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Chromosomes, Human, Pair 14

Known as: 14 chromosome, Chromosome 14 
The designation for each member of the fourteenth largest human autosomal chromosome pair. Chromosome 14 spans about 105 million base pairs and… 
National Institutes of Health

Related topics

Related topics

38 relations
AP5M1 geneATG2B geneC14orf119 geneCOX16 gene

Narrower (4)

Chromosome 14, trisomy mosaicRing Chromosome 14 SyndromeUniparental disomy, paternal, chromosome 14chromosome 14 trisomy syndrome

Broader (1)

Chromosomes, Human, 13-15

Papers overview

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Highly Cited
2008
Highly Cited
2008
Genomic and epigenetic alterations deregulate microRNA expression in human epithelial ovarian cancer
MicroRNAs (miRNAs) are an abundant class of small noncoding RNAs that function as negative gene regulators. miRNA deregulation is… 
Highly Cited
2008
Highly Cited
2008
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes
Human chromosome 14q32.2 carries a cluster of imprinted genes including paternally expressed genes (PEGs) such as DLK1 and RTL1… 
Highly Cited
1997
Highly Cited
1997
Alzheimer’s Presenilin Mutation Sensitizes Neural Cells to Apoptosis Induced by Trophic Factor Withdrawal and Amyloid β-Peptide: Involvement of Calcium and Oxyradicals
Most autosomal dominant inherited forms of early onset Alzheimer’s disease (AD) are caused by mutations in the presenilin-1 (PS-1… 
Highly Cited
1993
Highly Cited
1993
The gene for Machado–Joseph disease maps to human chromosome 14q
Machado–Joseph disease (MJD) is an autosomal dominant, multisystem neurodegenerative disorder involving predominantly cerebellar… 
Highly Cited
1992
Highly Cited
1992
Genetic evidence for a novel familial Alzheimer's disease locus on chromosome 14
Familial Alzheimer's disease (FAD) has been shown to be genetically heterogeneous, with a very small proportion of early onset… 
Highly Cited
1992
Highly Cited
1992
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3
Genetic linkage studies with chromosome 21 DNA markers and mutation analysis of the β–amyloid protein precursor gene located in… 
Highly Cited
1992
Highly Cited
1992
A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene
Although mutations in the β–amyloid precursor protein gene (APP) on chromosome 21 cause some cases of early–onset Alzheimer's… 
Highly Cited
1992
Highly Cited
1992
Four novel members of the connexin family of gap junction proteins. Molecular cloning, expression, and chromosome mapping.
Highly Cited
1983
Highly Cited
1983
Translocation and rearrangements of the c-myc oncogene locus in human undifferentiated B-cell lymphomas.
The locus for the cellular myc (c-myc) oncogene in humans is located on the region of chromosome 8 that is translocated to… 
Highly Cited
1979
Highly Cited
1979
Chromosomal location of the genes for human immunoglobulin heavy chains.
We have studied somatic cell hybrids between P3x63Ag8 mouse myeloma cells deficient in hypoxanthine phosphoribosyltransferase (EC… 
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