(Q24611761)

English

Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin

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scholarly article

1 reference

Europe PubMed Central

23 June 2017

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Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin (English)

1 reference

Europe PubMed Central

23 June 2017

0 references

1 reference

based on heuristic

inferred from title

Donna M. Martin

object named as

Donna M Martin

5

author given names

Donna M

author last names

Martin

1 reference

29 November 2023

author name string

David J Brown

1

author given names

David J

author last names

Brown

1 reference

Europe PubMed Central

23 June 2017

Theresa B Kim

2

author given names

Theresa B

author last names

Kim

1 reference

Europe PubMed Central

23 June 2017

Elizabeth M Petty

3

author given names

Elizabeth M

author last names

Petty

1 reference

Europe PubMed Central

23 June 2017

Catherine A Downs

4

author given names

Catherine A

author last names

Downs

1 reference

Europe PubMed Central

23 June 2017

Peter J Strouse

6

author given names

Peter J

author last names

Strouse

1 reference

Europe PubMed Central

23 June 2017

Sayoko E Moroi

7

author given names

Sayoko E

author last names

Moroi

1 reference

Europe PubMed Central

23 June 2017

Jeff M Milunsky

8

author given names

Jeff M

author last names

Milunsky

1 reference

Europe PubMed Central

23 June 2017

Marci M Lesperance

9

author given names

Marci M

author last names

Lesperance

1 reference

Europe PubMed Central

23 June 2017

language of work or name

0 references

publication date

27 June 2002

1 reference

Europe PubMed Central

23 June 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

23 June 2017

71

1 reference

Europe PubMed Central

23 June 2017

3

1 reference

Europe PubMed Central

23 June 2017

618-624

1 reference

Europe PubMed Central

23 June 2017

Human disease-causing NOG missense mutations: effects on noggin secretion, dimer formation, and bone morphogenetic protein binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

BMP4 is essential for lens induction in the mouse embryo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Noggin-mediated antagonism of BMP signaling is required for growth and patterning of the neural tube and somite

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

The Spemann organizer signal noggin binds and inactivates bone morphogenetic protein 4

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Identification of mammalian noggin and its expression in the adult nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

A DNA polymorphism discovery resource for research on human genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

7 April 2017

Evolution and classification of cystine knot-containing hormones and related extracellular signaling molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

27 September 2017

Developmental expression patterns of bone morphogenetic proteins, receptors, and binding proteins in the chick retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

27 September 2017

Animal-vegetal asymmetries influence the earliest steps in retina fate commitment in Xenopus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

30 May 2018

Congenital stapes ankylosis, broad thumbs, and hyperopia: report of a family and refinement of a syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

30 May 2018

The autosomal dominant syndrome with congenital stapes ankylosis, broad thumbs and hyperopia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

30 May 2018

Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

30 May 2018

Noggin and retinoic acid transform the identity of avian facial prominences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

28 November 2018

Bmp4 mediates apoptotic cell death in the developing chick eye.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

28 November 2018

Secreted noggin protein mimics the Spemann organizer in dorsalizing Xenopus mesoderm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

28 November 2018

An autosomal dominant inherited syndrome with congenital stapes ankylosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=379196

28 November 2018

Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism

1 reference

https://pubmed.ncbi.nlm.nih.gov/12089654

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

1 reference

https://api.crossref.org/works/10.1086%2F342067

7 January 2021

based on heuristic

inferred from DOI database lookup

Evolution and Classification of Cystine Knot-Containing Hormones and Related Extracellular Signaling Molecules

1 reference

https://api.crossref.org/works/10.1086%2F342067

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

23 June 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Europe PubMed Central

23 June 2017

ResearchGate publication ID

0 references

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