Zobrazeno 1 - 10
of 11
pro vyhledávání: '"David Duhl"'
Autor:
Zhenhai Gao, Nancy K. Pryer, William R. Sellers, Timothy Machajewski, David Duhl, Guoying Karen Yu, Darrin Stuart, Tinya Abrams, Michael R. Jensen, Pietro Taverna, Daniel L. Menezes
PDF file - 41K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4c4cfebd34aa8fa669aaf404fef0a16
https://doi.org/10.1158/1535-7163.22497132
https://doi.org/10.1158/1535-7163.22497132
Autor:
Zhenhai Gao, Nancy K. Pryer, William R. Sellers, Timothy Machajewski, David Duhl, Guoying Karen Yu, Darrin Stuart, Tinya Abrams, Michael R. Jensen, Pietro Taverna, Daniel L. Menezes
PDF file - 212K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a52e072c564f45f7e1b788dabd742bb3
https://doi.org/10.1158/1535-7163.22497135
https://doi.org/10.1158/1535-7163.22497135
Autor:
Sunghae Joo, Yoshihiro Takihara, Hideaki Ohta, Hugh W. Brock, Jeffrey A. Simon, Daihachiro Tomotsune, Michael Kyba, Barry M. Honda, Filippo Randazzo, David Duhl, Kazunori Shimada, Yoichi Matsuda, Manabu Shirai, Joel Berger
Publikováno v:
Scopus-Elsevier
The Polycomb group of (PcG) genes were originally described in Drosophila, but many PcG genes have mammalian homologs. Genetic studies in flies and mice show that mutations in PcG genes cause posterior transformations caused by failure to maintain re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ed38fba07f113fff48d8b5e3d781bc6
https://doi.org/10.1046/j.1432-0436.1999.6540229.x
https://doi.org/10.1046/j.1432-0436.1999.6540229.x
Autor:
Ruth E. Swiderski, Rivka Carmi, David Duhl, Susan W. Gorman, Neena B. Haider, Juliet W. Welch, Charles Searby, Uta Grieshammer, Song Leng, Esther A. Kim, Val C. Sheffield
Publikováno v:
Genomics. 59:150-160
Bardet-Biedl Syndrome (BBS) is a heterogeneous, autosomal recessive disorder characterized by mental retardation, obesity, retinitis pigmentosa, syndactyly and/or polydactyly, short stature, and hypogenitalism and is caused by mutations at a number o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e357caf8e86c7c897e141901cc19a2
https://doi.org/10.1006/geno.1999.5867
https://doi.org/10.1006/geno.1999.5867
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 307(3)
A chimeric protein comprised of melanocortin-4 receptor (MC4R) and the green fluorescent protein (GFP) was created for studying receptor/ligand localization and trafficking. The ligand binding affinities and second messenger stimulation induced by MC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66019d3feab567954215fce1078cf5eb
https://pubmed.ncbi.nlm.nih.gov/14534363
https://pubmed.ncbi.nlm.nih.gov/14534363
Autor:
Thomas L. Casavant, Val C. Sheffield, Kirk Mykytyn, Alfonso Baldi, Charles Searby, David Duhl, Gretel Beck, Mythreyi Shastri, Annick Raas-Rothschild, Susan W. Gorman, Ruth Riise, Khalil Elbedour, Neena B. Haider, Samuel G. Jacobson, Alessandro Iannaccone, Rivka Carmi, Edwin M. Stone, Terry A. Braun, Alan F. Wright
Bardet–Biedl syndrome (BBS, MIM 209900) is a heterogeneous autosomal recessive disorder characterized by obesity, pigmentary retinopathy, polydactyly, renal malformations, mental retardation, and hypogenitalism1,2,3,4. The disorder is also associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86b5bcdf1b5dd609bd9ac8da37c81680
http://hdl.handle.net/11591/190769
http://hdl.handle.net/11591/190769
Autor:
Ruth E. Swiderski, David Duhl, Rivka Carmi, Susan W. Gorman, Edwin M. Stone, Gretel Beck, Robin R. Hockey, Val C. Sheffield, Luan M. Streb, Samuel G. Jacobson, Artur V. Cideciyan, Jean Bennett, David B. Hanna, Neena B. Haider, Richard G. Weleber, Charles Searby, Alan F. Wright, Gerald A. Fishman
Publikováno v:
Nature genetics. 24(2)
Hereditary human retinal degenerative diseases usually affect the mature photoreceptor topography by reducing the number of cells through apoptosis, resulting in loss of visual function1. Only one inherited retinal disease, the enhanced S-cone syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c9a62ccb417533e6e03e45b3a09d1de
https://pubmed.ncbi.nlm.nih.gov/10655045
https://pubmed.ncbi.nlm.nih.gov/10655045
Publikováno v:
Genomics. 61(1)
TIAM1 is a guanine nucleotide exchange factor that was identified in a screen for genes that increase the invasiveness of T lymphoma cell lines (Habets et al., 1994, Cell 77(4): 537-549). We have identified a gene, T-cell lymphoma invasion and metast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5a1ad203bd7eddc2d69f68abca33d54
https://pubmed.ncbi.nlm.nih.gov/10512681
https://pubmed.ncbi.nlm.nih.gov/10512681
Publikováno v:
The Journal of Pharmacology and Experimental Therapeutics; December 2003, Vol. 307 Issue: 3 p870-7, 8p
Publikováno v:
Acta Metallurgica. 11:1-6
The diffusivities of iron, cobalt and nickel into otherwise pure gold were determined by the residual-activity technique, after checking this procedure against the better-known sectioning method for self-diffusion in gold. The results may be summariz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65efaa69497c0f7116ed823597d26d0e
https://doi.org/10.1016/0001-6160(63)90119-6
https://doi.org/10.1016/0001-6160(63)90119-6