Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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P1476

Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.

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P2093

Chi-Fan Yang

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

Chien-Ping Chiang

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Chun-Ping Chang

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Jer-Yuarn Wu

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Shuan-Pei Lin

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Weng Siong H'ng

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Yu-Hung Wu

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P2860

Functional amyloid formation within mammalian tissue.

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Osteoactivin, an anabolic factor that regulates osteoblast differentiation and function

nmb, a novel gene, is expressed in low-metastatic human melanoma cell lines and xenografts

Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis

Fast and accurate short read alignment with Burrows-Wheeler transform

Hematopoietic growth factor inducible neurokinin-1 type: a transmembrane protein that is similar to neurokinin 1 interacts with substance P

Gpnmb is induced in macrophages by IFN-gamma and lipopolysaccharide and acts as a feedback regulator of proinflammatory responses

Molecular cloning of a dendritic cell-associated transmembrane protein, DC-HIL, that promotes RGD-dependent adhesion of endothelial cells through recognition of heparan sulfate proteoglycans

Cloning and characterization of osteoactivin, a novel cDNA expressed in osteoblasts

P304

219-232

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P31

scholarly article

P356

10.1016/J.AJHG.2017.12.012

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P407

English

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P478

102

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P50

Yuan-Tsong Chen

P577

2018-01-09T00:00:00Z

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P698

29336782

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P932

5985536

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