B. Hosler

发表

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

L. Gudas, M. Rogers, B. Hosler, 1991, Development.

Supporting Online Material Materials and Methods Figs. S1 to S7 Tables S1 to S4 References Mutations in the Fus/tls Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

J L Haines, M A Pericak-Vance, J. Haines, 2022 .

A New Mating Compatibility Locus in PHYSARUM POLYCEPHALUM.

P. Youngman, G. Struhl, B. Hosler, 1979, Genetics.

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

H. Horvitz, J. De Belleroche, J. Belleroche, 2006, Neurology.

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

J. Grippo, L. Gudas, G. Larosa, 1989, Molecular and cellular biology.

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

P. Fishman, B. Hosler, J. W. Francis, 1995, The Journal of Biological Chemistry.

50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis

Robert H. Brown, S. Purcell, J. Glass, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

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

C. Kozak, L. Gudas, M. Rogers, 1993, Molecular and cellular biology.

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

H. Horvitz, Robert H. Brown, R. Orrell, 1996, Neuromuscular Disorders.

Identification of three novel mutations in the gene for Cu Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosis

H. Horvitz, Robert H. Brown, P. Sapp, 1995, Neuromuscular Disorders.

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis.

J. Haines, M. Pericak-Vance, H. Horvitz, 2003, American journal of human genetics.

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

Claire L. Simpson, R. Ophoff, H. Horvitz, 2009, Proceedings of the National Academy of Sciences.

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

J. Haines, M. Pericak-Vance, H. Horvitz, 2000, JAMA.

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

R. Schooley, D. Thorley-Lawson, B. Hosler, 1985, Virology.

A novel mutation in the spastin gene in a family with spastic paraplegia

M. Morita, D. McKenna-Yasek, B. Hosler, 2002, Neuroscience Letters.

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

B. Hosler, R. H. Brown, 1995, Advances in neurology.

Varicella-zoster virus gpI and herpes simplex virus gE: phosphorylation and Fc binding.

B. Hosler, D. Waters, C. Edson, 1987, Virology.

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

D. Thorley-Lawson, B. Hosler, D. Waters, 1985, Journal of virology.

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

J. Haines, D. McKenna-Yasek, B. Hosler, 1999, Neurology.

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

Pieter J. de Jong, Saeed Bohlega, Jing Liu, 1998, Nature Genetics.

Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis

H. Horvitz, D. Schoenfeld, M. Cudkowicz, 1997, Annals of neurology.

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

J. Haines, M. Pericak-Vance, Robert H. Brown, 2004, Neurogenetics.

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

J. Haines, H. Horvitz, M. Hamida, 1998, Neurogenetics.

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

S. Scherer, Robert H. Brown, M. Hayden, 2001, Nature Genetics.

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

S. Scherer, Robert H. Brown, M. Hayden, 2001, Nature Genetics.

Survival motor neuron protein in the nucleolus of mammalian neurons

C. Lorson, S. Baserga, Karen A. Wehner, 2002, Brain Research.

Chronic inhibition of superoxide dismutase produces apoptotic death of spinal neurons.

J. Rothstein, R. Kuncl, L. Bristol, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Motoneuron-specific NR3B gene

K. Kidd, J. Landers, W. Speed, 2008, Neurology.

Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.

P. D. de Jong, K. Bossie, J. Gingrich, 1998, Genomics.

Variants in the ALS2 gene are not associated with sporadic amyotrophic lateral sclerosis

Claire L. Simpson, Robert H. Brown, J. Powell, 2003, Neurogenetics.

Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes

P. Andersen, P. Sapp, D. McKenna-Yasek, 2006, Neuroscience Letters.

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

J. Haines, M. Pericak-Vance, H. Horvitz, 2009, Science.

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

M. Pericak-Vance, H. Horvitz, P. D. de Jong, 2009, Science.