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4q32
A chromosome band present on 4q
National Institutes of Health
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Related topics
Related topics
2 relations
Chromosomes
TLR2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Translocation breakpoints of chromosome 1 in male carriers: clinical features and implications for genetic counseling.
R. Wang
,
H. G. Zhang
,
+4 authors
R. Liu
Genetics and Molecular Research
2016
Corpus ID: 25942495
Reciprocal translocation is closely associated with male infertility and recurrent miscarriages. Balanced reciprocal…
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2013
2013
Ultra-Rare Mutation in Long-Range Enhancer Predisposes to Thyroid Carcinoma with High Penetrance
Huiling He
,
Wei Li
,
+24 authors
A. de la Chapelle
PLoS ONE
2013
Corpus ID: 18631001
Thyroid cancer shows high heritability but causative genes remain largely unknown. According to a common hypothesis the genetic…
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2010
2010
Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement
A. Tzschach
,
C. Menzel
,
+7 authors
V. Kalscheuer
American Journal of Medical Genetics. Part A
2010
Corpus ID: 205312478
Interstitial deletions of chromosome band 4q32 are rare. We report on a 22‐year‐old female patient with a de novo interstitial…
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2009
2009
Study of abnormal chromosome regions in esophageal squamous cell carcinoma by comparative genomic hybridization: relationship of lymph node metastasis and distant metastasis to selected abnormal…
N. Sakai
,
Y. Kajiyama
,
+5 authors
M. Tsurumaru
Diseases of the esophagus
2009
Corpus ID: 34325370
Squamous cell carcinoma of the esophagus (ESCC) has a poor prognosis among digestive tract cancers. Lymph node metastasis and…
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Review
2008
Review
2008
A comparison of genetic chromosomal loci for intracranial, thoracic aortic, and abdominal aortic aneurysms in search of common genetic risk factors.
Y. Ruigrok
,
R. Elias
,
C. Wijmenga
,
G. Rinkel
Cardiovascular pathology
2008
Corpus ID: 28770107
2004
2004
Loss of heterozygosity on chromosome 4q32–35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes
E. Sironi
,
A. Cerri
,
+5 authors
G. Simoni
Journal of cutaneous pathology
2004
Corpus ID: 2520678
Background: Studies on basal cell carcinoma (BCC) have demonstrated that patched gene and p53 gene located at 9q22.3 and 17p13…
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Highly Cited
2003
Highly Cited
2003
Classical Hodgkin lymphoma is associated with frequent gains of 17q
Daniel Chui
,
D. Hammond
,
M. Baird
,
Lesley A. Shield
,
R. Jackson
,
R. Jarrett
Genes, Chromosomes and Cancer
2003
Corpus ID: 17570646
The etiology of Hodgkin lymphoma (HL) is poorly understood, and studies of the genetics of this disease have been hampered by the…
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1999
1999
Assignment1 of TLL1 and TLL2, which encode human BMP-1/Tolloid-related metalloproteases, to chromosomes 4q32→q33 and 10q23→q24 and assignment of murine Tll2 to chromosome 19
I. Scott
,
T. G. Clark
,
+5 authors
D. Greenspan
Cytogenetic and Genome Research
1999
Corpus ID: 42081614
Bone morphogenetic protein-1 (BMP-1) and Tolloid (TLD) are prototypes of a family of metalloproteases with important functions in…
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1996
1996
Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1p36 and of CLCN3 to 4q32-q33 by in situ hybridization.
F. Saito-Ohara
,
S. Uchida
,
+4 authors
T. Ikeuchi
Genomics
1996
Corpus ID: 36386772
This report describes the localization of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to human chromosome…
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Highly Cited
1989
Highly Cited
1989
Chromosomal abnormalities in Hodgkin's disease.
H. Schouten
,
W. Sanger
,
M. Duggan
,
D. Weisenburger
,
K. Maclennan
,
J. Armitage
Blood
1989
Corpus ID: 2851286
Numerous neoplastic states have associated or causal cytogenetic abnormalities. In some cancers, specific chromosomal…
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