Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Jonas Gustafson"'
Publikováno v:
Case Reports in Genetics, Vol 2022 (2022)
Craniosynostosis, the premature fusion of the calvarial bones, has numerous etiologies. Among them, several involve mutations in genes related to the TGFb signaling pathway, a critical molecular mediator of human development. These TGFb pathway-assoc
Externí odkaz:
https://doaj.org/article/d5aaa8b618f342bcaf2d01ac4e626ada
Autor:
Daniela V. Luquetti, Carrie L. Heike, Ignacio Zarante, Andrew E. Timms, Jonas Gustafson, Harry Pachajoa, Gloria L. Porras‐Hurtado, Paola Ayala‐Ramirez, Milagros M. Duenas‐Roque, Natalia Jimenez, Lina M. Ibanez, Paula Hurtado‐Villa
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 10, Pp n/a-n/a (2020)
Abstract Background Craniofacial microsomia (CFM), also known as the oculo‐auriculo‐vertebral spectrum, comprises a variable phenotype with the most common features including microtia and mandibular hypoplasia on one or both sides, in addition to
Externí odkaz:
https://doaj.org/article/ac22a56482324882a03a2f67acf1ced2
Autor:
Zahra A. Aldawood, Luigi Mancinelli, Xuehui Geng, Shu-Chi A. Yeh, Roberta Di Carlo, Taiana C. Leite, Jonas Gustafson, Katarzyna Wilk, Joseph Yozgatian, Sasan Garakani, Seyed Hossein Bassir, Michael L. Cunningham, Charles P. Lin, Giuseppe Intini
Publikováno v:
Proceedings of the National Academy of Sciences. 120
In newborn humans, and up to approximately 2 y of age, calvarial bone defects can naturally regenerate. This remarkable regeneration potential is also found in newborn mice and is absent in adult mice. Since previous studies showed that the mouse cal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::456873283fc0217846d6f4500b203076
https://doi.org/10.1073/pnas.2120826120
https://doi.org/10.1073/pnas.2120826120