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This intronless gene encodes a member of the basic helix-loop-helix family of transcription factors, with similarity to Drosophila atonal gene that controls photoreceptor development. Zusätzlich bieten wir Ihnen ATOH7 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 66 products:
Human Polyclonal ATOH7 Primary Antibody für WB - ABIN531345
Prasov, Brown, Glaser: A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina. in PLoS ONE 2010
Show all 2 Pubmed References
Cow (Bovine) Polyclonal ATOH7 Primary Antibody für WB - ABIN2775072
McLellan, Langlands, Kealey: Exhaustive identification of human class II basic helix-loop-helix proteins by virtual library screening. in Mechanisms of development 2003
Zebrafish Polyclonal ATOH7 Primary Antibody für ELISA - ABIN451523
Kay, Link, Baier: Staggered cell-intrinsic timing of ath5 expression underlies the wave of ganglion cell neurogenesis in the zebrafish retina. in Development (Cambridge, England) 2005
Human Monoclonal ATOH7 Primary Antibody für ELISA, WB - ABIN531346
Prasov, Masud, Khaliq, Mehdi, Abid, Oliver, Silva, Lewanda, Brodsky, Borchert, Kelberman, Sowden, Dattani, Glaser: ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. in Human molecular genetics 2012
Human Polyclonal ATOH7 Primary Antibody für ELISA - ABIN451594
Brown, Dagenais, Chen, Glaser: Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. in Mammalian genome : official journal of the International Mammalian Genome Society 2002
Atoh7 indirectly impacts amacrine-cell division modes to regulate the right number of Barhl2 (zeige BARHL2 Antikörper)-expressing cells. Atoh7 itself influences the subtypes of Barhl2 (zeige BARHL2 Antikörper)-dependent amacrine cells.
Observations suggest that Irx2 (zeige IRX2 Antikörper) functions downstream of irx1a (zeige IRX1 Antikörper) to control shh (zeige SHH Antikörper) expression in the retina. Study proposed a novel transcriptional cascade of ath5-irx1a (zeige IRX1 Antikörper)-irx2a in the regulation of hedgehog (zeige SHH Antikörper) waves during vertebrate retinal development.
Staggered cell-intrinsic timing of ath5 expression underlies the wave of ganglion cell neurogenesis in the zebrafish retina.
Pou4f2 (zeige POU4F2 Antikörper) and Isl1 (zeige ISL1 Antikörper), are sufficient to specify the retinal ganglion cell fate in ATOH7 deficient mice
This study present evidence for a Pax6 (zeige PAX6 Antikörper)-Atoh7-Eya2 (zeige EYA2 Antikörper) pathway that acts downstream of Atoh7 but upstream of differentiation factor Pou4f2 (zeige POU4F2 Antikörper).
Notch (zeige NOTCH1 Antikörper) signaling controls the overall tempo of retinogenesis through Atoh7 and Neurog2 (zeige NEUROG2 Antikörper), by integrating cell fate specification, the wave of neurogenesis and the developmental status of cells ahead of this wave
The level of basic helix-loop-helix factor Math5 expression may determine the ultimate number of retinal ganglion cells.
Atoh7 acts dominantly in Neurod1-expressing retina progenitor cells to activate the retinal ganglion cell genetic program.
Results suggest that Math5 is not sufficient to stimulate retinal ganglion cell (RGC)fate.
new insights into Math5 function, ganglion cell development, and the mechanism of retinal fate determination were provided.
The present data demonstrates that the loss of ganglion cells in the Math5(-/-) mice is associated with a lack of retinal vascular development.
Report Math5 expression/function in retinal ganglion cells.
Data suggest that Math5 regulates the generation of multiple retinal cell types via different mechanisms during retinogenesis.
We evaluated 21 consanguineous NCRNA pedigrees and identified the causal mutations in known retinal genes in 13 out of our 21 families. We found mutations in ATOH7 in three families.
We discovered a novel SNP, rs56238729 (P = 1.22 x 10-13), in the ATOH7-PBLD (zeige PBLD Antikörper) region that is significantly associated with VCDR in Latino individuals.
The genotype and allele frequencies of the polymorphism in ATOH7 did not show any statistically significant association with primary open angle glaucomacompared to controls.
Familial linkage studies for primary angle-closure glaucoma have been performed and identified ATOH7 causative primary angle-closure glaucoma disease
Single nucleotide polymorphism in ATOH7 gene is associated with primary open angle glaucoma.
The significant association of three common variants in TMCO1 (zeige TMCO1 Antikörper), ATOH7, and CAV1 (zeige CAV1 Antikörper) with primary open angle, primary angle closure, and pseudoexfoliation glaucoma was found in Pakistani cohorts.
Mutations within the ATOH7 gene are not implicated in the pathogenesis of optic nerve hypoplasia in our patient cohort.
This study finds that ATOH7 is associated with optic disc size but not independently with cup/disk ratio.
a bHLH mutation in ATOH7 causes recessive persistent hyperplasia of the primary vitreous
findings document Mendelian mutations within ATOH7 and imply a role for this molecule in the development of structures at the front as well as the back of the eye; study provides further insights into the function of ATOH7, especially its importance in retinal vascular development and hyaloid regression
This intronless gene encodes a member of the basic helix-loop-helix family of transcription factors, with similarity to Drosophila atonal gene that controls photoreceptor development. Studies in mice suggest that this gene plays a central role in retinal ganglion cell and optic nerve formation. Mutations in this gene are associated with nonsyndromic congenital retinal nonattachment.
atonal homolog 7
, atonal homolog 7 (Drosophila)
, atonal homolog 5
, helix-loop-helix protein zATH-5
, protein atonal homolog 5
, protein atonal homolog 7
, protein lakritz
, helix-loop-helix protein mATH-5
, class A basic helix-loop-helix protein 13
, helix-loop-helix protein hATH-5
, Atonal Homolog 5
, atonal transcription factor homologue
, helix-loop-helix protein cATH-5