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1q21-q22

A chromosome band present on 1q
National Institutes of Health

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8 relations
ARHGEF2 wt AlleleChromosomesDARC wt AlleleFCRL1 wt Allele

Papers overview

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2016
2016
Homozygous mutations in NTRK 1 gene underlie congenital insensitivity to pain with anhidrosis in Pakistani families
Congenital insensitivity to pain with anhidrosis is a rare autosomal recessive disorder presenting with loss of pain sensation… 
2015
2015
Neuronal Misplacement in Schizophrenia
2014
2014
A novel NTRK1 mutation in a patient with congenital insensitivity to pain with anhidrosis
2005
2005
PDZK1 is a potential target for 1q21-q22 amplification frequently detected in drug resistant ovarian cancer(Oncology 1)
2005
2005
Myelin Protein Zero (MPZ) Gene Analysis in Korean Patients with Charcot-Marie-Tooth- Clinical and Electrophysiological Characteristics -
Background: Mutations in the myelin protein zero (MPZ) gene, which is located on chromosome 1q21-q22, is present in Charcot-Marie… 
2002
2002
Prenatal suffering and genetic variability as causative factors of schizophrenia and schizophrenia spectrum disorders phenotype
El objetivo general de la presente tesis fue estudiar marcadores de sufrimiento prenatal y genes candidatos como factores… 
2000
2000
[Comparative genomic hybridization for analysis of chromosomal changes in cisplatin-resistant ovarian cancer].
In our attempt to find characteristic genetic changes in resistant tumors, we screened the whole genome for gene aberrations in… 
Highly Cited
1999
Highly Cited
1999
Identification of the Human YVH1 Protein-tyrosine Phosphatase Orthologue Reveals a Novel Zinc Binding Domain Essential for in Vivo Function*
A human orthologue of the Saccharomyces cerevisiae YVH1 protein-tyrosine phosphatase is able to rescue the slow growth defect… 
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