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19q13.1
A chromosome band present on 19q
National Institutes of Health
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Related topics
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15 relations
19q
AXL wt Allele
CEBPA wt Allele
CLC wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2010
Highly Cited
2010
Association studies on 11 published colorectal cancer risk loci
S. Holst
,
S. Picelli
,
+24 authors
A. Lindblom
British Journal of Cancer
2010
Corpus ID: 12716909
Background:Recently, several genome-wide association studies (GWAS) have independently found numerous loci at which common single…
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2003
2003
Cytogenetic study of malignant triton tumor: a case report.
M. Haddadin
,
A. Hawkins
,
+4 authors
C. Griffin
Cancer Genetics and Cytogenetics
2003
Corpus ID: 27873512
2003
2003
Genetic alterations of lung adenocarcinoma in relation to smoking and ethnicity.
S. Sy
,
N. Wong
,
+6 authors
A. Yim
Lung Cancer
2003
Corpus ID: 28289028
1999
1999
Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1 using historical recombinants in Libyan Jewish cystinuria patients.
E. Pras
,
Y. Kreiss
,
Y. Frishberg
,
L. Prosen
,
I. Aksentijevich
,
D. Kastner
Genomics
1999
Corpus ID: 42223
Cystinuria is a genetic disease manifested by the development of kidney stones. In some patients, the disease is caused by…
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1999
1999
Linkage of type II and type III cystinuria to 19q13.1: codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone-forming phenotype.
M. L. Stoller
,
J. Bruce
,
C. Bruce
,
T. Foroud
,
S. C. Kirkwood
,
P. Stambrook
American journal of medical genetics
1999
Corpus ID: 44296953
Cystinuria, a renal tubule disease affecting urinary cystine excretion with or without kidney stone formation, previously was…
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1998
1998
A severe clinical and pathological variant of central core disease with possible autosomal recessive inheritance
A. Manzur
,
C. Sewry
,
J. Ziprin
,
V. Dubowitz
,
F. Muntoni
Neuromuscular Disorders
1998
Corpus ID: 30660234
1996
1996
Cytogenetic analysis of a case of myxoid liposarcoma with cartilaginous differentiation.
T. Dijkhuizen
,
W. Molenaar
,
H. Hoekstra
,
J. Wiersema
,
E. van den Berg
Cancer Genetics and Cytogenetics
1996
Corpus ID: 2568784
1996
1996
Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.
A. Olsen
,
A. Georgescu
,
S. Johnson
,
A. Carrano
Genomics
1996
Corpus ID: 22561646
We describe the assembly of a 1-Mb cosmid contig and restriction map spanning the candidate region for Finnish congenital…
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1995
1995
Mapping of the gene for hormone sensitive lipase (LIPE) to chromosome 19q13.1-->q13.2.
R. Levitt
,
Z. Liu
,
N. Nouri
,
D. Meyers
,
B. Brandriff
,
H. Mohrenweiser
Cytogenetics and Cell Genetics
1995
Corpus ID: 3315316
Free fatty acids are the major source of fuel for mammals, and hormone sensitive lipase (LIPE) plays a critical role in lipid…
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1990
1990
Localization of the receptor gene for type D simian retroviruses on human chromosome 19
Maja A. Sommerfelt
,
Brenda P. Williams
,
Á. McKnight
,
P. Goodfellow
,
Robin A. Weiss
Journal of Virology
1990
Corpus ID: 23271081
Simian retrovirus (SRV) serotypes 1 to 5 are exogenous type D viruses causing immune suppression in macaque monkeys. These…
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