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9q34.1

A chromosome band present on 9q
National Institutes of Health

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8 relations
ABL1 wt AlleleCDK9 wt AlleleCIZ1 wt AlleleChromosomes

Papers overview

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Review
2009
Review
2009
Mutations and polymorphisms in the human argininosuccinate synthetase (ASS1) gene
Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate… 
2005
2005
Loss of blood group A antigen expression in bladder cancer caused by allelic loss and/or methylation of the ABO gene
Correction to: Laboratory Investigation (2005) 85, 895–907. doi:10.1038/sj.labinvest.3700268 Following the publication of the… 
Highly Cited
2000
Highly Cited
2000
Nail-patella syndrome: identification of mutations in the LMX1B gene in Dutch families.
Nail-patella syndrome is an autosomal dominant disorder characterized by dyplasia of finger nails, skeletal anomalies, and… 
Highly Cited
1999
Highly Cited
1999
Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1.
We have isolated a human gene homologous to Drosophila melanogaster rotated abdomen, rt, a poorly viable recessive mutation… 
Highly Cited
1997
Highly Cited
1997
Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family
Idiopathic torsion dystonia is characterized by involuntary twisting movements and postures. One molecularly defined form with… 
Highly Cited
1995
Highly Cited
1995
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in…
Highly Cited
1995
Highly Cited
1995
Assignment of DAP1 and DAPK--genes that positively mediate programmed cell death triggered by IFN-gamma--to chromosome regions 5p12.2 and 9q34.1, respectively.
DAP-kinase (DAPK) and DAP1 were recently identified as positive mediators of IFN-{gamma}-induced programmed cell death. The… 
Highly Cited
1992
Highly Cited
1992
Construction of a GT polymorphism map of human 9q.
Highly Cited
1990
Highly Cited
1990
Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain
XERODERMA pigmentosum (XP) is an autosomal recessive disease, characterized by a high incidence of sunlight-induced skin cancer… 
1986
1986
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia.
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