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Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

The Journal of cell biology, 2012-10, Vol.199 (2), p.381-399

2012

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Combinatorial complexity of 5' alternative acetylcholinesterase transcripts and protein products

The Journal of biological chemistry, 2004-07, Vol.279 (28), p.29740-29751

2004

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Novel transgenic mice for inducible gene overexpression in pancreatic cells define glucocorticoid receptor-mediated regulations of beta cells

PloS one, 2012-02, Vol.7 (2), p.e30210

2012

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A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Nature genetics, 1997-02, Vol.15 (2), p.157-164

1997

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Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio‐oto‐renal (BOR) syndrome

Developmental dynamics, 1998-12, Vol.213 (4), p.486-499

1998

Volltextzugriff (PDF)

The giant spectrin [beta]V couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route

Human molecular genetics, 2013-09, Vol.22 (18), p.3773-3788

2013

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The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route

Human molecular genetics, 2013-09, Vol.22 (18), p.3773-3788

2013

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Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments

Scientific reports, 2018-01, Vol.8 (1), p.1968-12, Article 1968

2018

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SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous Tissue

Human molecular genetics, 1997-07, Vol.6 (7), p.1069-1077

1997

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Expression of myosin VIIA during mouse embryogenesis

Anatomy and Embryology, 1997-08, Vol.196 (2), p.159-170

1997

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The GABAergic Gudden's dorsal tegmental nucleus: A new relay for serotonergic regulation of sleep-wake behavior in the mouse

Neuropharmacology, 2018-08, Vol.138, p.315-330

2018

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A Subpopulation of Serotonergic Neurons That Do Not Express the 5‑HT1A Autoreceptor

ACS chemical neuroscience, 2013-01, Vol.4 (1), p.89-95

2013

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The zebrafish eya1 gene and its expression pattern during embryogenesis

Development genes and evolution, 1999-07, Vol.209 (7), p.399-410

1999

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On-line confocal imaging of the events leading to structural dedifferentiation of an axonal segment into a growth cone after axotomy

Journal of comparative neurology (1911), 2006-02, Vol.494 (5), p.705-720

2006

Volltextzugriff (PDF)

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice: Usher 1 retinal pathogenesis

The Journal of cell biology, 2012-10, Vol.199 (2), p.381-99

2012

Volltextzugriff (PDF)

When reverse genetics meets physiology: the use of site-specific recombinases in mice

FEBS Letters, 2002-10, Vol.529 (1), p.116-121

2002

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Human Usher 1B/Mouse shaker-1: The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor Cells

Human molecular genetics, 1996-08, Vol.5 (8), p.1171-1178

1996

Volltextzugriff (PDF)

Human Myosin VIIA Responsible for the Usher 1B Syndrome: A Predicted Membrane-Associated Motor Protein Expressed in Developing Sensory Epithelia

Proceedings of the National Academy of Sciences - PNAS, 1996-04, Vol.93 (8), p.3232-3237

1996

Volltextzugriff (PDF)

5-HT1A-iCre, a new transgenic mouse line for genetic analyses of the serotonergic pathway

Molecular and cellular neuroscience, 2007-09, Vol.36 (1), p.27-35

2007

Volltextzugriff (PDF)

Combinatorial Complexity of 5â² Alternative Acetylcholinesterase Transcripts and Protein Products

The Journal of biological chemistry, 2004-07, Vol.279 (28), p.29740

2004

Volltextzugriff (PDF)

Calcium channel blockers inhibit retinal degeneration in the retinal-degeneration-B mutant of Drosophila

Proceedings of the National Academy of Sciences - PNAS, 1992, Vol.89 (1), p.435-439

1992

Volltextzugriff (PDF)

Identification of novel PAX6 mutations in two families with bilateral aniridia

Human mutation, 1998, Vol.12 (2), p.138-138

1998

Volltextzugriff (PDF)

Accumulation of calcium in degenerating photoreceptors of several Drosophila mutants

Visual neuroscience, 1994-07, Vol.11 (4), p.763

1994

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Identification of a novel PAX6 gene mutation in an Aniridia patient

Human mutation, 1996, Vol.7 (4), p.377-377

1996

Volltextzugriff (PDF)

Study of oesophageal motility in Egyptian cirrhotic patients before and after prophylactic endoscopic variceal ligation

Arab journal of gastroenterology, 2009-06, Vol.10 (2), p.49-56

2009

Volltextzugriff (PDF)

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Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

Combinatorial complexity of 5' alternative acetylcholinesterase transcripts and protein products

Novel transgenic mice for inducible gene overexpression in pancreatic cells define glucocorticoid receptor-mediated regulations of beta cells

A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family

Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio‐oto‐renal (BOR) syndrome

The giant spectrin [beta]V couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route

The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route

Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments

SOX22 is a New Member of the SOX Gene Family, Mainly Expressed in Human Nervous Tissue

Expression of myosin VIIA during mouse embryogenesis

The GABAergic Gudden's dorsal tegmental nucleus: A new relay for serotonergic regulation of sleep-wake behavior in the mouse

A Subpopulation of Serotonergic Neurons That Do Not Express the 5‑HT1A Autoreceptor

The zebrafish eya1 gene and its expression pattern during embryogenesis

On-line confocal imaging of the events leading to structural dedifferentiation of an axonal segment into a growth cone after axotomy

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice: Usher 1 retinal pathogenesis

When reverse genetics meets physiology: the use of site-specific recombinases in mice

Human Usher 1B/Mouse shaker-1: The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor Cells

Human Myosin VIIA Responsible for the Usher 1B Syndrome: A Predicted Membrane-Associated Motor Protein Expressed in Developing Sensory Epithelia

5-HT1A-iCre, a new transgenic mouse line for genetic analyses of the serotonergic pathway

Combinatorial Complexity of 5â² Alternative Acetylcholinesterase Transcripts and Protein Products

Calcium channel blockers inhibit retinal degeneration in the retinal-degeneration-B mutant of Drosophila

Identification of novel PAX6 mutations in two families with bilateral aniridia

Accumulation of calcium in degenerating photoreceptors of several Drosophila mutants

Identification of a novel PAX6 gene mutation in an Aniridia patient

Study of oesophageal motility in Egyptian cirrhotic patients before and after prophylactic endoscopic variceal ligation

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