Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Robert Wisotzkey"'
Autor:
Ilya Kupershmidt, Qiaojuan Jane Su, Anoop Grewal, Suman Sundaresh, Inbal Halperin, James Flynn, Mamatha Shekar, Helen Wang, Jenny Park, Wenwu Cui, Gregory D Wall, Robert Wisotzkey, Satnam Alag, Saeid Akhtari, Mostafa Ronaghi
Publikováno v:
PLoS ONE, Vol 5, Iss 9 (2010)
The investigation of the interconnections between the molecular and genetic events that govern biological systems is essential if we are to understand the development of disease and design effective novel treatments. Microarray and next-generation se
Externí odkaz:
https://doaj.org/article/7572ea42529f40acacbad1e77fce7367
Autor:
Vilmundur Gudnason, Valur Emilsson, Oscar Puig, Matthew Akana, Rebecca Fox, Malgorzata Jaremko, Chihyu Chang, Ying Cai, Bolli Thorsson, Robert Wisotzkey, Michael Jansen, Greg Kellogg, Andrew Pollock, Elias F. Gudmundsson, Bonny Patel
Publikováno v:
Scandinavian journal of clinical and laboratory investigation. 80(6)
Familial hypercholesterolemia (FH) is a monogenic disease characterized by a lifelong exposure to high LDL-C levels that can lead to early onset coronary heart disease (CHD). The main causes of FH identified to date include loss-of-function mutations
Autor:
Malgorzata Jaremko, Alex Bisignano, Bonny Patel, Chihyu Chang, Robert Wisotzkey, Michael Jansen, Andrew Pollock, Rebecca Fox, Mohammad Niknazar, R. Shraga, Oscar Puig, Sasha Parets, Colby Hunter, Ying Cai, Gregory Kellogg, Matthew Akana
Publikováno v:
Journal of Assisted Reproduction and Genetics
Purpose To develop a comprehensive genetic test for female and male infertility in support of medical decisions during assisted reproductive technology (ART) protocols. Methods We developed a next-generation sequencing (NGS) gene panel consisting of
Autor:
Valur Emilsson, Greg Kellogg, Bonny Patel, Rebecca Fox, Malgorzata Jaremko, Vilmundur Gudnason, Ying Cai, Bolli Thorsson, Matthew Akana, Robert Wisotzkey, Michael Jansen, Chihyu Chang, Oscar Puig, Andrew Pollock, Elias F. Gudmundsson
Familial hypercholesterolemia (FH) is a monogenic disease characterized by a lifelong exposure to high LDL-C levels that can lead to early onset coronary heart disease (CHD). The main causes of FH identified to date include loss-of-function mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb6281c270907acdecec55bc4d4e00a4
Autor:
Ying Cai, Colby Hunter, Sasha Parets, Gregory Kellogg, Malgorzata Jaremko, Mohammad Niknazar, Rebecca Fox, Alex Bisignano, Oscar Puig, Chihyu Chang, Michael Jansen, Bonny Patel, Matthew Akana, Robert Wisotzkey, Andrew Pollock, R. Shraga
ObjectiveTo develop a comprehensive genetic test for female and male infertility in support of medical decisions during assisted reproductive technology (ART) protocols.DesignRetrospective analysis of results from 118 DNA samples with known variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd0c5d4c354544a4737f944e76cefa85
https://doi.org/10.1101/272419
https://doi.org/10.1101/272419
Autor:
Alexander Bisignano, Sasha Parets, Malgorzata Jaremko, Georges Duverger, Oscar Puig, Bonny Patel, Andrew Pollock, Chihyu Chang, R. Shraga, Gregory Kellogg, Mohammad Niknazar, Eugene Joseph, Robert Wisotzkey, Rebecca Fox
Publikováno v:
Journal of Clinical Oncology. 35:e13105-e13105
e13105 Background: Diagnosis of hereditary cancer syndromes involves time-consuming comprehensive clinical and laboratory work-up, however, timely and accurate diagnosis is pivotal to the clinical management of cancer patients. Germline genetic testi
Autor:
Yen Tran, Sriram Balasubramanian, Ralph Clover, Gary Hardiman, Karin Franz-Bacon, Abhijit Mazumder, Robert Wisotzkey
Publikováno v:
Nature Genetics. 23:32-32
Caenorhabditis elegans gene expression analysis using microarrays of covalently attached oligodeoxyribonucleotides