5q35

A chromosome band present on 5q
National Institutes of Health

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9 relations
CANX wt AlleleChromosomesGRM6 wt AlleleMAML1 wt Allele
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Papers overview

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2009
2009
Locus for familial migrainous vertigo disease maps to chromosome 5q35.
OBJECTIVES Migrainous vertigo (episodic vertigo associated with migraine) is sometimes inherited as an autosomal dominant trait… (More)
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2008
2008
Genetic Epidemiology of Paget’s Disease of Bone in Italy: sequestosome1/p62 Gene Mutational Test and Haplotype Analysis at 5q35 in a Large Representative Series of Sporadic and Familial Italian Cases…
Families affected by Paget’s disease of bone frequently harbor mutations in the SQSTM1/p62 gene. In this multicentric study we… (More)
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Highly Cited
2006
Highly Cited
2006
Promoter hypermethylation-mediated inactivation of multiple Slit-Robo pathway genes in cervical cancer progression
Cervical Cancer (CC) exhibits highly complex genomic alterations. These include hemizygous deletions at 4p15.3, 10q24, 5q35, 3p12… (More)
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2005
2005
Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome.
BACKGROUND Sotos syndrome is characterised by learning difficulties, overgrowth, and a typical facial appearance. Microdeletions… (More)
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Highly Cited
2005
Highly Cited
2005
A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics.
Evidence of the existence of major prostate cancer (PC)-susceptibility genes has been provided by multiple segregation analyses… (More)
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Highly Cited
2003
Highly Cited
2003
ALK-positive diffuse large B-cell lymphoma is associated with Clathrin-ALK rearrangements: report of 6 cases.
Expression of ALK protein by lymphoid cells and the description of variant anaplastic lymphoma kinase (ALK) translocations have… (More)
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Highly Cited
2002
Highly Cited
2002
Haploinsufficiency of NSD1 causes Sotos syndrome
We isolated NSD1 from the 5q35 breakpoint in an individual with Sotos syndrome harboring a chromosomal translocation. We… (More)
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Highly Cited
1999
Highly Cited
1999
A new fusion gene TPM3-ALK in anaplastic large cell lymphoma created by a (1;2)(q25;p23) translocation.
Anaplastic large cell lymphomas (ALCL) are frequently associated with the t(2;5)(p23;q35). This translocation fuses the… (More)
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Highly Cited
1999
Highly Cited
1999
The signal transducer and activator of transcription STAT5b gene is a new partner of retinoic acid receptor alpha in acute promyelocytic-like leukaemia.
Acute promyelocytic leukaemia (APL) exhibits a characteristic t(15;17) translocation that fuses the promyelocytic leukaemia (PML… (More)
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Highly Cited
1994
Highly Cited
1994
Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma.
The 2;5 chromosomal translocation occurs in most anaplastic large-cell non-Hodgkin's lymphomas arising from activated T… (More)
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