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Therapeutic Development in Charcot Marie Tooth Type 1 Disease

International journal of molecular sciences, 2021-06, Vol.22 (13), p.6755

2021

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A Rat Model of Clinically Relevant Extracorporeal Circulation Develops Early Organ Dysfunctions

International journal of molecular sciences, 2023-04, Vol.24 (8), p.7338

2023

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The Promoters of the Survival Motor Neuron Gene ( SMN) and Its Copy ( SMNc) Share Common Regulatory Elements

American journal of human genetics, 1999-05, Vol.64 (5), p.1365-1370

1999

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Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice

Molecular neurobiology, 2022-07, Vol.59 (7), p.4159-4178

2022

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Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

Human molecular genetics, 1994-12, Vol.3 (12), p.2093-2102

1994

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Gene targeting restricted to mouse striated muscle lineage

Nucleic acids research, 1999-10, Vol.27 (19), p.e27

1999

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Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

Human molecular genetics, 2000-03, Vol.9 (5), p.849-858

2000

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The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease

American journal of human genetics, 1997, Vol.60 (1), p.72-79

1997

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α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

Human genetics, 1997-06, Vol.99 (6), p.738-745

1997

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Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH

The EMBO journal, 1997-03, Vol.16 (5), p.1093-1102

1997

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Human colorectal cancer (CRC) antigen CO17-1A/GA733 encoded by adenovirus inhibits growth of established CRC cells in mice

The Journal of immunology (1950), 1997-07, Vol.159 (2), p.763

1997

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Assignment of the human syntaxin 1B gene (STX) to chromosome 16p11.2 by fluorescence in situ hybridization

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.551-553

1996

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1-02-11 Spinal muscular atrophy: Etiology and pathogenesis

Journal of the neurological sciences, 1997-09, Vol.150, p.S6-S6

1997

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Assignment of the Human Syntaxin 1B Gene (STX) to Chromosome 16p11.2 by Fluorescencein SituHybridization

Genomics (San Diego, Calif.), 1996-09, Vol.36 (3), p.551-553

1996

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Baculovirus recombinant expressing a secreted form of a transmembrane carcinoma-associated antigen

Cancer research (Chicago, Ill.), 1992-02, Vol.52 (4), p.815-821

1992

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Human Retinal Guanylate Cyclase (GUC2D) Maps to Chromosome 17p13.1

Genomics (San Diego, Calif.), 1994-07, Vol.22 (2), p.478-481

1994

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cDNA, Gene Structure, and Chromosomal Localization of Human GAR1 (CNCG3L), a Homolog of the Third Subunit of Bovine Photoreceptor cGMP-Gated Channel

Genomics (San Diego, Calif.), 1995-07, Vol.28 (1), p.32-38

1995

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Three new dinucleotide repeat polymorphisms on human chromosome 9: D9S970, D9S971, and D9S972

Human genetics, 1995-08, Vol.96 (2), p.237-238

1995

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Therapeutic Development in Charcot Marie Tooth Type 1 Disease

A Rat Model of Clinically Relevant Extracorporeal Circulation Develops Early Organ Dysfunctions

The Promoters of the Survival Motor Neuron Gene ( SMN) and Its Copy ( SMNc) Share Common Regulatory Elements

Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice

Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients

Gene targeting restricted to mouse striated muscle lineage

Nuclear targeting defect of SMN lacking the C-terminus in a mouse model of spinal muscular atrophy

The gene encoding p44, a subunit of the transcription factor TFIIH, is involved in large-scale deletions associated with Werdnig-Hoffmann disease

α-Satellite DNA methylation in normal individuals and in ICF patients : heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues

Cloning and characterization of p52, the fifth subunit of the core of the transcription/DNA repair factor TFIIH

Human colorectal cancer (CRC) antigen CO17-1A/GA733 encoded by adenovirus inhibits growth of established CRC cells in mice

Assignment of the human syntaxin 1B gene (STX) to chromosome 16p11.2 by fluorescence in situ hybridization

1-02-11 Spinal muscular atrophy: Etiology and pathogenesis

Assignment of the Human Syntaxin 1B Gene (STX) to Chromosome 16p11.2 by Fluorescencein SituHybridization

Baculovirus recombinant expressing a secreted form of a transmembrane carcinoma-associated antigen

Human Retinal Guanylate Cyclase (GUC2D) Maps to Chromosome 17p13.1

cDNA, Gene Structure, and Chromosomal Localization of Human GAR1 (CNCG3L), a Homolog of the Third Subunit of Bovine Photoreceptor cGMP-Gated Channel

Three new dinucleotide repeat polymorphisms on human chromosome 9: D9S970, D9S971, and D9S972

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