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CTSK wt Allele

Known as: CTSO1, CTS02, CTSO2 
Human CTSK wild-type allele is located in the vicinity of 1q21 and is approximately 12 kb in length. This allele, which encodes cathepsin K protein… 
National Institutes of Health

Related topics

Related topics

5 relations
1q21Bone remodelingHydrolysisProteolysis

Papers overview

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2019
2019
Paroxismal non-kinesigenic dyskinesia and hemidystonia associated with silent celiac disease
Review
2018
Review
2018
ZNF423: A New Player in Estrogen Receptor-Positive Breast Cancer
Preventive therapy can target hormone-responsive breast cancer (BC) by treatment with selective estrogen receptor modulators… 
2016
2016
Relationship of ZNF423 and CTSO with breast cancer risk in two randomised tamoxifen prevention trials
A case–control study from two randomised breast cancer prevention trials of tamoxifen and raloxifene (P-1 and P-2) identified… 
2015
2015
Abstract P5-05-02: Prognostic impact of single-nucleotide polymorphisms (SNPs) in or near the ZNF423 and CTSO genes in estrogen receptor (ER)-positive breast cancer patients receiving adjuvant…
Background : Selective estrogen receptor modulators (SERMs) can reduce the occurrence of breast cancer in high-risk women by 50… 
2013
2013
Vaccination with Recombinant Mycobacterium tuberculosis PknD Attenuates Bacterial Dissemination to the Brain in Guinea Pigs
Background We have previously identified Mycobacterium tuberculosis PknD to be an important virulence factor required for the… 
2003
2003
Picnodisostose: relato de dois casos
Pycnodysostosis (PYCD) is a rare autosomal recessive skeletal dysplasia, due to a defect in the gene encoding cathepsin K, and… 
1998
1998
Cloning and characterisation of the pknD gene encoding an eukaryotic-type protein kinase in the cyanobacterium Anabaena sp. PCC7120
Abstract Protein phosphorylation catalysed by protein kinases is an important mechanism for signal transduction in both… 
Review
1998
Review
1998
Pycnodysostosis: orofacial manifestations in two pediatric patients.
p ycnodysostosis (PKND) is a rare autosomal recessive skeletal abnormality acknowledged as a distinct entity by Maroteux and Lamy… 
1998
1998
Genomic structure and chromosomal localization of the human cathepsin O gene (CTSO).
The human gene encoding cathepsin O, a cysteine proteinase from the papain superfamily, has been cloned and its overall… 
1996
1996
Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genes
Abstract Pycnodysostosis (PKND) is a rare, autosomal recessive skeletal dysplasia, which has been mapped previously to a 4-cM… 
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