Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: PIP[original query] |
---|
Genetic variations observed in arterial and venous thromboembolism--relevance for therapy, risk prevention and prognosis. Clinical chemistry and laboratory medicine : CCLM / FESCC 2003 Apr 41 (4): 496-500. Harrington Dominic J, Malefora Agata, Schmeleva Veronika, Kapustin Sergey, Papayan Ludmila, Blinov Mikhail, Harrington Pip, Mitchell Mike, Savidge Geoffrey |
The A1166C polymorphism of the AT1 receptor gene is associated with collagen type I synthesis and myocardial stiffness in hypertensives. Journal of hypertension 2003 Nov 21 (11): 2085-92. Díez Javier, Laviades Concepción, Orbe Josune, Zalba Guillermo, López Begoña, González Arantxa, Mayor Gaspar, Páramo José A, Beloqui Osc |
Germline SDHB mutations and familial renal cell carcinoma. Journal of the National Cancer Institute 2008 Sep 100 (17): 1260-2. Ricketts Christopher, Woodward Emma R, Killick Pip, Morris Mark R, Astuti Dewi, Latif Farida, Maher Eamonn |
Genotype-phenotype correlations in VHL exon deletions. American journal of medical genetics. Part A 2009 Oct 149A (10): 2147-51. McNeill Alisdair, Rattenberry Eleanor, Barber Richard, Killick Pip, MacDonald Fiona, Maher Eamonn |
CLC- a novel susceptibility gene for allergic rhinitis? Allergy 2010 Feb 65 (2): 220-8. Bryborn M, Halldén C, Säll T, Cardell L |
Confirmation of two major polyarticular osteoarthritis (POA) phenotypes--differentiation on the basis of joint topography. Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society 2009 Jul 17 (7): 891-5. Carroll G J, Breidahl W H, Jazayeri |
The relationship of estrogen receptor-alpha and -beta genes with osteoarthritis of the hand. The Journal of rheumatology 2009 Dec 36 (12): 2772-9. Wise Barton L, Demissie Serkalem, Cupples L Adrienne, Felson David T, Yang Mei, Shearman Amanda M, Aliabadi Piran, Hunter David |
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. Human mutation 2010 Jan 31 (1): 41-51. Ricketts Christopher J, Forman Julia R, Rattenberry Eleanor, Bradshaw Nicola, Lalloo Fiona, Izatt Louise, Cole Trevor R, Armstrong Ruth, Kumar V K Ajith, Morrison Patrick J, Atkinson A Brew, Douglas Fiona, Ball Steve G, Cook Jackie, Srirangalingam Umasuthan, Killick Pip, Kirby Gail, Aylwin Simon, Woodward Emma R, Evans D Gareth R, Hodgson Shirley V, Murday Vicky, Chew Shern L, Connell John M, Blundell Tom L, Macdonald Fiona, Maher Eamonn |
Epistatic and functional interactions of catechol-o-methyltransferase (COMT) and AKT1 on neuregulin1-ErbB signaling in cell models. PloS one 2010 5 (5): e10789. Sei Yoshitatsu, Li Zhen, Song Jian, Ren-Patterson Renee, Tunbridge Elizabeth M, Iizuka Yukihiko, Inoue Masahiro, Alfonso Berenice T, Beltaifa Senda, Nakai Yoko, Kolachana Bhaskar S, Chen Jingshan, Weinberger Daniel |
Contribution of anti-CCP antibodies, proximal interphalangeal joint involvement, HLA-DRB1 shared epitope, and PADI4 as risk factors for the development of rheumatoid arthritis in palindromic rheumatism. Scandinavian journal of rheumatology 2010 Aug 39 (4): 287-91. Tamai M, Kawakami A, Iwamoto N, Arima K, Aoyagi K, Eguchi |
Type of CFTR mutation determines risk of pancreatitis in patients with cystic fibrosis. Gastroenterology 2011 Jan 140 (1): 153-61. Ooi Chee Y, Dorfman Ruslan, Cipolli Marco, Gonska Tanja, Castellani Carlo, Keenan Katherine, Freedman Steven D, Zielenski Julian, Berthiaume Yves, Corey Mary, Schibli Susanne, Tullis Elizabeth, Durie Peter |
Transforming growth factor ß 869C/T and interleukin 6 -174G/C polymorphisms relate to the severity and progression of bone-erosive damage detected by ultrasound in rheumatoid arthritis. Arthritis research & therapy 2011 13 (4): R111. Ceccarelli Fulvia, Perricone Carlo, Fabris Martina, Alessandri Cristiano, Iagnocco Annamaria, Fabro Cinzia, Pontarini Elena, De Vita Salvatore, Valesini Gui |
Additive effect of the AZGP1, PIP, S100A8 and UBE2C molecular biomarkers improves outcome prediction in breast carcinoma. International journal of cancer. Journal international du cancer 2014 Apr 134 (7): 1617-29. Parris Toshima Z, Kovács Anikó, Aziz Luaay, Hajizadeh Shahin, Nemes Szilárd, Semaan May, Forssell-Aronsson Eva, Karlsson Per, Helou Khal |
Impact of MYH6 variants in hypoplastic left heart syndrome. Physiological genomics 2016 12 48 (12): 912-921. Tomita-Mitchell Aoy, Stamm Karl D, Mahnke Donna K, Kim Min-Su, Hidestrand Pip M, Liang Huan Ling, Goetsch Mary A, Hidestrand Mats, Simpson Pippa, Pelech Andrew N, Tweddell James S, Benson D Woodrow, Lough John W, Mitchell Michael |
Variation at HLA-DPB1 is associated with dermatomyositis in Chinese population.
