Detalhe da pesquisa
1.
Estimation of DNA contamination and its sources in genotyped samples.
Genet Epidemiol
; 43(8): 980-995, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31452258
2.
SARS-CoV-2 receptor networks in diabetic and COVID-19-associated kidney disease.
Kidney Int
; 98(6): 1502-1518, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33038424
3.
Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
Am J Med Genet A
; 158A(4): 839-49, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22407726
4.
SARS-CoV-2 receptor networks in diabetic and COVID-19 associated kidney disease.
medRxiv
; 2020 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32511461
5.
Amplification and overexpression of the dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 2 (DYRK2) gene in esophageal and lung adenocarcinomas.
Cancer Res
; 63(14): 4136-43, 2003 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12874018
6.
The hepatocyte nuclear factor 3 alpha gene, HNF3alpha (FOXA1), on chromosome band 14q13 is amplified and overexpressed in esophageal and lung adenocarcinomas.
Cancer Res
; 62(18): 5273-9, 2002 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12234996
7.
Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.
Gene Expr Patterns
; 4(6): 611-9, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15465483
8.
Mutation of the FOXC2 gene in familial distichiasis.
J AAPOS
; 7(5): 354-7, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-14566319
9.
A novel VEGFR3 mutation causes Milroy disease.
Am J Med Genet A
; 143A(11): 1212-7, 2007 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17458866
10.
Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development.
Mamm Genome
; 13(2): 95-101, 2002 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-11889557
11.
FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.
Hum Mol Genet
; 12(10): 1179-85, 2003 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12719382