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Article

OSTM1 bone defect reveals an intercellular hematopoietic crosstalk.

The Journal of biological chemistry - 7 Nov 2008

Pata Monica, Héraud Céline, Vacher Jean

Abstract excerpt

The most severe form of bone autosomal recessive osteopetrosis both in humans and in the gray-lethal (gl/gl) mouse is caused by mutations in the Ostm1 gene. Although osteopetrosis is usually associated with a defect in the hematopoietic-derived osteoclast cells, this study determined that Ostm1 i...

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Share to CD8-Positive T-Lymphocytes
Share to Chromosomes, Artificial, Bacterial
Share to Genetic Diseases, Inborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hematopoiesis

Share to Hematopoietic Stem Cells

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Source

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Identifiers

PMID: 18790735
DOI: 10.1074/jbc.M805242200
PMCID: PMC2662145

Genes

OSTM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18790735-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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