Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 91 Records) |
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IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population. American journal of medical genetics. Part A 2012 Sep 158A (9): 2170-5. Brito Luciano A, Bassi Camila F S, Masotti Cibele, Malcher Carolina, Rocha Kátia M, Schlesinger David, Bueno Daniela F, Cruz Lucas A, Barbara Ligia K, Bertola Débora R, Meyer Diogo, Franco Diogo, Alonso Nivaldo, Passos-Bueno Maria Ri |
Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B. Thrombosis and haemostasis 2013 Jan 109 (1): 24-33. Radic Claudia Pamela, Rossetti Liliana Carmen, Abelleyro Miguel Martín, Candela Miguel, Pérez Bianco Raúl, de Tezanos Pinto Miguel, Larripa Irene Beatriz, Goodeve Anne, De Brasi Carlos Dani |
Interactive influences of ethnicity, endothelin-1 gene, and everyday discrimination upon nocturnal ambulatory blood pressure. Annals of behavioral medicine : a publication of the Society of Behavioral Medicine 2013 Jun 45 (3): 377-86. Gregoski Mathew J, Buxbaum Sarah G, Kapuku Gaston, Dong Yanbin, Zhu Haidong, Davis Mary, Gonto Kelsey, Treiber Frank |
Effects of a novel schizophrenia risk variant rs7914558 at CNNM2 on brain structure and attributional style. The British journal of psychiatry : the journal of mental science 2013 Dec . Rose EJ, Hargreaves A, Morris D, Fahey C, Tropea D, Cummings E, Caltagirone C, Bossù P, Chiapponi C, Piras F, Spalletta G, Gill M, Corvin A, Donohoe G |
A genome-wide association study of prostate cancer in West African men. Human genetics 2014 May 133 (5): 509-21. Cook Michael Blaise, Wang Zhaoming, Yeboah Edward D, Tettey Yao, Biritwum Richard B, Adjei Andrew A, Tay Evelyn, Truelove Ann, Niwa Shelley, Chung Charles C, Chokkalingam Annand P, Chu Lisa W, Yeager Meredith, Hutchinson Amy, Yu Kai, Rand Kristin A, Haiman Christopher A, , Hoover Robert N, Hsing Ann W, Chanock Stephen |
Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage. Stroke; a journal of cerebral circulation 2013 Feb 44 (2): 321-6. Falcone Guido J, Biffi Alessandro, Devan William J, Brouwers H Bart, Anderson Christopher D, Valant Valerie, Ayres Alison M, Schwab Kristin, Rost Natalia S, Goldstein Joshua N, Viswanathan Anand, Greenberg Steven M, Selim Magdy, Meschia James F, Brown Devin L, Worrall Bradford B, Silliman Scott L, Tirschwell David L, Rosand Jonathan, |
Association of aminoacyl-tRNA synthetases gene polymorphisms with the risk of congenital heart disease in the Chinese Han population. PloS one 2014 9 (10): e110072. Da Min, Feng Yu, Xu Jing, Hu Yuanli, Lin Yuan, Ni Bixian, Qian Bo, Hu Zhibin, Mo Xumi |
Functional characterisation of the osteoarthritis susceptibility locus at chromosome 6q14.1 marked by the polymorphism rs9350591. BMC medical genetics 2015 16 (1): 81. Johnson Katherine, Reynard Louise N, Loughlin Jo |
Meta-Analysis of the Reduction of Norovirus and Male-Specific Coliphage Concentrations in Wastewater Treatment Plants. Applied and environmental microbiology 2015 Jul 81 (14): 4669-81. Pouillot Régis, Van Doren Jane M, Woods Jacquelina, Plante Daniel, Smith Mark, Goblick Gregory, Roberts Christopher, Locas Annie, Hajen Walter, Stobo Jeffrey, White John, Holtzman Jennifer, Buenaventura Enrico, Burkhardt William, Catford Angela, Edwards Robyn, DePaola Angelo, Calci Kevin |
