Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Brian C. Gibbs"'
Autor:
Brian C. Gibbs, Rama Rao Damerla, Eszter K. Vladar, Bishwanath Chatterjee, Yong Wan, Xiaoqin Liu, Cheng Cui, George C. Gabriel, Maliha Zahid, Hisato Yagi, Heather L. Szabo-Rogers, Kaye L. Suyama, Jeffrey D. Axelrod, Cecilia W. Lo
Publikováno v:
Biology Open, Vol 5, Iss 3, Pp 323-335 (2016)
Planar cell polarity (PCP) is controlled by a conserved pathway that regulates directional cell behavior. Here, we show that mutant mice harboring a newly described mutation termed Beetlejuice (Bj) in Prickle1 (Pk1), a PCP component, exhibit developm
Externí odkaz:
https://doaj.org/article/c2fc0a651ddd4dd79f9745140bfe7151
Autor:
Madhavi K. Ganapathiraju, Shazina Saeed, D. Woodrow Benson, Dennis Kostka, Omar Khalifa, George C. Gabriel, Simon C. Watkins, Cecilia W. Lo, Kevin A. Peterson, Manush Saydmohammed, Karen L. de Mesy Bentley, Xiaoqin Liu, You Li, Yijen L. Wu, Lisa J. Martin, Nikolai Klena, Hisato Yagi, Maliha Zahid, Anchit Bhagat, Paul Grossfeld, Phillip J. Dexheimer, Bishwanath Chatterjee, William T. Pu, Stephen A. Murray, William A. Devine, George A. Porter, Brian C. Gibbs, Linda Leatherbury, Bruce J. Aronow, Zhaohan Chen, William T Reynolds, Molly Schwartz, Michael Tsang, Abha S. Bais
Publikováno v:
Nature Genetics. 49:1152-1159
Congenital heart disease (CHD) affects up to 1 % of live births1. Although a genetic etiology is indicated by an increased recurrence risk2,3, sporadic occurrence suggests that CHD genetics is complex4. Here, we show that hypoplastic left heart syndr
Autor:
Bishwanath Chatterjee, Brian C. Gibbs, Eszter K. Vladar, Cheng Cui, Hisato Yagi, Cecilia W. Lo, Heather L. Szabo-Rogers, Xiaoqin Liu, Yong Wan, Jeffrey D. Axelrod, Kaye Suyama, Maliha Zahid, George C. Gabriel, Rama Rao Damerla
Publikováno v:
Biology Open, Vol 5, Iss 3, Pp 323-335 (2016)
Biology Open
Biology Open
Planar cell polarity (PCP) is controlled by a conserved pathway that regulates directional cell behavior. Here, we show that mutant mice harboring a newly described mutation termed Beetlejuice (Bj) in Prickle1 (Pk1), a PCP component, exhibit developm
Proper control of multipotent/stem cell number and fate is essential for ensuing organ formation during development. β1-integrin, a subfamily of cell surface receptors, has a conserved role in maintenance of multipotent/stem cells, including renal p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4674f8b4f79f0e1308e7c4eefbc96baa
https://europepmc.org/articles/PMC5924717/
https://europepmc.org/articles/PMC5924717/
Autor:
Robert J. Bollo, Cecilia W. Lo, Brian C. Gibbs, Rama Rao Damerla, Stephanie Greene, Jason S. Hauptman, Aviva Katz
Publikováno v:
Journal of neurosurgery. Pediatrics. 21(6)
Myelomeningocele and gastroschisis, on their own, are both relatively common entities encountered in pediatric surgical care. Coexistence of these pathologies, however, is exceedingly rare. The authors report on 2 patients who presented with myelomen
Publikováno v:
Cold Spring Harbor perspectives in biology. 9(8)
A central role for cilia in congenital heart disease (CHD) was recently identified in a large-scale mouse mutagenesis screen. Although the screen was phenotype-driven, the majority of genes recovered were cilia-related, suggesting that cilia play a c
Autor:
Sharon H. O'Neil, George C. Gabriel, Brian C. Gibbs, Vincent Lee, Jodie K. Votava-Smith, Lisa Paquette, Vincent J. Schmithorst, Ashok Panigrahy, Cecilia W. Lo, William T Reynolds, Nikolai Klena, Giulio Zuccoli
Publikováno v:
Circulation. 132
Introduction: Mutant mouse models with congenital heart disease (CHD) were observed to have distinct brain dysplasia, prompting an assessment for brain anomalies in CHD patients. CHD infants with brain magnetic resonance imaging (MRI) assessments wer
Autor:
Thibaut Eguether, Bishwanath Chatterjee, Ramiah Subramanian, Jacques L. Michaud, George B. Witman, Cheng Cui, Jovenal T. San Agustin, Xiaoqin Liu, Cecilia W. Lo, Gregory J. Pazour, Branch Craige, Richard Francis, Brian C. Gibbs, You Li, Rama Rao Damerla, George C. Gabriel
Recent studies identified a previously uncharacterized gene C5ORF42 (JBTS17) as a major cause of Joubert syndrome (JBTS), a ciliopathy associated with cerebellar abnormalities and other birth defects. Here we report the first Jbts17 mutant mouse mode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6835c15859ceec684ff02bea4160ee74
https://europepmc.org/articles/PMC4476446/
https://europepmc.org/articles/PMC4476446/
Autor:
Brian C. Gibbs
Publikováno v:
Education Review, Vol 0, Iss 0 (2014)
Autor:
Jean-Pierre Cartron, Marie-Geneviève Mattei, Virginia Raynal, Pascal Bailly, Pierre Gane, Baya Cherif-Zahar, Yves Colin, Brian C. Gibbs
Publikováno v:
Nature genetics. 12(2)
The Rh antigen is a multi-subunit complex composed of Rh polypeptides and associated glycoproteins (Rh50, CD47, LW and glycophorin B); these interact in the red cell membrane and are lacking or severely reduced in Rhnull cells. As a result, individua