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16q24.3

A chromosome band present on 16q
National Institutes of Health

Related topics

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11 relations
16qCDT1 wt AlleleCPNE7 wt AlleleChromosomes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
F-box protein FBXO 31 directs degradation of MDM 2 to facilitate p 53-mediated growth arrest following genotoxic stress
box protein FBXO31 directs degradation of MDM2 to facilitate p53-mediated growth arrest following genotoxic stress" (2015… 
Highly Cited
2003
Highly Cited
2003
Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema
Primary lymphoedema is oedema that occurs as a consequence of a failure of lymph drainage and arises from an intrinsic… 
Highly Cited
2002
Highly Cited
2002
MID1, mutated in Opitz syndrome, encodes a ubiquitin ligase that targets phosphatase 2A for degradation
A Trockenbacher, V Suckow, J Foerster, J Winter, S Kraus, H-H Ropers, R Schneider & S Schweiger Nature Genet. 29, 287–294 (2001… 
Highly Cited
2002
Highly Cited
2002
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
M Tartaglia, E L Mehler, R. Goldberg, G Zampino, H G Brunner, H Kremer, I van der Burgt, A H Crosby, A Ion, S Jeffery, K Kalidas… 
Highly Cited
2000
Highly Cited
2000
Loss of heterozygosity at chromosomes 3, 6, 8, 11, 16, and 17 in ovarian cancer: correlation to clinicopathological variables.
Highly Cited
1999
Highly Cited
1999
A gene for lymphedema-distichiasis maps to 16q24.3.
Lymphedema-distichiasis (LD) is a dominantly inherited syndrome with onset of lymphedema at or just after puberty. Most affected… 
Highly Cited
1998
Highly Cited
1998
A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.
Hereditary spastic paraplegia is a genetically and phenotypically heterogeneous disorder. Both pure and complicated forms have… 
Highly Cited
1996
Highly Cited
1996
Erratum: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
J R L T Foe, M A Rooimans, L Bosnoyan-Collins, N Alon, M Wijker, L Parker, J Lightfoot, M Carreau, D F Callen, A Savoia, N C… 
Highly Cited
1994
Highly Cited
1994
Mapping of the gene encoding the melanocortin-1 (alpha-melanocyte stimulating hormone) receptor (MC1R) to human chromosome 16q24.3 by Fluorescence in situ hybridization.
[alpha]-Melanocyte stimulating hormone ([alpha]-MSH), a hormone originally named for its ability to regulate pigmentation of… 
Highly Cited
1993
Highly Cited
1993
The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3.
The gene for N-acetylgalactosamine-6-sulfatase, the deficiency of which results in Morquio A syndrome (mucopolysaccharidosis type… 
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