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9p23
A chromosome band present on 9p
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosome 9 Short Arm
Chromosomes
TYRP1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Characterization of gene rearrangements resulted from genomic structural aberrations in human esophageal squamous cell carcinoma KYSE150 cells.
J. Hao
,
Ting Gong
,
+6 authors
Ming-Rong Wang
Gene
2013
Corpus ID: 13265985
2011
2011
D9S168 microsatellite alteration predicts a poor prognosis in patients with clear cell renal cell carcinoma and correlates with the down‐regulation of protein tyrosine phosphatase receptor delta
Xiaopan Li
,
X. Tan
,
+6 authors
G. Cao
Cancer
2011
Corpus ID: 36849602
The role of microsatellite alterations in surgically excised tumors in predicting the prognosis of patients with clear cell renal…
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2011
2011
Complex chromosome rearrangement 46,XY, der(9)t(Y;9)(q12;p23) in a girl with sex reversal and mental retardation.
I-Wen Lee
,
Yen-Yin Chou
,
+4 authors
Shio‐Jean Lin
Urology
2011
Corpus ID: 19742508
2006
2006
Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 → pter and partial trisomy 1q41 → qter suggests neo‐telomere formation in stabilizing the deleted chromosome
L. Kulikowski
,
L. Christ
,
S. I. Nogueira
,
D. Brunoni
,
S. Schwartz
,
M. I. Melaragno
American Journal of Medical Genetics. Part A
2006
Corpus ID: 24979232
We report on a clinical and molecular cytogenetic study of a patient who presents a complex chromosomal rearrangement with two…
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Review
2005
Review
2005
Chromosomal Abnormalities and Glaucoma: A Case of Congenital Glaucoma with Trisomy 8q22-Qter/ Monosomy 9p23-Pter
A. Cohn
,
L. Kearns
,
R. Savarirayan
,
Jacinta Ryan
,
J. Craig
,
D. Mackey
Ophthalmic Genetics
2005
Corpus ID: 36831915
Purpose: To present a case of congenital glaucoma with an unbalanced translocation trisomy 8q22-qter/monosomy 9p23-pter…
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2001
2001
Constitutional genomic instability with inversions, duplications, and amplifications in 9p23-24 in BRCA2 mutation carriers.
L. Savelyeva
,
A. Claas
,
+5 authors
M. Schwab
Cancer Research
2001
Corpus ID: 25246736
Germ-line mutations of the BRCA2 gene (13q12-13) account for a large proportion of familial breast cancer cases in females and…
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2000
2000
Sensitivity and limitations of high throughput fluorescent microsatellite analysis for the detection of allelic imbalance: application in lung tumors.
T. Liloglou
,
P. Maloney
,
G. Xinarianos
,
S. Fear
,
J. Field
International Journal of Oncology
2000
Corpus ID: 6445558
We have used two hexaplex fluorescent microsatellite assays and analysis on an automatic sequencer to determine allelic imbalance…
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1998
1998
An interstitial tandem duplication of 9p23-24 coexists with a mutation in the BRCA2 gene in the germ line of three brothers with breast cancer.
L. Savelyeva
,
A. Claas
,
+5 authors
M. Schwab
Cancer Research
1998
Corpus ID: 23832647
Germ-line mutations of the BRCA2 gene account for the majority of families with both male and female breast cancer. However…
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1994
1994
Assignment of the true and processed genes for human glycine decarboxylase to 9p23-24 and 4q12.
M. Isobe
,
H. Koyata
,
T. Sakakibara
,
K. Momoi-Isobe
,
K. Hiraga
Biochemical and Biophysical Research…
1994
Corpus ID: 46047467
Southern analysis using a human glycine decarboxylase cDNA probe and genomic DNA preparations from Chinese hamster-human…
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1994
1994
DNA amplifications on chromosomes 7, 9 and 12 in glioblastoma detected by reverse chromosome painting.
U. Fischer
,
Bernd Wullich
,
H. Sattler
,
E. Göttert
,
K. Zang
,
E. Meese
European Journal of Cancer
1994
Corpus ID: 12268609
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