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CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development

PLoS genetics, 2009-08, Vol.5 (8), p.e1000607-e1000607

2009

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The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain

Neurobiology of disease, 2004-06, Vol.16 (1), p.29-40

2004

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Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain

The Journal of biological chemistry, 2009-07, Vol.284 (28), p.18980-18993

2009

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Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

Human molecular genetics, 2002-04, Vol.11 (8), p.885-891

2002

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Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain: POSSIBLE ROLE OF CLARIN-1 IN ORGANIZING THE ACTIN CYTOSKELETON

The Journal of biological chemistry, 2009-07, Vol.284 (28), p.18980-18993

2009

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Speech recognition and communication outcomes with cochlear implantation in Usher syndrome type 3

Otology & neurotology, 2012-01, Vol.33 (1), p.38-41

2012

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Alternative splice variants of the USH3A gene Clarin 1 (CLRN1)

European journal of human genetics : EJHG, 2011-01, Vol.19 (1), p.30-35

2011

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Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane

Molecular vision, 2009-09, Vol.15, p.1806-1818

2009

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Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3

Molecular biology of the cell, 2002-07, Vol.13 (7), p.2410-2420

2002

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Two Finnish USH1B patients with three novel mutations in myosin VIIA

Molecular vision, 2006-09, Vol.12, p.1093-1097

2006

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CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development: e1000607

PLoS genetics, 2009-08, Vol.5 (8)

2009

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Toward Cloning of a Novel Ataxia Gene: Refined Assignment and Physical Map of the IOSCA Locus (SCA8) on 10q24

Genomics (San Diego, Calif.), 1997-01, Vol.39 (2), p.185-191

1997

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Positional Cloning of the CLN5 Gene Defective in the Finnish Variant of the LINCL

Molecular genetics and metabolism, 1999-04, Vol.66 (4), p.324-328

1999

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Utilization of FISH in positional cloning: an example on 13q22

Genome research, 1996-10, Vol.6 (10), p.1002-1012

1996

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A Physical Map of the 6q14–q15 Region Harboring the Locus for the Lysosomal Membrane Sialic Acid Transport Defect

Genomics (San Diego, Calif.), 1996-10, Vol.37 (1), p.62-67

1996

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Developmental expression of palmitoyl protein thioesterase in normal mice

Brain research. Developmental brain research, 1999-12, Vol.118 (1), p.1-11

1999

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HLA Markers in a Community-based Rheumatoid Arthritis Series

Annals of medicine (Helsinki), 1997-08, Vol.29 (4), p.291-296

1997

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Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCLFinnish; CLN5)

Prenatal diagnosis, 1999-07, Vol.19 (7), p.685-688

1999

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CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development

The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain

Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain

Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

Clarin-1, Encoded by the Usher Syndrome III Causative Gene, Forms a Membranous Microdomain: POSSIBLE ROLE OF CLARIN-1 IN ORGANIZING THE ACTIN CYTOSKELETON

Speech recognition and communication outcomes with cochlear implantation in Usher syndrome type 3

Alternative splice variants of the USH3A gene Clarin 1 (CLRN1)

Disease-causing mutations in the CLRN1 gene alter normal CLRN1 protein trafficking to the plasma membrane

Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3

Two Finnish USH1B patients with three novel mutations in myosin VIIA

CLRN1 Is Nonessential in the Mouse Retina but Is Required for Cochlear Hair Cell Development: e1000607

Toward Cloning of a Novel Ataxia Gene: Refined Assignment and Physical Map of the IOSCA Locus (SCA8) on 10q24

Positional Cloning of the CLN5 Gene Defective in the Finnish Variant of the LINCL

Utilization of FISH in positional cloning: an example on 13q22

A Physical Map of the 6q14–q15 Region Harboring the Locus for the Lysosomal Membrane Sialic Acid Transport Defect

Developmental expression of palmitoyl protein thioesterase in normal mice

HLA Markers in a Community-based Rheumatoid Arthritis Series

Prenatal diagnosis of variant late infantile neuronal ceroid lipofuscinosis (vLINCLFinnish; CLN5)

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