Carotid Artery Diseases < Carrier Proteins < Cartilage

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 24.
[0-20] [0 - 20][0 - 24][20-23][20-40]

Ident.	Authors (with country if any)	Title
000440 (2015)	Mikko Muona ; Samuel F. Berkovic ; Leanne M. Dibbens ; Karen L. Oliver ; Snezana Maljevic ; Marta A. Bayly ; Tarja Joensuu ; Laura Canafoglia ; Silvana Franceschetti ; Roberto Michelucci ; Salla Markkinen ; Sarah E. Heron ; Michael S. Hildebrand ; Eva Andermann ; Frederick Andermann ; Antonio Gambardella ; Paolo Tinuper ; Laura Licchetta ; Ingrid E. Scheffer ; Chiara Criscuolo ; Alessandro Filla ; Edoardo Ferlazzo ; Jamil Ahmad ; Adeel Ahmad ; Betul Baykan ; Edith Said ; Meral Topcu ; Patrizia Riguzzi ; Mary D. King ; Cigdem Ozkara ; Danielle M. Andrade ; Bernt A. Engelsen ; Arielle Crespel ; Matthias Lindenau ; Ebba Lohmann ; Veronica Saletti ; João Massano ; Michael Privitera ; Alberto J. Espay ; Birgit Kauffmann ; Michael Duchowny ; Rikke S. M Ller ; Rachel Straussberg ; Zaid Afawi ; Bruria Ben-Zeev ; Kaitlin E. Samocha ; Mark J. Daly ; Steven Petrou ; Holger Lerche ; Aarno Palotie ; Anna-Elina Lehesjoki	A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.
000614 (2014)	Martial Mallaret ; Ouhaid Lagha-Boukbiza ; Saskia Biskup ; Izzie Jacques Namer ; Gabrielle Rudolf ; Mathieu Anheim ; Christine Tranchant	SPG15: a cause of juvenile atypical levodopa responsive parkinsonism.
000651 (2013)	Michael Zech ; Georg Nübling ; Florian Castrop ; Angela Jochim ; Eva C. Schulte ; Brit Mollenhauer ; Peter Lichtner ; Annette Peters ; Christian Gieger ; Thorsten Marquardt ; Marie T. Vanier ; Philippe Latour ; Hans Klünemann ; Claudia Trenkwalder ; Janine Diehl-Schmid ; Robert Perneczky ; Thomas Meitinger ; Konrad Oexle ; Bernhard Haslinger ; Stefan Lorenzl ; Juliane Winkelmann	Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders.
000784 (2013)	Julien Spatazza ; Elizabeth Di Lullo ; Alain Joliot ; Edmond Dupont ; Kenneth L. Moya ; Alain Prochiantz	Homeoprotein signaling in development, health, and disease: a shaking of dogmas offers challenges and promises from bench to bed.
000858 (2012)	Serge Maia ; Nicolas Arlicot ; Emilie Vierron ; Sylvie Bodard ; Jackie Vergote ; Denis Guilloteau ; Sylvie Chalon	Longitudinal and parallel monitoring of neuroinflammation and neurodegeneration in a 6-hydroxydopamine rat model of Parkinson's disease.
000923 (2011)	Lei Wang ; Ji-Feng Guo ; Wen-Wen Zhang ; Qian Xu ; Xing Zuo ; Chang-He Shi ; Lin-Zi Luo ; Jia Liu ; Liang Hu ; Ya-Cen Hu ; Xin-Xiang Yan ; Bei-Sha Tang	Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease.
000A82 (2010)	Suzanne Lesage ; Christel Condroyer ; Ebba Lohman ; André Troiano ; François Tison ; François Viallet ; Philippe Damier ; Christine Tranchant ; Marie Vidhaillet ; Anne-Marie Ouvrard-Hernandez ; Alexandra Dürr ; Alexis Brice	Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.
000A88 (2010)	Agnès Petit-Paitel	[GSK-3beta: a central kinase for neurodegenerative diseases?].
000B72 (2009)	Alexander Zimprich ; Claudia Schulte ; Eva Reinthaler ; Dietrich Haubenberger ; Jörg Balzar ; Peter Lichtner ; Salwa El Tawil ; S. Edris ; Thomas Foki ; Walter Pirker ; Regina Katzenschlager ; Gerhard Daniel ; Thomas Brücke ; Eduard Auff ; Thomas Gasser	PARK11 gene (GIGYF2) variants Asn56Ser and Asn457Thr are not pathogenic for Parkinson's disease.
000E74 (2006)	Emilie Giaime ; Claire Sunyach ; Magali Herrant ; Sébastien Grosso ; Patrick Auberger ; Pamela J. Mclean ; Frédéric Checler ; Cristine Alves Da Costa	Caspase-3-derived C-terminal product of synphilin-1 displays antiapoptotic function via modulation of the p53-dependent cell death pathway.
000F25 (2005)	Véronique Sgambato-Faure ; Virginie Buggia ; François Gilbert ; Daniel Lévesque ; Alim-Louis Benabid ; François Berger	Coordinated and spatial upregulation of arc in striatonigral neurons correlates with L-dopa-induced behavioral sensitization in dyskinetic rats.
001050 (2004)	Jean-Jacques Bacci ; Philippe Kachidian ; Lydia Kerkerian-Le Goff ; Pascal Salin	Intralaminar thalamic nuclei lesions: widespread impact on dopamine denervation-mediated cellular defects in the rat basal ganglia.
001085 (2003)	X. Drouot ; S. Moutereau ; J P Nguyen ; J P Lefaucheur ; A. Créange ; P. Remy ; F. Goldenberg ; M P D'Ortho	Low levels of ventricular CSF orexin/hypocretin in advanced PD.
001098 (2003)	Olga Corti ; Cornelia Hampe ; Hana Koutnikova ; Frédéric Darios ; Sandrine Jacquier ; Annick Prigent ; Jean-Charles Robinson ; Laurent Pradier ; Merle Ruberg ; Marc Mirande ; Etienne Hirsch ; Thomas Rooney ; Alain Fournier ; Alexis Brice	The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration.
001206 (2002)	A. Hartmann ; A. Mouatt-Prigent ; B A Faucheux ; Y. Agid ; E C Hirsch	FADD: A link between TNF family receptors and caspases in Parkinson's disease.
001239 (2001)	T. Poyot ; F. Condé ; M C Grégoire ; V. Frouin ; C. Coulon ; C. Fuseau ; F. Hinnen ; F. Dollé ; P. Hantraye ; M. Bottlaender	Anatomic and biochemical correlates of the dopamine transporter ligand 11C-PE2I in normal and parkinsonian primates: comparison with 6-[18F]fluoro-L-dopa.
001281 (2000)	C B Lücking ; A. Brice	Alpha-synuclein and Parkinson's disease.
001306 (2000)	E. Bezard ; M. Jaber ; F. Gonon ; A. Boireau ; B. Bloch ; C E Gross	Adaptive changes in the nigrostriatal pathway in response to increased 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurodegeneration in the mouse.
001341 (2000)	C. Périer ; M. Vila ; J. Féger ; Y. Agid ; E C Hirsch	Functional activity of zona incerta neurons is altered after nigrostriatal denervation in hemiparkinsonian rats.
001420 (1999)	S. Chalon ; P. Emond ; S. Bodard ; M P Vilar ; C. Thiercelin ; J C Besnard ; D. Guilloteau	Time course of changes in striatal dopamine transporters and D2 receptors with specific iodinated markers in a rat model of Parkinson's disease.
001436 (1999)	G. Mercier ; J C Turpin ; G. Lucotte	Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association found.

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