The Journal of dermatology 2016 Nov 43 (11): 1307-1313. Zhang Chang-E, Li Yang, Wang Zai-Xing, Gao Jin-Ping, Zhang Xiao-Guang, Zuo Xian-Bo, Sheng Yu-Jun, Chen Gang, Sun Liang-Dan, Zhang Xue-Jun, Xu Jin-Hua, Yang S |
ApoE4-associated phospholipid dysregulation contributes to development of Tau hyper-phosphorylation after traumatic brain injury. Scientific reports 2017 9 7 (1): 11372. Cao Jiqing, Gaamouch Farida El, Meabon James S, Meeker Kole D, Zhu Li, Zhong Margaret B, Bendik John, Elder Gregory, Jing Ping, Xia Jiahong, Luo Wenjie, Cook David G, Cai Dongmi |
Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations. BMC medical genetics 2018 7 19 (1): 113. Beke Artur, Piko Henriett, Haltrich Iren, Karcagi Veronika, Rigo Janos, Molnar Maria Judit, Fekete Györ |
pyseer: a comprehensive tool for microbial pangenome-wide association studies. Bioinformatics (Oxford, England) 2018 12 34 (24): 4310-4312. Lees John A, Galardini Marco, Bentley Stephen D, Weiser Jeffrey N, Corander Juk |
Metabolite profiling identified pipecolic acid as an important component of peanut seed resistance against Aspergillus flavus infection. Journal of hazardous materials 2020 10 404 (Pt A): 124155. Sharma Sandeep, Choudhary Babita, Yadav Sonam, Mishra Avinash, Mishra Vinod K, Chand Ramesh, Chen Chen, Pandey Shree |
Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia. Human reproduction (Oxford, England) 2020 1 35 (1): 240-252. Oud M S, Okutman Ö, Hendricks L A J, de Vries P F, Houston B J, Vissers L E L M, O'Bryan M K, Ramos L, Chemes H E, Viville S, Veltman J |
IKZF1 alterations are not associated with outcome in 498 adults with B-precursor ALL enrolled in the UKALL14 trial. Blood advances 2021 9 5 (17): 3322-3332. Mitchell Rachel J, Kirkwood Amy A, Barretta Emilio, Clifton-Hadley Laura, Lawrie Emma, Lee SooWah, Leongamornlert Daniel, Marks David I, McMillan Andrew K, Menne Tobias F, Papaemmanuil Elli, Patel Bela, Patrick Pip, Rowntree Clare J, Zareian Nahid, Alapi Krisztina Zuborne, Moorman Anthony V, Fielding Adele |
Genetic and genomic analysis of acute lymphoblastic leukemia in older adults reveals a distinct profile of abnormalities: analysis of 210 patients from the UKALL14 and UKALL60+ clinical trials. Haematologica 2021 11 107 (9): 2051-2063. Creasey Thomas, Barretta Emilio, Ryan Sarra L, Butler Ellie, Kirkwood Amy A, Leongamornlert Daniel, Papaemmanuil Elli, Patrick Pip, Clifton-Hadley Laura, Patel Bela, Menne Tobias, McMillan Andrew K, Harrison Christine J, Rowntree Clare J, Morley Nick, Marks David I, Fielding Adele K, Moorman Anthony |
Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
Environmental thallium exposure and the risk of early embryonic arrest among women undergoing in vitro fertilization: thallium exposure and polymorphisms of mtDNA gene interaction and potential cause exploring. Environmental science and pollution research international 2022 4 29 (41): 62648-62661. Liang Chunmei, Luo Guiying, Cao Yu, Li Danyang, Shen Lingchao, Zhang Zhikang, Jiang Tingting, Zong Kai, Liang Dan, Zou Weiwei, Xu Xiaofeng, Liu Yajing, Ji Dongmei, Cao Yunx |
Fine-mapping of intracranial aneurysm susceptibility based on a genome-wide association study. Scientific reports 2022 02 12 (1): 2717. Hong Eun Pyo, Youn Dong Hyuk, Kim Bong Jun, Ahn Jun Hyong, Park Jeong Jin, Rhim Jong Kook, Kim Heung Cheol, Hwang Gyojun, Jeon Hong Jun, Jeon Jin Pyeo |
Finnish-specific AKT2 gene variant leads to impaired insulin signalling in myotubes. Journal of molecular endocrinology 2022 11 70 (2): . Mäkinen Selina, Datta Neeta, Rangarajan Savithri, Nguyen Yen H, Olkkonen Vesa M, Latva-Rasku Aino, Nuutila Pirjo, Laakso Markku, Koistinen Heikki |
Elevated Levels of Toxic Bile Acids in Serum of Cystic Fibrosis Patients with CFTR Mutations Causing Pancreatic Insufficiency. International journal of molecular sciences 2022 10 23 (20): . Tabori Harold, Schneider Jochen, Lüth Stefan, Zagoya Carlos, Barucha Anton, Lehmann Thomas, Kauf Eberhard, Barth Astrid, Mainz Jochen |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: