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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… Expand
National Institutes of Health

Related topics

Related topics

38 relations
13qAleukemic Chronic Lymphocytic LeukemiaChromatinChromosome 13 Short Arm
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Narrower (6)

Chromosome 13 ringChromosome 13q deletion syndromeChromosome 13q trisomyPatau syndrome
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Broader (1)

Chromosomes, Human, 13-15

Papers overview

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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… Expand
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Highly Cited
2005
Highly Cited
2005
MicroRNA expression profiles classify human cancers
Recent work has revealed the existence of a class of small non-coding RNA species, known as microRNAs (miRNAs), which have… Expand
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Highly Cited
2005
Highly Cited
2005
A microRNA polycistron as a potential human oncogene
To date, more than 200 microRNAs have been described in humans; however, the precise functions of these regulatory, non-coding… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
1997
Highly Cited
1997
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.
Non-syndromic neurosensory autosomal recessive deafness (NSRD) is the most common form of genetic hearing loss. Previous studies… Expand
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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… Expand
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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… Expand
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