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Comparative expression profiling of 40 mouse cytochrome P450 genes in embryonic and adult tissues

Archives of biochemistry and biophysics, 2003-06, Vol.414 (1), p.91-100

2003

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Milroy disease and the VEGFR-3 mutation phenotype

Journal of Medical Genetics, 2005-02, Vol.42 (2), p.98-102

2005

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Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Journal of medical genetics, 2002-07, Vol.39 (7), p.478-483

2002

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Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Journal of medical genetics, 1999-04, Vol.36 (4), p.290-294

1999

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Optimization of Anthocyanin Extraction from Saffron Petals with Response Surface Methodology

Food analytical methods, 2016-07, Vol.9 (7), p.1993-2001

2016

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Localization of a Locus (GLC1B) for Adult-Onset Primary Open Angle Glaucoma to the 2cen–q13 Region

Genomics (San Diego, Calif.), 1996-08, Vol.36 (1), p.142-150

1996

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Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema

Journal of medical genetics, 2003-09, Vol.40 (9), p.697-703

2003

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Assignment of a Locus (GLC3A) for Primary Congenital Glaucoma (Buphthalmos) to 2p21 and Evidence for Genetic Heterogeneity

Genomics (San Diego, Calif.), 1995-11, Vol.30 (2), p.171-177

1995

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Recent Advances in Molecular Genetics of Glaucomas

Human molecular genetics, 1997-01, Vol.6 (10), p.1667-1677

SARFARAZI, M

1997

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Expression patterns of mouse and human CYP orthologs (families 1–4) during development and in different adult tissues

Archives of biochemistry and biophysics, 2005-04, Vol.436 (1), p.50-61

2005

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Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1

Human molecular genetics, 2005-03, Vol.14 (6), p.725-733

2005

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Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin

Science (American Association for the Advancement of Science), 2002-02, Vol.295 (5557), p.1077-1079

2002

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Physiological Significance and Expression of P450s in the Developing Eye

Drug metabolism reviews, 2006, Vol.38 (1-2), p.337-352

2006

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Family pedigree analysis of children with severe breath-holding spells

The Journal of pediatrics, 1997-04, Vol.130 (4), p.647-651

1997

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A Gene for Lymphedema-Distichiasis Maps to 16q24.3

American journal of human genetics, 1999-08, Vol.65 (2), p.427-432

1999

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Molecular genetics of primary congenital glaucoma

Eye, 2000-06, Vol.14 (3b), p.422-428

2000

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Identification of Three Different Truncating Mutations in Cytochrome P4501B1 (CYP1B1) as the Principal Cause of Primary Congenital Glaucoma (Buphthalmos) in Families Linked to the GLC3A Locus on Chromosome 2p21

Human molecular genetics, 1997-04, Vol.6 (4), p.641-647

1997

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Molecular cloning, genomic structure, and protein characterization of mouse optineurin

Genomics (San Diego, Calif.), 2005, Vol.85 (1), p.131-138

2005

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Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene

Investigative ophthalmology & visual science, 2005-08, Vol.46 (8), p.2816-2822

2005

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Localization of the Fourth Locus (GLC1E) For Adult-Onset Primary Open-Angle Glaucoma to the 10p15-p14 Region

American journal of human genetics, 1998-03, Vol.62 (3), p.641-652

1998

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Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1

American journal of human genetics, 1998-03, Vol.62 (3), p.573-584

1998

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Visual event related potentials modulated by contextually relevant and irrelevant olfactory primes

Chemical senses, 1999-04, Vol.24 (2), p.145-154

1999

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Papillary thyroid carcinoma associated with papillary renal neoplasia : Genetic linkage analysis of a distinct heritable tumor syndrome

The journal of clinical endocrinology and metabolism, 2000-05, Vol.85 (5), p.1758-1764

2000

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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

Nature genetics, 2000-08, Vol.25 (4), p.397-401

2000

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Molecular Genetics of Primary Congenital Glaucoma in Brazil

Investigative ophthalmology & visual science, 2002-06, Vol.43 (6), p.1820-1827

2002

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Comparative expression profiling of 40 mouse cytochrome P450 genes in embryonic and adult tissues

Milroy disease and the VEGFR-3 mutation phenotype

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Optimization of Anthocyanin Extraction from Saffron Petals with Response Surface Methodology

Localization of a Locus (GLC1B) for Adult-Onset Primary Open Angle Glaucoma to the 2cen–q13 Region

Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema

Assignment of a Locus (GLC3A) for Primary Congenital Glaucoma (Buphthalmos) to 2p21 and Evidence for Genetic Heterogeneity

Recent Advances in Molecular Genetics of Glaucomas

Expression patterns of mouse and human CYP orthologs (families 1–4) during development and in different adult tissues

Identification of a novel adult-onset primary open-angle glaucoma (POAG) gene on 5q22.1

Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin

Physiological Significance and Expression of P450s in the Developing Eye

Family pedigree analysis of children with severe breath-holding spells

A Gene for Lymphedema-Distichiasis Maps to 16q24.3

Molecular genetics of primary congenital glaucoma

Identification of Three Different Truncating Mutations in Cytochrome P4501B1 (CYP1B1) as the Principal Cause of Primary Congenital Glaucoma (Buphthalmos) in Families Linked to the GLC3A Locus on Chromosome 2p21

Molecular cloning, genomic structure, and protein characterization of mouse optineurin

Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene

Localization of the Fourth Locus (GLC1E) For Adult-Onset Primary Open-Angle Glaucoma to the 10p15-p14 Region

Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1

Visual event related potentials modulated by contextually relevant and irrelevant olfactory primes

Papillary thyroid carcinoma associated with papillary renal neoplasia : Genetic linkage analysis of a distinct heritable tumor syndrome

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

Molecular Genetics of Primary Congenital Glaucoma in Brazil

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