Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Haploinsufficiency of SAMD9L, an Endosome Fusion Facilitator, Causes Myeloid Malignancies in Mice Mimicking Human Diseases with Monosomy 7

1 Sept 2013

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Acute Myeloid Leukemia Research
Share to Cell Adhesion Molecules Research
Share to Neutrophil, Myeloperoxidase and Oxidative Mechanisms

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24029230
DOI: 10.1016/j.ccr.2013.08.011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Haploinsufficiency of SAMD9L, an Endosome Fusion Facilitator, Causes Myeloid Malignancies in Mice Mimicking Human Diseases with Monosomy 7PMID 24029230Read ↗

Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes.Semantic proximity Read ↗

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7.Semantic proximity Read ↗

Pediatric MDS and bone marrow failure-associated germline mutations in SAMD9 and SAMD9L impair multiple pathways in primary hematopoietic cells.Semantic proximity Read ↗

Germline SAMD9 mutation in siblings with monosomy 7 and myelodysplastic syndromeSemantic proximity Read ↗

The enigma of monosomy 7Semantic proximity Read ↗

A homozygous frameshift variant expands the clinical spectrum of SAMD9 gene defects.Semantic proximity Read ↗

Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7Semantic proximity Read ↗

Genetic and clinical spectrum of SAMD9 and SAMD9L syndromes: from variant interpretation to patient managementSemantic proximity Read ↗

Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7Semantic proximity Read ↗

SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.Semantic proximity Read ↗

Mutant Samd9l expression impairs hematopoiesis and induces bone marrow failure in miceSemantic proximity Read ↗

Essential role of MFSD1-GLMP-GIMAP5 in lymphocyte survival and liver homeostasisSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.