Zobrazeno 1 - 10
of 60
pro vyhledávání: '"A Kwitek-Black"'
Autor:
Gösele, Claudia, Hong, Liu, Kreitler, Thomas, Rossmann, Marlies, Hieke, Brigitte, Groß, Uwe, Kramer, Markus, Himmelbauer, Heinz, Bihoreau, Marie-Thérese, Kwitek-Black, Anne E, Twigger, Simon, Tonellato, Peter J, Jacob, Howard J, Schalkwyk, Leonard C, Lindpaintner, Klaus, Ganten, Detlev, Lehrach, Hans, Knoblauch, Margit
Publikováno v:
In Genomics 1 November 2000 69(3):287-294
Publikováno v:
In Molecular and Cellular Neuroscience August 1999 14(2):141-152
Autor:
Diana Maas, Masahiko Takahashi, Tohru Funahashi, Ahmed H. Kissebah, Anthony G. Comuzzie, Shinji Kihara, Daniel A. Cohen, Gabriele E. Sonnenberg, Howard J. Jacob, Sachiyo Tanaka, Yuji Matsuzawa, Anne E. Kwitek Black, John Blangero, Lisa J. Martin
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 86:4321-4325
Here we present the first genetic analysis of adiponectin levels, a newly identified adipocyte-derived protein. Recent work has suggested that adiponectin may play a role in mediating the effects of body weight as a risk factor for coronary artery di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be4ef7ba83287bea5c1a0a6d1f52b1ec
https://doi.org/10.1210/jcem.86.9.7878
https://doi.org/10.1210/jcem.86.9.7878
Autor:
D Maglott, Z Wang, J Lu, D Chen, J Ginster, M Shimoyama, J Tonellato, R Nigam, Fredrik Ståhl, P Long, Göran Levan, S Twigger, CF Chen, J Eppig, D Pasko, A Kwitek-Black, H Jacob, Gerhard Schuler
Publikováno v:
Journal of Molecular Medicine. 79:B1-B34
The Rat Genome Database (RGD) is a NIH funded project who’s stated mission is “to collect, consolidate, and integrate data generated from ongoing rat genetic and genomic research efforts and make these data widely available to the scientific comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a64e9209c9ad3d70c084844831246251
https://doi.org/10.1007/s001090170001
https://doi.org/10.1007/s001090170001
Autor:
Joseph M. Miano, Bradford C. Berk, Howard J. Jacob, Michael R. Aebly, Anne E. Kwitek-Black, Louise A. Kelly, Judith Haendeler, George Koike, Hesheng Ou, Brian C. Cholewa
Publikováno v:
Circulation Research. 87:881-887
Abstract —Retinoids exert antiproliferative and prodifferentiating effects in vascular smooth muscle cells (SMCs) and reduce neointimal mass in balloon-injured blood vessels. The mechanisms through which retinoids carry out these effects are unknow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c59072644fb0113b4cc3e07fde50af9
https://doi.org/10.1161/01.res.87.10.881
https://doi.org/10.1161/01.res.87.10.881
Autor:
Batsheva Bonne-Tamir, Arne M. Nystuen, A. Adato, M. Korostishevsky, Val C. Sheffield, Hagar Kalinsky, Anne E. Kwitek-Black, E. Seroussi
Publikováno v:
American Journal of Physical Anthropology. 104:193-200
We have previously reported significant linkage between markers on 11q13.5 and Usher syndrome type 1 (USH1B) in a large Samaritan kindred. USH1B is an autosomal recessive disease characterized by profound congenital sensorineural deafness, vestibular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f6f44804b3b772301b2310b808a0a05
https://doi.org/10.1002/(sici)1096-8644(199710)104:2<193::aid-ajpa5>3.0.co
https://doi.org/10.1002/(sici)1096-8644(199710)104:2<193::aid-ajpa5>3.0.co
Autor:
Rivka Carmi, Edwin M. Stone, Khalil Elbedour, Val C. Sheffield, Anne E. Kwitek-Black, Tatiana Rokhlina, Darryl Y. Nishimura
Publikováno v:
Human Molecular Genetics. 4:9-13
Bardet-Biedl syndrome is a heterogeneous autosomal recessive disorder characterized by obesity, mental retardation, polydactyly, retinitis pigmentosa and hypogonadism. Patients with this disorder also have a high incidence of hypertension, diabetes m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b40eec00c879d0f7d66ab8b4ccc45a
https://doi.org/10.1093/hmg/4.1.9
https://doi.org/10.1093/hmg/4.1.9
Autor:
Geoffrey M. Duyk, Anne E. Kwitek-Black, Khalil Elbedour, Ruti Parvari, Chandra Naidu Yandava, Val C. Sheffield, Rivka Carmi, Edwin M. Stone, Kenneth H. Buetow
Publikováno v:
Nature Genetics. 5:392-396
Bardet-Biedl syndrome is an autosomal recessive disorder characterized by mental retardation, obesity, retinitis pigmentosa, polydactyly and hypogonadism. Other findings include hypertension, diabetes mellitus and renal and cardiovascular anomalies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04acd050a15dfbe47b803d43139aa168
https://doi.org/10.1038/ng1293-392
https://doi.org/10.1038/ng1293-392
Autor:
A E, Kwitek-Black
Publikováno v:
Lab animal. 29(3)
Two hundred years of physiological and pharmaceutical studies and a decade of transgenic technology and genomic resources have made the laboratory rat a major model for biomedical research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46cf4102d643bb5cbff8c5b34dcf9699
https://pubmed.ncbi.nlm.nih.gov/11375646
https://pubmed.ncbi.nlm.nih.gov/11375646
Autor:
M. Bento Soares, Chad A. Roberts, Jack M. Gardiner, Anne E. Kwitek-Black, Jie Zhang, Howard J. Jacob, Val C. Sheffield, Thomas L. Casavant, Todd E. Scheetz, Nichole Butters, Christine L. Sun, Clay Birkett, Darryl Y. Nishimura, Michael R. Raymond, Ann McClain
Publikováno v:
Genome research. 11(3)
The rat provides excellent physiological and biochemical models for the study of genetically complex human disease, including hypertension (Hilbert et al. 1991; Jacob et al. 1991), renal disease (Brown et al. 1996), behavioral disorders (Moisan et al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26fccea179e2cb44ba5df95bbb6893dc
https://pubmed.ncbi.nlm.nih.gov/11230173
https://pubmed.ncbi.nlm.nih.gov/11230173