gender < gene < genera

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 56.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000073 (2013)	Wassilios G. Meissner [France] ; Marie Fernet [France] ; Jérôme Couturier [France] ; Janet Hall [France] ; Anthony Laugé [France] ; Patrick Henry [France] ; Dominique Stoppa-Lyonnet [France] ; François Tison [France]	Isolated generalized dystonia in biallelic missense mutations of the ATM gene
000219 (2012)	Mun-Gwan Hong [Suède] ; Chandra A. Reynolds [États-Unis] ; Adina L. Feldman [Suède] ; Mikael Kallin [Suède] ; Jean-Charles Lambert [France] ; Philippe Amouyel [France] ; Erik Ingelsson [Suède] ; Nancy L. Pedersen [Suède] ; Jonathan A. Prince [Suède]	Genome‐wide and gene‐based association implicates FRMD6 in alzheimer disease
000222 (2012)	Ryosuke Miyamoto [Japon] ; Satoshi Goto [Japon] ; Wataru Sako [Japon] ; Ai Miyashiro [Japon] ; Isabelle Kim [France] ; Fabienne Escande [France] ; Masafumi Harada [Japon] ; Ryoma Morigaki [Japon] ; Kotaro Asanuma [Japon] ; Yoshifumi Mizobuchi [Japon] ; Shinji Nagahiro [Japon] ; Yuishin Izumi [Japon] ; Ryuji Kaji [Japon]	Generalized dystonia in a patient with a novel mutation in the GLUD1 gene
000375 (2011)	Y. Halder [Allemagne] ; Eric Largy [France] ; Martin Benzler [Allemagne] ; Martin Teulade-Fichou [France, Allemagne] ; Martin Hartig [Allemagne]	Efficient Suppression of Gene Expression by Targeting 5′‐UTR‐Based RNA Quadruplexes with Bisquinolinium Compounds
000479 (2010)	Yannick Campion [France] ; Henry Neel [France] ; Thierry Gostan [France] ; Johann Soret [France] ; Rémy Bordonné [France]	Specific splicing defects in S. pombe carrying a degron allele of the Survival of Motor Neuron gene
000675 (2009)	Solenn Legallic [France] ; Jacqueline Bou [France] ; Sadeq Haouzir [France] ; Gabrielle Allio [France] ; Caroline Demily [France] ; Michel Petit [France] ; Thierry Frebourg [France] ; Florence Thibaut [France] ; Dominique Campion [France]	No pathogenic rearrangement within the DISC 1 gene in psychosis
000679 (2009)	S. Lesage [France] ; C. Condroyer [France] ; A. Lannuzel [France] ; E. Lohmann [France] ; A. Troiano [France] ; F. Tison [France] ; P. Damier [France] ; S. Thobois [France] ; A-M Ouvrard-Hernandez [France] ; S. Rivaud-Péchoux [France] ; C. Brefel-Courbon [France] ; A. Destée [France] ; C. Tranchant [France] ; M. Romana ; L. Leclere [France] ; A. Dürr [France] ; A. Brice [France]	Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson’s disease
000685 (2009)	Diane Doummar [France] ; Fabienne Clot [France] ; Marie Vidailhet [France] ; Alexandra Afenjar [France] ; Alexandra Durr [France] ; Alexis Brice [France] ; Cyril Mignot [France] ; Agnès Guet [France] ; Thierry Billette De Villemeur [France] ; Diana Rodriguez [France]	Infantile hypokinetic‐hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene
000891 (2007)	Stéphane Fénart ; Frédéric Austerlitz [France] ; Joël Cuguen ; Jean-François Arnaud	Long distance pollen‐mediated gene flow at a landscape level: the weed beet as a case study
000924 (2007)	Suzanne Lesage [France] ; Periquet Magali [France] ; Ebba Lohmann [France] ; Lucette Lacomblez [France] ; Helio Teive [Brésil] ; Sabine Janin [France] ; Pierre-Yves Cousin [France] ; Alexandra Dürr [France] ; Alexis Brice [France]	Deletion of the parkin and PACRG gene promoter in early‐onset parkinsonism
000928 (2007)	Lorraine N. Clark [États-Unis] ; Eneli Haamer [Estonie] ; Helen Mejia-Santana [États-Unis] ; Juliette Harris [États-Unis] ; Suzanne Lesage [France] ; Alexandra Durr [France] ; Sabine Janin Bs [France] ; Katja Hedrich [Allemagne] ; Elan D. Louis [États-Unis] ; Lucien J. Cote [États-Unis] ; Howard Andrews [États-Unis] ; Stanley Fahn [États-Unis] ; Cheryl Waters [États-Unis] ; Blair Ford [États-Unis] ; Steven Frucht [États-Unis] ; William Scott [États-Unis] ; Christine Klein [Allemagne] ; Alexis Brice [France] ; Hanno Roomere [Estonie] ; Ruth Ottman [États-Unis] ; Karen Marder [États-Unis]	Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene
