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11q13.1
A chromosome band present on 11q
National Institutes of Health
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Related topics
Related topics
13 relations
BAD wt Allele
C11orf20 wt Allele
CHKA wt Allele
Chromosomes
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Generation of two MEN1 knockout lines from a human embryonic stem cell line.
Yanli Liu
,
Aynisahan Ruzi
,
+10 authors
Yin-xiong Li
Stem Cell Research
2017
Corpus ID: 22714510
2015
2015
Deletion of 11q12.3-11q13.1 in a patient with intellectual disability and childhood facial features resembling Cornelia de Lange syndrome.
M. I. Boyle
,
C. Jespersgaard
,
+4 authors
Z. Tümer
Gene
2015
Corpus ID: 27962232
Review
2014
Review
2014
An Introduction of Genetics in Otosclerosis
Arnold J. N. Bittermann
,
I. Wegner
,
Bo Jan Noordman
,
R. Vincent
,
G. J. van der Heijden
,
W. Grolman
Otolaryngology Head & Neck Surgery
2014
Corpus ID: 5478575
Objective To present an easy to read systematic review concerning the genetic etiology of otosclerosis to help health care…
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Review
2011
Review
2011
CST6 (cystatin E/M)
D. Keppler
2011
Corpus ID: 86088839
Review on CST6 (cystatin E/M), with data on DNA, on the protein encoded, and where the gene is implicated.
2010
2010
Paraganglioma in a 13-year-old girl: a novel SDHB gene mutation in the family?
Z. Musil
,
A. Puchmajerová
,
+7 authors
M. Kohoutová
Cancer Genetics and Cytogenetics
2010
Corpus ID: 27441888
Review
2007
Review
2007
Molecular characterization of the renal organic anion transporter 1
G. Burckhardt
,
N. Wolff
,
A. Bahn
Cell Biochemistry and Biophysics
2007
Corpus ID: 22064119
Organic anions of diverse chemical structures are secreted in renal proximal tubules. The first step in secretion, uptake of…
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2003
2003
11q13 Alterations in two cases of hibernoma: Large heterozygous deletions and rearrangement breakpoints near GARP in 11q13.5
G. Maire
,
A. Forus
,
+5 authors
F. Pedeutour
Genes, Chromosomes and Cancer
2003
Corpus ID: 13606852
Hibernomas are rare, benign tumors with a histological appearance resembling that of brown adipose tissue. The diagnosis of…
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2003
2003
Isolated familial somatotropinomas: clinical and genetic considerations.
L. Frohman
Transactions of the American Clinical and…
2003
Corpus ID: 37396277
The majority of somatotropinomas (GH-secreting pituitary adenomas) are sporadic, through a few occur with a familial aggregation…
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1997
1997
Fine mapping of the MLK-3 gene within 11q13 and its exclusion as the MEN1 susceptibility gene
N. Lassam
,
Zheng Lin
,
+4 authors
C. Larsson
Human Genetics
1997
Corpus ID: 37807539
Abstract MLK-3 kinase is a widely expressed serine/ threonine kinase that bears multiple protein interaction domains and…
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1992
1992
De novo complex chromosome rearrangement in identical twins with multiple congenital anomalies
Y. Wakita
,
K. Narahara
,
+5 authors
Y. Seino
Human Genetics
1992
Corpus ID: 32839479
SummaryA de novo and apparently balanced complex chromosome rearrangement (CCR) was found in monozygotic (MZ) twin infants with…
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