The Lacrimal Gland Transcriptome Is an Unusually Rich Source of Rare and Poorly Characterized Gene … - Full text - MIT Libraries
AM Ozyildirim, GJ Wistow, J Gao, J Wang, DP … - Investigative Ophthalmology & Visual Science, 2005 - iovs.org
... 3–5 gene pairs) of putative TFAP2A (AP-2 ), ELK1, FOXF2, FOXF1, FOXC1, FOXL1, SRY,
HAND1, and YY1 sites and a few others (2 or fewer gene pairs). ...
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Table 2. Gene Mutations Demonstrating Cardiac Phenotypes
N Phenotype - ahavj.ahajournals.org
... Foxc1 (Fkh1/forkhead box C1), Aortic arch abnormalities, 68. ... Hand1 (eHand/heart and
neural crest derivatives expressed 1), Looping abnormality, 97, 98. ...
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Autosomal dominant inheritance of left ventricular outflow tract obstruction - Full text - MIT Libraries
MW Wessels, RMF Berger, IME Frohn-Mulder, JW Roos- … - American Journal of Medical Genetics Part A, 2005 - doi.wiley.com
... LR axis Abu -Issa et al. [2002 ] Foxc1 I AA*, C oA, VSD, valve anomalies Winn ier
et al. ... Pa zneka s et al. [2003 ] Hand1 HLV Firulli et al. [19 98] Jagged1 ...
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Development Gone Awry - Full text - MIT Libraries
CH Disease - Circulation Research, 2004 - circresaha.org
... 68 Interestingly, Foxc1 and Foxc2 can function downstream of sonic hedgehog in ... The
bHLH transcription factor gene Hand1 is predominantly restricted to the left ...
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Coordinated Changes in Classes of Ribosomal Protein Gene Expression Is Associated with Light-Induced … - Full text - MIT Libraries
R Grewal, J Stepczynski, R Kelln, T Erickson, R … - Investigative Ophthalmology & Visual Science, 2004 - iovs.org
... Evi-1, Lmo2 complex, c-Rel, GATA-1, Comp-1, Nkx2-5, and Hand1/E47 ... 68 Mutations in
several members of the Fox TF gene family (FoxC1, FoxE3, FoxL2, and FoxC2) are ...
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