Mesenchymal Stromal Cells Derived From Crohn's Patients Deploy Indoleamine 2,3-dioxygenase-mediated Immune Suppression, Independent of Autophagy. Molecular therapy : the journal of the American Society of Gene Therapy 2015 Jul 23 (7): 1248-61. Chinnadurai Raghavan, Copland Ian B, Ng Spencer, Garcia Marco, Prasad Mahadev, Arafat Dalia, Gibson Greg, Kugathasan Subra, Galipeau Jacqu |
KIT D816V-mutated bone marrow mesenchymal stem cells in indolent systemic mastocytosis are associated with disease progression. Blood 2015 Nov . Garcia-Montero Andres C, Jara-Acevedo Maria, Alvarez-Twose Ivan, Teodosio Cristina, Sanchez-Muñoz Laura, Muñiz Carmen, Muñoz-Gonzalez Javier I, Mayado Andrea, Matito Almudena, Caldas Carolina, Morgado Jose M, Escribano Luis, Orfao Alber |
Demographics, clinical characteristics, IFNL3- and IFNL4- polymorphisms in a cohort of hepatitis C patients from Puerto Rico. Puerto Rico health sciences journal 2014 Dec 33 (4): 177-83. Morales-Vásquez Lilliana, Miranda-Avalo Edgar I, Rodríguez-Medina José R, Quiñones-Badillo Yomarid, Marqués-Lespier Juan, Muñoz-Acabá José, Pastrana Rafael, Pérez-Cardona Cynthia M, Yamamura Yasuhiro, Torres Esther |
Detection of Mycobacterium tuberculosis genome in vitreous fluid of eyes with multifocal serpiginoid choroiditis. Ophthalmology 2015 1 122 (4): 840-50. Bansal Reema, Sharma Kusum, Gupta Amod, Sharma Aman, Singh Mini P, Gupta Vishali, Mulkutkar Samyak, Dogra Mohit, Dogra Mangat R, Kamal Shivali, Sharma Surya Parkash, Fiorella Paul |
Genetic variants in multisynthetase complex genes are associated with DNA damage levels in Chinese populations. Mutation research 2016 Jan 786 8-13. Liu Jia, Zhu Meng, Chen Weihong, Xie Kaipeng, Shen Wei, Yuan Jing, Cheng Yang, Geng Liguo, Wang Yuzhuo, Jin Guangfu, Dai Juncheng, Ma Hongxia, Du Jiangbo, Wang Meilin, Zhang Zhengdong, Hu Zhibin, Wu Tangchun, Shen Hongbi |
Association of DARS gene polymorphisms with the risk of isolated ventricular septal defects in the Chinese Han population. Italian journal of pediatrics 2016 Nov 42 (1): 102. Feng Yu, Chen Runsen, Mo Xumi |
Exome sequencing identifies a novel mutation in GJA8 associated with inherited cataract in a Chinese family. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie 2016 Oct . Ren Mei, Yang Xin Guang, Dang Xiao Jie, Xiao Jin |
Mutations in KARS cause early-onset hearing loss and leukoencephalopathy: Potential pathogenic mechanism. Human mutation 2017 9 38 (12): 1740-1750. Zhou Xiao-Long, He Long-Xia, Yu Li-Jia, Wang Yong, Wang Xi-Jin, Wang En-Duo, Yang T |
Frequently used bioinformatics tools overestimate the damaging effect of allelic variants. Genes and immunity 2017 12 20 (1): 10-22. Andersen Line Lykke, Terczy?ska-Dyla Ewa, Mørk Nanna, Scavenius Carsten, Enghild Jan J, Höning Klara, Hornung Veit, Christiansen Mette, Mogensen Trine H, Hartmann Ru |
Genetic variations of bone marrow mesenchymal stromal cells derived from acute leukemia and myelodysplastic syndrome by targeted deep sequencing. Leukemia research 2017 Sep 62 23-28. Azuma Kenko, Umezu Tomohiro, Imanishi Satoshi, Asano Michiyo, Yoshizawa Seiichiro, Katagiri Seiichiro, Ohyashiki Kazuma, Ohyashiki Junko |
Analysis of Mesenchymal Stromal Cell Engraftment After Allogeneic HSCT in Pediatric Patients: A Large Multicenter Study. Journal of pediatric hematology/oncology 2018 Sep . Castello Laura M, Leone Marco, Adamini Aloe, Castiglia Sara, Mareschi Katia, Ferrero Ivana, Marco De Gobbi, Carnevale-Schianca Fabrizio, Fagioli Franca, Berger Massi |
