Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 210,064,151 papers from all fields of science
Search
Sign In
Create Free Account
10q24
A chromosome band present on 10q
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
20 relations
10q
ABCC2 wt Allele
CYP2C18 wt Allele
CYP2C9 wt Allele
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2013
Highly Cited
2013
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
T. Fingerlin
,
Elissa Murphy
,
+47 authors
D. Schwartz
Nature Genetics
2013
Corpus ID: 13134257
We performed a genome-wide association study of non-Hispanic, white individuals with fibrotic idiopathic interstitial pneumonias…
Expand
Highly Cited
2009
Highly Cited
2009
Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.
A. Shuldiner
,
J. O’Connell
,
+14 authors
P. Gurbel
JAMA
2009
Corpus ID: 34634643
CONTEXT Clopidogrel therapy improves cardiovascular outcomes in patients with acute coronary syndromes and following percutaneous…
Expand
Highly Cited
2005
Highly Cited
2005
Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas
J. Reifenberger
,
M. Wolter
,
+7 authors
G. Reifenberger
British Journal of Dermatology
2005
Corpus ID: 2288761
Background Basal cell carcinoma (BCC) of the skin is the most common human cancer. The genetic alterations underlying BCC…
Expand
Review
2003
Review
2003
PTEN signaling pathways in melanoma
Heng Wu
,
V. Goel
,
F. Haluska
Oncogene
2003
Corpus ID: 22705785
Phosphatase and tensin homolog deleted in from chromosome ten (PTEN), initially also known as mutated in multiple advanced…
Expand
Highly Cited
2003
Highly Cited
2003
Autosomal Dominant Lateral Temporal Epilepsy: Clinical Spectrum, New Epitempin Mutations, and Genetic Heterogeneity in Seven European Families
R. Michelucci
,
J. Poza
,
+21 authors
C. Nobile
Epilepsia
2003
Corpus ID: 5975397
Summary: Purpose: To describe the clinical and genetic findings of seven additional pedigrees with autosomal dominant lateral…
Expand
Highly Cited
2002
Highly Cited
2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy.
J. Morante-Redolat
,
A. Gorostidi-Pagola
,
+24 authors
A. López de Munain
Human Molecular Genetics
2002
Corpus ID: 17324377
Autosomal dominant lateral temporal epilepsy (EPT; OMIM 600512) is a form of epilepsy characterized by partial seizures, usually…
Expand
Highly Cited
1998
Highly Cited
1998
A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors
O. Chernova
,
R. Somerville
,
J. Cowell
Oncogene
1998
Corpus ID: 2475026
Loss of heterozygosity for 10q23–26 is seen in over 80% of glioblastoma multiforme tumors. We have used a positional cloning…
Expand
Highly Cited
1996
Highly Cited
1996
A human canalicular multispecific organic anion transporter (cMOAT) gene is overexpressed in cisplatin-resistant human cancer cell lines with decreased drug accumulation.
K. Taniguchi
,
M. Wada
,
+7 authors
M. Kuwano
Cancer Research
1996
Corpus ID: 16808247
By targeting the ATP binding conserved domain in three ATP binding cassette superfamily proteins (P-glycoprotein, multidrug…
Expand
Highly Cited
1991
Highly Cited
1991
HOX11, a homeobox-containing T-cell oncogene on human chromosome 10q24.
M. Kennedy
,
R. González-Sarmiento
,
+4 authors
T. Rabbitts
Proceedings of the National Academy of Sciences…
1991
Corpus ID: 20167498
A common chromosomal abnormality in childhood T-cell acute leukemia is a translocation, t(10;14) (q24;q11), that together with…
Expand
Highly Cited
1991
Highly Cited
1991
Deregulation of a homeobox gene, HOX11, by the t(10;14) in T cell leukemia.
M. Hatano
,
C. Roberts
,
M. Minden
,
W. Crist
,
S. Korsmeyer
Science
1991
Corpus ID: 20793074
Molecular cloning of the t(10;14)(q24;q11) recurrent breakpoint of T cell acute lymphoblastic leukemia has demonstrated a…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE