(Q24629855)

6

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Colin E. Willoughby

object named as

Colin E Willoughby

7

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author name string

Anne E Hughes

1

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Malcolm Campbell

3

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Judith Lechner

4

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Durga P Dash

American Journal of Human Genetics

5

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language of work or name

English

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publication date

11 November 2011

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published in

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volume

89

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issue

5

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page(s)

628-33

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cites work

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

Identification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridia

7 April 2017

1 reference

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Fast and accurate short read alignment with Burrows-Wheeler transform

7 April 2017

1 reference

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MicroRNA-184 antagonizes microRNA-205 to maintain SHIP2 levels in epithelia

7 April 2017

1 reference

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Apoptosis in the initiation, modulation and termination of the corneal wound healing response

7 April 2017

1 reference

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SH2-containing 5'-inositol phosphatase, SHIP2, regulates cytoskeleton organization and ligand-dependent down-regulation of the epidermal growth factor receptor

7 April 2017

1 reference

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MicroRNA expression detected by oligonucleotide microarrays: system establishment and expression profiling in human tissues

7 April 2017

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7 April 2017

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MicroRNA targets in Drosophila

7 April 2017

1 reference

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7 April 2017

1 reference

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7 April 2017

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7 April 2017

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The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14

7 April 2017

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MicroRNAs of the mammalian eye display distinct and overlapping tissue specificity

7 April 2017

1 reference

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Mammalian tissue oxygen levels modulate iron-regulatory protein activities in vivo

7 April 2017

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7 April 2017

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SSAHA: a fast search method for large DNA databases

7 April 2017

1 reference

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7 April 2017

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A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

27 September 2017

1 reference

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microRNAs and genetic diseases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss.

27 September 2017

1 reference

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27 September 2017

1 reference

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VSX1: a gene for posterior polymorphous dystrophy and keratoconus

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

Keratocyte apoptosis associated with keratoconus

27 September 2017

1 reference

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A 48-year clinical and epidemiologic study of keratoconus

27 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

27 September 2017

https://api.crossref.org/works/10.1016%2FJ.AJHG.2011.09.014

inferred from DOI database lookup

7 January 2021

based on heuristic

DnaJA4 is a SREBP-regulated chaperone involved in the cholesterol biosynthesis pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

Mutational screening of VSX1 in keratoconus patients from the European population.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

Familial keratoconus with cataract: linkage to the long arm of chromosome 15 and exclusion of candidate genes.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3213395

Fine mapping of the keratoconus with cataract locus on chromosome 15q and candidate gene analysis

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21996275

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2011.09.014

1 reference

1 reference

1 reference

PubMed publication ID

21996275

1 reference