Membrane Potentials < Membrane Proteins < Membrane Transport Proteins

Facettes :

List of bibliographic references indexed by Membrane Proteins

Number of relevant bibliographic references: 25.
[0-20] [0 - 20][0 - 25][20-24][20-40]

Ident.	Authors (with country if any)	Title
000546 (2014)	Charlotte Delay [Canada] ; Cyntia Tremblay ; Elodie Brochu ; Sarah Paris-Robidas ; Vincent Emond ; Ali H. Rajput ; Alex Rajput ; Frédéric Calon	Increased LINGO1 in the cerebellum of essential tremor patients.
000563 (2014)	Martin B. Delatycki [Australie] ; Geneieve Tai ; Louise Corben ; Eppie M. Yiu ; Marguerite V. Evans-Galea ; Sarah E M. Stephenson ; Lyle Gurrin ; Katrina J. Allen ; David Lynch ; Paul J. Lockhart	HFE p.C282Y heterozygosity is associated with earlier disease onset in Friedreich ataxia.
000582 (2014)	Edina Silajdži [Suède] ; Radu Constantinescu ; Björn Holmberg ; Maria Björkqvist ; Oskar Hansson	Flt3 ligand does not differentiate between Parkinsonian disorders.
000866 (2013)	Chang-He Shi ; Shi-Lei Sun ; Jun-Ling Wang ; Ai-Qin Liu ; Wang Miao ; Chandra Avinash ; Xiao Mao ; Bei-Sha Tang ; Yu-Ming Xu	PRRT2 gene mutations in familial and sporadic paroxysmal kinesigenic dyskinesia cases.
000898 (2013)	Yi-Chun Chen [Taïwan] ; Yun-Shien Lee ; Chen-Chang Shih ; Tony Wu ; Chiung-Mei Chen	Mutations of proline-rich transmembrane protein-2 and paroxysmal kinesigenic dyskinesia in Taiwan.
000A80 (2013)	Virginie Lambrecq ; Florence Riant ; Elisabeth Tournier-Lasserve ; Véronique Michel ; Pierre Burbaud	Caffeine improved paroxysmal dyskinesia caused by the PRRT2 mutation.
000D95 (2012)	Anne Weissbach [Allemagne] ; Katharina Siegesmund ; Norbert Brüggemann ; Alexander Schmidt ; Meike Kasten ; Irene Pichler ; Hiltrud Muhle ; Ebba Lohmann ; Thora Lohnau ; Eberhard Schwinger ; Johann Hagenah ; Ulrich Stephani ; Peter P. Pramstaller ; Christine Klein ; Katja Lohmann	Exome sequencing in a family with restless legs syndrome.
001242 (2011)	Benjamin Dehay	α-synuclein, a prion-like protein.
001598 (2011)	Oswaldo Lorenzo-Betancor [Espagne] ; Lluís Samaranch [Espagne] ; Elena García-Martín [Espagne] ; Sebastián Cervantes [Espagne] ; José A. G. Agúndez [Espagne] ; Félix J. Jiménez-Jiménez [Espagne] ; Hortensia Alonso-Navarro [Espagne] ; Antonio Luengo [Espagne] ; Francisco Coria [Espagne] ; Elena Lorenzo [Espagne] ; Jaione Irigoyen [Espagne] ; Pau Pastor [Espagne]	LINGO1 gene analysis in Parkinson's disease phenotypes
001C13 (2010)	Sandra Thier [Allemagne] ; Delia Lorenz [Allemagne] ; Michael Nothnagel [Allemagne] ; Giovanni Stevanin [France] ; Alexandra Dürr [France] ; Almut Nebel [Allemagne] ; Stefan Schreiber [Allemagne] ; Gregor Kuhlenb Umer [Allemagne] ; Günther Deuschl [Allemagne] ; Stephan Klebe [Allemagne]	LINGO1 polymorphisms are associated with essential tremor in Europeans
002064 (2009)	Dietrich Haubenberger [Autriche] ; Christoph Hotzy [Autriche] ; Walter Pirker [Autriche] ; Regina Katzenschlager [Autriche] ; Thomas Brücke [Autriche] ; Fritz Zimprich [Autriche] ; Eduard Auff [Autriche] ; Alexander Zimprich [Autriche]	Role of LINGO1 polymorphisms in Parkinson's disease
002805 (2008)	Guilherme G. Riccioppo Rodrigues ; Ruth H. Walker [États-Unis] ; Alexis Brice [France] ; Cécile Cazeneuve [France] ; Odile Russaouen [France] ; Helio A. G. Teive [Brésil] ; Renato Puppi Munhoz [Brésil] ; Nilson Becker [Brésil] ; Salmo Raskin [Brésil] ; Lineu Cesar Werneck [Brésil] ; Wilson Marques Junior ; Vitor Tumas	Huntington's disease‐like 2 in Brazil—Report of 4 patients