000960 (2006)	M. Sharma [Allemagne] ; J C Mueller [Allemagne] ; A. Zimprich [Autriche] ; P. Lichtner [Allemagne] ; A. Hofer [Allemagne] ; P. Leitner [Allemagne] ; S. Maass [Allemagne] ; D. Berg [Allemagne] ; A. Dürr [France] ; V. Bonifati [Italie] ; G. De Michele [Pays-Bas] ; B. Oostra [Italie] ; A. Brice [France] ; N W Wood [Royaume-Uni] ; B. Muller-Myhsok [Allemagne] ; T. Gasser [Allemagne]	The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson’s disease in European populations
000961 (2006)	Thomas H. Gillingwater ; Thomas M. Wishart ; Philip E. Chen ; Jane E. Haley ; Kevin Robertson ; Stephen H.-F. Macdonald ; Susan Middleton ; Kolja Wawrowski [États-Unis] ; Michael J. Shipston ; Shlomo Melmed [États-Unis] ; David J. A. Wyllie ; Paul A. Skehel ; Michael P. Coleman [Royaume-Uni] ; Richard R. Ribchester	The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells
000990 (2006)	Pablo Iba N Ez ; Suzanne Lesage ; Ebba Lohmann ; Ste Phane Thobois ; Giuseppe De Michele [Italie] ; Michel Borg [France] ; Yves Agid [France] ; Alexandra Du Rr ; Alexis Brice	Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa
000994 (2006)	Alexis-Pierre Bemelmans [France, Suisse] ; Isabelle Husson [France] ; Muriel Jaquet [Suisse] ; Jacques Mallet [France] ; Barry E. Kosofsky [France, États-Unis] ; Pierre Gressens [France]	Lentiviral‐mediated gene transfer of brain‐derived neurotrophic factor is neuroprotective in a mouse model of neonatal excitotoxic challenge
000995 (2006)	Manuel Schiff [France] ; Manuele Miné [France] ; Michèle Brivet [France] ; Cécile Marsac [France] ; Monique Elmaleh-Bergés [France] ; Philippe Evrard [France] ; Hélène Ogier De Baulny [France]	Leigh's disease due to a new mutation in the PDHX gene
000A38 (2006)	A. Guénégou [France] ; B. Leynaert [France] ; J. Bénessiano [France] ; I. Pin [France] ; P. Demoly [France] ; F. Neukirch [France] ; J. Boczkowski [France] ; M. Aubier [France]	Association of lung function decline with the heme oxygenase-1 gene promoter microsatellite polymorphism in a general population sample. Results from the European Community Respiratory Health Survey (ECRHS), France
000A52 (2006)	Martine Barkats [France] ; Philippe Horellou [France] ; Philippe Colin [France] ; Stéphanie Millecamps [France] ; Nicole Faucon-Biguet [France] ; Jacques Mallet [France]	1‐methyl‐4‐phenylpyridinium neurotoxicity is attenuated by adenoviral gene transfer of human Cu/Zn superoxide dismutase
000A53 (2005)	E. Guérin [France] ; G. Marquet [France] ; A. Burgun [France] ; O. Loréal [France] ; L. Berti-Equille [France] ; U. Leser [Allemagne] ; F. Moussouni [France]	Integrating and Warehousing Liver Gene Expression Data and Related Biomedical Resources in GEDAW
000A54 (2005)	E. Guérin [France] ; G. Marquet [France] ; A. Burgun [France] ; O. Loréal [France] ; L. Berti-Equille [France] ; U. Leser [Allemagne] ; F. Moussouni [France]	Integrating and Warehousing Liver Gene Expression Data and Related Biomedical Resources in GEDAW
000B13 (2005)	Abdelaziz Tlili [Tunisie] ; Ilhem Charfedine [Tunisie] ; Imed Lahmar [Tunisie] ; Zaineb Benzina [Tunisie] ; Ben Amor Mohamed [Tunisie] ; Dominique Weil [France] ; Nabil Idriss [Tunisie] ; Mohamed Drira [Tunisie] ; Saber Masmoudi [Tunisie] ; Hammadi Ayadi [Tunisie]	Identification of a novel frameshift mutation in the DFNB31/WHRN gene in a Tunisian consanguineous family with hereditary non‐syndromic recessive hearing loss

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