Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development (2018)
- Authors:
- USP affiliated authors: ZATZ, MAYANA - IB ; CEIDE, ROSELI MARIA ZECHI - HRAC ; BERTOLA, DÉBORA ROMEO - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidades: IB; HRAC
- DOI: 10.3389/fgene.2018.00149
- Subjects: DISOSTOSE CRÂNIOFACIAL; DOENÇAS GENÉTICAS; CROMOSSOMOS; METILAÇÃO DE DNA; MALFORMAÇÕES; ANORMALIDADES CRANIOFACIAIS; GENÉTICA MÉDICA
- Keywords: Acrofacial dysostosis; Non-coding region; Haplotype; Expansion; Crossing-over
- Language: Inglês
- Imprenta:
- Source:
- Título: Frontiers in Genetics
- ISSN: 1664-8021
- Volume/Número/Paginação/Ano: v. 9, art. 149, p. 1-8, Apr. 2018
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
HSIA, Gabriella S. P et al. Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development. Frontiers in Genetics, v. 9, p. 1-8, 2018Tradução . . Disponível em: https://doi.org/10.3389/fgene.2018.00149. Acesso em: 28 dez. 2025. -
APA
Hsia, G. S. P., Musso, C. M., Alvizi, L., Brito, L. A., Kobayashi, G. S., Pavanello, R. C. M., et al. (2018). Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development. Frontiers in Genetics, 9, 1-8. doi:10.3389/fgene.2018.00149 -
NLM
Hsia GSP, Musso CM, Alvizi L, Brito LA, Kobayashi GS, Pavanello RCM, Zatz M, Gardham A, Wakeling E, Zechi-Ceide RM, Bertola D, Passos-Bueno MR. Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development [Internet]. Frontiers in Genetics. 2018 ; 9 1-8.[citado 2025 dez. 28 ] Available from: https://doi.org/10.3389/fgene.2018.00149 -
Vancouver
Hsia GSP, Musso CM, Alvizi L, Brito LA, Kobayashi GS, Pavanello RCM, Zatz M, Gardham A, Wakeling E, Zechi-Ceide RM, Bertola D, Passos-Bueno MR. Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development [Internet]. Frontiers in Genetics. 2018 ; 9 1-8.[citado 2025 dez. 28 ] Available from: https://doi.org/10.3389/fgene.2018.00149 - EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome
- Craniosynostosis in pycnodysostosis: broadening the spectrum of the cranial flat bone abnormalities
- Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries
- Challenges in the orthodontic treatment of a patient with pycnodysostosis
- A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder
- Obesity in pycnodysostosis due to UPD1: possible effect of an imprinted gene on chromosome 1
- A review of craniofacial disorders caused by spliceosomal defects
- Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
- Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes
- Molecular biology enhancing our understanding and improving the prevention of hereditary myopathies in the brazilian population
Informações sobre o DOI: 10.3389/fgene.2018.00149 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
