Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: ARSB[original query] |
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Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients. Journal of inherited metabolic disease 2006 1 28 (6): 1027-34. Petry M F G, Nonemacher K, Sebben J C, Schwartz I V D, Azevedo A C M, Burin M G, de Rezende A R, Kim C A, Giugliani R, Leistner-Segal |
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.
PloS one 2009 4 (8): e6501. Potkin Steven G, Guffanti Guia, Lakatos Anita, Turner Jessica A, Kruggel Frithjof, Fallon James H, Saykin Andrew J, Orro Alessandro, Lupoli Sara, Salvi Erika, Weiner Michael, Macciardi Fabio, |
Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk. The Journal of clinical endocrinology and metabolism 2014 Oct 99 (10): E2084-92. Figlioli Gisella, Köhler Aleksandra, Chen Bowang, Elisei Rossella, Romei Cristina, Cipollini Monica, Cristaudo Alfonso, Bambi Franco, Paolicchi Elisa, Hoffmann Per, Herms Stefan, Kalemba Micha?, Kula Dorota, Pastor Susana, Marcos Ricard, Velázquez Antonia, Jarz?b Barbara, Landi Stefano, Hemminki Kari, Försti Asta, Gemignani Federi |
Genetics of Plasminogen Activator Inhibitor-1 (PAI-1) in a Ghanaian Population. PloS one 2015 10 (8): e0136379. White Marquitta J, Kodaman Nuri M, Harder Reed H, Asselbergs Folkert W, Vaughan Douglas E, Brown Nancy J, Moore Jason H, Williams Scott |
Genomics and response to long-term oxygen therapy in chronic obstructive pulmonary disease.
Journal of molecular medicine (Berlin, Germany) 2018 Dec 96 (12): 1375-1385. Seo Minseok, Qiu Weiliang, Bailey William, Criner Gerard J, Dransfield Mark T, Fuhlbrigge Anne L, Reilly John J, Scholand Mary Beth, Castaldi Peter, Chase Robert, Parker Margaret, Saferali Aabida, Yun Jeong H, Crapo James D, Cho Michael H, Beaty Terri H, Silverman Edwin K, Hersh Craig |
Identification of eleven different mutations including six novel, in the arylsulfatase B gene in Iranian patients with mucopolysaccharidosis type VI. Molecular biology reports 2019 4 46 (3): 3417-3426. Jafaryazdi Rokhsareh, Shams Sedigheh, Isaian Anna, Setoodeh Aria, Teimourian Shahr |
Genotype by environment interactions for chronic wasting disease in farmed US white-tailed deer. G3 (Bethesda, Md.) 2022 5 12 (7): . Seabury Christopher M, Lockwood Mitchell A, Nichols Tracy |
Epidemiology and Genetics of Mucopolysaccharidosis Type VI in Russia. Frontiers in molecular biosciences 2022 2 8 780184. Voskoboeva Elena, Semyachkina Alla, Miklyaev Ochir, Gamzatova Amina, Mikhaylova Svetlana, Vashakmadze Nato, Baydakova Galina, Omzar Olga, Pichkur Natalia, Zakharova Ekaterina, Kutsev Serg |
Genetic and environmental factors driving congenital solitary functioning kidney. Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2023 9 . Sander Groen In 't Woud, Marleen M H J van Gelder, Iris A L M van Rooij, Wout F J Feitz, Nel Roeleveld, Michiel F Schreuder, Loes F M van der Zanden, |
Genetic predisposition to differentiated thyroid cancer among Polish population. Polish archives of internal medicine 2024 1 . Martyna Borowczyk, Mateusz Sypniewski, Joanna Szyda, Ma?gorzata Braszka, Katarzyna Ziemnicka, Marek Rucha?a, Michalina Oszywa, Zbigniew J Król, Paula Dobo |
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- Page last updated:Apr 22, 2024
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