(Q34700522)

4 August 2017

title

Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in mice (English)

1 reference

4 August 2017

Anna Kyunglim Park

1

1 reference

4 August 2017

Ryan P Liegel

2

1 reference

4 August 2017

Adam Ronchetti

3

1 reference

4 August 2017

Allison D Ebert

4

1 reference

4 August 2017

Aron Geurts

5

1 reference

4 August 2017

Duska J Sidjanin

6

1 reference

4 August 2017

publication date

5 December 2014

1 reference

4 August 2017

1 reference

4 August 2017

volume

15

1 reference

4 August 2017

page(s)

135

1 reference

Creative Commons Attribution 4.0 International

4 August 2017

copyright license

start time

1 December 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4266191/fullTextXML

inferred from PubMed Central ID database lookup

cites work

A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Hepatitis C virus infection activates an innate pathway involving IKK-α in lipogenesis and viral assembly

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Mutation spectrum in RAB3GAP1, RAB3GAP2, and RAB18 and genotype-phenotype correlations in warburg micro syndrome and Martsolf syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Loss-of-function mutations in RAB18 cause Warburg micro syndrome.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

A homozygous RAB3GAP2 mutation causes Warburg Micro syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Phenotypic variability in Micro syndrome: report of new cases.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

TBC1D20 is a Rab1 GTPase-activating protein that mediates hepatitis C virus replication

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Analysis of GTPase-activating proteins: Rab1 and Rab43 are key Rabs required to maintain a functional Golgi complex in human cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Rab3 GTPase-activating protein regulates synaptic transmission and plasticity through the inactivation of Rab3

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Micro syndrome in Muslim Pakistan children

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Use of peanut agglutinin to assess the acrosomal status and the zona pellucida-induced acrosome reaction in stallion spermatozoa

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Perinuclear cytoskeleton of acrosome-less spermatids in the blind sterile mutant mouse

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

MICRO syndrome: an entity distinct from COFS syndrome.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Congenital cataract, microphthalmia, hypoplasia of corpus callosum and hypogenitalism: report and review of Micro syndrome.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Characterization and expression of a stage specific antigen by monoclonal antibody TRA 54 in testicular germ cells

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4266191

Blind-sterile: a new mutation on chromosome 2 of the house mouse

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25476608

12 December 2020

inferred from PubMed ID database lookup

Failure of acrosome assembly in a male sterile mouse mutant

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25476608

12 December 2020

inferred from PubMed ID database lookup

Genetic localization of Hao-1, blind-sterile (bs), and Emv-13 on mouse chromosome 2

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25476608

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1186/PREACCEPT-1869361155145443

reason for deprecated rank

redirect

1 reference

10.1186/S12863-014-0135-2

4 August 2017

1 reference

SciGraph

https://scigraph.springernature.com/pub.10.1186/s12863-014-0135-2

Dimensions Publication ID

9 September 2019

1 reference

https://scigraph.springernature.com/pub.10.1186/s12863-014-0135-2

9 September 2019

1 reference

4 August 2017

1 reference