Expression of Meis2, a Knotted-related murine homeobox gene, indicates a role in the differentiation … - Full text - MIT Libraries
F Cecconi, G Proetzel, G Alvarez-Bolado, D Jay, P … - Dev. Dyn, 1997 - doi.wiley.com
... proteins of plants (see references above), in the murine TGIF, and in ... The expression
of Pax3 spatially and temporally precedes expression of myogenic markers ...
Cited by 20 - Web Search - doi.wiley.com - ncbi.nlm.nih.gov

A genomewide survey of developmentally relevant genes in Ciona intestinalis - Full text - MIT Libraries
S Wada, M Tokuoka, E Shoguchi, K Kobayashi, A Di … - Dev Genes Evol, 2003 - springerlink.com
... and Mix of the Paired class, POU-I, III, V and VI of the POU class, Lhx6/7 of the
LIM class, TGIF of the ... Pax3/7 Pax3/7 genewise.209.17.1 36362 Q96H85 Pax-3 99 ...
Cited by 22 - Web Search - ncbi.nlm.nih.gov

Six family genesÐstructure and function as transcription factors and their roles in development - Full text - MIT Libraries
K Kawakami, S Sato, H Ozaki, K Ikeda - BioEssays - doi.wiley.com
... other genes implicated in HPE, such as Shh, (33) Zic2, (34) and TGIF (35) have ...
expression of Pax3, Six (Six1, Six4) and Eya (Eya1, Eya2) is observed in somites ...
Cited by 55 - Web Search - doi.wiley.com - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Homeodomain revisited: a lesson from disease-causing mutations - Full text - MIT Libraries
YI Chi - Human Genetics, 2005 - springerlink.com
... Holoprosencephaly TGIF 602630 Homeodomain (35–97) P63R R90C PS/DB DB ... Waardenburg
syndrome PAX3 606597 193500 Paired box-homeodomain (219–278) F238S V265F ...
Web Search - ncbi.nlm.nih.gov

Septo-Optic Dysplasia and Related Malformations
MT Dattani - Hypothalamic-pituitary development: genetic and clinical …, 2001 - content.karger.com
... and combined hormone deficiencies), PAX2 (renal-coloboma syndrome), PAX3 (Waardenberg
syndrome type I ... these are Sonic Hedgehog (SHH), ZIC2, TGIF and SIX3. ...
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Status of the Human Malformation Map: 2002
JC CAREY, DH VISKOCHIL - American Journal of Medical Genetics (Semin. Med. Genet.), 2002 - doi.wiley.com
... Holoprosencephaly-3 142945 600725 7q36 SHH Sonic hedgehog Holoprosencephaly-4
142946 602630 18p11 TGIF TG-interacting factor Holoprosencephaly ...
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Homeobox genes in the developing mouse brain - Full text - MIT Libraries
JY Vollmer, RG Clerc - J Neurochem, 1998 - blackwell-synergy.com
... et al., 1990), MATa2 (Goutte and Johnson, 1988), and TGIF (Bertolino et a ... Altered
pigmented retina, coloboma, altered inner ear patterning Pax3 (splotch) Loss-of ...
Cited by 12 - Web Search - ncbi.nlm.nih.gov

Central Nervous System Embryogenesis and Its Failures - Full text - MIT Libraries
FL Lacbawan, M Muenke - Pediatric and Developmental Pathology, 2002 - springerlink.com
... stricted expression during CNS development. Pax3, Pax6, and Pax7 are expressed
early in devel- opment. Except for Pax6, which is ...
Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Induction and specification of midbrain dopaminergic cells: focus on SHH, FGF8, and TGF-β - Full text - MIT Libraries
ERK Krieglstein - Cell Tissue Res, 2004 - springerlink.com
... Shh (Echelard et al. 1993). Apparently, dorsal markers, such as Pax3 (Tremblay
et al. 1996), a homeobox-containing transcription ...
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Malformations of the Craniofacial Region: Evolutionary, Embryonic, Genetic, and Clinical …
M MICHAEL COHEN JR - American Journal of Medical Genetics (Semin. Med. Genet.), 2002 - doi.wiley.com
... Waardenburg syndrome, type 1 2q37 PAX3 Waardenburg syndrome, type 2 3p12-p14 MITF ...
Holoprosencephaly 18p11.3 TGIF Peutz-Jeghers syndrome 19p13.3 STK11 ...
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Limb anomalies and craniofacial syndromes II. Gene regulation of morphogenetic and dysmorphogenetic …
FN Synodinos, MJ Papagrigorakis - grortho.gr
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Hox Genes and Their Candidate Downstream Targets in the Developing Central Nervous System
ZN Akin, AJ Nazarali - springerlink.com
Page 1. Cellular and Molecular Neurobiology, Vol. 25, Nos. 3/4, June 2005 (
C 2005) DOI: 10.1007/s10571-005-3971-9 Hox Genes and ...
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