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Multiplex PCR: Critical Parameters and Step-by-Step Protocol

BioTechniques, 1997-09, Vol.23 (3), p.504-511

1997

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Long-term disease-free survival after nonmyeloablative cyclophosphamide fludarabine conditioning and related unrelated allotransplantation for acute myeloid leukemia myelodysplasia

Bone marrow transplantation (Basingstoke), 2010-08, Vol.45 (8), p.1300-1308

2010

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Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library

Brain research. Molecular brain research., 1994-09, Vol.25 (3), p.183-191

1994

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An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy

The American journal of pathology, 1998-06, Vol.152 (6), p.1415-1420

1998

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Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease

Neurology, 1996-11, Vol.47 (5), p.1333

1996

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Pelizaeus-Merzbacher Disease: Tight Linkage to Proteolipid Protein Gene Exon Variant

Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (23), p.9427-9430

1989

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A male child with the rumpshaker mutation, X‐linked spastic paraplegia/Pelizaeus‐Merzbacher disease and lysinuria

Journal of inherited metabolic disease, 1997-11, Vol.20 (6), p.811-816

1997

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Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred

American journal of human genetics, 1993-06, Vol.52 (6), p.1053-1056

1993

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Salivary Androgen-binding Protein Variation in Mus and Other Rodents

The Journal of heredity, 1991-11, Vol.82 (6), p.453-458

1991

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AhaII polymorphism in human X-linked proteolipid protein gene (PLP)

Nucleic acids research, 1991-11, Vol.19 (21), p.6057-6057

1991

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165 Prior protein (PrP) residue 129 Val in Gerstmann-Sträussler-Scheinker (GSS) disease with mutation PRNP P102L

Neurobiology of aging, 1996, Vol.17 (4), p.S42-S42

1996

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Mouse Transgenes in Human Cells Detect Specific Base Substitutions

Proceedings of the National Academy of Sciences - PNAS, 1990-11, Vol.87 (21), p.8675-8679

1990

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Linkage of the indiana kindred variant of Gerstmann-Sträussler-Scheinker disease to a mutation in the prion protein gene ( [formula omitted])

Neurobiology of aging, 1992, Vol.13, p.S70-S70

1992

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Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain

Brain research. Molecular brain research., 1994-09, Vol.25 (3), p.192-199

1994

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Cellular distribution of the RNA transcripts of a newly discovered gene in the brain of normal, weaver, Purkinje cell degeneration and reeler mutant mice as evidenced by in situ hybridization histochemistry

Brain research. Molecular brain research., 1993-06, Vol.18 (4), p.321-328

1993

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Analysis of maize alcohol dehydrogenase by native-SDS two dimensional electrophoresis and autoradiography

Molecular & general genetics, 1979, Vol.169 (1), p.7-12

1979

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Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene

American journal of medical genetics, 1995-02, Vol.55 (4), p.402-404

1995

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In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease

American journal of medical genetics, 1995-02, Vol.55 (4), p.405-407

1995

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Assessment of Nutritional Intake During Space Flight and Space Flight Analogs

Procedia food science, 2013, Vol.2, p.27-34

2013

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Multiplex PCR: Critical Parameters and Step-by-Step Protocol

Long-term disease-free survival after nonmyeloablative cyclophosphamide fludarabine conditioning and related unrelated allotransplantation for acute myeloid leukemia myelodysplasia

Novel cDNA clones obtained by antibody screening of a mouse cerebellar cDNA expression library

An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy

Adult-onset neurodegenerative disorder due to proteolipid protein gene mutation in the mother of a man with Pelizaeus-Merzbacher disease

Pelizaeus-Merzbacher Disease: Tight Linkage to Proteolipid Protein Gene Exon Variant

A male child with the rumpshaker mutation, X‐linked spastic paraplegia/Pelizaeus‐Merzbacher disease and lysinuria

Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred

Salivary Androgen-binding Protein Variation in Mus and Other Rodents

AhaII polymorphism in human X-linked proteolipid protein gene (PLP)

165 Prior protein (PrP) residue 129 Val in Gerstmann-Sträussler-Scheinker (GSS) disease with mutation PRNP P102L

Mouse Transgenes in Human Cells Detect Specific Base Substitutions

Linkage of the indiana kindred variant of Gerstmann-Sträussler-Scheinker disease to a mutation in the prion protein gene ( [formula omitted])

Molecular characterization of a novel cDNA from murine cerebellum, developmental expression, and distribution in brain

Cellular distribution of the RNA transcripts of a newly discovered gene in the brain of normal, weaver, Purkinje cell degeneration and reeler mutant mice as evidenced by in situ hybridization histochemistry

Analysis of maize alcohol dehydrogenase by native-SDS two dimensional electrophoresis and autoradiography

Pelizaeus-Merzbacher disease in a family of Portuguese origin caused by a point mutation in exon 5 of the proteolipid protein gene

In-frame deletion in the proteolipid protein gene of a family with Pelizaeus-Merzbacher disease

Assessment of Nutritional Intake During Space Flight and Space Flight Analogs

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