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5q35.1
A chromosome band present on 5q
National Institutes of Health
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Related topics
Related topics
7 relations
Chromosomes
DRD1 wt Allele
MIR218-2 wt Allele
PTTG1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature.
A. Zrhidri
,
I. Jaouad
,
+5 authors
A. Sefiani
Gene
2017
Corpus ID: 25641293
Highly Cited
2013
Highly Cited
2013
Down-regulation of miR-218-2 and its host gene SLIT3 cooperate to promote invasion and progression of thyroid cancer.
H. Guan
,
G. Wei
,
+5 authors
Yanbing Li
Journal of Clinical Endocrinology and Metabolism
2013
Corpus ID: 207087287
CONTEXT The functional relationships between intronic microRNAs (miRNAs) and their host genes in thyroid cancer remain unclear…
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Highly Cited
2010
Highly Cited
2010
Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.
Z. Iqbal
,
P. Cejudo-Martı́n
,
+19 authors
H. van Bokhoven
American Journal of Human Genetics
2010
Corpus ID: 1028570
Highly Cited
2010
Highly Cited
2010
Duplication of the SLIT3 Locus on 5q35.1 Predisposes to Major Depressive Disorder
J. Glessner
,
Kai Wang
,
+10 authors
H. Hakonarson
PLoS ONE
2010
Corpus ID: 16716594
Major depressive disorder (MDD) is a common psychiatric and behavioral disorder. To discover novel variants conferring risk to…
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2006
2006
Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1
D. Koolen
,
J. Herbergs
,
+7 authors
B. Vries
Journal of Human Genetics
2006
Corpus ID: 22501547
AbstractHoloprosencephaly (HPE) is the most common developmental defect affecting the forebrain and midface in humans. The…
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Highly Cited
2003
Highly Cited
2003
The cardiac homeobox gene NKX2-5 is deregulated by juxtaposition with BCL11B in pediatric T-ALL cell lines via a novel t(5;14)(q35.1;q32.2).
S. Nagel
,
M. Kaufmann
,
H. Drexler
,
R. MacLeod
Cancer Research
2003
Corpus ID: 2268494
A cryptic chromosome rearrangement, t(5;14)(q35.1;q32.2), recently identified in pediatric acute lymphoblastic leukemia (ALL…
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1992
1992
Exclusion of close linkage of bipolar disorder to dopamine D1 and D2 receptor gene markers.
P. Mitchell
,
L. Selbie
,
+4 authors
J. Shine
Journal of Affective Disorders
1992
Corpus ID: 3783113
Highly Cited
1990
Highly Cited
1990
A human D1 dopamine receptor gene is located on chromosome 5 at q35.1 and identifies an EcoRI RFLP.
D. Grandy
,
Q. Zhou
,
+4 authors
M. Litt
American Journal of Human Genetics
1990
Corpus ID: 24486374
Dopaminergic neurons have been shown to affect voluntary movement, hormone secretion, and emotional tone. Mediating these…
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Highly Cited
1988
Highly Cited
1988
A Ki-1 (CD30)-positive human cell line (Karpas 299) established from a high-grade non-Hodgkin's lymphoma, showing a 2;5 translocation and rearrangement of the T-cell receptor beta-chain gene
P. Fischer
,
E. Nacheva
,
+4 authors
A. Karpas
1988
Corpus ID: 222252212
We describe the characterization of a new human cell line, Karpas 299 (K299), established from blast cells in the peripheral…
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Highly Cited
1988
Highly Cited
1988
A Ki-1 (CD30)-positive human cell line (Karpas 299) established from a high-grade non-Hodgkin's lymphoma, showing a 2;5 translocation and rearrangement of the T-cell receptor beta-chain gene.
P. Fischer
,
E. Nacheva
,
+4 authors
A. Karpas
Blood
1988
Corpus ID: 1973901
We describe the characterization of a new human cell line, Karpas 299 (K299), established from blast cells in the peripheral…
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