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9q22.3
A chromosome band present on 9q
National Institutes of Health
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4 relations
Chromosomes
FANCC wt Allele
PTCH1 wt Allele
XPA wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies
S. Reichert
,
Kristin Zelley
,
K. Nichols
,
M. Eberhard
,
E. Zackai
,
J. Martinez-Poyer
American Journal of Medical Genetics. Part A
2015
Corpus ID: 24712488
9q22.3 microdeletion syndrome is a well‐described contiguous deletion syndrome with features of Gorlin syndrome and other…
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2011
2011
Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features
K. Izumi
,
A. Hahn
,
L. Christ
,
C. Curtis
,
D. Neilson
American Journal of Medical Genetics. Part A
2011
Corpus ID: 377150
Partial trisomy 9q involving the duplication of band 9q22 is manifested by a constellation of symptoms including short stature…
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2006
2006
Allelic loss at Drosophila patched gene is highly prevalent in Basal and squamous cell carcinomas of the skin.
H. Danaee
,
M. Karagas
,
K. Kelsey
,
A. Perry
,
H. Nelson
Journal of Investigative Dermatology
2006
Corpus ID: 2065546
The human homolog of the Drosophila Patched gene (PTCH), located at chromosome 9q22.3, is frequently altered in both nevoid basal…
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2004
2004
Accelerated Induction of Bladder Cancer in Patched Heterozygous Mutant Mice
S. Hamed
,
H. Larue
,
+4 authors
Y. Fradet
Cancer Research
2004
Corpus ID: 15309317
The PATCHED (PTC) gene is recognized as a tumor suppressor in basal cell carcinoma. Mapping of a minimal region of deletion at…
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1998
1998
Mutation analysis of the human homologue of drosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin
L. Eklund
,
E. Lindström
,
+5 authors
P. Söderkvist
Molecular Carcinogenesis
1998
Corpus ID: 37944465
The human homologue of Drosophila patched (PTCH), located at chromosome 9q22.3, was recently identified as a candidate tumor…
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1998
1998
Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and female-specific tissues and its chromosomal localization to 9q22.3.
J. Nishiu
,
T. Tanaka
,
Y. Nakamura
Genomics
1998
Corpus ID: 25615681
We isolated by the differential display technique a novel gene that was expressed abundantly in adipose and female-specific…
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1998
1998
Allelic Loss on Chromosome 9q Is Associated with Lymph Node Metastasis of Primary Breast Cancer
K. Minobe
,
M. Onda
,
+4 authors
M. Emi
Japanese journal of cancer research : Gann
1998
Corpus ID: 13708282
Frequent allelic losses on chromosome 9 are seen in a wide variety of human tumors; moreover, two genes (P16 and PTC) whose…
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1996
1996
cDNA cloning of a novel WD repeat protein mapping to the 9q22.3 chromosomal region.
P. Zaphiropoulos
,
R. Toftgård
DNA and Cell Biology
1996
Corpus ID: 32703549
To identify expressed sequences from the candidate genomic region of the nevoid basal cell carcinoma syndrome (9q22.3), the CpG…
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1996
1996
An EST and STS-based YAC contig map of human chromosome 9q22.3.
N. Lench
,
Elizabeth A.R. Telford
,
S. E. Andersen
,
T. Moynihan
,
Philip A. Robinson
,
A. F. Markham
Genomics
1996
Corpus ID: 30902881
We have isolated 48 yeast artificial chromosome (YAC) clones from a 4 cM/27 cR region of human chromosome 9q22.3 encompassed by…
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1995
1995
Fructose-1,6-bisphosphatase: genetic and physical mapping to human chromosome 9q22.3 and evaluation in non-insulin-dependent diabetes mellitus.
C. B. Rothschild
,
B. Freedman
,
+7 authors
S. Fajans
Genomics
1995
Corpus ID: 40991019
PCR primers specific to the human liver fructose-1,6-bisphosphatase (FBP) gene were designed and used to isolate a cosmid clone…
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