Vinodh Narayanan : rechercher sur Z-Library

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Articles (37)
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Epigenetics, Autism Spectrum, and Neurodevelopmental Disorders

Rangasamy, Sampathkumar, DâMello, Santosh R., Narayanan, Vinodh

Journal:

Neurotherapeutics

Année:

2013

Langue:

english

Fichier:

PDF, 590 KB

english, 2013

Mutation analysis of the M6b gene in patients with Rett syndrome

Narayanan, Vinodh, Olinsky, Shari, Dahle, Elizabeth, Naidu, Sakkubai, Zoghbi, Huda Y.

Journal:

American Journal of Medical Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 72 KB

english, 1998

Expression of members of the proteolipid protein gene family in the developing murine central nervous system

Yan, Yimin, Narayanan, Vinodh, Lagenaur, Carl

Journal:

The Journal of Comparative Neurology

Année:

1996

Langue:

english

Fichier:

PDF, 2.05 MB

english, 1996

Expression of a synapse-associated membrane protein, P84/SHPS-1, and its ligand, IAP/CD47, in mouse retina

Mi, Zhi Ping, Jiang, Peihua, Weng, Wei Li, Lindberg, Frederik P., Narayanan, Vinodh, Lagenaur, Carl F.

Journal:

The Journal of Comparative Neurology

Année:

2000

Langue:

english

Fichier:

PDF, 1.15 MB

english, 2000

Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1

Dr Sinan Çomu, Vinodh Narayanan, Michael Giuliani

Journal:

Annals of Neurology

Année:

1996

Langue:

english

Fichier:

PDF, 338 KB

english, 1996

Partial Structure and Mapping of the Human Myelin P2 Protein Gene

Vinodh Narayanan, Benedetta Ripepi, Ethylin Wang Jabs, Anita Hawkins, Constance Griffin, Gihan Tennekoon

Journal:

Journal of Neurochemistry

Année:

1994

Langue:

english

Fichier:

PDF, 474 KB

english, 1994

Evidence for population variation inTSC1andTSC2gene expression

Garilyn M Jentarra, Stephen G Rice, Shannon Olfers, David Saffen, Vinodh Narayanan

Journal:

BMC Medical Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 3.47 MB

english, 2011

Mapping of the human P84 gene to the subtelomeric region of chromosome 20p

Chad Eckert, Shari Olinsky, James Cummins, Dietrich Stephan, Vinodh Narayanan

Journal:

Somatic Cell and Molecular Genetics

Année:

1997

Langue:

english

Fichier:

PDF, 708 KB

english, 1997

Structure of the Mouse Myelin P2 Protein Gene

Vinodh Narayanan, Klaus H. Kaestner, Gihan I. Tennekoon

Journal:

Journal of Neurochemistry

Année:

1991

Langue:

english

Fichier:

PDF, 697 KB

english, 1991

Identification of Somatic Chromosomal Abnormalities in Hypothalamic Hamartoma Tissue at the GLI3 Locus

David W. Craig, Abraham Itty, Corrie Panganiban, Szabolcs Szelinger, Michael C. Kruer, Aswin Sekar, David Reiman, Vinodh Narayanan, Dietrich A. Stephan, John F. Kerrigan

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 735 KB

english, 2008

Genetic Aspects of Neurocutaneous Disorders

Garilyn Jentarra, Shannon L. Snyder, Vinodh Narayanan

Journal:

Seminars in Pediatric Neurology

Année:

2006

Langue:

english

Fichier:

PDF, 224 KB

english, 2006

Ataxia With Oculomotor Apraxia

Wei Liu, Vinodh Narayanan

Journal:

Seminars in Pediatric Neurology

Année:

2008

Langue:

english

Fichier:

PDF, 625 KB

english, 2008

Genetics and Child Neurology: What Every Trainee/Resident Should Know

Vinodh Narayanan

Journal:

Seminars in Pediatric Neurology

Année:

2011

Langue:

english

Fichier:

PDF, 143 KB

english, 2011

Maturational changes in cell surface antigen expression in the mouse retina and optic pathway

Zhi-Ping Mi, Weili Weng, Mark H Hankin, Vinodh Narayanan, Carl F Lagenaur

Journal:

Developmental Brain Research

Année:

1998

Langue:

english

Fichier:

PDF, 4.76 MB

english, 1998

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

Garilyn M Jentarra, Shannon L Olfers, Stephen G Rice, Nishit Srivastava, Gregg E Homanics, Mary Blue, SakkuBai Naidu, Vinodh Narayanan

Journal:

