Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: GNB1[original query] |
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A screen for mutations in the transducin gene GNB1 in patients with autosomal dominant retinitis pigmentosa. Molecular vision 2006 12 (): 1496-8. Mylvaganam Geetha H, McGee Terri L, Berson Eliot L, Dryja Thaddeus |
Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the beta-subunit of transducin with digenic disease. Molecular vision 2007 13 (): 287-92. Gao Yong-Qing, Danciger Michael, Ozgul Riza Köksal, Gribanova Yekaterina, Jacobson Samuel, Farber Debora |
Association of genetic variations in GNB1 with response to peginterferon plus ribavirin therapy for chronic hepatitis C in a Chinese population in Taiwan. BMC gastroenterology 2012 12 (1): 167. Lim Yun-Ping, Tsai Fuu-Jen, Liao Wen-Ling, Tien Ni, Hung Dong-Zong, Peng Cheng-Yuan, Wan L |
Genetic variation in the parasympathetic signaling pathway in patients with reflex syncope. Genetics and molecular research : GMR 2013 12 (3): 2601-10. Holmegard H N, Benn M, Mehlsen J, Haunsø |
Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature. American journal of medical genetics. Part A 2018 9 176 (11): 2259-2275. Hemati Parisa, Revah-Politi Anya, Bassan Haim, Petrovski Slavé, Bilancia Colleen G, Ramsey Keri, Griffin Nicole G, Bier Louise, Cho Megan T, Rosello Monica, Lynch Sally Ann, Colombo Sophie, Weber Astrid, Haug Marte, Heinzen Erin L, Sands Tristan T, Narayanan Vinodh, Primiano Michelle, Aggarwal Vimla S, Millan Francisca, Sattler-Holtrop Shannon G, Caro-Llopis Alfonso, Pillar Nir, Baker Janice, Freedman Rebecca, Kroes Hester Y, Sacharow Stephanie, Stong Nick, Lapunzina Pablo, Schneider Michael C, Mendelsohn Nancy J, Singleton Amanda, Loik Ramey Valerie, Wou Karen, Kuzminsky Alla, Monfort Sandra, Weiss Monica, Doyle Samantha, Iglesias Alejandro, Martinez Francisco, Mckenzie Fiona, Orellana Carmen, van Gassen Koen L I, Palomares Maria, Bazak Lily, Lee Andy, Bircher Ana, Basel-Vanagaite Lina, Hafström Maria, Houge Gunnar, , , Goldstein David B, Anyane-Yeboa Kwa |
Novel West syndrome candidate genes in a Chinese cohort. CNS neuroscience & therapeutics 2018 4 24 (12): 1196-1206. Peng Jing, Wang Ying, He Fang, Chen Chen, Wu Li-Wen, Yang Li-Fen, Ma Yu-Ping, Zhang Wen, Shi Zi-Qing, Chen Chao, Xia Kun, Guo Hui, Yin Fei, Pang N |
Genome-Wide Copy Number Variation Association Study of Atrial Fibrillation Related Thromboembolic Stroke. Journal of clinical medicine 2019 Mar 8 (3): . Hsieh Chia-Shan, Huang Pang-Shuo, Chang Sheng-Nan, Wu Cho-Kai, Hwang Juey-Jen, Chuang Eric Y, Tsai Chia- |
Clonal myelopoiesis promotes adverse outcomes in chronic kidney disease. Leukemia 2021 8 36 (2): 507-515. Dawoud Ahmed A Z, Gilbert Rodney D, Tapper William J, Cross Nicholas C |
Genomic Analysis of Korean Patient With Microcephaly. Frontiers in genetics 2021 2 11 543528. Lee Jiwon, Park Jong Eun, Lee Chung, Kim Ah Reum, Kim Byung Joon, Park Woong-Yang, Ki Chang-Seok, Lee Jeeh |
Identification of Candidate Genes for Pigmentation in Camels Using Genotyping-by-Sequencing. Animals : an open access journal from MDPI 2022 5 12 (9): . Bitaraf Sani Morteza, Zare Harofte Javad, Banabazi Mohammad Hossein, Faraz Asim, Esmaeilkhanian Saeid, Naderi Ali Shafei, Salim Nader, Teimoori Abbas, Bitaraf Ahmad, Zadehrahmani Mohammad, Burger Pamela Anna, Asadzadeh Nader, Silawi Mohammad, Taghipour Sheshdeh Afsaneh, Mohammad Nazari Behrouz, Faghihi Mohammad Ali, Roudbari Zah |
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- Page last updated:Apr 29, 2024
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