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 Scholar Results 1 - 14 of 14 for FOXC1 and NF1. (0.05 seconds) 

FOXC1 Transcriptional Regulatory Activity Is Impaired by PBX1 in a Filamin A-Mediated Manner - Full text - MIT Libraries
FB Berry, MA O'Neill, M Coca-Prados, MA Walter - Mol Cell Biol, 2005 - mcb.asm.org
... Potential interactions between FOXC1 and PBX and NF1 were identified. ... (C) FOXC1
transcriptional activity is unaffected by NF1-A in M2 and A7 cells. ...
Web Search - pubmedcentral.nih.gov - dx.doi.org - ncbi.nlm.nih.gov - all 5 versions »

Ophthalmic genetics/inherited eye disease.
TL Young - Current Opinion in Ophthalmology, 2003 - co-ophthalmology.com
... of heterozygosity, MFS Marfan syndrome, MRI magnetic resonance imaging, NF1
neurofibromatosis type ... FOXC1 is a forkhead gene located at chromosome 6p25, and was ...
Web Search - co-ophthalmology.com - ncbi.nlm.nih.gov - Get it from MIT Libraries

Status of the Human Malformation Map: 2002
JC CAREY, DH VISKOCHIL - American Journal of Medical Genetics (Semin. Med. Genet.), 2002 - doi.wiley.com
... ligands (FGFR1-3), signal transduction pathway genes (NF1), extracellular matrix ...
Axenfeld anomaly 601090 601090 6p25 FOXC1 Forkhead, Drosophila, homolog-like 7 ...
Web Search - ncbi.nlm.nih.gov - Get it from MIT Libraries

Table 2. Gene Mutations Demonstrating Cardiac Phenotypes
N Phenotype - ahavj.ahajournals.org
... 93. Foxc1 (Fkh1/forkhead box C1), Aortic arch abnormalities, 68. Foxc2 ... 102.
Nf1 (neurofibromatosis 1), EC cushion defect, DORV, 32. Nfatc ...
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Foxp1 regulates cardiac outflow tract and endocardial cushion morphogenesis and myocyte …
B Wang, J Weidenfeld, MM Lu, S Maika, WA Kuziel, … - bio.utexas.edu
... Nf1 has an essential role in endothelial cells ... The murine winged helix transcription
factors, Foxc1 and Foxc2, are both required for cardiovascular development ...
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Molecular markers of cardiac endocardial cushion development - Full text - MIT Libraries
AD Gitler, MM Lu, YQ Jiang, JA Epstein, PJ Gruber - Developmental Dynamics, 2003 - doi.wiley.com
... 2003. Nf1 has an essential role in endothelial cells. ... The murine winged helix tran-
scription factors, Foxc1 and Foxc2, are both required for cardiovascular de ...
Cited by 6 - Web Search - uphs.upenn.edu - ncbi.nlm.nih.gov

Transcriptional regulation of cardiac development: implications for congenital heart disease and … - Full text - MIT Libraries
JA Epstein, CA Buck - Pediatr Res, 2000 - pedresearch.org
... will be of interest to determine whether somatic mutations in the NF1 gene account ...
enzyme 1 (61) and by the winged helix transcription factors Foxc1 (Mf1) and ...
Cited by 19 - Web Search - pedresearch.org - ncbi.nlm.nih.gov

FOXP 2: novel exons, splice variants, and CAG repeat length stability - Full text - MIT Libraries
H Bruce, R Margolis - Human Genetics, 2002 - springerlink.com
... s1, there are no SP1, NRSE, WT, RREBP1, GC Box, Egr-1/NGF1-A, AP2, NF1, Elk-1 ... 2000);
anterior chamber defects asso- ciated with glaucoma (FOXC1; Nishimura et al ...
Cited by 11 - Web Search - ruccs.rutgers.edu - ncbi.nlm.nih.gov

Genetic effects on human cognition: lessons from the study of mental retardation syndromes - Full text - MIT Libraries
P Nokelainen, J Flint - Journal of Neurology Neurosurgery & Psychiatry, 2002 - jnnp.bmjjournals.com
... The protein encoded by the NF1 gene, known as neurofibromin, contains a domain ... 108–
113 Duplications involving FOXC1 are known to cause defects of the ...
Cited by 2 - Web Search - well.ox.ac.uk - dx.doi.org - ncbi.nlm.nih.gov - all 7 versions »

REVIEW ARTICLES Transcriptional Regulation of Cardiac Development: Implications for Congenital Heart …
JA EPSTEIN, CA BUCK - PEDIATRIC RESEARCH, 2000 - uphs.upenn.edu
... will be of interest to determine whether somatic mutations in the NF1 gene account ...
enzyme 1 (61) and by the winged helix transcription factors Foxc1 (Mf1) and ...
View as HTML - Web Search - Get it from MIT Libraries

Development Gone Awry - Full text - MIT Libraries
CH Disease - Circulation Research, 2004 - circresaha.org
... 34 Nf1 cardiac defects are due to a primary role for neurofibromin in ... 62,64–67 Mutations
in two related forkhead transcription factors, Foxc1 and Foxc2, can ...
Cached - Web Search - circres.ahajournals.org - ahavj.ahajournals.org - uphs.upenn.edu - all 8 versions »

Development & Communication
S Kuure, F Naillat, T Jukkola, R Trokovic, M Palgi … - biocenter.helsinki.fi
... Progression of calvarial bone development requires Foxc1 regulation of Msx2 and
Alx4. ... The role of the NF1 gene in intercellular communication and tumoral cell ...
View as HTML - Web Search - biocenter.helsinki.fi

PlexinA2 and semaphorin signaling during cardiac neural crest development - Full text - MIT Libraries
CB Brown, L Feiner, MM Lu, J Li, X Ma, AL Webber, … - Development, 2001 - dev.biologists.org
... 1998 ), Neurofibromatosis type 1 (Nf1; Brannan et al., 1994 ; Jacks et al., 1994 ),
Connexin 43 (Cx43; also called Gjal; Lo et al., 1999 ), Foxc1 and Foxc2 ...
Cited by 34 - Web Search - uphs.upenn.edu - dev.biologists.org - ncbi.nlm.nih.gov

TYPE XVIII AND XV COLLAGENS: PRIMARY STRUCTURE OF HUMAN ALPHA1 (XVIII) CHAIN, PHENOTYPIC STUDIES OF …
CDN MICE - herkules.oulu.fi
Page 1. TYPE XVIII AND XV COLLAGENS: PRIMARY STRUCTURE OF HUMAN ALPHA1(XVIII) CHAIN,
PHENOTYPIC STUDIES OF TYPE XVIII COLLAGEN SINGLE NULL AND TYPE XVIII AND XV ...
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