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CERKL gene
Known as:
CERKL
, CERAMIDE KINASE-LIKE
, ceramide kinase like
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This gene plays a role in apoptosis.
National Institutes of Health
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Related topics
Related topics
3 relations
Apoptosis
Ceramide Kinase-like Protein
Negative Regulation of Apoptosis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Novel CERKL variant in consanguineous Jordanian pedigrees with inherited retinal dystrophies.
B. Azab
,
Raghda Barham
,
+10 authors
A. Awidi
Canadian Journal of Ophthalmology-journal…
2019
Corpus ID: 73726904
2017
2017
CERKL isoforms are differentially expressed in retinal cells
R. Gonzàlez-Duarte
,
R. Andrés
,
+5 authors
G. Marfany
2017
Corpus ID: 90343312
2016
2016
Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry
A. Cassidy
,
S. Brugnatelli
,
C. Ayuso
,
A. Avila-Fernandez
,
D. Zeller
,
D. Lester
2016
Corpus ID: 90580722
2016
2016
A novel homozygous c.1154+3_1151+6delAAGT mutation in CERKL causes autosomal recessive retinitis pigmentosa with a special phenotype in a consanguineous Tunisian Family
L. Matri
,
Y. Falfoul
,
+4 authors
A. Chebil
2016
Corpus ID: 78832391
2015
2015
Clinical aspects of Autosomic Recessive Retinitis Pigmentosa Caused by USH2A Mutations in Consanguineous Tunisian Families
A. Chebil
,
L. Largueche
,
+4 authors
L. Matri
2015
Corpus ID: 74643709
Purpose To assess the clinical phenotype in consanguineous Tunisian families with non syndromic autosomic recessive retinitis…
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2010
2010
Effects of fibroblastic and endothelial extracellular matrices on corneal endothelial cells.
P. Hsieh
,
J. Baum
Investigative Ophthalmology and Visual Science
2010
Corpus ID: 44342958
Extracellular matrices (ECM) isolated from chick embryo fibroblast and human and rabbit corneal stromal cells induce polarization…
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2009
2009
CERKL Mutations Cause Retina-Wide Cone and Rod Disease With Prominent Maculopathy
T. Aleman
,
A. Cideciyan
,
+7 authors
S. Jacobson
2009
Corpus ID: 83440717
2008
2008
CERKL mutations and associated phenotypes in seven Spanish families with autosomal recessive retinitis pigmentosa.
A. Avila-Fernandez
,
R. Riveiro-Alvarez
,
+7 authors
C. Ayuso
Investigative Ophthalmology and Visual Science
2008
Corpus ID: 7602381
PURPOSE Retinitis pigmentosa (RP) is a genetically heterogeneous group of inherited retinopathies. Up to now, 39 genes and loci…
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2008
2008
A missense mutation (p.R106S) in the nuclear localization signal sequence of CERKL causes autosomal recessive retinal degeneration
Manir Ali
,
V. Ramprasad
,
+7 authors
C. Inglehearn
2008
Corpus ID: 82326396
2008
2008
Molecular modelling: a tool for understanding the cytoplasm–nucleus–nucleolus shuttling of the ceramide kinase-like protein
Leila Ayadi
,
I. Ben-Rebeh
,
H. Ayadi
,
S. Masmoudi
2008
Corpus ID: 56224729
Ceramide kinase like (CERKL) is a protein implicated in the pathology of retinitis pigmentosa. In this study, the 3D predicted…
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