moiety < molecular < molecules

Facettes :

List of bibliographic references indexed by molecular

Number of relevant bibliographic references: 23.
[0-20] [0 - 20][0 - 23][20-22][20-40]

Ident.	Authors (with country if any)	Title
000840 (2010)	C. Savio Chan [États-Unis] ; Tracy S. Gertler [États-Unis] ; D. James Surmeier [États-Unis]	A molecular basis for the increased vulnerability of substantia nigra dopamine neurons in aging and Parkinson's disease
000A30 (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
000B05 (2009)	H. F. Harbo [Norvège] ; J. Finsterer [Autriche] ; J. Baets [Belgique] ; C. Van Broeckhoven [Belgique] ; S. Di Donato [Italie] ; B. Fontaine [France] ; P. De Jonghe [Belgique] ; A. Lossos [Israël] ; T. Lynch [Irlande (pays)] ; C. Mariotti [Italie] ; L. Schöls [Allemagne] ; A. Spinazzola [Italie] ; Z. Szolnoki [Hongrie] ; S. J. Tabrizi [Royaume-Uni] ; C. Tallaksen [Norvège] ; M. Zeviani [Italie] ; J. Burgunder [Suisse] ; T. Gasser [Allemagne]	EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington’s disease, Parkinson’s disease and dystonias
000C44 (2008)	John Svaren [États-Unis] ; Dies Meijer [Pays-Bas]	The molecular machinery of myelin gene transcription in Schwann cells
000D45 (2008)	Peter Jenner [Royaume-Uni]	Molecular mechanisms of L-DOPA-induced dyskinesia
000D46 (2008)	Yi Wei Lu [Singapour] ; Eng-King Tan [Singapour]	Molecular biology changes associated with LRRK2 mutations in Parkinson's disease
001009 (2007)	M. C. Shih [Brésil] ; A. C. Felicio [Brésil] ; C. De Oliveira Godeiro-Junior [Brésil] ; P. De Carvalho Aguiar [Brésil] ; L. A. F. De Andrade [Brésil] ; H. B. Ferraz ; R. A. Bressan [Brésil]	Molecular imaging in hereditary forms of parkinsonism
001012 (2007)	Michelle L. Block [États-Unis] ; Luigi Zecca [Italie] ; Jau-Shyong Hong [États-Unis]	Microglia-mediated neurotoxicity: uncovering the molecular mechanisms
001386 (2005)	Bego A Diosdado ; Erica Van Oort ; Cisca Wijmenga	“Coelionomics”: towards understanding the molecular pathology of coeliac disease
001465 (2005)	Sonia Gandhi [Royaume-Uni] ; Nicholas W. Wood [Royaume-Uni]	Molecular pathogenesis of Parkinson's disease
001466 (2005)	Paul J. Muchowski [États-Unis] ; Jennifer L. Wacker [États-Unis]	Modulation of neurodegeneration by molecular chaperones
001689 (2003)	Jeffrey L. Cummings [États-Unis]	Toward a molecular neuropsychiatry of neurodegenerative diseases
001701 (2003)	Kah Leong Lim ; Valina L. Dawson [États-Unis] ; Ted M. Dawson [États-Unis]	The Cast of Molecular Characters in Parkinson's Disease
001741 (2003)	Carl J. Vaughan ; Yolanda Hom ; Daniel A. Okin ; Deborah A. Mcdermott ; Bruce B. Lerman [États-Unis] ; Craig T. Basson	Molecular Genetic Analysis of PRKAG2 in Sporadic Wolff‐Parkinson‐White Syndrome
001A58 (2001)	H. Watkins [Royaume-Uni]	Hypertrophic cardiomyopathy: from molecular and genetic mechanisms to clinical management
001B81 (2000)	Christian Rohlff [Royaume-Uni]	Proteomics in molecular medicine: Applications in central nervous systems disorders
001C01 (2000)	Fred W. Van Leeuwen [Pays-Bas] ; David F. Fischer [Pays-Bas] ; Darlene Kamel [Pays-Bas] ; Jacqueline A. Sluijs [Pays-Bas] ; Marc A. F. Sonnemans [Pays-Bas] ; Rob Benne [Pays-Bas] ; Dick F. Swaab [Pays-Bas] ; Ahmad Salehi [Pays-Bas] ; Elly M. Hol [Pays-Bas]	Molecular misreading: a new type of transcript mutation expressed during aging
001C02 (2000)	M. Jimenez Del Rio [Colombie] ; C. Velez-Pardo [Colombie]	Molecular mechanism of monoamine toxicity in Parkinson’s disease: hypothetical cell death model
001C03 (2000)	Fred W. Van Leeuwen [Pays-Bas] ; David F. Fischer [Pays-Bas] ; Rob Benne [Pays-Bas] ; Elly M. Hol [Pays-Bas]	Molecular Misreading: A New Type of Transcript Mutation in Gerontology
002156 (1996)	U. Müller [Allemagne] ; B. Graeber [Allemagne]	Neurogenetic diseases: molecular diagnosis and therapeutic approaches
002425 (1994)	S. Umeki [Japon]	Mechanisms for the activation/electron transfer of neutrophil NADPH-oxidase complex and molecular pathology of chronic granulomatous disease

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