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10q23-q24
A chromosome band present on 10q
National Institutes of Health
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Related topics
Related topics
5 relations
10q
CYP26A1 wt Allele
Chromosomes
DNTT 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
Mutations in HPSE2 cause urofacial syndrome.
S. Daly
,
J. Urquhart
,
+18 authors
W. Newman
American journal of human genetics
2010
Corpus ID: 25847199
Urinary voiding dysfunction in childhood, manifesting as incontinence, dysuria, and urinary frequency, is a common condition…
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Review
2003
Review
2003
Can a congenital dysfunctional bladder be diagnosed from a smile? The Ochoa syndrome updated
B. Ochoa
Pediatric Nephrology
2003
Corpus ID: 24698524
During the last 40 years over 100 patients have been reported with a dysfunctional lower urinary tract associated with a peculiar…
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Highly Cited
2002
Highly Cited
2002
Polymorphisms of insulin degrading enzyme gene are not associated with Alzheimer's disease
Mekki Boussaha
,
D. Hannequin
,
P. Verpillat
,
A. Brice
,
D. Campion
Neuroscience Letters
2002
Corpus ID: 25775809
To date, allele 4 of the apolipoprotein E gene is the only risk factor that has been robustly associated with Alzheimer's disease…
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Highly Cited
2001
Highly Cited
2001
Molecular Cloning and Characterization of a Novel Mammalian Endo-apyrase (LALP1)*
J. Shi
,
T. Kukar
,
+8 authors
J. X. She
The Journal of Biological Chemistry
2001
Corpus ID: 24301471
Here we describe the cloning, localization, and characterization of a novel mammalian endo-apyrase (LALP1) in human and mouse…
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Highly Cited
2000
Highly Cited
2000
Chromosomal Imbalances in Brain Metastases of Solid Tumors
I. Petersen
,
Alfredo Hidalgo
,
+9 authors
A. Deimling
Brain pathology
2000
Corpus ID: 21284041
Metastases account for approximately 50% of the malignant tumors in the brain. In order to identify structural alterations that…
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1999
1999
Construction of a physical and transcript map for a 1-Mb genomic region containing the urofacial (Ochoa) syndrome gene on 10q23-q24 and localization of the disease gene within two overlapping BAC…
C. Wang
,
J. Shi
,
+5 authors
J. X. She
Genomics
1999
Corpus ID: 36638651
Urofacial (Ochoa) syndrome is an autosomal recessive disease characterized by distorted facial expression and urinary…
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Highly Cited
1997
Highly Cited
1997
Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.
R. Yee
,
L. Sullivan
,
+5 authors
S. Daiger
Genomics
1997
Corpus ID: 22717979
Corneal dystrophy of the anterior basement membrane is a heterogeneous set of diseases characterized by painful, recurrent…
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1997
1997
Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24.
C. Wang
,
B. Hawkins-Lee
,
B. Ochoa
,
R. D. Walker
,
J. X. She
American journal of human genetics
1997
Corpus ID: 24495049
The urofacial (Ochoa) syndrome (UFS) is a rare autosomal recessive disease characterized by congenital obstructive uropathy and…
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Highly Cited
1989
Highly Cited
1989
Clustering of breakpoints on chromosome 10 in acute T-cell leukemias with the t(10;14) chromosome translocation.
J. Kagan
,
L. Finger
,
J. Letofsky
,
J. Finan
,
P. Nowell
,
C. Croce
Proceedings of the National Academy of Sciences…
1989
Corpus ID: 22595137
The T-cell receptor (TCR) alpha/delta chain locus on chromosome 14q11 is nonrandomly involved in translocations and inversions in…
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1987
1987
Alpha-chain locus of the T-cell antigen receptor is involved in the t(10;14) chromosome translocation of T-cell acute lymphocytic leukemia.
J. Kagan
,
J. Finan
,
J. Letofsky
,
E. Besa
,
P. Nowell
,
C. Croce
Proceedings of the National Academy of Sciences…
1987
Corpus ID: 41768164
Human leukemic T cells carrying a t(10;14)(q24;q11) chromosome translocation were fused with mouse leukemic T cells, and the…
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