G, Mustafa Stefan, Wagner Oswald, Coutinho António, Penha-Gonçalves Carl |
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Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease.
Heart rhythm : the official journal of the Heart Rhythm Society 2009 Dec 6 (12): 1745-50. Tseng Zian H, Vittinghoff Eric, Musone Stacy L, Lin Feng, Whiteman Dean, Pawlikowska Ludmila, Kwok Pui-Yan, Olgin Jeffrey E, Aouizerat Bradley |
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Genetic determinants of immune-response to a polysaccharide vaccine for typhoid.
The HUGO journal 2009 Dec 3 (1-4): 1-4. Majumder PP, Staats HF, Sarkar-Roy N, Varma B, Ghosh T, Maiti S, Narayanasamy K, Whisnant CC, Stephenson JL, Wagener DK |
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High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 Dec 24 (12): 2039-49. Yerges Laura M, Klei Lambertus, Cauley Jane A, Roeder Kathryn, Kammerer Candace M, Moffett Susan P, Ensrud Kristine E, Nestlerode Cara S, Marshall Lynn M, Hoffman Andrew R, Lewis Cora, Lang Thomas F, Barrett-Connor Elizabeth, Ferrell Robert E, Orwoll Eric S, Zmuda Joseph M, |
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Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.
American journal of human genetics 2009 Nov 85 (5): 628-42. Talmud Philippa J, Drenos Fotios, Shah Sonia, Shah Tina, Palmen Jutta, Verzilli Claudio, Gaunt Tom R, Pallas Jacky, Lovering Ruth, Li Kawah, Casas Juan Pablo, Sofat Reecha, Kumari Meena, Rodriguez Santiago, Johnson Toby, Newhouse Stephen J, Dominiczak Anna, Samani Nilesh J, Caulfield Mark, Sever Peter, Stanton Alice, Shields Denis C, Padmanabhan Sandosh, Melander Olle, Hastie Claire, Delles Christian, Ebrahim Shah, Marmot Michael G, Smith George Davey, Lawlor Debbie A, Munroe Patricia B, Day Ian N, Kivimaki Mika, Whittaker John, Humphries Steve E, Hingorani Aroon D, , , |
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Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging.
PLoS genetics 2009 Oct 5 (10): e1000685. Wheeler Heather E, Metter E Jeffrey, Tanaka Toshiko, Absher Devin, Higgins John, Zahn Jacob M, Wilhelmy Julie, Davis Ronald W, Singleton Andrew, Myers Richard M, Ferrucci Luigi, Kim Stuart |
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Genetic susceptibility to respiratory syncytial virus bronchiolitis in preterm children is associated with airway remodeling genes and innate immune genes.
The Pediatric infectious disease journal 2009 Apr 28 (4): 333-5. Siezen Christine L E, Bont Louis, Hodemaekers Hennie M, Ermers Marieke J, Doornbos Gerda, Van't Slot Ruben, Wijmenga Ciska, Houwelingen Hans C van, Kimpen Jan L L, Kimman Tjeerd G, Hoebee Barbara, Janssen Ri |
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Sclera-related gene polymorphisms in high myopia.
Molecular vision 2009 15 1655-63. Lin Hui-Ju, Wan Lei, Tsai Yuhsin, Liu Su-Ching, Chen Wen-Chi, Tsai Shih-Wei, Tsai Fuu-J |
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Association of polymorphisms in complement component C3 gene with susceptibility to systemic lupus erythematosus.
Rheumatology (Oxford, England) 2008 Feb 47 (2): 158-64. Miyagawa H, Yamai M, Sakaguchi D, Kiyohara C, Tsukamoto H, Kimoto Y, Nakamura T, Lee J-H, Tsai C-Y, Chiang B-L, Shimoda T, Harada M, Tahira T, Hayashi K, Horiuchi |
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Genetic susceptibility to respiratory syncytial virus bronchiolitis is predominantly associated with innate immune genes.
