Detalhe da pesquisa
1.
Defining novel causal SNPs and linked phenotypes at melanoma-associated loci.
Hum Mol Genet
; 31(17): 2845-2856, 2022 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35357426
2.
Genomic Characterization of a Rare, de Novo Unbalanced ins(3;1)(p25.3;q21.3q23.3) in a Female Child with Multiple Congenital Anomalies.
Cytogenet Genome Res
; 160(10): 579-588, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33152732
3.
Paracrine stimulation of P2X7 receptor by ATP activates a proliferative pathway in ovarian carcinoma cells.
J Cell Biochem
; 115(11): 1955-66, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24913779
4.
Clinical Exome Sequencing Enables Congenital Sialidosis Type II Diagnosis in Two Siblings Presenting with Unreported Clinical Features from a Rare Homozygous Sequence Variant p.(Tyr370Cys) in NEU1.
Mol Syndromol
; 12(4): 250-257, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34421504
5.
Acral lentiginous melanoma: Basic facts, biological characteristics and research perspectives of an understudied disease.
Pigment Cell Melanoma Res
; 34(1): 59-71, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32330367