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RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1

PloS one, 2014-09, Vol.9 (9), p.e107324-e107324

2014

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Biochemistry of Tau in Alzheimer's disease and related neurological disorders

Expert review of proteomics, 2008-04, Vol.5 (2), p.207-224

2008

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Myotonic Dystrophy: an RNA Toxic Gain of Function Tauopathy?

Advances in experimental medicine and biology, 2019-01, Vol.1184, p.207-216

2019

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ETR-3 represses Tau exons 2/3 inclusion, a splicing event abnormally enhanced in myotonic dystrophy type I

Journal of neuroscience research, 2006-09, Vol.84 (4), p.852-859

2006

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Brain pathology in myotonic dystrophy: when tauopathy meets spliceopathy and RNAopathy

Frontiers in molecular neuroscience, 2014-01, Vol.6, p.57

2014

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Regulation of human MAPT gene expression

Molecular neurodegeneration, 2015-07, Vol.10 (1), p.28-28, Article 28

2015

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Analysis of Exonic Regions Involved in Nuclear Localization, Splicing Activity, and Dimerization of Muscleblind-like-1 Isoforms

The Journal of biological chemistry, 2011-05, Vol.286 (18), p.16435-16446

2011

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Evidence of a balance between phosphorylation and O-GlcNAc glycosylation of Tau proteins—a role in nuclear localization

Biochimica et biophysica acta, 2003-01, Vol.1619 (2), p.167-176

2003

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Immunodetection of Tau microtubule-associated protein in human sperm and testis

Asian journal of andrology, 2014-11, Vol.16 (6), p.927-928

2014

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Transcriptional regulation of the human ST6GAL2 gene in cerebral cortex and neuronal cells

Glycoconjugate journal, 2010-01, Vol.27 (1), p.99-114

2010

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Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1

Biochimica et biophysica acta, 2006-04, Vol.1762 (4), p.460-467

2006

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O-glycosylation of the nuclear forms of Pax-6 products in quail neuroretina cells

Journal of cellular biochemistry, 2002, Vol.85 (1), p.208-218

2002

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Defining the human sperm microtubulome: an integrated genomics approach

Biology of reproduction, 2017-01, Vol.96 (1), p.93-106

2017

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Tau pathology modulates Pin1 post-translational modifications and may be relevant as biomarker

Neurobiology of aging, 2013-03, Vol.34 (3), p.757-769

2013

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Altered splicing of Tau in DM1 is different from the foetal splicing process

FEBS letters, 2009-02, Vol.583 (4), p.675-679

2009

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Effect of okadaic acid on O-linked N-acetylglucosamine levels in a neuroblastoma cell line

Biochimica et biophysica acta, 1999-10, Vol.1472 (1), p.71-81

1999

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Synthesis and Regulation of Apolipoprotein E during the Differentiation of Human Neuronal Precursor NT2/D1 Cells into Postmitotic Neurons

Experimental neurology, 2000-12, Vol.166 (2), p.415-421

2000

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Alzheimer-specific epitope of AT100 in transfected cell lines with tau: toward an efficient cell model of tau abnormal phosphorylation

Neuroscience letters, 1998-10, Vol.255 (1), p.13-16

1998

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Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2

Biochimica et biophysica acta, 2014-04, Vol.1842 (4), p.654-664

2014

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Synthesis of apolipoprotein E (ApoE) mRNA by human neuronal-type SK N SH-SY 5Y cells and its regulation by nerve growth factor and ApoE

Neuroscience letters, 1999-04, Vol.265 (2), p.147-150

1999

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Crystallization, enzymatic cleavage, and the polarity of the adenovirus type 2 fiber

Virology (New York, N.Y.), 1987-11, Vol.161 (1), p.121-128

1987

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Functional and structural effects of an Ala to Val mutation in the adenovirus serotype 2 fibre

Journal of molecular biology, 1991-02, Vol.217 (3), p.477-486

1991

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Human adenovirus-host cell interactions: comparative study with members of subgroups B and C

Journal of Virology, 1990-08, Vol.64 (8), p.3661-3673

1990

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O-GlcNAc glycosylation and neurological disorders

Advances in experimental medicine and biology, 2003, Vol.535, p.189

2003

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RBFOX1 cooperates with MBNL1 to control splicing in muscle, including events altered in myotonic dystrophy type 1

Biochemistry of Tau in Alzheimer's disease and related neurological disorders

Myotonic Dystrophy: an RNA Toxic Gain of Function Tauopathy?

ETR-3 represses Tau exons 2/3 inclusion, a splicing event abnormally enhanced in myotonic dystrophy type I

Brain pathology in myotonic dystrophy: when tauopathy meets spliceopathy and RNAopathy

Regulation of human MAPT gene expression

Analysis of Exonic Regions Involved in Nuclear Localization, Splicing Activity, and Dimerization of Muscleblind-like-1 Isoforms

Evidence of a balance between phosphorylation and O-GlcNAc glycosylation of Tau proteins—a role in nuclear localization

Immunodetection of Tau microtubule-associated protein in human sperm and testis

Transcriptional regulation of the human ST6GAL2 gene in cerebral cortex and neuronal cells

Brain-specific change in alternative splicing of Tau exon 6 in myotonic dystrophy type 1

O-glycosylation of the nuclear forms of Pax-6 products in quail neuroretina cells

Defining the human sperm microtubulome: an integrated genomics approach

Tau pathology modulates Pin1 post-translational modifications and may be relevant as biomarker

Altered splicing of Tau in DM1 is different from the foetal splicing process

Effect of okadaic acid on O-linked N-acetylglucosamine levels in a neuroblastoma cell line

Comment les acteurs moléculaires de la pathologie Alzheimer permettent de comprendre la démence ? Quelles conséquences diagnostiques et thérapeutiques ?

Synthesis and Regulation of Apolipoprotein E during the Differentiation of Human Neuronal Precursor NT2/D1 Cells into Postmitotic Neurons

Alzheimer-specific epitope of AT100 in transfected cell lines with tau: toward an efficient cell model of tau abnormal phosphorylation

Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2

Synthesis of apolipoprotein E (ApoE) mRNA by human neuronal-type SK N SH-SY 5Y cells and its regulation by nerve growth factor and ApoE

Crystallization, enzymatic cleavage, and the polarity of the adenovirus type 2 fiber

Functional and structural effects of an Ala to Val mutation in the adenovirus serotype 2 fibre

Human adenovirus-host cell interactions: comparative study with members of subgroups B and C

O-GlcNAc glycosylation and neurological disorders

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