The Journal of infectious diseases 2007 Sep 196 (6): 826-34. Janssen Riny, Bont Louis, Siezen Christine L E, Hodemaekers Hennie M, Ermers Marieke J, Doornbos Gerda, van 't Slot Ruben, Wijmenga Ciska, Goeman Jelle J, Kimpen Jan L L, van Houwelingen Hans C, Kimman Tjeerd G, Hoebee Barba |
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Transforming growth factor-beta(2) polymorphisms are associated with childhood atopic asthma.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2007 Aug 37 (8): 1165-74. Hatsushika K, Hirota T, Harada M, Sakashita M, Kanzaki M, Takano S, Doi S, Fujita K, Enomoto T, Ebisawa M, Yoshihara S, Sagara H, Fukuda T, Masuyama K, Katoh R, Matsumoto K, Saito H, Ogawa H, Tamari M, Nakao |
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Investigation of TGFB2 as a candidate gene in multiple sclerosis and Parkinson's disease.
Journal of neurology 2007 Jul 254 (7): 846-8. Goris A, Williams-Gray C H, Foltynie T, Brown J, Maranian M, Walton A, Compston D A S, Barker R A, Sawcer S |
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Variant alleles of TGFB1 and TGFBR2 are associated with a decreased risk of gastric cancer in a Chinese population.
International journal of cancer. Journal international du cancer 2007 Mar 120 (6): 1330-5. Jin G, Wang L, Chen W, Hu Z, Zhou Y, Tan Y, Wang J, Hua Z, Ding W, Shen J, Zhang Z, Wang X, Xu Y, Shen H |
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No associations between genetic polymorphisms of TGF-beta, PAI-1, and COL1A1, and bone mineral density in Caucasian females.
Endocrine regulations 2006 Dec 40 (4): 107-12. Hubacek Jaroslav A, Weichetova Marketa, Bohuslavova Romana, Skodova Zdena, Stepan Jan J, Adamkova Ve |
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A novel functional polymorphism in the transforming growth factor-beta2 gene promoter and tumor progression in breast cancer.
Cancer research 2006 Aug 66 (15): 7554-61. Beisner Julia, Buck Miriam B, Fritz Peter, Dippon Jürgen, Schwab Matthias, Brauch Hiltrud, Zugmaier Gerhard, Pfizenmaier Klaus, Knabbe Corneli |
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Transforming growth factor-beta gene polymorphisms in sarcoidosis patients with and without fibrosis.
Chest 2006 Jun 129 (6): 1584-91. Kruit Adrian, Grutters Jan C, Ruven Henk J T, van Moorsel Coline H M, Weiskirchen Ralf, Mengsteab Senait, van den Bosch Jules M |
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Analysis of candidate genes in celiac disease: a tool to identify life-threatening associated genes?
Rejuvenation research 2006 9 (1): 153-6. Nuzzo Domenico, Cataldo Francesco, Scola Letizia, Forte Giusi Irma, Crivello Antonio, Giacalone Antonio, Accomando Salvatore, Barbieri Rainer, Candore Giuseppina, Caruso Calogero, Lio Domeni |
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Genetic susceptibility to keloid disease: transforming growth factor beta receptor gene polymorphisms are not associated with keloid disease.
Experimental dermatology 2004 Feb 13 (2): 120-4. Bayat A, Bock O, Mrowietz U, Ollier WE, Ferguson MW |
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Polymorphisms of transforming growth factor-beta1 and transforming growth factor-beta1 type II receptor genes are associated with acute graft-versus-host disease in children with HLA-matched sibling bone marrow transplantation.
Bone marrow transplantation 2002 Nov 30 (10): 665-71. Hattori H, Matsuzaki A, Suminoe A, Ihara K, Nagatoshi Y, Sakata N, Kawa K, Okamura J, Hara |
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Transforming growth factor-12 polymorphism and systemic lupus erythematosus.
The Journal of rheumatology 2002 Jun 29 (6): 1189-91. Alansari Aliya, Hajeer Ali, Teh Lee-Suan, Bayat Ardeshir, Mysercough Anne, Gül Ahmet, Inanc Murat, Ordi-Ros Jose, Ollier Willi |
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Gene/environment causes of cleft lip and/or palate.
Clinical genetics 2002 Apr 61 (4): 248-56. Murray J |
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Genetic susceptibility in Dupuytren's disease: lack of association of a novel transforming growth factor beta(2) polymorphism in Dupuytren's disease.
Journal of hand surgery (Edinburgh, Scotland) 2002 Feb 27 (1): 47-9. Bayat A, Alansar A, Hajeer A H, Shah M, Watson J S, Stanley J K, Ferguson M W J, Ollier W E |
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