Divergent pathways in COS-7 cells mediate defective internalization and intracellular routing of truncated G-CSFR forms in SCN/AML - Wikidata - wikimedia - TriplyDB

Divergent pathways in COS-7 cells mediate defective internalization and intracellular routing of truncated G-CSFR forms in SCN/AML

Divergent pathways in COS-7 cells mediate defective internalization and intracellular routing of truncated G-CSFR forms in SCN/AML

http://www.wikidata.org/entity/Q33344491

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miR-155 is associated with the leukemogenic potential of the class IV granulocyte colony-stimulating factor receptor in CD34⁺ progenitor cells.

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P2860

Divergent pathways in COS-7 cells mediate defective internalization and intracellular routing of truncated G-CSFR forms in SCN/AML

http://www.wikidata.org/entity/Q33344491

description

2008 nî lūn-bûn

@nan

2008 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2008年の論文

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2008年論文

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2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

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name

Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@ast

Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@en

type

label

Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@ast

Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@en

prefLabel

Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@ast

Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@en

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JOURNAL.PONE.0002452

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Divergent pathways in COS-7 ce ...... ncated G-CSFR forms in SCN/AML

@en

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Alexander Copelan

http://www.w3.org/2001/XMLSchema#string

Belinda R Avalos

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Daniel C Link

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Megan Loveland

http://www.w3.org/2001/XMLSchema#string

Melissa G Hunter

http://www.w3.org/2001/XMLSchema#string

Morgan McLemore

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A single amino acid substitution in the exoplasmic domain of the human growth hormone (GH) receptor confers familial GH resistance (Laron syndrome) with positive GH-binding activity by abolishing receptor homodimerization

Functional domains of the granulocyte colony-stimulating factor receptor

Expression cloning of a human granulocyte colony-stimulating factor receptor: a structural mosaic of hematopoietin receptor, immunoglobulin, and fibronectin domains

Signals for sorting of transmembrane proteins to endosomes and lysosomes

A mutation in the insulin receptor gene that impairs transport of the receptor to the plasma membrane and causes insulin-resistant diabetes.

A single-base substitution in the proximal Sp1 site of the human low density lipoprotein receptor promoter as a cause of heterozygous familial hypercholesterolemia.

Distinct patterns of mutations occurring in de novo AML versus AML arising in the setting of severe congenital neutropenia.

Protein targeting by tyrosine- and di-leucine-based signals: evidence for distinct saturable components

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Severe congenital neutropenia terminating in acute myeloid leukemia: disease progression associated with mutations in the granulocyte-colony stimulating factor receptor gene.

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e2452

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scholarly article

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10.1371/JOURNAL.PONE.0002452

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6

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2008-06-18T00:00:00Z

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5295307

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18560579

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2409964

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