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4q35.1
A chromosome band present on 4q
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
ING2 wt Allele
SORBS2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2017
Highly Cited
2017
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
P. Law
,
S. Berndt
,
+94 authors
S. Slager
Nature Communications
2017
Corpus ID: 4395109
Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains…
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Highly Cited
2012
Highly Cited
2012
Genotype–phenotype analysis of 4q deletion syndrome: Proposal of a critical region
E. Strehle
,
Linbo Yu
,
+20 authors
Taosheng Huang
American Journal of Medical Genetics. Part A
2012
Corpus ID: 12015247
Chromosome 4q deletion syndrome (4q‐ syndrome) is a rare condition, with an estimated incidence of 1 in 100,000. Although…
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Highly Cited
2010
Highly Cited
2010
Identification and molecular characterization of two novel chromosomal deletions associated with autism
Wei-Hsien Chien
,
S. S. Gau
,
+6 authors
C-H Chen
Clinical Genetics
2010
Corpus ID: 31814116
Chien W‐H, Gau SS‐F, Wu Y‐Y, Huang Y‐S, Fang J‐S, Chen Y‐J, Soong W‐T, Chiu Y‐N, Chen C‐H. Identification and molecular…
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2009
2009
Frequent deletion of ING2 locus at 4q35.1 associates with advanced tumor stage in head and neck squamous cell carcinoma
S. Borkosky
,
M. Gunduz
,
+9 authors
N. Nagai
Journal of Cancer Research and Clinical Oncology
2009
Corpus ID: 1669404
BackgroundLoss of heterozygosity (LOH) in the ING family members has been shown in head and neck squamous cell carcinoma (HNSCC…
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Highly Cited
2005
Highly Cited
2005
Genome-wide aberrations in pancreatic adenocarcinoma.
N. Nowak
,
D. Gaile
,
+6 authors
A. Maitra
Cancer Genetics and Cytogenetics
2005
Corpus ID: 25559801
2005
2005
Regulation of myeloid leukemia factor-1 interacting protein (MLF1IP) expression in glioblastoma
S. Hanissian
,
B. Teng
,
+4 authors
J. Robertson
Brain Research
2005
Corpus ID: 30594722
Highly Cited
2004
Highly Cited
2004
Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.
Anren Li
,
X. Jiao
,
+15 authors
J. Hejtmancik
American Journal of Human Genetics
2004
Corpus ID: 20269654
Bietti crystalline corneoretinal dystrophy (BCD) is an autosomal recessive retinal dystrophy characterized by multiple glistening…
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Highly Cited
2003
Highly Cited
2003
CLDN23 gene, frequently down-regulated in intestinal-type gastric cancer, is a novel member of CLAUDIN gene family.
Masuko Katoh
,
M. Katoh
International Journal of Molecular Medicine
2003
Corpus ID: 34720180
Microarray analyses combined with laser-capture microdissection have been applied for risk assessments of gastric cancer as well…
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Highly Cited
1995
Highly Cited
1995
Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a).
S. Slaugenhaupt
,
A. Roca
,
C. B. Liebert
,
M. Altherr
,
J. Gusella
,
S. Reppert
Genomics
1995
Corpus ID: 19842500
The pineal hormone melatonin elicits potent circadian and reproductive effects in mammals. We report the chromosomal location of…
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Highly Cited
1994
Highly Cited
1994
Structure and regulation of the human interferon regulatory factor 1 (IRF-1) and IRF-2 genes: implications for a gene network in the interferon system
H. Harada
,
E. Takahashi
,
S. Itoh
,
K. Harada
,
T. Hori
,
T. Taniguchi
Molecular and Cellular Biology
1994
Corpus ID: 43469122
Interferon regulatory factor 1 (IRF-1) and IRF-2 are structurally similar DNA-binding factors which were originally identified as…
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