Chromosomes, Human, Pair 13

Known as: 13 chromosome, 13 chromosomes, Chromosome 13 
The designation for each member of the thirteenth largest human autosomal chromosome pair. Chromosome 13 spans about 113 million base pairs and… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1962-2018
05019622018

Related topics

Related topics

38 relations
13qAleukemic Chronic Lymphocytic LeukemiaChromatinChromosome 13 Short Arm
(More)

Narrower (6)

Chromosome 13 ringChromosome 13q deletion syndromeChromosome 13q trisomyPatau syndrome
(More)

Broader (1)

Chromosomes, Human, 13-15

Related mentions per year

Related mentions per year

1936-2019
19401960198020002020
Chromosomes, Human, Pair 13
physiological aspects
Microbiological
13q
Patau syndrome
refractory plasma cell neoplasm

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Spread of artemisinin resistance in Plasmodium falciparum malaria.
BACKGROUND Artemisinin resistance in Plasmodium falciparum has emerged in Southeast Asia and now poses a threat to the control… (More)
  • figure 2
  • table 3
Is this relevant?
Highly Cited
2005
Highly Cited
2005
c-Myc-regulated microRNAs modulate E2F1 expression
MicroRNAs (miRNAs) are 21–23 nucleotide RNA molecules that regulate the stability or translational efficiency of target messenger… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
1999
Highly Cited
1999
MRP4: A previously unidentified factor in resistance to nucleoside-based antiviral drugs
Dideoxynucleosides, which are potent inhibitors of HIV reverse transcriptase and other viral DNA polymerases, are a common… (More)
  • figure 1
  • table 1
  • figure 2
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Connexin-26 mutations in sporadic and inherited sensorineural deafness.
BACKGROUND Hearing impairment affects one infant in 1000 and 4% of people aged younger than 45 years. Congenital deafness is… (More)
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.
Schizophrenia is a common disorder characterized by psychotic symptoms; diagnostic criteria have been established. Family, twin… (More)
Is this relevant?
Highly Cited
1998
Highly Cited
1998
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired
Holoprosencephaly (HPE) is the most common structural anomaly of the human brain and is one of the anomalies seen in patients… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
1996
Highly Cited
1996
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
The BRCA2 gene on chromosome 13 has been shown to be associated with familial male and female breast cancer. Here we describe a… (More)
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma
We have determined that PAX3 (found previously to be mutated in Waardenburg syndrome) is the chromosome 2 locus rearranged by the… (More)
Is this relevant?
Highly Cited
1993
Highly Cited
1993
Fusion of a fork head domain gene to PAX3 in the solid tumour alveolar rhabdomyosarcoma
We have examined the structure and expression of the products associated with the t(2;13)(q35;q14) translocation associated with… (More)
Is this relevant?
Highly Cited
1983
Highly Cited
1983
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
Inheritance of a mutation at the Rb-1 locus, which has been mapped to band q14 of human chromosome 13, results in predisposition… (More)
Is this relevant?