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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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X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene

Journal of medical genetics, 2006-08, Vol.43 (8), p.699-704

2006

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Anti-clarin-1 AAV-delivered ribozyme induced apoptosis in the mouse cochlea

Hearing research, 2007-08, Vol.230 (1), p.9-16

2007

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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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Efficient Construction of a Physical Map by Fiber-Fish of the CLN5 Region: Refined Assignment and Long-Range Contig Covering the Critical Region on 13q22

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.71-78

1996

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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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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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The Visual Assignment of Genes by Fiber-Fish: BTF3 Protein Homologue Gene (BTF3) and a Novel Pseudogene of Human RNA Helicase A (DDX9P) on 13q22

Genomics (San Diego, Calif.), 1997-09, Vol.44 (3), p.355-357

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

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

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

2009

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Hydrogen Bonding Effects on the Surface Structure and Photoelectrochemical Properties of Nanostructured SnO2 Electrodes Modified with Porphyrin and Fullerene Composites

The journal of physical chemistry. B, 2005-10, Vol.109 (39), p.18465-18474

2005

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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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Lysosomal localization of the neuronal ceroid lipofuscinosis CLN5 protein

X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene

Anti-clarin-1 AAV-delivered ribozyme induced apoptosis in the mouse cochlea

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

Efficient Construction of a Physical Map by Fiber-Fish of the CLN5 Region: Refined Assignment and Long-Range Contig Covering the Critical Region on 13q22

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

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

The Visual Assignment of Genes by Fiber-Fish: BTF3 Protein Homologue Gene (BTF3) and a Novel Pseudogene of Human RNA Helicase A (DDX9P) on 13q22

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)

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

Hydrogen Bonding Effects on the Surface Structure and Photoelectrochemical Properties of Nanostructured SnO2 Electrodes Modified with Porphyrin and Fullerene Composites

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

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