Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Polymorphic variation"'
Autor:
Michael A. Gbadegesin, Olabode E. Omotoso, Timothy A. O. Oluwasola, Clement A. Okolo, Opeyemi Soremekun, Gabriel O. Ogun, Abideen O. Oluwasola, Oyeronke A. Odunola
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Factors contributing to the pathogenesis and progression of cervical cancer include poor attitude to screening and health intervention, late presentation, among others. Mutations in p53 gene have been attributed to several cancer
Externí odkaz:
https://doaj.org/article/d905e024feee4fb5a5434a581df20379
Publikováno v:
Human Genomics, Vol 3, Iss 2, Pp 106-120 (2009)
Abstract Succinic semialdehyde dehydrogenase (SSADH; aldehyde dehydrogenase 5A1 [ALDH5A1]; locus 6p22) occupies a central position in central nervous system (CNS) neurotransmitter metabolism as one of two enzymes necessary for γ-aminobutyric acid (G
Externí odkaz:
https://doaj.org/article/036703f35410463c8067216c15a78b1c
Autor:
Manly, B. F. J.
Publikováno v:
Biometrics, 1983 Mar 01. 39(1), 13-27.
Externí odkaz:
https://www.jstor.org/stable/2530803
Akademický článek
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Akademický článek
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Akademický článek
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Autor:
Piero Portincasa, Fatemeh Hadizadeh, Gerardo Nardone, Giovanni Barbara, Lars Engstrand, Ghazaleh Assadi, Anna Andreasson, Louise B. Thingholm, Emeran A. Mayer, Lars Agréus, Lena Diekmann, John F. Baines, Martin Heine, Mauro D'Amato, Rosario Cuomo, Ottmar Distl, Ute Philipp, Aldona Dlugosz, Vincenzo Stanghellini, Magnus Simrén, Pontus Karling, Eva Maria Kuech, Andre Franke, C. Dierks, Matteo Neri, Michael Camilleri, Maria Henström, Maren von Köckritz-Blickwede, Ferdinando Bonfiglio, Susanna Walter, Hassan Y. Naim, Bodil Ohlsson, Mary E. Money, Greger Lindberg, Meriem Belheouane, Peter T. Schmidt, Lin Chang, Joseph Rafter, Paolo Usai-Satta, Francesca Galeazzi, Massimo Bellini, Femke-Anouska Heinsen, Tenghao Zheng
Publikováno v:
Gut
ObjectiveIBS is a common gut disorder of uncertain pathogenesis. Among other factors, genetics and certain foods are proposed to contribute. Congenital sucrase–isomaltase deficiency (CSID) is a rare genetic form of disaccharide malabsorption charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bbaf7cf787cb86498166072005d30a1
http://hdl.handle.net/11568/948647
http://hdl.handle.net/11568/948647
Autor:
Nicholas J. Talley, Aldona Dlugosz, Arthur Beyder, Anna Andreasson, Tenghao Zheng, Ghazaleh Assadi, Mauro D'Amato, Lars Agréus, Gianrico Farrugia, Peter T. Schmidt, Susanna Walter, Ferdinando Bonfiglio, Mira M. Wouters, Greger Lindberg, Magnus Simrén, Joseph Rafter, Maria Henström, Fatemeh Hadizadeh, Luis Bujanda, Pontus Karling, Bodil Ohlsson
Publikováno v:
Gut
Recently in Gut , genetic variation affecting ion channels activity has been highlighted in relation to bowel function and the biology of stool frequency.1 It is also known that 2% of patients with IBS carry functional missense mutations in the volta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6189d87cf0f9e1ba91a2a119415da169
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-139620
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-139620
Autor:
Hisashi Ogawa, Takahiro Sakai, Akishi Onishi, Shin-ichi Itoh, Hisao Kobayashi, Yoshiko Emi, Akichika Mikami, Kenichi Terao, Hiroo Imai, Atsuko Saito, Toshifumi Udono, Satoshi Koike, Migaku Teramoto, Yoshinori Shichida, Osamu Takenaka
Publikováno v:
Vision Research. 45:1225-1235
We determined the structures of long (L)-wavelength-sensitive and middle (M)-wavelength-sensitive opsin gene array of 58 male chimpanzees and we investigated relative sensitivity to red and green lights by electroretinogram flicker photometry. One su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9400bb77c524d13926ca8f99d152e461
https://doi.org/10.1016/j.visres.2004.11.016
https://doi.org/10.1016/j.visres.2004.11.016
Autor:
Charal Eakavhibata, Kenji Kitahara, Puttipongse Varavudhi, Miki Ida-Hosonuma, Hiroo Imai, Akitoshi Hanazawa, Hidehiko Komatsu, Achmad Farajallah, Satoshi Koike, Akishi Onishi, Tetsuo Yamamori, Yoshinori Shichida, Akichika Mikami, Shunji Goto, Osamu Takenaka, Bambang Suryobroto
Publikováno v:
Vision Research. 42:281-292
We analyzed variations in long (L)- and middle (M)-wavelength-sensitive opsin gene loci in crab-eating monkeys. Unlike humans, most monkeys have a single L and a single M gene. Two variant genotypes, one with only one opsin gene (dichromatic) and one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33c4ebef0b0a86d0446b5b90acbe3c39
https://doi.org/10.1016/s0042-6989(01)00293-0
https://doi.org/10.1016/s0042-6989(01)00293-0