Detalhe da pesquisa
1.
Chromosome Transplantation: Correction of the Chronic Granulomatous Disease Defect in Mouse Induced Pluripotent Stem Cells.
Stem Cells
; 37(7): 876-887, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30895693
2.
Molecular and clinical heterogeneity in CLCN7-dependent osteopetrosis: report of 20 novel mutations.
Hum Mutat
; 31(1): E1071-80, 2010 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-19953639
3.
Chromosome Transplantation: A Possible Approach to Treat Human X-linked Disorders.
Mol Ther Methods Clin Dev
; 17: 369-377, 2020 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32099849
4.
Brain lipid composition in grey-lethal mutant mouse characterized by severe malignant osteopetrosis.
Glycoconj J
; 26(6): 623-33, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18781385
5.
SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.
J Bone Miner Res
; 28(5): 1041-9, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23280965
6.
Prognostic potential of precise molecular diagnosis of Autosomal Recessive Osteopetrosis with respect to the outcome of bone marrow transplantation.
Cytotechnology
; 58(1): 57-62, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19002772