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9q22.1
A chromosome band present on 9q
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
NTRK2 wt Allele
SHC3 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2008
Review
2008
Genome-Wide Linkage Analysis of Lipids in the HyperGEN Study: An Investigation of the Effects of Lipid-Lowering Medications
A. Kraja
2008
Corpus ID: 51757577
The blood lipid levels are often distorted by the use of anti-hyperlipidemic medications. To investigate this medication effect…
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2004
2004
Frequent loss of heterozygosity on chromosome 9 in Chinese esophageal squamous cell carcinomas.
Yang Lichun
,
Cecilia Man Ching Tang
,
Kwok Wai Lau
,
M. Lung
Cancer Letters
2004
Corpus ID: 31204046
2004
2004
Functional investigation of tumor suppressive role of chromosome 9 in esophageal squamous cell carcinoma.
L. C. Yang
,
J. C. Tang
,
G. Srivastava
,
E. Stanbridge
,
M. Lung
Journal of Clinical Oncology
2004
Corpus ID: 6229356
9571 Background: Esophageal carcinoma (EC) is a very deadly disease, but its molecular basis for tumorigenesis is still largely…
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2000
2000
Assignment1 of human GADD45G to chromosome 9q22.1→q22.3 by radiation hybrid mapping
R. Gong
,
L. Yu
,
+5 authors
S. Zhao
Cytogenetic and Genome Research
2000
Corpus ID: 45495955
The growth arrest and DNA damage inducible (GADD) genes represent a family of genes that were identified on the basis of rapid…
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2000
2000
RNF20,a Human Novel RING Finger Protein Expressed High in the Testis Located in 9q22.1-22.3
Hai Wu
,
K. Ying
,
+5 authors
Sheng-dong Huang
2000
Corpus ID: 203860217
A novel RING finger gene was isolated from screening a human fetal brain cDNA library. In additional, two bipartite nuclear…
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2000
2000
A FAMILY WITH AUTOSOMAL DOMINANT MUTILATING NEUROPATHY NOT LINKED TO EITHER 3q13-q22 OR 9q22 LOCI
E. Bellone
,
E. Maria
,
+8 authors
P. Mandich
2000
Corpus ID: 71782541
The clinical separation of CMT2 from HSAN I may be difficult in some kindreds in which the sensory and motor symptoms and…
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Highly Cited
1999
Highly Cited
1999
Loss of heterozygosity at chromosome 9p21 (INK4-p14ARF locus): homozygous deletions and mutations in the p16 and p14ARF genes in sporadic primary melanomas.
R. Kumar
,
J. Smeds
,
B. Lundh Rozell
,
K. Hemminki
Melanoma research
1999
Corpus ID: 36246510
Loss of heterozygosity (LOH) was determined in 45 sporadic primary melanomas at six polymorphic microsatellite markers that flank…
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1998
1998
Involvement of 9q22.1–31.3 region in pyloric stenosis
P. Maraschio
,
E. Maserati
,
L. Seghezzi
,
R. Tupler
,
M. P. Verri
,
L. Tiepolo
Clinical Genetics
1998
Corpus ID: 26402957
To the Editor: A chromosome 9q22.1 -q3 1.3 direct duplication was found in a 40-year-old patient in a screening program for…
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1996
1996
Molecular anatomy of human chromosome 9: comparative mapping of the immunoglobulin processed pseudogene C epsilon 3 (IGHEP2) in primates.
H. Tanabe
,
T. Ishida
,
S. Ueda
,
T. Sofuni
,
H. Mizusawa
Cytogenetics and Cell Genetics
1996
Corpus ID: 20752877
Karyotypic homology in relation to human chromosome 9 (HSA 9) was studied through comparative mapping of the immunoglobulin…
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Review
1994
Review
1994
De novo interstitial deletions of 9q22.1-22.3 in two unrelated cases with different phenotype
A. Mohamed
,
E. Bawle
,
J. Conard
1994
Corpus ID: 80755708
Deletions involving the long arm of chromosome 9 are rare. A recent review, particularly with deletions of 9q22-32 region, failed…
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