Case report: Y; 6 translocation with deletion of 6p.
OD Klein, K Backstrand, PD Cotter, E Marco, E … - Clinical Dysmorphology, 2005 - clindysmorphol.com
... The paternal karyotype was 46,XY with the SRY locus present at Yp11 ... presumably due
to haploinsufficiency for the forkhead transcription factor FOXC1 (Mirza et al ...
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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). ...
Web Search - dx.doi.org - iovs.org - ncbi.nlm.nih.gov

Status of the Human Malformation Map: 2002
JC CAREY, DH VISKOCHIL - American Journal of Medical Genetics (Semin. Med. Genet.), 2002 - doi.wiley.com
... Axenfeld anomaly 601090 601090 6p25 FOXC1 Forkhead, Drosophila, homolog-like 7 ...
Campomelic dysplasia 114290 114290 17q24.3-q25.1 SOX9 SRY-box 9 ...
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Eyes: Variety, Development and Evolution - Full text - MIT Libraries
RD Fernald - Brain Behavior and Evolution, 2004 - content.karger.com
... paired domain; eya, eyes absent; eyg, eye gone homeodomain; FOXC1, forkhead box
gene ... fold homeobox; so, sine oculus homeodomain/six domain; SOX2, SRY, box with ...
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Eyes: Variety, Development and Evolution - Full text - MIT Libraries
F Alert, RG Northcutt, C San Diego, MS Northcutt, … - Brain, Behavior and Evolution, 2004 - content.karger.com
... paired domain; eya, eyes absent; eyg, eye gone homeodomain; FOXC1, forkhead box
gene ... fold homeobox; so, sine oculus homeodomain/six domain; SOX2, SRY, box with ...
Web Search - dx.doi.org - content.karger.com - karger.com

Transcriptional regulation of cardiac development: implications for congenital heart disease and … - Full text - MIT Libraries
JA Epstein, CA Buck - Pediatr Res, 2000 - pedresearch.org
... Transcriptional regulators such as NFATc, the Sry-related homeobox gene Sox4, and
the ... 1 (61) and by the winged helix transcription factors Foxc1 (Mf1) and ...
Cited by 19 - Web Search - pedresearch.org - ncbi.nlm.nih.gov

Evolving eyes.
RD FERNALD - Int. J. Dev. Biol, 2004 - stanford.edu
... paired domain, eya-eyes absent, eyg-eye gone homeodomain, FOXC1-forkhead box ... neural
fold homeobox, so-sine oculus homeodomain/six domain, SOX2-SRY-box with ...
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REVIEW ARTICLES Transcriptional Regulation of Cardiac Development: Implications for Congenital Heart …
JA EPSTEIN, CA BUCK - PEDIATRIC RESEARCH, 2000 - uphs.upenn.edu
... Transcriptional regulators such as NFATc, the Sry- related homeobox gene Sox4, and
the ... 1 (61) and by the winged helix transcription factors Foxc1 (Mf1) and ...
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Novel transcription factors in human CD34 antigen-positive hematopoietic cells - Full text - MIT Libraries
I Gomes, TT Sharma, S Edassery, N Fulton, BG Mar, … - Blood, 2002 - bloodjournal.org
Page 1. HEMATOPOIESIS Novel transcription factors in human CD34 antigen–positive
hematopoietic cells Ignatius Gomes, Tiffany T. Sharma ...
Cited by 3 - Web Search - bloodjournal.org - dx.doi.org - ncbi.nlm.nih.gov - all 7 versions »

The molecular control of renal branching morphogenesis: current knowledge and emerging insights - Full text - MIT Libraries
TD Piscione, ND Rosenblum, C Boudreau-Lariviere, R … - Differentiation, 2002 - ingentaconnect.com
... Spontaneous mutations Congenital Foxc1 ch , forkhead/ ureteral anomalies
ureter development eye, skeleton, heart (Kume et al., 2000) ...
Cited by 15 - Web Search - ingentaconnect.com - ncbi.nlm.nih.gov

Long-Range Control of Gene Expression: Emerging Mechanisms and Disruption in Disease - Full text - MIT Libraries
DA Kleinjan, V van Heyningen - The American Journal of Human Genetics, 2005 - journals.uchicago.edu
... Lehmann et al. 2003). FOXC1 (previously, FKHL7) lies in a cluster of forkhead
genes on chromosome 6p25. Mutations cause ocular malformations ...
Cited by 9 - Web Search - ncbi.nlm.nih.gov

Development & Communication
S Kuure, F Naillat, T Jukkola, R Trokovic, M Palgi … - biocenter.helsinki.fi
... Irma Thesleff. (2003). Progression of calvarial bone development requires
Foxc1 regulation of Msx2 and Alx4. Dev. Biol. 262:75-87. 6 ...
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Molecular Mechanisms of Human Embryogenesis: Developmental Pathogenesis of Renal Tract Malformations - Full text - MIT Libraries
AS Woolf, PJD Winyard - Pediatric and Developmental Pathology, 2002 - springerlink.com
... Transcription factors: BF2 [28], EMX2 [29], EYA1 [30,31], hepatocyte nuclear
factors (HNF) [32], FOXc1 and FOXc2 [33], HOXa11 and ...
Cited by 8 - Web Search - ncbi.nlm.nih.gov

Developmental gene expression profiling of mammalian, fetal orofacial tissue
P Mukhopadhyay, RM Greene, W Zacharias, MC … - Birth Defects Research Part A Clinical and Molecular …, 2004 - doi.wiley.com
Page 1. Original Articles Developmental Gene Expression Profiling of Mammalian,
Fetal Orofacial Tissue Partha Mukhopadhyay, 1 Robert ...
Cited by 3 - Web Search - louisville.edu - louisville.edu - ncbi.nlm.nih.gov - Get it from MIT Libraries

E ARLY E YE D EVELOPMENT IN V ERTEBRATES - Full text - MIT Libraries
RL Chow, RA Lang - Annual Review of Cell and Developmental Biology, 2001 - cellbio.annualreviews.org
Annual Reviews tagline graphic, ...
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Twist is required for patterning the cranial nerves and maintaining the viability of mesodermal … - Full text - MIT Libraries
MS Ota, DAF Loebel, MP O'Rourke, N Wong, B Tsoi, … - Developmental Dynamics, 2004 - doi.wiley.com
... 2C,D), Foxc1/ Mf1, Foxc2/Mfh1, Hoxb8, and Fgf8 (data not shown) and of the
region- alized expression within the somite of Uncx4.1 (Fig. ...
Cited by 1 - Web Search - ncbi.nlm.nih.gov