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19q13.2-q13.3
A chromosome band present on 19q
National Institutes of Health
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Related topics
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3 relations
19q
Chromosomes
ERCC1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
Co-expression of ERCC 1 and Snail is a prognostic but not predictive factor of cisplatin-based neoadjuvant chemotherapy for bladder cancer
A. Kawashima
,
H. Takayama
,
+12 authors
A. Tsujimura
2012
Corpus ID: 145024900
Neoadjuvant chemotherapy (NC) for bladder cancer has been reported to significantly improve the 5-year survival rate. The aim of…
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2002
2002
3-Methylglutaconic aciduria type III in a non-Iraqi-Jewish kindred: clinical and molecular findings.
R. Kleta
,
F. Skovby
,
E. Christensen
,
T. Rosenberg
,
W. Gahl
,
Y. Anikster
Molecular Genetics and Metabolism
2002
Corpus ID: 44840792
2002
2002
Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study
K. Reunanen
,
S. Finnilä
,
+10 authors
P. Tienari
Journal of Neuroimmunology
2002
Corpus ID: 1559539
1996
1996
Cloning of the VASP (vasodilator-stimulated phosphoprotein) genes in human and mouse: structure, sequence, and chromosomal localization.
M. Zimmer
,
T. Fink
,
+4 authors
U. Walter
Genomics
1996
Corpus ID: 11693748
The genes encoding the vasodilator-stimulated phosphoprotein (VASP) in human and mouse were isolated, and major parts were…
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1995
1995
Assignment of the gastric inhibitory polypeptide receptor gene (GIPR) to chromosome bands 19q13.2-q13.3 by fluorescence in situ hybridization.
M. Stoffel
,
A. Fernald
,
M. L. Le Beau
,
G. Bell
Genomics
1995
Corpus ID: 35713686
The gastric inhibitory polypeptide receptor gene (GIPR) was localized, using fluorescence in situ hybridization (FISH), to human…
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Highly Cited
1992
Highly Cited
1992
Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.
W. Flejter
,
W. Flejter
,
L. McDaniel
,
D. Johns
,
E. Friedberg
,
R. Schultz
Proceedings of the National Academy of Sciences…
1992
Corpus ID: 10802879
Cultured cells from individuals afflicted with the genetically heterogeneous autosomal recessive disorder xeroderma pigmentosum…
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Review
1992
Review
1992
cDNA surveying of specific tissue expression of human chromosome 19 sequences.
P. W. Dunne
,
S. W. Wang
,
T. Ashizawa
,
M. Perryman
,
H. F. Epstein
Genomics
1992
Corpus ID: 44676026
1992
1992
Characterization of a complex chromosomal rearrangement maps the locus for In vitro complementation of xeroderma pigmentosum group D to human chromosome band 19q 13
W. Flejter
,
L. McDaniel
,
M. Askari
,
E. Friedberg
,
R. Schultz
Genes, Chromosomes and Cancer
1992
Corpus ID: 25412673
Microcell‐mediated chromosome transfer (MMCT) is a powerful genetic technique that permits the transfer of a single chromosome…
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Review
1991
Review
1991
VII International Congress on Neuromuscular Diseases Munich, Germany 16–22 September, 1990
A. Ceballos-Baumann
,
Linda Castell
Journal of Muscle Research and Cell Motility
1991
Corpus ID: 31335931
s were published as a supplement fo Vol. 98 of the Journal of the Neurological Sciences. A total of 2143 people ffom 52 countries…
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1988
1988
NcoI RFLP at the creatine kinase-muscle type gene locus (CKMM, chromosome 19).
M. Coerwinkel-Driessen
,
J. Schepens
,
P. V. van Zandvoort
,
B. V. van Oost
,
E. Mariman
,
B. Wieringa
Nucleic Acids Research
1988
Corpus ID: 8954299
A 3.2 kbp human genomic DNA fragment (BamHI-Sau3A) of the 3{prime} untranslated and 3{prime} flanking region of the CKMM gene was…
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