Zobrazeno 1 - 10
of 2 248
pro vyhledávání: '"craniofacial development"'
Autor:
Mauco Gil Rosas, Cielo Centola, Mercedes Torres, Valeria S. Mouguelar, Aldana P. David, Ernesto J. Piga, Dennis Gomez, Nora B. Calcaterra, Pablo Armas, Gabriela Coux
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract Treacle ribosome biogenesis factor 1 (TCOF1) is responsible for about 80% of mandibular dysostosis (MD) cases. We have formerly identified a correlation between TCOF1 and CNBP (CCHC-type zinc finger nucleic acid binding protein) expression i
Externí odkaz:
https://doaj.org/article/a8ac98edac9b43569ec36254c43366e8
Autor:
Wafaa Yahia Alghonemy, Abdelmonem Awad Hegazy, Fayig Elmigdadi, Gamal Abdel Nasser Atia, Mai Badreldin Helal
Publikováno v:
Translational Research in Anatomy, Vol 37, Iss , Pp 100338- (2024)
Background: The interaction of cell populations and synchronization of cell signaling pathways during craniofacial development can cause malformations such as facial clefts when interrupted by teratogenic agents including synthetic corticosteroids. T
Externí odkaz:
https://doaj.org/article/7060c89920234a0ea334d402ed5e55e3
Autor:
Yulin Dai, Toshiyuki Itai, Guangsheng Pei, Fangfang Yan, Yan Chu, Xiaoqian Jiang, Seth M. Weinberg, Nandita Mukhopadhyay, Mary L. Marazita, Lukas M. Simon, Peilin Jia, Zhongming Zhao
Publikováno v:
HGG Advances, Vol 5, Iss 3, Pp 100312- (2024)
Summary: Orofacial clefts (OFCs) are among the most common human congenital birth defects. Previous multiethnic studies have identified dozens of associated loci for both cleft lip with or without cleft palate (CL/P) and cleft palate alone (CP). Alth
Externí odkaz:
https://doaj.org/article/1674e572859a430fb03d3eef41dde83f
Autor:
Marek Hampl, Nela Jandová, Denisa Lusková, Monika Nováková, Tereza Szotkowská, Štěpán Čada, Jan Procházka, Jiri Kohoutek, Marcela Buchtová
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 6 (2024)
Externí odkaz:
https://doaj.org/article/da1c92341f2c4e39bd23cffe0800a750
Autor:
Sarah Widmer, Franz R. Seefried, Irene M. Häfliger, Heidi Signer-Hasler, Christine Flury, Cord Drögemüller
Publikováno v:
Journal of Dairy Science, Vol 106, Iss 12, Pp 8969-8978 (2023)
ABSTRACT: Shortening of the mandible (brachygnathia inferior) is a congenital, often inherited and variably expressed craniofacial anomaly in domestic animals including cattle. Brachygnathia inferior can lead to poorer animal health and welfare and r
Externí odkaz:
https://doaj.org/article/e1b95967bf6e4b2aa63de1c865b41099
Autor:
Motoki Tamura, Ryota Ishikawa, Yuki Nakanishi, Juan Pascual-Anaya, Makiko Fukui, Takashi Saitou, Fumiaki Sugahara, Filippo M. Rijli, Shigeru Kuratani, Daichi G. Suzuki, Yasunori Murakami
Publikováno v:
Zoological Letters, Vol 9, Iss 1, Pp 1-14 (2023)
Abstract The evolutionary origin of the jaw remains one of the most enigmatic events in vertebrate evolution. The trigeminal nerve is a key component for understanding jaw evolution, as it plays a crucial role as a sensorimotor interface for the effe
Externí odkaz:
https://doaj.org/article/bde9a43fe6224220b93d3a215aca3ce5
Autor:
Jaaved Mohammed, Neha Arora, Harold S Matthews, Karissa Hansen, Maram Bader, Susan Walsh, John R Shaffer, Seth M Weinberg, Tomek Swigut, Peter Claes, Licia Selleri, Joanna Wysocka
Publikováno v:
eLife, Vol 13 (2024)
Genome-wide association studies (GWAS) identified thousands of genetic variants linked to phenotypic traits and disease risk. However, mechanistic understanding of how GWAS variants influence complex morphological traits and can, in certain cases, si
Externí odkaz:
https://doaj.org/article/2cc1a2d4cf454d649f23f3d5f8c28b50
Autor:
Sabrina C. Fox, Andrew J. Waskiewicz
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Humans and other jawed vertebrates rely heavily on their craniofacial skeleton for eating, breathing, and communicating. As such, it is vital that the elements of the craniofacial skeleton develop properly during embryogenesis to ensure a high qualit
Externí odkaz:
https://doaj.org/article/e0f53aef72f54b47802baa664012b95e
Publikováno v:
Journal of Developmental Biology, Vol 12, Iss 3, p 19 (2024)
Frontonasal malformations are caused by a failure in the growth of the frontonasal prominence during development. Although genetic studies have identified genes that are crucial for frontonasal development, it remains largely unknown how these genes
Externí odkaz:
https://doaj.org/article/f659729d1c364b5b8ab6c00fdabff578
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 11 (2023)
Externí odkaz:
https://doaj.org/article/2ad85e8b832e4ac49786259528a894f4