Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Christopher P. Raab"'
Autor:
Brice Nzigou Mombo, Brent M. Bijonowski, Christopher A. Raab, Stephan Niland, Katrin Brockhaus, Marc Müller, Johannes A. Eble, Seraphine V. Wegner
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract E-cadherin-based cell-cell adhesions are dynamically and locally regulated in many essential processes, including embryogenesis, wound healing and tissue organization, with dysregulation manifesting as tumorigenesis and metastasis. However,
Externí odkaz:
https://doaj.org/article/95180b5c11be448fa2645bf8fa403228
Autor:
Yu Hsuan Carol Yang, Linford JB Briant, Christopher A Raab, Sri Teja Mullapudi, Hans-Martin Maischein, Koichi Kawakami, Didier YR Stainier
Publikováno v:
eLife, Vol 11 (2022)
The importance of pancreatic endocrine cell activity modulation by autonomic innervation has been debated. To investigate this question, we established an in vivo imaging model that also allows chronic and acute neuromodulation with genetic and optog
Externí odkaz:
https://doaj.org/article/8318e81bacd3497db430df08c5ba1ed2
Autor:
Christopher P, Raab
Publikováno v:
Primary Care: Clinics in Office Practice. 38:681-691
Passive immunization employs preformed antibodies provided to an individual that can prevent or treat infectious diseases. There are several situations in which passive immunization can be used: for persons with congenital or acquired immunodeficienc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb5fef74bdadf254cdaedbbc73c2f02b
https://doi.org/10.1016/j.pop.2011.07.006
https://doi.org/10.1016/j.pop.2011.07.006
Publikováno v:
Primary Care: Clinics in Office Practice. 36:671-684
Childhood cancer is uncommon but remains the leading cause of disease-related death in children. Symptoms are often vague or insidious; they may suggest a more common alternative diagnosis, and they are quite different from those associated with adul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec204ad3297d1e4caebddc215470029b
https://doi.org/10.1016/j.pop.2009.07.002
https://doi.org/10.1016/j.pop.2009.07.002
Autor:
Daniele Ghezzi, Mark A. Johnson, Mai Tsukikawa, Xiaowu Gai, Satish Srinivasan, Claire A. Sheldon, Thomas Meitinger, Eric A. Pierce, Christopher P. Raab, Emily Place, Aurelio Reyes, Mustafa A. Salih, Wolfgang Sperl, Alan J. Robinson, Holger Prokisch, Lee-Jun C. Wong, Caroline Biagosch, Erzsebet Polyak, Massimo Zeviani, Johannes A. Mayr, Emtethal Al-Jishi, Rossella Parini, Tobias B. Haack, Marni J. Falk, Charles Bean, Costanza Lamperti, Thomas Wieland, Matteo Gorza, Hanan E. Shamseldin, Julian Ostrovsky, Peter Freisinger, Fowzan S. Alkuraya, Neal Sondheimer, Martina Huemer, Vassiliki Konstantopoulou, Sara Vidoni, Francesca Furlan, Laura S. Kremer, Tim M. Strom, Mark B. Consugar
Publikováno v:
American journal of human genetics. 93(3)
Whole-exome sequencing and autozygosity mapping studies, independently performed in subjects with defective combined mitochondrial OXPHOS-enzyme deficiencies, identified a total of nine disease-segregating FBXL4 mutations in seven unrelated mitochond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26aee8ac4a7da89a007e50bce7d4b937
https://pubmed.ncbi.nlm.nih.gov/23993194
https://pubmed.ncbi.nlm.nih.gov/23993194