Detalhe da pesquisa
1.
Analysis of copy loss and gain variations in Holstein cattle autosomes using BeadChip SNPs.
BMC Genomics
; 11: 673, 2010 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-21114805
2.
Selection criteria for genetic assessment of patients with familial melanoma.
J Am Acad Dermatol
; 61(4): 677.e1-14, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19751883
3.
Features associated with germline CDKN2A mutations: a GenoMEL study of melanoma-prone families from three continents.
J Med Genet
; 44(2): 99-106, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-16905682
4.
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL.
Cancer Res
; 66(20): 9818-28, 2006 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17047042
5.
The Y152X MC1R gene mutation: occurrence in ethnically diverse Jewish malignant melanoma patients.
Melanoma Res
; 17(2): 105-8, 2007 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-17496785
6.
[Gene silencing RNAi technology: possible application to therapy].
Harefuah
; 145(2): 156-9, 163, 2006 Feb.
Artigo
em Hebraico
| MEDLINE | ID: mdl-16509424
7.
A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone families.
Eur J Hum Genet
; 11(4): 288-96, 2003 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12700603
8.
Polymorphisms in the NPY2R gene show significant associations with BMI that are additive to FTO, MC4R, and NPFFR2 gene effects.
Obesity (Silver Spring)
; 19(11): 2241-7, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21818152