Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Samer Nuwayhid"'
Autor:
Beverly A. Karpinski, Thomas M. Maynard, Matthew S. Fralish, Samer Nuwayhid, Irene E. Zohn, Sally A. Moody, Anthony-S. LaMantia
Publikováno v:
Disease Models & Mechanisms, Vol 7, Iss 2, Pp 245-257 (2014)
We assessed feeding-related developmental anomalies in the LgDel mouse model of chromosome 22q11 deletion syndrome (22q11DS), a common developmental disorder that frequently includes perinatal dysphagia – debilitating feeding, swallowing and nutrit
Externí odkaz:
https://doaj.org/article/3d1c470eb871483a8acf2cece0a1d79e
Autor:
William A. Gahl, Elizabeth A. Burke, Yajun Tang, Melissa G. Dominguez, Ron A. Deckelbaum, May Christine V. Malicdan, Michael Podgorski, Brian Zambrowicz, James R. Lupski, Christopher J. Scheonherr, Wendy K. Chung, Dennis Delgado, Aris N. Economides, John Dronzek, Nicholas W. Gale, Richard A. Gibbs, Prasad Sarangapani, Samer Nuwayhid, Matthew C. Franklin, Harikiran Nistala, Shek Man Chim, Claudia Gonzaga-Jauregui, Saathyaki Rajamani, Ender Karaca, Marjorie Withers
Publikováno v:
Human Molecular Genetics
Neurodevelopmental disorder with microcephaly, hypotonia and variable brain anomalies (NMIHBA) is an autosomal recessive neurodevelopmental and neurodegenerative disorder characterized by global developmental delay and severe intellectual disability.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0571f97e78204efd705fe7ef33c99a53
http://europepmc.org/articles/PMC7788287
http://europepmc.org/articles/PMC7788287
Autor:
Samer Nuwayhid, Harikiran Nistala, Saathyaki Rajamani, Richard A. Gibbs, Christopher J. Scheonherr, Dennis Delgado, Yajun Tang, James R. Lupski, John Dronzek, May Christine V. Malicdan, Matthew C. Franklin, Michael Podgorski, Ender Karaca, Claudia Gonzaga-Jauregui, Melissa G. Dominguez, Ron A. Deckelbaum, Marjorie Withers, Wendy K. Chung, Aris N. Economides, Brian Zambrowicz, Elizabeth A. Burke, Shek Man Chim, Nicholas W. Gale, William A. Gahl, Prasad Sarangapani
Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies (NMIHBA) is an autosomal recessive neurodevelopmental and neurodegenerative disorder characterized by global developmental delay and severe intellectual disability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09a25f9eed0ffba184f5c372d32b5a24
https://doi.org/10.1101/2020.03.02.973909
https://doi.org/10.1101/2020.03.02.973909
Somitogenesis and subsequent axial skeletal development is regulated by the interaction of pathways that determine the periodicity of somite formation, rostrocaudal somite polarity and segment identity. Here we use a hypomorphic mutant mouse line to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f761d6b13c74b6f6549173af2194ce54
https://europepmc.org/articles/PMC5209264/
https://europepmc.org/articles/PMC5209264/