Protein Subunits < Protein-Serine-Threonine Kinases < Proteins

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List of bibliographic references

Number of relevant bibliographic references: 103.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000319 (2015)	Fatma Nabli ; Samia Ben Sassi ; Rim Amouri ; John E. Duda ; Matthew J. Farrer ; Fayçal Hentati	Motor phenotype of LRRK2-associated Parkinson's disease: a Tunisian longitudinal study.
000339 (2015)	Andrew B. West	Ten years and counting: moving leucine-rich repeat kinase 2 inhibitors to the clinic.
000442 (2014)	Roberta Allegra ; Sara Tunesi ; Roberto Cilia ; Gianni Pezzoli ; Stefano Goldwurm	LRRK2-G2019S mutation is not associated with an increased cancer risk: a kin-cohort study.
000485 (2014)	Gilad Yahalom ; Yael Orlev ; Oren S. Cohen ; Evgenia Kozlova ; Eitan Friedman ; Rivka Inzelberg ; Sharon Hassin-Baer	Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation.
000489 (2014)	Sheila M. Fleming ; Alberto J. Espay	Ribosomal s15: A novel therapeutic target for Parkinson's disease.
000593 (2014)	Avner Thaler ; Moran Artzi ; Anat Mirelman ; Yael Jacob ; Rick C. Helmich ; Bart F L. Van Nuenen ; Tanya Gurevich ; Avi Orr-Urtreger ; Karen Marder ; Susan Bressman ; Bastiaan R. Bloem ; Talma Hendler ; Nir Giladi ; Dafna Ben Bashat	A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriers.
000646 (2014)	Javier Ruiz-Martínez ; Patricia De La Riva ; Maria C. Rodríguez-Oroz ; Elisabet Mondrag N Rezola ; Alberto Bergareche ; Ana Gorostidi ; Belen Gago ; Ainara Estanga ; Nerea Larra Aga ; Cristina Sarasqueta ; Adolfo L Pez De Munain ; José F. Martí Mass	Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2.
000665 (2013)	Eldad Melamed	The G2019S LRRK2 mutation: another morbid burden for Ashkenazi Jews may provide new insights on sporadic Parkinson's disease.
000675 (2013)	Ryosuke Takahashi ; Hodaka Yamakado	Genetic correction will be a standard method for the patient-derived ips cell research?
000676 (2013)	Roy N. Alcalay ; Anat Mirelman ; Rachel Saunders-Pullman ; Ming-X Tang ; Helen Mejia Santana ; Deborah Raymond ; Ernest Roos ; Martha Orbe-Reilly ; Tanya Gurevich ; Anat Bar Shira ; Mali Gana Weisz ; Kira Yasinovsky ; Maayan Zalis ; Avner Thaler ; Andres Deik ; Matthew James Barrett ; Jose Cabassa ; Mark Groves ; Ann L. Hunt ; Naomi Lubarr ; Marta San Luciano ; Joan Miravite ; Christina Palmese ; Rivka Sachdev ; Harini Sarva ; Lawrence Severt ; Vicki Shanker ; Matthew Carrington Swan ; Jeannie Soto-Valencia ; Brooke Johannes ; Robert Ortega ; Stanley Fahn ; Lucien Cote ; Cheryl Waters ; Pietro Mazzoni ; Blair Ford ; Elan Louis ; Oren Levy ; Llency Rosado ; Diana Ruiz ; Tsvyatko Dorovski ; Michael Pauciulo ; William Nichols ; Avi Orr-Urtreger ; Laurie Ozelius ; Lorraine Clark ; Nir Giladi ; Susan Bressman ; Karen S. Marder	Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations.
000746 (2013)	Anat Mirelman ; Talia Heman ; Kira Yasinovsky ; Avner Thaler ; Tanya Gurevich ; Karen Marder ; Susan Bressman ; Anat Bar-Shira ; Avi Orr-Urtreger ; Nir Giladi ; Jeffrey M. Hausdorff	Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation.
