Detalhe da pesquisa
1.
Biallelic variants in NOS3 and GUCY1A3, the two major genes of the nitric oxide pathway, cause moyamoya cerebral angiopathy.
Hum Genomics
; 17(1): 24, 2023 03 20.
Artigo
Inglês
| MEDLINE | ID: mdl-36941667
2.
Novel Chronic Mouse Model of Cerebral Cavernous Malformations.
Stroke
; 51(4): 1272-1278, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-31992178
3.
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy.
Stroke
; 50(4): 789-796, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-30908154
4.
Network-based analysis of omics data: the LEAN method.
Bioinformatics
; 33(5): 701-709, 2017 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27797778
5.
De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy.
J Med Genet
; 54(8): 550-557, 2017 08.
Artigo
Inglês
| MEDLINE | ID: mdl-28343148
6.
Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoya.
Am J Hum Genet
; 88(6): 718-728, 2011 Jun 10.
Artigo
Inglês
| MEDLINE | ID: mdl-21596366
7.
Developmental timing of CCM2 loss influences cerebral cavernous malformations in mice.
J Exp Med
; 208(9): 1835-47, 2011 Aug 29.
Artigo
Inglês
| MEDLINE | ID: mdl-21859843