(Q34462197)

2 August 2017

title

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse (English)

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2 August 2017

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Phillip Hahn

4

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Carsten Drepper

object named as

Carsten Drepper

2

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Martin Hafner

object named as

Martin Hafner

7

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author name string

Thomas Schmitt-John

1

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2 August 2017

Anke Mussmann

3

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2 August 2017

Melanie Kuhlmann

5

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Cora Thiel

6

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Andreas Lengeling

8

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2 August 2017

Peter Heimann

9

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Julie M Jones

10

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Miriam H Meisler

11

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2 August 2017

Harald Jockusch

12

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2 August 2017

language of work or name

English

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publication date

23 October 2005

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2 August 2017

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2 August 2017

volume

37

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2 August 2017

issue

11

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2 August 2017

page(s)

1213-1215

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https://scigraph.springernature.com/pub.10.1038/ng1661

2 August 2017

exact match

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cites work

An hereditary motor neurone disease with progressive denervation of muscle in the mouse: the mutant 'wobbler'.

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Defect of sperm assembly in a neurological mutant of the mouse, wobbler (WR).

21 January 2018

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Wobbler, a mutation affecting motoneuron survival and gonadal functions in the mouse, maps to proximal chromosome 11

21 January 2018

1 reference

Comparative transcription map of the wobbler critical region on mouse chromosome 11 and the homologous region on human chromosome 2p13-14.

21 January 2018

1 reference

Spinal muscular atrophy gene wobbler of the mouse: evidence from chimeric spinal cord and testis for cell-autonomous function.

21 January 2018

1 reference

Vps51p mediates the association of the GARP (Vps52/53/54) complex with the late Golgi t-SNARE Tlg1p

21 January 2018

1 reference

Identification, characterization and cytogenetic mapping of a yeast Vps54 homolog in rat and mouse.

21 January 2018

1 reference

Characterization of the human GARP (Golgi associated retrograde protein) complex

21 January 2018

1 reference

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome

21 January 2018

1 reference

Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles

21 January 2018

1 reference

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

21 January 2018

1 reference

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

21 January 2018

1 reference

Murine motor neuron disease (the wobbler mouse): degeneration and regeneration of the lower motor neuron.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/NG1661

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2 August 2017

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