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7p21

A chromosome band present on 7p
National Institutes of Health

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3 relations
Chromosome 7 Short ArmChromosomesIL6 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Role of interleukin-6 -174 G/C promoter polymorphism in trace metal levels of autopsy kidney and liver tissues.
2010
2010
Gain of CBL-interacting protein, a possible alternative to CBL mutations in myeloid malignancies
Gain of CBL-interacting protein, a possible alternative to CBL mutations in myeloid malignancies 
2004
2004
A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21
SummaryA tiny interstitial delection of 7p was found in a 5-month-old boy with a craniosynostosis and many anomalies. His… 
Highly Cited
1998
Highly Cited
1998
Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locus
AbstractA polymorphic dinucleotide (CA) sequence was isolated from a genomic clone containing the human interleukin 6 (interferon… 
Review
1998
Review
1998
Cytogenetics of uterine sarcomas: presentation of eight new cases and review of the literature.
Tissue from 14 uterine tumor samples from eight patients-four with endometrial stromal sarcoma (ESS), two with leiomyosarcoma… 
1994
1994
Human arylhydrocarbon receptor: functional expression and chromosomal assignment to 7p21.
We isolated the human arylhydrocarbon receptor (AhR) cDNA from a human lung cDNA library, by using mouse AhR cDNA as a labeled… 
1994
1994
Chromosomal localization of the human AHR locus encoding the structural gene for the Ah receptor to 7p21-->p15.
The AHR locus encodes the structural gene for the Ah receptor, a ligand activated transcription factor that regulates the… 
1993
1993
Cytogenetic evidence that the Saethre-Chotzen gene maps to 7p21.2.
Evidence for the location of the Saethre-Chotzen acrocephalosyndactyly mutation on 7p21-22 is based on genetic linkage studies in… 
1992
1992
Karyotype at relapse following allogeneic bone marrow transplantation for chronic myelogenous leukemia.
1976
1976
Mental retardation, malformation syndrome and partial 7p monosomy [45, XX, tdic (7;15) (p21;pll)]
A mentally retarded and malformed girl is described. Her karyotype was 45, XX, tdic(7;15) (p21;p11), i.e. she was monosomic for… 
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