The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects.

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The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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The skeletal phenotype of acho ...... lusively by cartilage defects.

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The skeletal phenotype of acho ...... lusively by cartilage defects.

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The skeletal phenotype of acho ...... lusively by cartilage defects.

@en

The skeletal phenotype of acho ...... lusively by cartilage defects.

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The skeletal phenotype of acho ...... lusively by cartilage defects.

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The skeletal phenotype of acho ...... lusively by cartilage defects.

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P1476

The skeletal phenotype of acho ...... lusively by cartilage defects.

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P2093

Alexander G Robling

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Devin K Schweppe

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Ian M Bird

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Julia F Charles

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Matthew L Warman

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Patrick J Smits

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Susie H Kim

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P2860

The Golgin GMAP210/TRIP11 anchors IFT20 to the Golgi complex

Two classes of proteins dependent on either the presence or absence of thyroid hormone for interaction with the thyroid hormone receptor

Two splice variants of Golgi-microtubule-associated protein of 210 kDa (GMAP-210) differ in their binding to the cis-Golgi network

Lrp5 functions in bone to regulate bone mass

GMAP-210, A cis-Golgi network-associated protein, is a minus end microtubule-binding protein

Vesicle-mediated export from the ER: COPII coat function and regulation

An approach to correlate tandem mass spectral data of peptides with amino acid sequences in a protein database

The Wnt co-receptor LRP5 is essential for skeletal mechanotransduction but not for the anabolic bone response to parathyroid hormone treatment

Functions and mechanics of dynein motor proteins

Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210

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scholarly article

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10.1242/DEV.156588

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English

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P478

145

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Joana Caetano-Lopes

Steven P Gygi

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2018-01-08T00:00:00Z

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P698

29180569

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cartilage

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5825869

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