(Q28273868)

2

0 references

Osman Demirhan

3

0 references

Defne Aruoba

4

0 references

N Humphrey

5

0 references

S Mundlos

European Journal of Human Genetics

6

0 references

language of work or name

English

0 references

publication date

September 2008

0 references

published in

0 references

volume

16

0 references

issue

9

0 references

page(s)

1070-4

0 references

cites work

Structures and functions of multiligand lipoprotein receptors: macrophage scavenger receptors and LDL receptor-related protein (LRP).

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

Cerebellar hypoplasia and quadrupedal locomotion in humans as a recessive trait mapping to chromosome 17p

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

The Dysequilibrium Syndrome – A genetic study

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Nonprogressive cerebellar disorder with mental retardation and autosomal recessive inheritance in Hutterites

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Autosomal recessive cerebellar hypoplasia in the Hutterite population.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Disequilibrium syndrome in Montana Hutterites.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Identification of a nonsense mutation in the very low-density lipoprotein receptor gene (VLDLR) in an Iranian family with dysequilibrium syndrome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Mouse very low-density lipoprotein receptor (VLDLR): gene structure, tissue-specific expression and dietary and developmental regulation

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Reelin signaling is necessary for a specific step in the migration of hindbrain efferent neurons

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Divergent roles of ApoER2 and Vldlr in the migration of cortical neurons

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Reelin is a ligand for lipoprotein receptors

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

The Pafah1b complex interacts with the reelin receptor VLDLR

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Cortical development: receiving reelin

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Reelin is a detachment signal in tangential chain-migration during postnatal neurogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Disabled-1-regulated adhesion of migrating neurons to radial glial fiber contributes to neuronal positioning during early corticogenesis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Normal plasma lipoproteins and fertility in gene-targeted mice homozygous for a disruption in the gene encoding very low density lipoprotein receptor

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.73

7 January 2021