(Q41923113)

14 October 2017

CIT, a gene involved in neurogenic cytokinesis, is mutated in human primary microcephaly (English)

1 reference

14 October 2017

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

author name string

Khalid M Al-Harbi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Sabri A M Alhijji

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Alia M Albalawi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Essa Alharby

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Amr Eldardear

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

Mohammed I Samman

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

publication date

12 August 2016

1 reference

14 October 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

volume

135

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

issue

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

12 June 2020

page(s)

1199-1207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27519304%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-016-1724-0

12 June 2020

exact match

0 references

cites work

Citron kinase is required for postnatal neurogenesis in the hippocampus

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Citron kinase controls a molecular network required for midbody formation in cytokinesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

ASPM is a major determinant of cerebral cortical size

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Interactive visual analysis of SNP data for rapid autozygosity mapping in consanguineous families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Citron rho-interacting kinase, a novel tissue-specific ser/thr kinase encompassing the Rho-Rac-binding protein Citron

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Defective neurogenesis in citron kinase knockout mice by altered cytokinesis and massive apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Molecular genetics of human primary microcephaly: an overview.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Kinetochore KMN network gene CASC5 mutated in primary microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

KIF14 and citron kinase act together to promote efficient cytokinesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Splice site prediction in Arabidopsis thaliana pre-mRNA by combining local and global sequence information

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

easyLINKAGE-Plus--automated linkage analyses using large-scale SNP data

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Identification of microcephalin, a protein implicated in determining the size of the human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

In silico prediction of splice-altering single nucleotide variants in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Many roads lead to primary autosomal recessive microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Dissecting the role of Rho-mediated signaling in contractile ring formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

STIL on my small brain: a new gene for microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Spliceman--a computational web server that predicts sequence variations in pre-mRNA splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Mutations in CENPE define a novel kinetochore-centromeric mechanism for microcephalic primordial dwarfism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Deletion of the citron kinase gene selectively affects the number and distribution of interneurons in barrelfield cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

WDR62 is associated with the spindle pole and is mutated in human microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

ASPM and citron kinase co-localize to the midbody ring during cytokinesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Improved splice site detection in Genie

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

HomozygosityMapper--an interactive approach to homozygosity mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Tissue-specific control of midbody microtubule stability by Citron kinase through modulation of TUBB3 phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

A primary microcephaly protein complex forms a ring around parental centrioles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Chelerythrine perturbs lamellar actomyosin filaments by selective inhibition of myotonic dystrophy kinase-related Cdc42-binding kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Characterization and prediction of alternative splice sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Maximum entropy modeling of short sequence motifs with applications to RNA splicing signals.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Microcephalin encodes a centrosomal protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-016-1724-0

Citron-kinase, a protein essential to cytokinesis in neuronal progenitors, is deleted in the flathead mutant rat.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27519304