دنبال کردن
Uta Francke
Uta Francke
Professor of Genetics, Stanford University
ایمیل تأیید شده در stanford.edu
عنوان
نقل شده توسط
نقل شده توسط
سال
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
RE Amir, IB Van den Veyver, M Wan, CQ Tran, U Francke, HY Zoghbi
Nature genetics 23 (2), 185-188, 1999
61301999
Tyrosine Kinase Receptor with Extensive Homology to EGF Receptor Shares Chromosomal Location with neu Oncogene
L Coussens, TL Yang-Feng, YC Liao, E Chen, A Gray, J McGrath, ...
Science 230 (4730), 1132-1139, 1985
26771985
Human proto‐oncogene c‐kit: a new cell surface receptor tyrosine kinase for an unidentified ligand.
Y Yarden, WJ Kuang, T Yang‐Feng, L Coussens, S Munemitsu, TJ Dull, ...
The EMBO journal 6 (11), 3341-3351, 1987
20611987
Structure of the receptor for platelet-derived growth factor helps define a family of closely related growth factor receptors
Y Yarden, JA Escobedo, WJ Kuang, TL Yang-Feng, TO Daniel, ...
Nature 323 (6085), 226-232, 1986
14481986
Multiple, distinct forms of bovine and human protein kinase C suggest diversity in cellular signaling pathways
L Coussens, PJ Parker, L Rhee, TL Yang-Feng, E Chen, MD Waterfield, ...
Science 233 (4766), 859-866, 1986
13681986
Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
JMJ Derry, HD Ochs, U Francke
Cell 78 (4), 635-644, 1994
13161994
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
M Koenig, AH Beggs, M Moyer, S Scherpf, K Heindrich, T Bettecken, ...
American journal of human genetics 45 (4), 498, 1989
12831989
Wiskott–Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
M Symons, JMJ Derry, B Karlak, S Jiang, V Lemahieu, F McCormick, ...
Cell 84 (5), 723-734, 1996
10731996
The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome
A Aruffo, M Farrington, D Hollenbaugh, XU Li, A Milatovich, S Nonoyama, ...
Cell 72 (2), 291-300, 1993
10091993
Cloning, Sequencing, and Expression of the Gene Coding for the Human Platelet α2-Adrenergic Receptor
BK Kobilka, H Matsui, TS Kobilka, TL Yang-Feng, U Francke, MG Caron, ...
Science 238 (4827), 650-656, 1987
10031987
cDNA for the human beta 2-adrenergic receptor: a protein with multiple membrane-spanning domains and encoded by a gene whose chromosomal location is shared with that of the …
BK Kobilka, RA Dixon, T Frielle, HG Dohlman, MA Bolanowski, IS Sigal, ...
Proceedings of the National Academy of Sciences 84 (1), 46-50, 1987
9341987
Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion
VM Riccardi, E Sujansky, AC Smith, U Francke
Pediatrics 61 (4), 604-610, 1978
9261978
NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21
JR Arron, MM Winslow, A Polleri, CP Chang, H Wu, X Gao, JR Neilson, ...
Nature 441 (7093), 595-600, 2006
8112006
Identification of a gene (GPR30) with homology to the G-protein-coupled receptor superfamily associated with estrogen receptor expression in breast cancer
C Carmeci, DA Thompson, HZ Ring, U Francke, RJ Weigel
Genomics 45 (3), 607-617, 1997
7431997
The neu Gene: an erbB-Homologous Gene Distinct from and Unlinked to the Gene Encoding the EGF Receptor
AL Schechter, MC Hung, L Vaidyanathan, RA Weinberg, TL Yang-Feng, ...
Science 229 (4717), 976-978, 1985
7341985
An intronless gene encoding a potential member of the family of receptors coupled to guanine nucleotide regulatory proteins
BK Kobilka, T Frielle, S Collins, T Yang-Feng, TS Kobilka, U Francke, ...
Nature 329 (6134), 75-79, 1987
7261987
Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study
L Faivre, G Collod-Beroud, BL Loeys, A Child, C Binquet, E Gautier, ...
The American Journal of Human Genetics 81 (3), 454-466, 2007
6332007
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
CB Do, JY Tung, E Dorfman, AK Kiefer, EM Drabant, U Francke, ...
PLoS genetics 7 (6), e1002141, 2011
6282011
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots
M Wan, SSJ Lee, X Zhang, I Houwink-Manville, HR Song, RE Amir, ...
The American Journal of Human Genetics 65 (6), 1520-1529, 1999
6101999
The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A
PI Patel, BB Roa, AA Welcher, R Schoener-Scott, BJ Trask, L Pentao, ...
Nature genetics 1 (3), 159-165, 1992
5931992
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مقاله‌ها 1–20