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5q34-q35
A chromosome band present on 5q
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
FLT4 wt Allele
chromosome 5q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Possible association between a haplotype of the GABA-A receptor alpha 1 subunit gene (GABRA1) and mood disorders
Y. Horiuchi
,
J. Nakayama
,
+8 authors
T. Arinami
Biological Psychiatry
2004
Corpus ID: 12192191
2004
2004
PRELI (protein of relevant evolutionary and lymphoid interest) is located within an evolutionarily conserved gene cluster on chromosome 5q34-q35 and encodes a novel mitochondrial protein.
E. J. Fox
,
Sally A Stubbs
,
Jimmy Kyaw Tun
,
J. Leek
,
A. Markham
,
S. Wright
The Biochemical journal
2004
Corpus ID: 36439822
The characterization of mitochondrial proteins is important for the understanding of both normal cellular function and…
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Highly Cited
2000
Highly Cited
2000
Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinase.
A. Irrthum
,
M. Karkkainen
,
K. Devriendt
,
K. Alitalo
,
M. Vikkula
American journal of human genetics
2000
Corpus ID: 37540124
Hereditary lymphedema is a chronic swelling of limbs due to dysfunction of lymphatic vessels. An autosomal dominant, congenital…
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2000
2000
Molecular genetic analysis of malignant ovarian germ cell tumors.
S. Faulkner
,
M. Friedlander
Gynecologic oncology
2000
Corpus ID: 27278064
OBJECTIVE Relatively little is known about the molecular mechanisms involved in the initiation and progression of ovarian germ…
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Highly Cited
1998
Highly Cited
1998
Hereditary lymphedema: evidence for linkage and genetic heterogeneity.
R. Ferrell
,
K. L. Levinson
,
+4 authors
D. Finegold
Human molecular genetics
1998
Corpus ID: 16767232
Hereditary or primary lymphedema is a developmental disorder of the lymphatic system which leads to a disabling and disfiguring…
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Highly Cited
1998
Highly Cited
1998
Phenotypic and genotypic heterogeneity in familial Milroy lymphedema.
M. Witte
,
R. Erickson
,
+5 authors
C. Witte
Lymphology
1998
Corpus ID: 40937863
Familial Milroy lymphedema (ML) is classified as an autosomal dominant disorder characterized by peripheral edema of the lower…
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Highly Cited
1996
Highly Cited
1996
Molecular Cloning, Chromosomal Mapping, and Characterization of the Human Cardiac-Specific Homeobox Gene hCsx
D. Turbay
,
S. B. Wechsler
,
K. Blanchard
,
S. Izumo
Molecular medicine
1996
Corpus ID: 16489338
BackgroundCsx/Nkx2.5, a murine nonclustered homeobox gene expressed primarily in the heart, has significant sequence similarity…
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1996
1996
Partial deletion of the long arm of chromosome 5: a fluorescence in situ hybridization study using band-specific painting probes generated by chromosome microdissection.
I. Tigaud
,
C. Charrin
,
R. Berger
,
P. Jonveaux
Cancer genetics and cytogenetics
1996
Corpus ID: 32574585
1995
1995
Mapping of the alpha 4 subunit gene (GABRA4) to human chromosome 4 defines an alpha 2-alpha 4-beta 1-gamma 1 gene cluster: further evidence that modern GABAA receptor gene clusters are derived from…
P. McLean
,
D. Farb
,
S. Russek
Genomics
1995
Corpus ID: 11024619
We demonstrated previously that an alpha 1-beta 2-gamma 2 gene cluster of the gamma-aminobutyric acid (GABAA) receptor is located…
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Highly Cited
1994
Highly Cited
1994
Mapping of the beta 2 subunit gene (GABRB2) to microdissected human chromosome 5q34-q35 defines a gene cluster for the most abundant GABAA receptor isoform.
S. Russek
,
D. Farb
Genomics
1994
Corpus ID: 2414726
The gamma-aminobutyric acid receptor (GABAAR) is a multisubunit Cl- channel that mediates most fast inhibitory synaptic…
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