(Q24681625)

22 June 2017

title

Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration. (English)

1 reference

22 June 2017

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1 reference

13

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22 June 2017

Mariz Vainzof

11

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Hans Lassmann

object named as

Hans Lassmann

8

0 references

Mayana Zatz

12

object named as

Mayana Zatz

1 reference

22 June 2017

Wolfgang M Schmidt

1

1 reference

22 June 2017

Cornelia Kraus

2

1 reference

22 June 2017

Harald Höger

3

1 reference

22 June 2017

Sonja Hochmeister

4

1 reference

22 June 2017

Felicitas Oberndorfer

5

1 reference

22 June 2017

Manuela Branka

6

1 reference

22 June 2017

Sonja Bingemann

7

1 reference

22 June 2017

Markus Müller

9

1 reference

22 June 2017

Lúcia Inês Macedo-Souza

10

1 reference

22 June 2017

Reginald E Bittner

14

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22 June 2017

language of work or name

English

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publication date

15 June 2007

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22 June 2017

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22 June 2017

volume

8

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22 June 2017

issue

7

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22 June 2017

page(s)

691-697

1 reference

describes a project that uses

22 June 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC1905899/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905899

Genome-wide atlas of gene expression in the adult mouse brain

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905899

Cex1p is a novel cytoplasmic component of the Saccharomyces cerevisiae nuclear tRNA export machinery

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905899

Identification and characterization of the human protein kinase-like gene NTKL: mitosis-specific centrosomal localization of an alternatively spliced isoform

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905899

Cloning and preliminary characterization of a 105 kDa protein with an N-terminal kinase-like domain

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1905899

The ataxia-ome: connecting disease proteins of the cerebellum.

28 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.EMBOR.7401001

Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.EMBOR.7401001

A new quantitative PCR multiplex assay for rapid analysis of chromosome 17p11.2-12 duplications and deletions leading to HMSN/HNPP.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FSJ.EMBOR.7401001

The mouse mutation muscle deficient (mdf) is characterized by a progressive motoneuron disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17571074

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A high-resolution genetic map of mouse chromosome 19 encompassing the muscle-deficient osteochondrodystrophy (mdf-ocd) region

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17571074

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/SJ.EMBOR.7401001

1 reference

22 June 2017

0 references

1 reference