Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development (Q24657446)

https://scigraph.springernature.com/pub.10.1007/s00335-001-2101-3

inferred from page(s)

published in

Mammalian Genome

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volume

13

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issue

2

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page(s)

95-101

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exact match

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cites work

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

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Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

7 April 2017

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Active conservation of noncoding sequences revealed by three-way species comparisons

7 April 2017

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Identification of a photoreceptor cell-specific nuclear receptor

7 April 2017

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Preservation of duplicate genes by complementary, degenerative mutations

7 April 2017

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A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene

7 April 2017

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Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor

7 April 2017

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

7 April 2017

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Interactions between heterologous helix-loop-helix proteins generate complexes that bind specifically to a common DNA sequence

7 April 2017

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A physical map of the human genome

7 April 2017

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Recognition by Max of its cognate DNA through a dimeric b/HLH/Z domain

7 April 2017

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Math5 is required for retinal ganglion cell and optic nerve formation

7 April 2017

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Requirement for math5 in the development of retinal ganglion cells

7 April 2017

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Math1: an essential gene for the generation of inner ear hair cells

7 April 2017

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Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10

7 April 2017

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De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis

7 April 2017

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Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration

7 April 2017

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Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

7 April 2017

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The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

7 April 2017

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BLAST 2 Sequences, a new tool for comparing protein and nucleotide sequences

7 April 2017

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VISTA : visualizing global DNA sequence alignments of arbitrary length

7 April 2017

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The "initiator" as a transcription control element

7 April 2017

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Correlations among amino acid sites in bHLH protein domains: an information theoretic analysis

7 April 2017

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The role of basic helix-loop-helix genes in vertebrate retinogenesis

9 May 2017

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The basic helix-loop-helix protein family: comparative genomics and phylogenetic analysis

28 September 2017

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Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects

28 September 2017

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The Ath5 proneural genes function upstream of Brn3 POU domain transcription factor genes to promote retinal ganglion cell development

28 September 2017

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28 September 2017

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Conserved noncoding sequences are reliable guides to regulatory elements.

28 September 2017

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Doing the MATH: is the mouse a good model for fly development?

28 September 2017

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Analysis of mammalian central nervous system gene expression and function using bacterial artificial chromosome-mediated transgenesis

28 September 2017

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Identification of a Coordinate Regulator of Interleukins 4, 13, and 5 by Cross-Species Sequence Comparisons

28 September 2017

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Autoregulation and multiple enhancers control Math1 expression in the developing nervous system

28 September 2017

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Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

28 September 2017

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Functional evolution of the Ultrabithorax protein

28 September 2017

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Gene duplication: past, present and future

28 September 2017

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Gene duplication and the uniqueness of vertebrate genomes circa 1970-1999.

28 September 2017

1 reference

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Causes of visual impairment among students at the Alabama School for the Blind

28 September 2017

1 reference

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The clinical and morphologic spectrum of optic nerve hypoplasia

28 September 2017

1 reference

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The roles of intrinsic and extrinsic cues and bHLH genes in the determination of retinal cell fates

28 September 2017

1 reference

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Xath5 participates in a network of bHLH genes in the developing Xenopus retina

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Neuronal type information encoded in the basic-helix-loop-helix domain of proneural genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Aplasia of the optic nerve in two cases of partial trisomy 10q24-ter.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

atonal is a proneural gene that directs chordotonal organ formation in the Drosophila peripheral nervous system

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

HLH proteins, fly neurogenesis, and vertebrate myogenesis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Discrimination between related DNA sites by a single amino acid residue of Myc-related basic-helix-loop-helix proteins

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Single amino acid substitutions alter helix-loop-helix protein specificity for bases flanking the core CANNTG motif

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Aplasia of the Optic Nerve and Disk

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Math5 encodes a murine basic helix-loop-helix transcription factor expressed during early stages of retinal neurogenesis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Encyclopedia of the mouse genome VII. Mouse chromosome 10.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Bilateral aplasia of the optic nerves, chiasm, and tracts in an otherwise healthy infant.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Comparable rates of gene loss and functional divergence after genome duplications early in vertebrate evolution

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Evolution of distinct developmental functions of three Drosophila genes by acquisition of different cis-regulatory regions

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Retinal ganglion cell genesis requires lakritz, a Zebrafish atonal Homolog.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Proprioceptor pathway development is dependent on Math1.

28 November 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

The basic helix-loop-helix transcription factors LIN-32 and HLH-2 function together in multiple steps of a C. elegans neuronal sublineage.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Midline signals regulate retinal neurogenesis in zebrafish.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Transcriptional regulation of atonal during development of the Drosophila peripheral nervous system.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Posterior segment neovascularization associated with optic nerve aplasia

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Atonal is the proneural gene for Drosophila photoreceptors.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Role of the proneural gene, atonal, in formation of Drosophila chordotonal organs and photoreceptors.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2262845

Some new terms for duplicated genes

28 November 2018

1 reference

12 December 2020

Evolution of bHLH transcription factors: modular evolution by domain shuffling?

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12 December 2020

Giving in to the blues

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12 December 2020

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12 December 2020

The canine copper toxicosis locus is not syntenic with ATP7B or ATX1 and maps to a region showing homology to human 2p21

1 reference

12 December 2020