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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

Science (American Association for the Advancement of Science), 2009-02, Vol.323 (5918), p.1205-1208

2009

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A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

Neurology, 2006-03, Vol.66 (6), p.839

2006

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Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

Annals of neurology, 1997-02, Vol.41 (2), p.210-221

1997

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Nature genetics, 1998-09, Vol.20 (1), p.31-36

1998

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A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Nature genetics, 2001-10, Vol.29 (2), p.166-173

2001

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Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

JAMA : the journal of the American Medical Association, 2000-10, Vol.284 (13), p.1664

2000

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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Nature genetics, 1998-09, Vol.20 (1), p.31-36

1998

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Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis

Annals of neurology, 1998-05, Vol.43 (5), p.645-653

1998

Volltextzugriff (PDF)

Specific expression of a retinoic acid-regulated, zinc-finger gene, Rex-1, in preimplantation embryos, trophoblast and spermatocytes

Development (Cambridge), 1991-11, Vol.113 (3), p.815-824

1991

Volltextzugriff (PDF)

Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele

Neurology, 2008-02, Vol.70 (9), p.666

2008

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Chronic Inhibition of Superoxide Dismutase Produces Apoptotic Death of Spinal Neurons

Proceedings of the National Academy of Sciences - PNAS, 1994-05, Vol.91 (10), p.4155-4159

1994

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Expression of REX-1, a gene containing zinc finger motifs, is rapidly reduced by retinoic acid in F9 teratocarcinoma cells

Molecular and Cellular Biology, 1989-12, Vol.9 (12), p.5623-5629

1989

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A Video Camera Model Identification System Using Deep Learning and Fusion

ICASSP 2019 - 2019 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP), 2019, p.8271-8275

2019

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Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22

Neurology, 1999-02, Vol.52 (3), p.510

1999

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An octamer motif contributes to the expression of the retinoic acid-regulated zinc finger gene Rex-1 (Zfp-42) in F9 teratocarcinoma cells

Molecular and Cellular Biology, 1993-05, Vol.13 (5), p.2919-2928

1993

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CuZn Superoxide Dismutase (SOD-1):Tetanus Toxin Fragment C Hybrid Protein for Targeted Delivery of SOD-1 to Neuronal Cells (∗)

The Journal of biological chemistry, 1995-06, Vol.270 (25), p.15434-15442

1995

Volltextzugriff (PDF)

Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13

Genomics (San Diego, Calif.), 1998-04, Vol.49 (1), p.23-29

1998

Volltextzugriff (PDF)

Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

American journal of human genetics, 2003-08, Vol.73 (2), p.397-403

2003

Volltextzugriff (PDF)

Cross-reactivity between herpes simplex virus glycoprotein B and a 63,000-dalton varicella-zoster virus envelope glycoprotein

Journal of Virology, 1985-10, Vol.56 (1), p.333-336

1985

Volltextzugriff (PDF)

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33

Neurogenetics, 1998-12, Vol.2 (1), p.34-42

1998

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Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis

Neuromuscular disorders : NMD, 1996-10, Vol.6 (5), p.361-366

1996

Volltextzugriff (PDF)

Superoxide dismutase and oxygen radical neurotoxicity

Current opinion in neurology, 1996-12, Vol.9 (6), p.486-491

1996

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Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis

Neurogenetics, 2004-12, Vol.5 (4), p.209-213

2004

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Copper/zinc superoxide dismutase mutations and free radical damage in amyotrophic lateral sclerosis

Advances in neurology, 1995, Vol.68, p.41

1995

Volltextzugriff (PDF)

Varicella-zoster virus envelope glycoproteins: Biochemical characterization and identification in clinical material

Virology (New York, N.Y.), 1985-08, Vol.145 (1), p.62-71

1985

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis

Specific expression of a retinoic acid-regulated, zinc-finger gene, Rex-1, in preimplantation embryos, trophoblast and spermatocytes

Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele

Chronic Inhibition of Superoxide Dismutase Produces Apoptotic Death of Spinal Neurons

Expression of REX-1, a gene containing zinc finger motifs, is rapidly reduced by retinoic acid in F9 teratocarcinoma cells

A Video Camera Model Identification System Using Deep Learning and Fusion

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22

An octamer motif contributes to the expression of the retinoic acid-regulated zinc finger gene Rex-1 (Zfp-42) in F9 teratocarcinoma cells

CuZn Superoxide Dismutase (SOD-1):Tetanus Toxin Fragment C Hybrid Protein for Targeted Delivery of SOD-1 to Neuronal Cells (∗)

Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13

Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

Cross-reactivity between herpes simplex virus glycoprotein B and a 63,000-dalton varicella-zoster virus envelope glycoprotein

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33

Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis

Superoxide dismutase and oxygen radical neurotoxicity

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis

Copper/zinc superoxide dismutase mutations and free radical damage in amyotrophic lateral sclerosis

Varicella-zoster virus envelope glycoproteins: Biochemical characterization and identification in clinical material

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