Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7 (Q24328884)

GOA release 2020-03-11

endosomal vesicle fusion

1 reference

GOA release 2020-03-11

author name string

Akiko Nagamachi

1

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Hirotaka Matsui

2

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Hiroya Asou

3

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Yuko Ozaki

4

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Daisuke Aki

5

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Akinori Kanai

6

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Keiyo Takubo

7

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Toshio Suda

8

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Takuro Nakamura

9

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Linda Wolff

10

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Hiroaki Honda

11

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Toshiya Inaba

The small GTPase rab5 functions as a regulatory factor in the early endocytic pathway

12

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language of work or name

English

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publication date

9 September 2013

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published in

Cancer Cell

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volume

24

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issue

3

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page(s)

305-17

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cites work

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Identification of a common microdeletion cluster in 7q21.3 subband among patients with myeloid leukemia and myelodysplastic syndrome

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Acquisition of G₀ state by CD34-positive cord blood cells after bone marrow transplantation

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Poly-ADP ribosylation of Miki by tankyrase-1 promotes centrosome maturation

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A 5' untranslated region containing the IRES element in the Runx1 gene is required for angiogenesis, hematopoiesis and leukemogenesis in a knock-in mouse model

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Transformation of congenital neutropenia into monosomy 7 and acute nonlymphoblastic leukemia in a child treated with granulocyte colony-stimulating factor

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Monosomy 7 and 7q- associated with myeloid malignancy

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PDGF-regulated rab4-dependent recycling of alphavbeta3 integrin from early endosomes is necessary for cell adhesion and spreading

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7 January 2021

Involvement of the endosomal autoantigen EEA1 in homotypic fusion of early endosomes.

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The Rab5 effector EEA1 is a core component of endosome docking

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7 January 2021

Functional Characterization of SAMD9, a Protein Deficient in Normophosphatemic Familial Tumoral Calcinosis

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7 January 2021

The Samd9L Gene: Transcriptional Regulation and Tissue-Specific Expression in Mouse Development

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Deletion 5q in myelodysplastic syndrome: a paradigm for the study of hemizygous deletions in cancer

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JHDM1B/FBXL10 is a nucleolar protein that represses transcription of ribosomal RNA genes

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A GTPase-activating protein controls Rab5 function in endocytic trafficking

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Normophosphatemic familial tumoral calcinosis is caused by deleterious mutations in SAMD9, encoding a TNF-alpha responsive protein

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Genetics of therapy-related myelodysplasia and acute myeloid leukemia

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Hypermethylation of the Ink4b locus in murine myeloid leukemia and increased susceptibility to leukemia in p15(Ink4b)-deficient mice

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Both AML1 and EVI1 oncogenic components are required for the cooperation of AML1/MDS1/EVI1 with BCR/ABL in the induction of acute myelogenous leukemia in mice

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Overexpression/enhanced kinase activity of BCR/ABL and altered expression of Notch1 induced acute leukemia in p210BCR/ABL transgenic mice

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The delivery of endocytosed cargo to lysosomes

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Identification of genes that synergize with Cbfb-MYH11 in the pathogenesis of acute myeloid leukemia

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Granulocyte colony-stimulating factor preferentially stimulates proliferation of monosomy 7 cells bearing the isoform IV receptor

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Hemp, an mbt domain-containing protein, plays essential roles in hematopoietic stem cell function and skeletal formation

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Proteomics analysis of Ring1B/Rnf2 interactors identifies a novel complex with the Fbxl10/Jhdm1B histone demethylase and the Bcl6 interacting corepressor

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A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis

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Loss of T-cell protein tyrosine phosphatase induces recycling of the platelet-derived growth factor (PDGF) beta-receptor but not the PDGF alpha-receptor

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R-Ras regulates exocytosis by Rgl2/Rlf-mediated activation of RalA on endosomes.

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Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice.

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Downregulation of Bim, a proapoptotic relative of Bcl-2, is a pivotal step in cytokine-initiated survival signaling in murine hematopoietic progenitors

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Roles of Bim in apoptosis of normal and Bcr-Abl-expressing hematopoietic progenitors

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Retroviral insertional mutagenesis identifies genes that collaborate with NUP98-HOXD13 during leukemic transformation.

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EVI1 induces myelodysplastic syndrome in mice

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High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients

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Trib1 and Evi1 cooperate with Hoxa and Meis1 in myeloid leukemogenesis.

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AML1 mutations induced MDS and MDS/AML in a mouse BMT model

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High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated.

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Risk factors for evolution of acquired aplastic anemia into myelodysplastic syndrome and acute myeloid leukemia after immunosuppressive therapy in children

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Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse

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Sorting of EGF and transferrin at the plasma membrane and by cargo-specific signaling to EEA1-enriched endosomes

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Identifiers

DOI

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Consolidated OpenCitations Corpus – April 2017

release_sbzheq3eoffddjudchqcca36y4

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/sbzheq3eoffddjudchqcca36y4

24 November 2022

mapped directly with Wikidata item

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

24029230

1 reference

Consolidated OpenCitations Corpus – April 2017