Familial Atypical Mole Melanoma Syndrome

Known as: DNS, familial atypical multiple mole melanoma syndrome, MLM 
An inherited condition marked by the following: (1) one or more first- or second-degree relatives (parent, sibling, child, grandparent, grandchild… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1952-2017
010020030019522016

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Highly Cited
2007
Highly Cited
2007
MicroRNAs (miRNAs) are evolutionarily conserved, 18- to 25-nucleotide, non-protein coding transcripts that posttranscriptionally… (More)
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Highly Cited
2004
Highly Cited
2004
Parkinson's disease (PD) pathology is characterized by the degeneration of midbrain dopamine neurons (DNs) ultimately leading to… (More)
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Highly Cited
2002
Highly Cited
2002
BACKGROUND Hereditary pancreatic carcinoma shows extant phenotypic and genotypic heterogeneity as evidenced by its integral… (More)
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Highly Cited
2000
Highly Cited
2000
Familial atypical multiple mole melanoma (FAMMM) is an autosomal dominant disease characterized by the familial occurrence of… (More)
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Highly Cited
1997
Highly Cited
1997
The cause of neurodegeneration in Huntington's disease (HD) is unknown. Patients with HD have an expanded NH2-terminal… (More)
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Highly Cited
1996
Highly Cited
1996
We have identified several genes that are required for various morphogenetic processes during gastrulation and tail formation… (More)
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Highly Cited
1995
Highly Cited
1995
The p16 gene (CDKN2) which is localized on chromosome 9p21, is deleted in a significant number of sporadic cancers1–3. Moreover… (More)
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Highly Cited
1994
Highly Cited
1994
A locus for familial melanoma, MLM, has been mapped within the same interval on chromosome 9p21 as the gene for a putative cell… (More)
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1983
1983
The familial atypical multiple mole-melanoma syndrome (FAMMM) is characterised by an autosomal dominantly inherited… (More)
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1983
1983
Genetic analysis was performed on four kindreds with clinical and pathological verification of the FAMMM syndrome. There were 80… (More)
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