Ngā hua rapu kaituhi

1

FMR1: A gene with three faces mā Ben A. Oostra, Rob Willemsen

I whakaputaina 2009

Whiwhi kuputuhi katoa
Revisão

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2

Fragile X syndrome: From protein function to therapy mā Claudia Bagni, Ben A. Oostra

I whakaputaina 2013

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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3

Microsatellite repeat instability and neurological disease mā Judith R. Brouwer, Rob Willemsen, Ben A. Oostra

I whakaputaina 2009

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Revisão

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4

The <i>FMR1</i> gene and fragile X‐associated tremor/ataxia syndrome mā Judith R. Brouwer, Rob Willemsen, Ben A. Oostra

I whakaputaina 2008

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Revisão

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5

Cloning, Characterization and Properties of Plasmids Containing CGG Triplet Repeats from the FMR-1 Gene mā Miho Shimizu, Robert Gellibolian, Ben A. Oostra, Robert D. Wells

I whakaputaina 1996

Whiwhi kuputuhi katoa
Artigo

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6

Characterization of the human lysosomal α-glucosidase gene mā Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Arnold Reuser, Ben A. Oostra

I whakaputaina 1990

Whiwhi kuputuhi katoa
Artigo

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7

Deletion loop mutagenesis: a novel method for the construction of point mutations using deletion mutants mā Daniel Kalderon, Ben A. Oostra, Barry K. Ely, Alan E. Smith

I whakaputaina 1982

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Artigo

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8

Potential therapeutic interventions for fragile X syndrome mā Josien Levenga, Femke M.S. de Vrij, Ben A. Oostra, Rob Willemsen

I whakaputaina 2010

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Revisão

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9

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments mā Elisabetta Tabolacci, Roberta Pietrobono, Umberto Moscato, Ben A. Oostra, Pietro Chiurazzi, Giovanni Neri

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

Human lysosomal alpha-glucosidase. Characterization of the catalytic site mā M M Hermans, Marian A. Kroos, J. Van Beeumen, Ben A. Oostra, Arnold Reuser

I whakaputaina 1991

Whiwhi kuputuhi katoa
Artigo

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11

The fragile X syndrome. mā Bert Ba de Vries, D. J. J. Halley, Ben A. Oostra, Martinus F. Niermeijer

I whakaputaina 1998

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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12

Synergistic Effect of Histone Hyperacetylation and DNA Demethylation in the Reactivation of the FMR1 Gene mā Pietro Chiurazzi, Maria Grazia Pomponi, Roberta Pietrobono, C.E. Bakker, Giovanni Neri, Ben A. Oostra

I whakaputaina 1999

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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13

Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P mā Filippo Tamanini, Leontine van Unen, Cathy Bakker, Nicoletta Sacchi, H. Galjaard, Ben A. Oostra, A. T. Hoogeveen

I whakaputaina 1999

Whiwhi kuputuhi katoa
Artigo

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14

A Mutation in the Interferon-γ –Receptor Gene and Susceptibility to Mycobacterial Infection mā Melanie J. Newport, Clare Huxley, Sara Huston, Catherine M. Hawrylowicz, Ben A. Oostra, Robert Williamson, Michael Levin

I whakaputaina 1996

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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15

Transport of Fragile X Mental Retardation Protein via Granules in Neurites of PC12 Cells mā Yolanda de Diego‐Otero, Lies‐Anne Severijnen, Gert van Cappellen, Mariëtte Schrier, Ben A. Oostra, Rob Willemsen

I whakaputaina 2002

Whiwhi kuputuhi katoa
Artigo

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16

Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome mā S Musumeci, Paolo Bosco, Giuseppe Calabrese, Cathy Bakker, Giovanni Battista De Sarro, Maurizio Elia, Raffaele Ferri, Ben A. Oostra

I whakaputaina 2000

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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17

Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome mā Leonardo Restivo, Francesca Ferrari, Enrica Passino, Carmelo Sgobio, Jörg Bock, Ben A. Oostra, Claudia Bagni, Martine Ammassari‐Teule

I whakaputaina 2005

Whiwhi kuputuhi katoa
Artigo

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18

A Reduced Number of Metabotropic Glutamate Subtype 5 Receptors Are Associated with Constitutive Homer Proteins in a Mouse Model of Fragile X Syndrome mā Rosario Giuffrida, S Musumeci, Simona D’Antoni, C. Bonaccorso, Anna Maria Giuffrida‐Stella, Ben A. Oostra, Maria Vincenza Catania

I whakaputaina 2005

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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19

Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of <i>Fmr1</i> knockout mice mā Yair Pilpel, Alexander Kolleker, Sven Berberich, Melanie Ginger, Andreas Frick, Edwin Mientjes, Ben A. Oostra, Peter H. Seeburg

I whakaputaina 2008

Whiwhi kuputuhi katoa
Artigo

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20

Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia mā Marialuisa Quadri, Giovanni Cossu, Valeria Saddi, Erik Simons, Daniela Murgia, Maurizio Melis, Anna Ticca, Ben A. Oostra, Vincenzo Bonifati

I whakaputaina 2011

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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Ngā hua rapu - Ben A. Oostra

FMR1: A gene with three faces mā Ben A. Oostra, Rob Willemsen

Fragile X syndrome: From protein function to therapy mā Claudia Bagni, Ben A. Oostra

Microsatellite repeat instability and neurological disease mā Judith R. Brouwer, Rob Willemsen, Ben A. Oostra

The <i>FMR1</i> gene and fragile X‐associated tremor/ataxia syndrome mā Judith R. Brouwer, Rob Willemsen, Ben A. Oostra

Cloning, Characterization and Properties of Plasmids Containing CGG Triplet Repeats from the FMR-1 Gene mā Miho Shimizu, Robert Gellibolian, Ben A. Oostra, Robert D. Wells

Characterization of the human lysosomal α-glucosidase gene mā Lies H. Hoefsloot, Marianne Hoogeveen‐Westerveld, Arnold Reuser, Ben A. Oostra

Deletion loop mutagenesis: a novel method for the construction of point mutations using deletion mutants mā Daniel Kalderon, Ben A. Oostra, Barry K. Ely, Alan E. Smith

Potential therapeutic interventions for fragile X syndrome mā Josien Levenga, Femke M.S. de Vrij, Ben A. Oostra, Rob Willemsen

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments mā Elisabetta Tabolacci, Roberta Pietrobono, Umberto Moscato, Ben A. Oostra, Pietro Chiurazzi, Giovanni Neri

Human lysosomal alpha-glucosidase. Characterization of the catalytic site mā M M Hermans, Marian A. Kroos, J. Van Beeumen, Ben A. Oostra, Arnold Reuser

The fragile X syndrome. mā Bert Ba de Vries, D. J. J. Halley, Ben A. Oostra, Martinus F. Niermeijer

Synergistic Effect of Histone Hyperacetylation and DNA Demethylation in the Reactivation of the FMR1 Gene mā Pietro Chiurazzi, Maria Grazia Pomponi, Roberta Pietrobono, C.E. Bakker, Giovanni Neri, Ben A. Oostra

Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P mā Filippo Tamanini, Leontine van Unen, Cathy Bakker, Nicoletta Sacchi, H. Galjaard, Ben A. Oostra, A. T. Hoogeveen

A Mutation in the Interferon-γ –Receptor Gene and Susceptibility to Mycobacterial Infection mā Melanie J. Newport, Clare Huxley, Sara Huston, Catherine M. Hawrylowicz, Ben A. Oostra, Robert Williamson, Michael Levin

Transport of Fragile X Mental Retardation Protein via Granules in Neurites of PC12 Cells mā Yolanda de Diego‐Otero, Lies‐Anne Severijnen, Gert van Cappellen, Mariëtte Schrier, Ben A. Oostra, Rob Willemsen

Audiogenic Seizures Susceptibility in Transgenic Mice with Fragile X Syndrome mā S Musumeci, Paolo Bosco, Giuseppe Calabrese, Cathy Bakker, Giovanni Battista De Sarro, Maurizio Elia, Raffaele Ferri, Ben A. Oostra

Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome mā Leonardo Restivo, Francesca Ferrari, Enrica Passino, Carmelo Sgobio, Jörg Bock, Ben A. Oostra, Claudia Bagni, Martine Ammassari‐Teule

A Reduced Number of Metabotropic Glutamate Subtype 5 Receptors Are Associated with Constitutive Homer Proteins in a Mouse Model of Fragile X Syndrome mā Rosario Giuffrida, S Musumeci, Simona D’Antoni, C. Bonaccorso, Anna Maria Giuffrida‐Stella, Ben A. Oostra, Maria Vincenza Catania

Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of <i>Fmr1</i> knockout mice mā Yair Pilpel, Alexander Kolleker, Sven Berberich, Melanie Ginger, Andreas Frick, Edwin Mientjes, Ben A. Oostra, Peter H. Seeburg

Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson’s disease in Sardinia mā Marialuisa Quadri, Giovanni Cossu, Valeria Saddi, Erik Simons, Daniela Murgia, Maurizio Melis, Anna Ticca, Ben A. Oostra, Vincenzo Bonifati

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