Detalhe da pesquisa
1.
Dominant Missense Variants in SREBF2 are Associated with Complex Dermatological, Neurological, and Skeletal Abnormalities.
Genet Med
; : 101174, 2024 Jun 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38847193
2.
Molecular Dissection of Somatic Skeletal Disease in Neurofibromatosis Type 1.
J Bone Miner Res
; 38(2): 288-299, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36459048
3.
Neurofibromin deficiency-associated transcriptional dysregulation suggests a novel therapy for tibial pseudoarthrosis in NF1.
J Bone Miner Res
; 29(12): 2636-42, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24932921
4.
High-concentration of BMP2 reduces cell proliferation and increases apoptosis via DKK1 and SOST in human primary periosteal cells.
Bone
; 54(1): 141-50, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23360788
5.
Acute BMP2 upregulation following induction of ischemic osteonecrosis in immature femoral head.
Bone
; 53(1): 239-47, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23219944
6.
Structure-function relationships in the stereospecific and manganese-dependent 3,4-dihydroxyphenylalanine/tyrosine-sulfating activity of human monoamine-form phenol sulfotransferase, SULT1A3.
J Biol Chem
; 278(3): 1525-32, 2003 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-12424257