A neuronal VLDLR variant lacking the third complement-type repeat exhibits high capacity binding of apoE containing lipoproteins (Q24646231)

1

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Oliver Tiebel

2

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M Cecilia Ljungberg

3

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Merry Sullivan

4

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Hye-Jeong Lee

5

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Tomoya Terashima

6

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Rongying Li

7

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Kunihisa Kobayashi

8

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Hui-Chen Lu

9

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Lawrence Chan

10

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Kazuhiro Oka

11

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language of work or name

English

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publication date

18 June 2009

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number of pages

11

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Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans

inferred from page(s)

published in

Brain Research

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volume

1276

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page(s)

11-21

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cites work

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Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplification

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The Very Low Density Lipoprotein Receptor Mediates the Cellular Catabolism of Lipoprotein Lipase and Urokinase-Plasminogen Activator Inhibitor Type I Complexes

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28 November 2018

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28 November 2018

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28 November 2018

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28 November 2018

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Identifiers

DOI

1 reference

1 reference

1 reference

PubMed publication ID

19393635

1 reference