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PTCH2 gene
Known as:
Patched 2 Gene
, PATCHED, DROSOPHILA, HOMOLOG OF, 2
, patched 2
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This gene plays a role in intercellular communication, embryonic structure development, and in tumorigenesis.
National Institutes of Health
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Related topics
Related topics
8 relations
Basal cell carcinoma
Desmoplastic Medulloblastoma
Intercellular Communication Process
Ligand Binding
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PTCH2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Germline mutation PTCH2 1172-1173delCT in Chinese population with early-onset breast cancer.
Lixi Li
,
Chun-xiao Li
,
+9 authors
Bing-he Xu
Journal of Clinical Oncology
2019
Corpus ID: 190910697
e13049 Background: Early-onset breast cancer has more aggressive clinicopathological characteristics and worse prognosis. The…
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2019
2019
Hedgehog signalling network gene status analysis in paediatric intracranial germ cell tumours.
Dominika Kuleszo
,
B. Lipska-Ziętkiewicz
,
+7 authors
E. Iżycka-Świeszewska
Folia Neuropathologica
2019
Corpus ID: 203849284
INTRODUCTION Germ cell tumours (GCTs) in the children comprise a group of tumours that originate from primordial germ cells but…
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2018
2018
Interaction of the primordial germ cell-specific protein C2EIP with PTCH2 directs differentiation of embryonic stem cells via HH signaling activation
Qisheng Zuo
,
K. Jin
,
Jiuzhou Z. Song
,
Yani Zhang
,
Guohong Chen
,
Bichun Li
Cell Death and Disease
2018
Corpus ID: 256600761
Although many marker genes for germ cell differentiation have been identified, genes that specifically regulate primordial germ…
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2017
2017
Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype
Shoko Onodera
,
A. Saito
,
+7 authors
T. Azuma
PLoS ONE
2017
Corpus ID: 6341331
Gorlin syndrome is a genetic disorder of autosomal dominant inheritance that predisposes the affected individual to a variety of…
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2017
2017
Congenital embryonal rhabdomyosarcoma caused by heterozygous concomitant PTCH1 and PTCH2 germline mutations
Julia Taeubner
,
T. Brozou
,
+8 authors
M. Kuhlen
European Journal of Human Genetics
2017
Corpus ID: 256612078
The sonic hedgehog (SHH) signaling pathway has been shown to play important roles in embryogenesis, cell proliferation as well as…
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2011
2011
PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas
D. C. Santos
,
P. Zaphiropoulos
,
C. F. Neto
,
E. Pimentel
,
J. Sanches
,
I. R. Ruiz
International Journal of Dermatology
2011
Corpus ID: 25154633
Background Basal cell carcinomas (BCCs) are the most frequent human cancer that results from malignant transformation of basal…
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Review
2011
Review
2011
PTCH2 (patched homolog 2 (Drosophila))
P. Zaphiropoulos
2011
Corpus ID: 9773160
Review on PTCH2 (patched homolog 2 (Drosophila)), with data on DNA, on the protein encoded, and where the gene is implicated.
2009
2009
A Susceptibility Locus on 1 p 32 – 1 p 34 for Congenital Macrostomia in a Chinese Family and Identification of a Novel PTCH 2 Mutation
Zhipeng Fan
,
Juan Du
,
+6 authors
Songlin Wang
2009
Corpus ID: 42923045
A Susceptibility Locus on 1p32–1p34 for Congenital Macrostomia in a Chinese Family and Identification of a Novel PTCH2 Mutation…
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2009
2009
[Studies on keratocystic odontogenic tumors].
Tie‐Jun Li
,
Li-Sha Sun
,
+5 authors
Li-li Xu
Beijing da xue xue bao. Yi xue ban = Journal of…
2009
Corpus ID: 24832233
Keratocystic odontogenic tumors (KCOTs, previously known as odontogenic keratocysts) are aggressive, noninflammatory jaw lesions…
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2000
2000
Patched 2, located in 1p32-34, is not mutated in high stage neuroblastoma tumors.
A. Jögi
,
F. Abel
,
+5 authors
H. Axelson
International Journal of Oncology
2000
Corpus ID: 22975075
Neuroblastoma is a childhood malignancy originating from cells of the sympathetic nervous system, exhibiting a marked diversity…
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