BMC Neuroscience

Année:

2010

Langue:

english

Fichier:

PDF, 4.75 MB

english, 2010

Cognitive dysfunction inNF1knock-out mice may result from altered vesicular trafficking of APP/DRD3 complex

Elizabeth A Donarum, Rebecca F Halperin, Dietrich A Stephan, Vinodh Narayanan

Journal:

BMC Neuroscience

Année:

2006

Langue:

english

Fichier:

PDF, 496 KB

english, 2006

Gene Expression Profiling in Postmortem Rett Syndrome Brain: Differential Gene Expression and Patient Classification

Carlo Colantuoni, Ok-Hee Jeon, Karim Hyder, Alex Chenchik, Anis H. Khimani, Vinodh Narayanan, Eric P. Hoffman, Walter E. Kaufmann, SakkuBai Naidu, Jonathan Pevsner

Journal:

Neurobiology of Disease

Année:

2001

Langue:

english

Fichier:

PDF, 953 KB

english, 2001

Misplaced peripherally inserted central catheter: an unusual cause of stroke

Sumit Parikh, Vinodh Narayanan

Journal:

Pediatric Neurology

Année:

2004

Langue:

english

Fichier:

PDF, 117 KB

english, 2004

Tuberous sclerosis complex: genetics to pathogenesis

Vinodh Narayanan

Journal:

Pediatric Neurology

Année:

2003

Langue:

english

Fichier:

PDF, 136 KB

english, 2003

Friedreich’s ataxia

Gulay Alper, Vinodh Narayanan

Journal:

Pediatric Neurology

Année:

2003

Langue:

english

Fichier:

PDF, 183 KB

english, 2003

Apoptosis in development and disease of the nervous system: 1. Naturally occurring cell death in the developing nervous system

Vinodh Narayanan

Journal:

Pediatric Neurology

Année:

1997

Langue:

english

Fichier:

PDF, 487 KB

english, 1997

Fuzzy assessment of FMEA for rotary switches: a case study

Vinodh, S., Aravindraj, S., Sathya Narayanan, Ravi, Yogeshwaran, N.

Journal:

The TQM Journal

Année:

2012

Langue:

english

Fichier:

PDF, 220 KB

english, 2012

Molecular cloning of M6: Identification of a PLP/DM20 gene family

Yan, Yimin, Lagenaur, Carl, Narayanan, Vinodh

Journal:

Neuron

Année:

1993

Langue:

english

Fichier:

PDF, 2.16 MB

english, 1993

Electrophysiological Phenotypes of MeCP2 A140V Mutant Mouse Model

Ma, Lu-Yao, Wu, Chen, Jin, Yu, Gao, Ming, Li, Guo-Hui, Turner, Dharshaun, Shen, Jian-Xin, Zhang, Shi-Jiang, Narayanan, Vinodh, Jentarra, Garilyn, Wu, Jie

Journal:

CNS Neuroscience & Therapeutics

Année:

2014

Langue:

english

Fichier:

PDF, 483 KB

english, 2014

Comparison of Anterior Cerebral Artery Blood Flow Velocity and Cerebral Blood Flow during Hypoxia

Rosenberg, Adam A, Narayanan, Vinodh, Douglas Jones, M

Journal:

Pediatric Research

Année:

1985

Langue:

english

Fichier:

PDF, 421 KB

english, 1985

KCNQ2 encephalopathy

Millichap, John J., Park, Kristen L., Tsuchida, Tammy, Ben-Zeev, Bruria, Carmant, Lionel, Flamini, Robert, Joshi, Nishtha, Levisohn, Paul M., Marsh, Eric, Nangia, Srishti, Narayanan, Vinodh, Ortiz-Gon

Journal:

Neurology: Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 574 KB

english, 2016

Dystonia in ATP2B3 -associated X-linked spinocerebellar ataxia

Feyma, Timothy, Ramsey, Keri, Huentelman, Matthew J., Craig, David W., Padilla-Lopez, Sergio, Narayanan, Vinodh, Kruer, Michael C.

Journal:

Movement Disorders

Année:

2016

Langue:

english

Fichier:

PDF, 143 KB

english, 2016

A gain-of-function mutation in the GRIK2 gene causes neurodevelopmental deficits

Guzmán, Yomayra F., Ramsey, Keri, Stolz, Jacob R., Craig, David W., Huentelman, Mathew J., Narayanan, Vinodh, Swanson, Geoffrey T.