Gene Polymorphisms in Cardiovascular Disease and Cancer. Angiology 2018 Jan 3319718774693. Katsiki Niki, Kolovou MSc Vana, Tsipis Md PhD Aggelos, Mihas Md PhD Constantinos, Vartela Md Vasiliki, Koutelou Md PhD Maria, Manolopoulou Dionisia, Leondiadis Md PhD Evangelos, Iakovou Md PhD Ioannis, Mavrogieni Md PhD Sophia, Kolovou Md PhD Genove |
Association of IL1RAP-related genetic variation with cerebrospinal fluid concentration of Alzheimer-associated tau protein. Scientific reports 2019 Feb 9 (1): 2460. Zettergren Anna, Höglund Kina, Kern Silke, Thorvaldsson Valgeir, Johan Skoog Msc, Hansson Oskar, Andreasen Niels, Bogdanovic Nenad, Blennow Kaj, Skoog Ingmar, Zetterberg Henr |
Multi-tissue epigenetic analysis of the osteoarthritis susceptibility locus mapping to the plectin gene PLEC. Osteoarthritis and cartilage 2020 6 28 (11): 1448-1458. Sorial A K, Hofer I M J, Tselepi M, Cheung K, Parker E, Deehan D J, Rice S J, Loughlin |
LncRNA MSC-AS1 Is a Diagnostic Biomarker and Predicts Poor Prognosis in Patients With Gastric Cancer by Integrated Bioinformatics Analysis. Frontiers in medicine 2021 12 8 795427. Yang Wei, Ge Fusheng, Lu Shuaibing, Shan Zhiming, Peng Liangqun, Chai Junhui, Liu Hongxing, Li Baodong, Zhang Zhandong, Huang Jinxi, Hua Yawei, Zhang Yongl |
Inflammatory Bowel Disease Risk Variants Are Associated with an Increased Risk of Skin Cancer. Inflammatory bowel diseases 2022 1 28 (11): 1667-1676. Cushing Kelly C, Du Xiaomeng, Chen Yanhua, Stetson L C, Kuppa Annapurna, Chen Vincent L, Kahlenberg J Michelle, Gudjonsson Johann E, Vanderwerff Brett, Higgins Peter D R, Speliotes Elizabeth |
Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women.
Human reproduction (Oxford, England) 2022 3 37 (5): 1069-1082. Verdiesen Renée M G, van der Schouw Yvonne T, van Gils Carla H, Verschuren W M Monique, Broekmans Frank J M, Borges Maria C, Gonçalves Soares Ana L, Lawlor Deborah A, Eliassen A Heather, Kraft Peter, Sandler Dale P, Harlow Siobán D, Smith Jennifer A, Santoro Nanette, Schoemaker Minouk J, Swerdlow Anthony J, Murray Anna, Ruth Katherine S, Onland-Moret N Charlot |
Genetic analysis of low-grade adenosquamous carcinoma of the breast progressing to high-grade metaplastic carcinoma. Breast cancer research and treatment 2023 8 . Kae Kawachi, Xiaoyan Tang, Rika Kasajima, Takashi Yamanaka, Eigo Shimizu, Kotoe Katayama, Rui Yamaguchi, Kazuaki Yokoyama, Kiyoshi Yamaguchi, Yoichi Furukawa, Satoru Miyano, Seiya Imoto, Emi Yoshioka, Kota Washimi, Yoichiro Okubo, Shinya Sato, Tomoyuki Yokose, Yohei Miya |
Comprehensive Scrna-Seq Analysis and Identification of CD8_+T Cell related Gene Markers for Predicting Prognosis and Drug Resistance of Hepatocellular Carcinoma. Current medicinal chemistry 2023 11 . Lu Cao, Muqi Liu, Xiaoqian Ma, Pengfei Rong, Juan Zhang, Wei Wa |
Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations. HGG advances 2023 1 4 (1): 100166. Zieger Hanna K, Weinhold Leonie, Schmidt Axel, Holtgrewe Manuel, Juranek Stefan A, Siewert Anna, Scheer Annika B, Thieme Frederic, Mangold Elisabeth, Ishorst Nina, Brand Fabian U, Welzenbach Julia, Beule Dieter, Paeschke Katrin, Krawitz Peter M, Ludwig Kerstin |
The Effect of Race/Ethnicity and MED12 Mutation on the Expression of Long Non-Coding RNAs in Uterine Leiomyoma and Myometrium. International journal of molecular sciences 2024 1 25 (2): . Tsai-Der Chuang, Nhu Ton, Shawn Rysling, Drake Boos, Omid Khorr |
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- Page last updated:Apr 22, 2024
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