Zobrazeno 1 - 10
of 129
pro vyhledávání: '"Victor A David"'
Autor:
Markus H Kuehn, Koren A Lipsett, Marilyn Menotti-Raymond, S Scott Whitmore, Todd E Scheetz, Victor A David, Stephen J O'Brien, Zhongyuan Zhao, Jackie K Jens, Elizabeth M Snella, N Matthew Ellinwood, Gillian J McLellan
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0161517 (2016)
[This corrects the article DOI: 10.1371/journal.pone.0154412.].
Externí odkaz:
https://doaj.org/article/ab671746dddc4054b18fe907d152c6d9
Autor:
Markus H Kuehn, Koren A Lipsett, Marilyn Menotti-Raymond, S Scott Whitmore, Todd E Scheetz, Victor A David, Stephen J O'Brien, Zhongyuan Zhao, Jackie K Jens, Elizabeth M Snella, N Matthew Ellinwood, Gillian J McLellan
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0154412 (2016)
The glaucomas are a group of diseases characterized by optic nerve damage that together represent a leading cause of blindness in the human population and in domestic animals. Here we report a mutation in LTBP2 that causes primary congenital glaucoma
Externí odkaz:
https://doaj.org/article/90a109b3da564685acc545e18fecb7b1
Autor:
Alexsandra Schneider, Corneliu Henegar, Kenneth Day, Devin Absher, Constanza Napolitano, Leandro Silveira, Victor A David, Stephen J O'Brien, Marilyn Menotti-Raymond, Gregory S Barsh, Eduardo Eizirik
Publikováno v:
PLoS Genetics, Vol 11, Iss 2, p e1004892 (2015)
Morphological variation in natural populations is a genomic test bed for studying the interface between molecular evolution and population genetics, but some of the most interesting questions involve non-model organisms that lack well annotated refer
Externí odkaz:
https://doaj.org/article/3ed94a881fbe4592b69cdf4bab6c34ee
Autor:
Minzhong Tang, James A Lautenberger, Xiaojiang Gao, Efe Sezgin, Sher L Hendrickson, Jennifer L Troyer, Victor A David, Li Guan, Carl E McIntosh, Xiuchan Guo, Yuming Zheng, Jian Liao, Hong Deng, Michael Malasky, Bailey Kessing, Cheryl A Winkler, Mary Carrington, Guy Dé The, Yi Zeng, Stephen J O'Brien
Publikováno v:
PLoS Genetics, Vol 8, Iss 11, p e1003103 (2012)
Nasopharyngeal carcinoma (NPC) is an epithelial malignancy facilitated by Epstein-Barr Virus infection. Here we resolve the major genetic influences for NPC incidence using a genome-wide association study (GWAS), independent cohort replication, and h
Externí odkaz:
https://doaj.org/article/1edc549c0a9c4d51b8cdb10f72acd624
Autor:
Alexsandra Schneider, Victor A David, Warren E Johnson, Stephen J O'Brien, Gregory S Barsh, Marilyn Menotti-Raymond, Eduardo Eizirik
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e50386 (2012)
The occurrence of melanism (darkening of the background coloration) is documented in 13 felid species, in some cases reaching high frequencies at the population level. Recent analyses have indicated that it arose multiple times in the Felidae, with t
Externí odkaz:
https://doaj.org/article/8ec7c920bc764df49746c5dc35f8fc87
Autor:
Yasuko Ishida, Taras K Oleksyk, Nicholas J Georgiadis, Victor A David, Kai Zhao, Robert M Stephens, Sergios-Orestis Kolokotronis, Alfred L Roca
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e20642 (2011)
Conservation strategies for African elephants would be advanced by resolution of conflicting claims that they comprise one, two, three or four taxonomic groups, and by development of genetic markers that establish more incisively the provenance of co
Externí odkaz:
https://doaj.org/article/49130cd4e3e64baabf449922ad61369c
Akademický článek
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Autor:
Yu Toyoda, Sung Kweon Cho, Velibor Tasic, Kateřina Pavelcová, Jana Bohatá, Hiroshi Suzuki, Victor A. David, Jaeho Yoon, Anna Pallaiova, Jana Šaligová, Darryl Nousome, Raul Cachau, Cheryl A. Winkler, Tappei Takada, Blanka Stibůrková
Publikováno v:
Frontiers in Genetics, Vol 13 (2023)
Renal hypouricemia (RHUC) is a pathological condition characterized by extremely low serum urate and overexcretion of urate in the kidney; this inheritable disorder is classified into type 1 and type 2 based on causative genes encoding physiologicall
Externí odkaz:
https://doaj.org/article/ecdfaf66f7f345c7b069c74d26b40df9
Akademický článek
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Autor:
Jaeho Yoon, Raul Cachau, Victor A. David, Mary Thompson, Wooram Jung, Sun-Ha Jee, Ira O. Daar, Cheryl A. Winkler, Sung-Kweon Cho
Publikováno v:
Biomedicines, Vol 9, Iss 9, p 1172 (2021)
Renal hypouricemia is a rare genetic disorder. Hypouricemia can present as renal stones or exercise-induced acute renal failure, but most cases are asymptomatic. Our previous study showed that two recessive variants of SLC22A12 (p.Trp258*, pArg90His)
Externí odkaz:
https://doaj.org/article/28a8b408d6c846c0924b1082e6396227