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Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71

Neurobiology of disease, 2011-07, Vol.43 (1), p.134-141

2011

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Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions

PloS one, 2009-08, Vol.4 (8), p.e6574-e6574

2009

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Regeneration and Transdifferentiation Potential of Muscle‐Derived Stem Cells Propagated as Myospheres

Stem cells (Dayton, Ohio), 2006-07, Vol.24 (7), p.1769-1778

2006

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Dystrophin-dependent and -independent AQP4 pools are expressed in the mouse brain

Glia, 2008-06, Vol.56 (8), p.869-876

2008

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Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy

The EMBO journal, 2007-01, Vol.26 (2), p.481-493

2007

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Dystrophin deficiency in Drosophila reduces lifespan and causes a dilated cardiomyopathy phenotype

Aging cell, 2008-04, Vol.7 (2), p.237-249

2008

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Farewell to Professor David Yaffe – A Pillar of the Myogenesis Field

European journal of translational myology, 2020-08

2020

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Cloned myogenic cells can transdifferentiate in vivo into neuron-like cells

PloS one, 2010-01, Vol.5 (1), p.e8814-e8814

2010

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Correction: Role of Mental Retardation-Associated Dystrophin-Gene Product Dp71 in Excitatory Synapse Organization, Synaptic Plasticity and Behavioral Functions

PloS one, 2010-01, Vol.5 (1)

2010

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Dp71 The most abundant non-muscle product of the Dystrophin gene

Frontiers in human neuroscience, 2013, Vol.7

2013

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The dystrophin / utrophin homologues in Drosophila and in sea urchin

Gene, 2001-01, Vol.263 (1-2), p.17-29

2001

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A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene

Human molecular genetics, 1993-11, Vol.2 (11), p.1883-1888

1993

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Dystrophin Dp71 Expression Is Down-regulated during Myogenesis

The Journal of biological chemistry, 2005-02, Vol.280 (7), p.5290-5299

2005

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Kir4.1 and AQP4 associate with Dp71- and utrophin-DAPs complexes in specific and defined microdomains of Müller retinal glial cell membrane

Glia, 2008-04, Vol.56 (6), p.597-610

2008

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Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina

Human molecular genetics, 2003-07, Vol.12 (13), p.1543-1554

2003

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Farewell to Professor David Yaffe - A pillar of the myogenesis field

European journal of translational myology, 2020-09, Vol.30 (3), p.9306

2020

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The Drosophila homologue of the dystrophin gene – Introns containing promoters are the major contributors to the large size of the gene

FEBS letters, 2005-10, Vol.579 (24), p.5365-5371

2005

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Specificity of expression of the muscle and brain dystrophin gene promoters in muscle and brain cells

Neuron (Cambridge, Mass.), 1990-12, Vol.5 (6), p.881-888

1990

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The Cellular Prion Protein Colocalizes with the Dystroglycan Complex in the Brain

Journal of neurochemistry, 2000-11, Vol.75 (5), p.1889-1897

2000

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Dystrophin Dp71 expression is down-regulated during myogenesis: role of Sp1 and Sp3 on the Dp71 promoter activity

The Journal of biological chemistry, 2005-02, Vol.280 (7), p.5290

2005

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Muscle-specific activation of a methylated chimeric actin gene

Cell, 1986-08, Vol.46 (3), p.409-416

1986

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Characterization and cell type distribution of a novel, major transcript of the Duchenne Muscular Dystrophy gene

Differentiation (London), 1992-04, Vol.49 (3), p.187-193

1992

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Targeted Inactivation of Dp71, the Major Non-Muscle Product of the DMD Gene: Differential Activity of the Dp71 Promoter during Development

Human molecular genetics, 1999-01, Vol.8 (1), p.1-10

1999

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A 71-Kilodalton Protein is a Major Product of the Duchenne Muscular Dystrophy Gene in Brain and Other Nonmuscle Tissues

Proceedings of the National Academy of Sciences - PNAS, 1992-06, Vol.89 (12), p.5346-5350

1992

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Acute pathophysiological effects of muscle-expressed Dp71 transgene on normal and dystrophic mouse muscle

Journal of applied physiology (1985), 2003-11, Vol.95 (5), p.1861-1866

2003

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Altered presynaptic ultrastructure in excitatory hippocampal synapses of mice lacking dystrophins Dp427 or Dp71

Role of mental retardation-associated dystrophin-gene product Dp71 in excitatory synapse organization, synaptic plasticity and behavioral functions

Regeneration and Transdifferentiation Potential of Muscle‐Derived Stem Cells Propagated as Myospheres

Dystrophin-dependent and -independent AQP4 pools are expressed in the mouse brain

Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy

Dystrophin deficiency in Drosophila reduces lifespan and causes a dilated cardiomyopathy phenotype

Farewell to Professor David Yaffe – A Pillar of the Myogenesis Field

Cloned myogenic cells can transdifferentiate in vivo into neuron-like cells

Correction: Role of Mental Retardation-Associated Dystrophin-Gene Product Dp71 in Excitatory Synapse Organization, Synaptic Plasticity and Behavioral Functions

Dp71 The most abundant non-muscle product of the Dystrophin gene

The dystrophin / utrophin homologues in Drosophila and in sea urchin

A housekeeping type promoter, located in the 3' region of the Duchenne muscular dystrophy gene, controls the expression of Dp71, a major product of the gene

Dystrophin Dp71 Expression Is Down-regulated during Myogenesis

Kir4.1 and AQP4 associate with Dp71- and utrophin-DAPs complexes in specific and defined microdomains of Müller retinal glial cell membrane

Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina

Farewell to Professor David Yaffe - A pillar of the myogenesis field

The Drosophila homologue of the dystrophin gene – Introns containing promoters are the major contributors to the large size of the gene

Specificity of expression of the muscle and brain dystrophin gene promoters in muscle and brain cells

The Cellular Prion Protein Colocalizes with the Dystroglycan Complex in the Brain

Dystrophin Dp71 expression is down-regulated during myogenesis: role of Sp1 and Sp3 on the Dp71 promoter activity

Muscle-specific activation of a methylated chimeric actin gene

Characterization and cell type distribution of a novel, major transcript of the Duchenne Muscular Dystrophy gene

Targeted Inactivation of Dp71, the Major Non-Muscle Product of the DMD Gene: Differential Activity of the Dp71 Promoter during Development

A 71-Kilodalton Protein is a Major Product of the Duchenne Muscular Dystrophy Gene in Brain and Other Nonmuscle Tissues

Acute pathophysiological effects of muscle-expressed Dp71 transgene on normal and dystrophic mouse muscle

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