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Mutations in the γ-Actin Gene ( ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

American journal of human genetics, 2003-11, Vol.73 (5), p.1082-1091

2003

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Association and linkage of α-2A adrenergic receptor gene polymorphisms with childhood ADHD

Molecular psychiatry, 2005-06, Vol.10 (6), p.572-580

2005

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A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression

Clinical genetics, 2010-09, Vol.78 (3), p.267-274

2010

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Depressive symptoms in mid‐pregnancy, lifetime stressors and the 5‐HTTLPR genotype

Genes, brain and behavior, 2007-07, Vol.6 (5), p.453-464

2007

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Genetic mutation in pontocerebellar hypoplasia

Clinical genetics, 2010-02, Vol.77 (2), p.197-199

2010

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Human β-Mannosidase cDNA Characterization and First Identification of a Mutation Associated with Human β-Mannosidosis

Human molecular genetics, 1998-01, Vol.7 (1), p.75-83

1998

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Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD

Molecular psychiatry, 2005-06, Vol.10 (6), p.572-580

2005

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A New Locus for Late-Onset, Progressive, Hereditary Hearing Loss DFNA20 Maps to 17q25

Genomics (San Diego, Calif.), 2000-01, Vol.63 (1), p.1-6

2000

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Caprine β-Mannosidase: Sequencing and Characterization of the cDNA and Identification of the Molecular Defect of Caprine β-Mannosidosis

Genomics (San Diego, Calif.), 1996-10, Vol.37 (1), p.51-56

1996

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Bovine kidney β-mannosidase : purification and characterization

Biochemical journal, 1993-01, Vol.289 (2), p.343-347

1993

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Molecular Diagnostics for Cystic Fibrosis

Clinics in laboratory medicine, 1997-03, Vol.17 (1), p.59-72

Friderici, Karen H.

1997

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Purification and characterization of goat lysosomal beta-mannosidase using monoclonal and polyclonal antibodies

The Journal of biological chemistry, 1992-03, Vol.267 (9), p.6178-6182

1992

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Beta-mannosidase maps to cattle Chromosome 6

Mammalian genome, 1996-06, Vol.7 (6), p.474-474, Article 474

1996

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Identification of a bovine β-mannosidosis mutation and detection of two β-mannosidase pseudogenes

Mammalian genome, 1999-12, Vol.10 (12), p.1137-1141

1999

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Molecular cloning and characterization of bovine beta-mannosidase

The Journal of biological chemistry, 1995-02, Vol.270 (8), p.3841-3848

1995

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SNP Discovery and Haplotype Analysis in the Segmentally Duplicated DRD5 Coding Region

Annals of human genetics, 2009-05, Vol.73 (3), p.274-282

2009

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Expression of GJB2 and GJB6 Is Reduced in a Novel DFNB1 Allele

American journal of human genetics, 2006-07, Vol.79 (1), p.174-179

2006

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Oxidation of branched chain amino acids by isolated hearts and diaphragms of the rat. The effect of fatty acids, glucose, and pyruvate respiration

The Journal of biological chemistry, 1972-12, Vol.247 (24), p.8085-8096

1972

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β-Mannosidosis mice: a model for the human lysosomal storage disease

Human molecular genetics, 2006-02, Vol.15 (3), p.493-500

2006

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Life stressors and 5-HTTLPR interaction in relation to midpregnancy depressive symptoms among African-American women

Psychiatric genetics, 2011-12, Vol.21 (6), p.271-280

2011

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Determination of genotypic frequency of caprine mucopolysaccharidosis IIID

Journal of veterinary diagnostic investigation, 1998-04, Vol.10 (2), p.181-183

1998

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Presence of 5'-terminal cap structures in virus-specific RNA from feline leukemia virus-infected cells

Journal of Virology, 1978-05, Vol.26 (2), p.226-235

1978

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Association and linkage of -2A adrenergic receptor gene polymorphisms with childhood ADHD

Molecular psychiatry, 2005-06, Vol.10 (6), p.572-580

2005

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d-Valine medium maintains prolactin production in primary culture

Molecular and cellular endocrinology, 1982-01, Vol.28 (3), p.613-626

1982

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Connexin 26 35delG does not represent a mutational hotspot

Human genetics, 2003-07, Vol.113 (1), p.18-23

2003

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Mutations in the γ-Actin Gene ( ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)

Association and linkage of α-2A adrenergic receptor gene polymorphisms with childhood ADHD

A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression

Depressive symptoms in mid‐pregnancy, lifetime stressors and the 5‐HTTLPR genotype

Genetic mutation in pontocerebellar hypoplasia

Human β-Mannosidase cDNA Characterization and First Identification of a Mutation Associated with Human β-Mannosidosis

Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD

A New Locus for Late-Onset, Progressive, Hereditary Hearing Loss DFNA20 Maps to 17q25

Caprine β-Mannosidase: Sequencing and Characterization of the cDNA and Identification of the Molecular Defect of Caprine β-Mannosidosis

Bovine kidney β-mannosidase : purification and characterization

Molecular Diagnostics for Cystic Fibrosis

Purification and characterization of goat lysosomal beta-mannosidase using monoclonal and polyclonal antibodies

Beta-mannosidase maps to cattle Chromosome 6

Identification of a bovine β-mannosidosis mutation and detection of two β-mannosidase pseudogenes

Molecular cloning and characterization of bovine beta-mannosidase

SNP Discovery and Haplotype Analysis in the Segmentally Duplicated DRD5 Coding Region

Expression of GJB2 and GJB6 Is Reduced in a Novel DFNB1 Allele

Oxidation of branched chain amino acids by isolated hearts and diaphragms of the rat. The effect of fatty acids, glucose, and pyruvate respiration

β-Mannosidosis mice: a model for the human lysosomal storage disease

Life stressors and 5-HTTLPR interaction in relation to midpregnancy depressive symptoms among African-American women

Determination of genotypic frequency of caprine mucopolysaccharidosis IIID

Presence of 5'-terminal cap structures in virus-specific RNA from feline leukemia virus-infected cells

Association and linkage of -2A adrenergic receptor gene polymorphisms with childhood ADHD

d-Valine medium maintains prolactin production in primary culture

Connexin 26 35delG does not represent a mutational hotspot

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