Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Débora Varela"'
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract CDKL5 deficiency disorder (CDD) is a rare neurodevelopmental condition characterized primarily by seizures and impairment of cognitive and motor skills. Additional phenotypes include microcephaly, dysmorphic facial features, and scoliosis. M
Externí odkaz:
https://doaj.org/article/46d980a8572d48188c6f5d09a2d1af0a
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 100990- (2021)
Externí odkaz:
https://doaj.org/article/c0e018561b8f43f0a874acaff174faaa
Publikováno v:
Genome. 65:513-523
Optineurin (OPTN) is involved in a variety of mechanisms, such as autophagy, vesicle trafficking, and nuclear factor kappa-B (NF-κB) signaling. Mutations in the OPTN gene have been associated with different pathologies, including glaucoma, amyotroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd27509a3e2e713ec7d1eaa29eadc716
https://doi.org/10.1139/gen-2022-0019
https://doi.org/10.1139/gen-2022-0019
Publikováno v:
The international journal of biochemistrycell biology. 154
Mutations in Zinc finger 687 (ZNF687) were associated with Paget's disease of bone (PDB), a disease charac-terized by increased bone resorption and excessive bone formation. It was suggested that ZNF687 plays a role in bone differentiation and develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::711260c24faee0dbda5e1c07820297ff
https://pubmed.ncbi.nlm.nih.gov/36372390
https://pubmed.ncbi.nlm.nih.gov/36372390
Publikováno v:
Bone Reports, Vol 14, Iss, Pp 100990-(2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::953052c55924fcb8a0c7eaf6a63edae8
http://www.sciencedirect.com/science/article/pii/S235218722100245X
http://www.sciencedirect.com/science/article/pii/S235218722100245X
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
T-box 5 (TBX5) protein belongs to the T-box family whose members play a crucial role in cell-type specification, morphogenesis and organogenesis. TBX5 is a transcription factor important for cardiac development and upper limbs formation and its haplo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a2339155cbee1b22f3d5acea7de7454
https://hdl.handle.net/10400.1/17035
https://hdl.handle.net/10400.1/17035
Autor:
Magalhães, Débora Varela
Publikováno v:
Biblioteca Digital de Teses e Dissertações da UNIFORUniversidade de FortalezaUNIFOR.
Made available in DSpace on 2019-04-05T23:07:50Z (GMT). No. of bitstreams: 0 Previous issue date: 2006-07-05
The scarcity of researches about credit risk in Brazil has obstructed a consistent evaluation of the behavior on the part of the financi
The scarcity of researches about credit risk in Brazil has obstructed a consistent evaluation of the behavior on the part of the financi
Externí odkaz:
https://uol.unifor.br/oul/ObraBdtdSiteTrazer.do?method=trazer&ns=true&obraCodigo=73413
http://dspace.unifor.br/handle/tede/73413
http://dspace.unifor.br/handle/tede/73413