Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Andrea Richter"'
Autor:
Marc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath Christopher Lionel, Guylaine D'Amours, Emmanuelle Lemyre, Rebecca Cullum, Jean-Luc Bigras, Maryse Thibeault, Philippe Chetaille, Alexandre Montpetit, Paul Khairy, Bert Overduin, Sabine Klaassen, Pamela Hoodless, Philip Awadalla, Julie Hussin, Youssef Idaghdour, Mona Nemer, Alexandre F. R. Stewart, Cornelius Boerkoel, Stephen W. Scherer, Andrea Richter, Marie-Pierre Dubé, Gregor Andelfinger
Publikováno v:
PLoS Genetics, Vol 9, Iss 3 (2013)
Externí odkaz:
https://doaj.org/article/5fedba472a7542699aadf367acb12b14
Autor:
Marc-Phillip Hitz, Louis-Philippe Lemieux-Perreault, Christian Marshall, Yassamin Feroz-Zada, Robbie Davies, Shi Wei Yang, Anath Christopher Lionel, Guylaine D'Amours, Emmanuelle Lemyre, Rebecca Cullum, Jean-Luc Bigras, Maryse Thibeault, Philippe Chetaille, Alexandre Montpetit, Paul Khairy, Bert Overduin, Sabine Klaassen, Pamela Hoodless, Philip Awadalla, Julie Hussin, Youssef Idaghdour, Mona Nemer, Alexandre F R Stewart, Cornelius Boerkoel, Stephen W Scherer, Andrea Richter, Marie-Pierre Dubé, Gregor Andelfinger
Publikováno v:
PLoS Genetics, Vol 8, Iss 9, p e1002903 (2012)
Left-sided congenital heart disease (CHD) encompasses a spectrum of malformations that range from bicuspid aortic valve to hypoplastic left heart syndrome. It contributes significantly to infant mortality and has serious implications in adult cardiol
Externí odkaz:
https://doaj.org/article/ee55faf916ca4893a8ac7573ae006f14
Publikováno v:
Bildung und Erziehung. 73:91-98
Autor:
Andrea Richter, Thomas Becker, Danielle E. Martin, Mark J. Hackett, Jitraporn Vongsvivut, Buddhika N. Dorakumbura, Wilhelm van Bronswjik, Simon W. Lewis, Rhiannon E. Boseley, Mark J. Tobin
Publikováno v:
The Analyst. 143:4027-4039
Latent fingermarks are an important form of crime-scene trace evidence and their usefulness may be increased by a greater understanding of the effect of chemical distribution within fingermarks on the sensitivity and robustness of fingermark detectio
Autor:
Andrea Richter
Publikováno v:
Bildung und Erziehung. 68:385-398
Autor:
Chris Paola, Amelia D. Mindich, Riley M Howes, Andrea Richter-Sanchez, Ifunanya B. Obidi, Emi Ito
Publikováno v:
Geological Society of America Abstracts with Programs.
Autor:
Sabine Henkes, Andrea Richter
»Aus dem Spieglein an der Wand sprach die ›Böse Königin Anorexia‹ zu mir: ›Du bist nicht die Schönste und Klügste im ganzen Land! Du bist zu dick!‹ Ich nahm mir die Worte der Bösen Königin zu Herzen und aß immer weniger, bis ich sehr
Autor:
Peter S. McPherson, Claude Prévost, J.P. Bouchard, Nicolas Dupré, Jean Mathieu, Antoine Duquette, J. Demers-Lamarche, I. Thiffault, Marie-Josée Dicaire, Geneviève Bernard, Laura Montermini, Martine Tétreault, A. Montpetit, Bernard Brais, Roxanne Larivière, Andrea Richter, Kalle Gehring, Jocelyne Mercier, K.N. Huang, Grant A. Mitchell
Publikováno v:
Europe PubMed Central
Background:The growing number of spastic ataxia of Charlevoix-Saguenay (SACS) gene mutations reported worldwide has broadened the clinical phenotype of autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS). The identification of Quebec A
Autor:
Andrea Schlicksupp, Susanne Mükusch, Christoph Körber, Jochen Kuhse, M. S. Kaiser, Joachim Kirsch, Andrea Richter, Thomas Kuner
Publikováno v:
Molecular and Cellular Neuroscience. 50:250-259
Collybistin (Cb) is a brain specific guanine nucleotide exchange factor that interacts with the inhibitory postsynaptic scaffold protein gephyrin. Cb is essential for the postsynaptic clustering of gephyrin and major GABA(A) receptor subtypes during
Autor:
Emily C. Deane, Esmeralda G. M. Vermeulen, Francois Blondeau, Nadya Nossova, Rébecca Gaudet, Eric A. Shoubridge, J. Paul Chapple, George A. Prenosil, Michael R. Duchen, Kalle Gehring, Peter S. McPherson, Andrea Richter, R. Anne McKinney, David A. Parfitt, Bernard Brais, Roxanne Larivière, Martine Girard
Publikováno v:
Proceedings of the National Academy of Sciences. 109:1661-1666
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a childhood-onset neurological disease resulting from mutations in the SACS gene encoding sacsin, a 4,579-aa protein of unknown function. Originally identified as a founder disease