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Soluble Calcium-Activated Nucleotidase 1
Known as:
CANT1
, Apyrase Homolog
, SCAN-1
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Soluble calcium-activated nucleotidase 1 (401 aa, ~45 kDa) is encoded by the human CANT1 gene. This protein plays a role in nucleotide hydrolysis.
National Institutes of Health
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Related topics
Related topics
9 relations
CANT1 gene
CANT1 wt Allele
Enzyme Gene
Hydrolysis
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
LncRNA CANT1 suppresses retinoblastoma progression by repellinghistone methyltransferase in PI3Kγ promoter
Hongyan Ni
,
P. Chai
,
+7 authors
Xianqun Fan
Cell Death and Disease
2020
Corpus ID: 218484182
Retinoblastoma (RB) is the most common malignant intraocular tumor of childhood. Recent studies have shown that long noncoding…
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2019
2019
Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification
Chiara Paganini
,
Luca Monti
,
+11 authors
A. Rossi
Matrix Biology
2019
Corpus ID: 53566358
2017
2017
MED resulting from recessively inherited mutations in the gene encoding calcium‐activated nucleotidase CANT1
K. Balasubramanian
,
Bing Li
,
+8 authors
D. Cohn
American Journal of Medical Genetics. Part A
2017
Corpus ID: 38651547
Multiple Epiphyseal Dysplasia (MED) is a relatively mild skeletal dysplasia characterized by mild short stature, joint pain, and…
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2015
2015
A novel CANT1 mutation in three Indian patients with Desbuquois dysplasia Kim type.
Ankur Singh
,
O. Kim
,
A. Iida
,
W. Park
,
S. Ikegawa
,
S. Kapoor
European Journal of Medical Genetics
2015
Corpus ID: 37033875
Highly Cited
2014
Highly Cited
2014
XYLT1 mutations in Desbuquois dysplasia type 2.
C. Bui
,
C. Huber
,
+7 authors
V. Cormier-Daire
American Journal of Human Genetics
2014
Corpus ID: 44344000
2012
2012
Further Delineation of CANT1 Phenotypic Spectrum and Demonstration of Its Role in Proteoglycan Synthesis
M. Nizon
,
C. Huber
,
+27 authors
V. Cormier-Daire
Human Mutation
2012
Corpus ID: 1256773
Desbuquois dysplasia (DD) is characterized by antenatal and postnatal short stature, multiple dislocations, and advanced carpal…
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2012
2012
IMPAD1 mutations in two Catel‐Manzke like patients
M. Nizon
,
Y. Alanay
,
+6 authors
Prof. Valérie Cormier‐Daire
American Journal of Medical Genetics. Part A
2012
Corpus ID: 32435552
Catel–Manzke syndrome is characterized by hyperphalangism with bilateral deviation of the index fingers and micrognathia with or…
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2011
2011
A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
J. Dai
,
O. Kim
,
+14 authors
S. Ikegawa
Journal of Human Genetics
2011
Corpus ID: 205165577
Desbuquois dysplasia (DBQD) is a severe skeletal dysplasia of autosomal recessive inheritance. DBQD is classified into types 1…
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2010
2010
CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant
T. Furuichi
,
J. Dai
,
+13 authors
S. Ikegawa
Journal of Medical Genetics
2010
Corpus ID: 19572116
Background Desbuquois dysplasia (DD) is a recessively inherited condition characterised by short stature, generalised skeletal…
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2006
2006
Xenopus apyrase (xapy), a secreted nucleotidase that is expressed during early development.
C. Devader
,
R. Webb
,
G. Thomas
,
L. Dale
Gene
2006
Corpus ID: 9148379
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