An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.

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An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.

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http://www.wikidata.org/entity/Q38753637

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

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name

An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.

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label

An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.

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prefLabel

An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1.

@en

P1476

An LPL-specific monoclonal antibody, 88B8, that abolishes the binding of LPL to GPIHBP1

@en

P2093

Alaleh Mapar

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

André Bensadoun

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

Anne P Beigneux

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

Christopher M Allan

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

Constance Voss

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

Cuiwen He

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

Katsuyuki Nakajima

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

Kazuya Miyashita

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

Loren G Fong

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

Masami Murakami

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

P2860

Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defects

Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase

GPIHBP1 is responsible for the entry of lipoprotein lipase into capillaries

Glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 plays a critical role in the lipolytic processing of chylomicrons

Expression cloning and characterization of a novel glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein, GPI-HBP1

Multimerization of glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) and familial chylomicronemia from a serine-to-cysteine substitution in GPIHBP1 Ly6 domain

Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia.

Childhood-onset chylomicronaemia with reduced plasma lipoprotein lipase activity and mass: identification of a novel GPIHBP1 mutation.

GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemia.

Lipoprotein lipase domain function.

P304

1889-1898

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P31

scholarly article

P356

10.1194/JLR.M070813

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P433

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

P478

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

P50

Michael Ploug

Xuchen Hu

Stephen G. Young

P577

2016-08-05T00:00:00Z

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

P698

27494936

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

P932

5036369

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