Journal:

Neurology: Genetics

Année:

2017

Langue:

english

Fichier:

PDF, 966 KB

english, 2017

Spatial molecular epidemiology of carbapenem resistant and New Delhi Metallo Beta-lactamase ( bla NDM) producing Escherichia coli strains from farmed piglets of India

Pruthvishree, B.S., Vinodh Kumar, O.R., Sinha, D.K., Malik, Y.P.S., Dubal, Z., Desingu, P.A., Shivakumar, M., Krishnaswamy, Narayanan, Singh, B.R.

Journal:

Journal of Applied Microbiology

Année:

2017

Langue:

english

Fichier:

PDF, 1.12 MB

english, 2017

Phenotypic Variability and mTOR Pathway Gene Aberrations in Familial Tuberous Sclerosis

Liang, Winnie, Sekar, Shobana, Nasser, Sara, Adkins, Jonathan, Cuyugan, Lori, Enriquez, Daniel, Rangasamy, Sampath, Narayanan, Vinodh

Journal:

Journal of Pediatric Neurology

Année:

2017

Langue:

english

Fichier:

PDF, 263 KB

english, 2017

Molecular characterisation of bla OXA48 carbapenemase, extended spectrum beta −lactamase (ESBL) and Shiga toxin producing Escherichia coli isolated from farm piglets of India

Nirupama, K.R., Kumar, O.R.Vinodh, Pruthvishree, B.S., Sinha, D.K., Murugan, M.Senthil, Krishnaswamy, Narayanan, Singh, B.R.

Journal:

Journal of Global Antimicrobial Resistance

Année:

2018

Langue:

english

Fichier:

PDF, 679 KB

english, 2018

Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing

Szelinger, Szabolcs, Malenica, Ivana, Corneveaux, Jason J., Siniard, Ashley L., Kurdoglu, Ahmet A., Ramsey, Keri M., Schrauwen, Isabelle, Trent, Jeffrey M., Narayanan, Vinodh, Huentelman, Matthew J.,

Journal:

PLoS ONE

Année:

2014

Langue:

english

Fichier:

PDF, 1.74 MB

english, 2014

Short-term Safety of mTOR Inhibitors in infants and very young children with Tuberous Sclerosis Complex (TSC): Multicentre Clinical Experience

Krueger, Darcy A., Capal, Jamie K., Curatolo, Paolo, Devinsky, Orrin, Ess, Kevin, Tzadok, Michal, Koenig, Mary K., Narayanan, Vinodh, Ramos, Federico, Jozwiak, Sergiusz, de Vries, Petrus, Jansen, Anna

Journal:

European Journal of Paediatric Neurology

Année:

2018

Langue:

english

Fichier:

PDF, 25.63 MB

english, 2018

A novel variant in TAF1 affects gene expression and is associated with X-linked TAF1 intellectual disability syndrome

Hurst, Sarah E., Liktor-Busa, Erika, Moutal, Aubin, Parker, Sara, Rice, Sydney, Szelinger, Szabolcs, Senner, Grant, Hammer, Michael F., Johnstone, Laurel, Ramsey, Keri, Narayanan, Vinodh, Perez-Miller

Journal:

Neuronal Signaling

Année:

2018

Langue:

english

Fichier:

PDF, 1.41 MB

english, 2018

Utilizing RNA and Outlier Analysis to Identify an Intronic Splice‐Altering Variant in AP4S1 in a Sibling Pair with Progressive Spastic Paraplegia

McCullough, Carmel G, Szelinger, Szabolcs, Belnap, Newell, Ramsey, Keri, Schrauwen, Isabelle, Claasen, Ana M, Burke, Leah W, Siniard, Ashley L, Huentelman, Matthew J, Narayanan, Vinodh, Craig, David W

Journal:

Human Mutation

Année:

2019

Langue:

english

Fichier:

PDF, 981 KB

english, 2019

Front Cover, Volume 41, Issue 2

McCullough, Carmel G., Szelinger, Szabolcs, Belnap, Newell, Ramsey, Keri, Schrauwen, Isabelle, Claasen, Ana M., Burke, Leah W., Siniard, Ashley L., Huentelman, Matthew J., Narayanan, Vinodh, Craig, Da

Journal:

Human Mutation

Année:

2020

Fichier:

PDF, 1.44 MB

2020

Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex

Wie, Jinhong, Bharthur, Apoorva, Wolfgang, Morgan, Narayanan, Vinodh, Ramsey, Keri, Aranda, Kimberly, Zhang, Qi, Zhou, Yandong, Ren, Dejian

Journal:

Nature Communications

Année:

2020

Fichier:

PDF, 2.40 MB

2020