Presphenoidal synchondrosis fusion in DBA/2J mice (Q30458724)

15 August 2017

Presphenoidal synchondrosis fusion in DBA/2J mice (English)

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15 August 2017

4

Margot E Bowen

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15 August 2017

Allysa Adams

1

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15 August 2017

Brandeis McBratney-Owen

2

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15 August 2017

Brittany Newby

3

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15 August 2017

Bjorn R Olsen

5

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15 August 2017

Matthew L Warman

6

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15 August 2017

21 November 2012

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15 August 2017

9

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based on heuristic

inferred from page(s)

published in

Mammalian Genome

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15 August 2017

24

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15 August 2017

1-2

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15 August 2017

54-62

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describes a project that uses

15 August 2017

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3560942/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

exact match

https://scigraph.springernature.com/pub.10.1007/s00335-012-9437-8

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cites work

Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing

1 reference

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Mouse genomic variation and its effect on phenotypes and gene regulation

14 July 2018

1 reference

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Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome

14 July 2018

1 reference

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A framework for variation discovery and genotyping using next-generation DNA sequencing data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

The Sequence Alignment/Map format and SAMtools

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Fast and accurate short read alignment with Burrows-Wheeler transform

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Morphology and physiology of the epiphyseal growth plate

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Noncanonical frizzled signaling regulates cell polarity of growth plate chondrocytes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Growth of cranial synchondroses and sutures requires polycystin-1.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Conditional Kif3a ablation causes abnormal hedgehog signaling topography, growth plate dysfunction, and excessive bone and cartilage formation during mouse skeletogenesis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Indian and sonic hedgehogs regulate synchondrosis growth plate and cranial base development and function

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Aneurysm syndromes caused by mutations in the TGF-beta receptor

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Structure and function of ETAA16: a novel cell surface antigen in Ewing's tumours

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Altered hematopoiesis in glypican-3-deficient mice results in decreased osteoclast differentiation and a delay in endochondral ossification

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Mutations in the human TWIST gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Progress toward understanding craniofacial malformations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Craniosynostosis: genes and mechanisms

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

Ext1-dependent heparan sulfate regulates the range of Ihh signaling during endochondral ossification

14 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-012-9437-8

Factors regulating endochondral ossification in the spheno-occipital synchondrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-012-9437-8

Roles of the primary cilium component Polaris in synchondrosis development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-012-9437-8

Genetic architecture of the mouse hippocampus: identification of gene loci with selective regional effects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-012-9437-8

Abnormalities in cartilage and bone development in the Apert syndrome FGFR2(+/S252W) mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-012-9437-8

Wnt5a and Wnt5b exhibit distinct activities in coordinating chondrocyte proliferation and differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00335-012-9437-8

Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT).

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

The role of the cranial base in facial growth: experimental craniofacial synostosis in the rabbit

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3560942

10.1007/S00335-012-9437-8

26 November 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

1 reference