000767 (2013)	John Mckinley ; Alan Mccarthy ; Timothy Lynch	Pathogenic LRRK2 mutations in nuclear ageing--a new organelle to study in Parkinson's disease.
000777 (2013)	Soraya Bardien ; Janine Blanckenberg ; Lize Van Der Merwe ; Matthew J. Farrer ; Owen A. Ross	Patient-control association study of the Leucine-Rich repeat kinase 2 (LRRK2) gene in South African Parkinson's disease patients.
000797 (2013)	Michael G. Heckman ; Alexandra I. Soto-Ortolaza ; Jan O. Aasly ; Nadine Abahuni ; Grazia Annesi ; Justin A. Bacon ; Soraya Bardien ; Maria Bozi ; Alexis Brice ; Laura Brighina ; Jonathan Carr ; Marie-Christine Chartier-Harlin ; Efthimios Dardiotis ; Dennis W. Dickson ; Nancy N. Diehl ; Alexis Elbaz ; Carlo Ferrarese ; Brian Fiske ; J Mark Gibson ; Rachel Gibson ; Georgios M. Hadjigeorgiou ; Nobutaka Hattori ; John P A. Ioannidis ; Magdalena Boczarska-Jedynak ; Barbara Jasinska-Myga ; Beom S. Jeon ; Yun Joong Kim ; Christine Klein ; Rejko Kruger ; Elli Kyratzi ; Suzanne Lesage ; Chin-Hsien Lin ; Timothy Lynch ; Demetrius M. Maraganore ; George D. Mellick ; Eugénie Mutez ; Christer Nilsson ; Grzegorz Opala ; Sung Sup Park ; Simona Petrucci ; Andreas Puschmann ; Aldo Quattrone ; Manu Sharma ; Peter A. Silburn ; Young Ho Sohn ; Leonidas Stefanis ; Vera Tadic ; Jessie Theuns ; Hiroyuki Tomiyama ; Ryan J. Uitti ; Enza Maria Valente ; Christine Van Broeckhoven ; Simone Van De Loo ; Demetrios K. Vassilatis ; Carles Vilari O-Güell ; Linda R. White ; Karin Wirdefeldt ; Zbigniew K. Wszolek ; Ruey-Meei Wu ; Faycal Hentati ; Matthew J. Farrer ; Owen A. Ross	Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium.
000856 (2013)	Aikaterina Angeli ; Niccolo E. Mencacci ; Raquel Duran ; Iciar Aviles-Olmos ; Zinovia Kefalopoulou ; Joseph Candelario ; Sarah Rusbridge ; Jennifer Foley ; Priyanka Pradhan ; Marjan Jahanshahi ; Ludvic Zrinzo ; Marwan Hariz ; Nicholas W. Wood ; John Hardy ; Patricia Limousin ; Tom Foltynie	Genotype and phenotype in Parkinson's disease: lessons in heterogeneity from deep brain stimulation.
000942 (2013)	Benjamin Dehay ; Marta Martinez-Vicente ; Guy A. Caldwell ; Kim A. Caldwell ; Zhenyue Yue ; Mark R. Cookson ; Christine Klein ; Miquel Vila ; Erwan Bezard	Lysosomal impairment in Parkinson's disease.
000993 (2013)	Christopher H. Hawkes	Comment to letter: "Identical twins with LRRK2 mutation discordant for Parkinson's disease".
000A06 (2013)	John Hardy	Reply to Letter: Identical twins with leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.
000A60 (2013)	Natalja Funk ; Peter Wieghofer ; Sabrina Grimm ; Richard Schaefer ; Hans-Jörg Bühring ; Thomas Gasser ; Saskia Biskup	Characterization of peripheral hematopoietic stem cells and monocytes in Parkinson's disease.
000A88 (2013)	Ignacio F. Mata ; Victoria Alvarez ; Renee Ribacoba ; Jon Infante ; María Sierra ; Pilar G Mez-Garre ; Pablo Mir ; Sarah Waldherr ; Dora Yearout ; Cyrus P. Zabetian	Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.
000A96 (2013)	Andrew B. Singleton ; Matthew J. Farrer ; Vincenzo Bonifati	The genetics of Parkinson's disease: progress and therapeutic implications.

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