002806 (2008)	Edward J. Wild [Royaume-Uni] ; Ese E. Mudanohwo [Royaume-Uni] ; Mary G. Sweeney [Royaume-Uni] ; Susanne A. Schneider [Royaume-Uni] ; Jon Beck [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Martin N. Rossor [Royaume-Uni] ; Mary B. Davis [Royaume-Uni] ; Sarah J. Tabrizi [Royaume-Uni]	Huntington's disease phenocopies are clinically and genetically heterogeneous
002A03 (2008)	Bart P. C. Van De Warrenburg [Royaume-Uni, Pays-Bas] ; Andrew J. Church [Royaume-Uni] ; Davide Martino [Royaume-Uni, Italie] ; Paul M. Candler [Royaume-Uni] ; Kailash P. Bhatia [Royaume-Uni] ; Gavin Giovannoni [Royaume-Uni] ; Niall P. Quinn [Royaume-Uni]	Antineuronal antibodies in Parkinson's disease
003059 (2007)	Giovanni Fabbrini [Italie] ; Massimo Pasquini [Italie] ; Cinzia Aurilia [Italie] ; Isabella Berardelli [Italie] ; Guido Breedveld [Pays-Bas] ; Ben A. Oostra [Pays-Bas] ; Vincenzo Bonifati [Pays-Bas] ; Alfredo Berardelli [Italie]	A large Italian family with Gilles de la Tourette syndrome: Clinical study and analysis of the SLITRK1 gene
003064 (2007)	Soraya Bardien [Afrique du Sud] ; Fatima Abrahams [Afrique du Sud] ; Himla Soodyall [Afrique du Sud] ; Lize Van Der Merwe [Afrique du Sud] ; Jacquie Greenberg [Afrique du Sud] ; Tinus Brink [Afrique du Sud] ; Jonathan Carr [Afrique du Sud]	A South African mixed ancestry family with Huntington disease‐like 2: Clinical and genetic features
003308 (2006)	Satoshi Kaneko [Japon] ; Toshitaka Kawarai [Canada] ; Edwin Yip [Canada] ; Shabnam Salehi-Rad [Canada] ; Christine Sato [Canada] ; Antonio Orlacchio [Italie] ; Giorgio Bernardi [Italie] ; Yan Liang [Canada] ; Hiroshi Hasegawa [Canada] ; Ekaterina Rogaeva [Canada] ; Peter St George-Hyslop [Canada]	Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia
003531 (2006)	Renato P. Munhoz [Brésil] ; Toshitaka Kawarai [Canada] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Christine Sato [Canada] ; Yan Liang [Canada] ; Peter H. St. George-Hyslop [Canada] ; Ekaterina Rogaeva [Canada]	Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus)
003553 (2006)	Alberto L. Rosa [Argentine, États-Unis] ; Irma Molina [Argentine] ; Valeria Kowaljow [Argentine] ; Cecilia B. Conde [Argentine]	Brisk deep‐tendon reflexes as a distinctive phenotype in an argentinean spinocerebellar ataxia type 2 pedigree
003612 (2006)	Toshiaki Takahashi [Japon] ; Masashi Aoki [Japon] ; Takashi Imai [Japon] ; Masaru Yoshioka [Japon] ; Hidehiko Konno [Japon] ; Shuichi Higano [Japon] ; Yoshiaki Onodera [Japon] ; Hiroshi Saito [Japon] ; Itaru Kimura [Japon] ; Yasuto Itoyama [Japon]	A case of dysferlinopathy presenting choreic movements
003827 (2005)	C. Warren Olanow [États-Unis] ; Joseph Jankovic [États-Unis]	Neuroprotective therapy in Parkinson's disease and motor complications: A search for a pathogenesis‐targeted, disease‐modifying strategy

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/Mesh.i -k "Membrane Proteins" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/Mesh.i  \
                -Sk "Membrane Proteins" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Exploration
   |type=    indexItem
   |index=    Mesh.i
   |clé=    Membrane Proteins
}}

---

This area was generated with Dilib version V0.6.23. Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024