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Role of Histone Methyltransferase G9a in CpG Methylation of the Prader-Willi Syndrome Imprinting Center

The Journal of biological chemistry, 2003-04, Vol.278 (17), p.14996-15000

2003

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Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein

The Journal of biological chemistry, 2004-09, Vol.279 (39), p.41208-41217

2004

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Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndrome

Neurobiology of disease, 2005-11, Vol.20 (2), p.471-478

2005

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Cell-free DNA is more sensitive than cell-free mRNA as a marker for evaluation of fetal-maternal hemorrhage

Clinical chemistry (Baltimore, Md.), 2006-11, Vol.52 (11), p.2121-2123

2006

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From Electrophysiology to Chromatin: A Bottom-Up Approach to Angelman Syndrome

Annals of the New York Academy of Sciences, 2004-12, Vol.1030 (1), p.599-611

2004

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Imprinting centers, chromatin structure, and disease

Journal of cellular biochemistry, 2005-05, Vol.95 (2), p.226-233

2005

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Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

Neurobiology of disease, 2002-03, Vol.9 (2), p.149-159

2002

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Genomic Organization of theUBE3A/E6-AP Gene and Related Pseudogenes

Genomics (San Diego, Calif.), 1998-01, Vol.47 (1), p.101-107

1998

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A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus

Nature (London), 1993-07, Vol.364 (6436), p.448-450

1993

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Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice

Neurobiology of disease, 2002-03, Vol.9 (2), p.149-159

2002

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Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene

The Lancet (British edition), 1992-02, Vol.339 (8789), p.366-367

1992

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Effects of a low dose of melatonin on sleep in children with Angelman syndrome

Journal of Pediatric Endocrinology and Metabolism, 1999-01, Vol.12 (1), p.57

1999

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Genetics beyond Mendel: Understanding nontraditional inheritance patterns

Postgraduate medicine, 2000-09, Vol.108 (3), p.131-138

Wagstaff, Joseph

2000

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Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

Nucleic acids research, 2005-01, Vol.33 (13), p.3976-3984

2005

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Meiosis in Haploid Yeast

Proceedings of the National Academy of Sciences - PNAS, 1982-05, Vol.79 (9), p.2986-2990

1982

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Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABA A receptor β 3 -subunit gene

The Lancet (British edition), 1992-02, Vol.339 (8789), p.366

1992

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Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region: Carlton VEH, Knisely AS, Freimer NB. Hum Mol Genet 1995; 4: 1049–1053

Hepatology (Baltimore, Md.), 1995, Vol.22 (5), p.1611-1613

1995

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FISH ordering of reference markers and of the gene for the α5 subunit of the γ-aminobutyric acid receptor (GABRA5) within the Angelman and Prader–Willi syndrome chromosomal regions

Human molecular genetics, 1993-02, Vol.2 (2), p.183-189

1993

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High-resolution mapping of the γ-aminobutyric acid receptor subunit β3 and α5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients

American journal of human genetics, 1993, Vol.52 (6), p.1216-1229

1993

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Income Tax Consciousness under Withholding

Southern economic journal, 1965-07, Vol.32 (1), p.73-80

Van Wagstaff, Joseph

1965

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Closing in on a “familial cholestasis gene”

Hepatology (Baltimore, Md.), 1995-11, Vol.22 (5), p.1611-1613

1995

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Neurologic complications in galactosemia

Pediatric neurology, 1992-05, Vol.8 (3), p.217-220

1992

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Evidence for two pathways of meiotic intrachromosomal recombination in yeast

Proceedings of the National Academy of Sciences - PNAS, 1989-09, Vol.86 (18), p.7072-7076

1989

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Severe folate deficiency and pancytopenia in a nutritionally deprived infant with homocystinuria caused by cystathionine beta-synthase deficiency

The Journal of pediatrics, 1991, Vol.118 (4), p.569-572

1991

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A cluster of three GABA sub(A) receptor subunit genes is deleted in a neurological mutant of the mouse p locus

Nature (London), 1993-07, Vol.364 (6436), p.448-450

1993

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Role of Histone Methyltransferase G9a in CpG Methylation of the Prader-Willi Syndrome Imprinting Center

Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein

Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndrome

Cell-free DNA is more sensitive than cell-free mRNA as a marker for evaluation of fetal-maternal hemorrhage

From Electrophysiology to Chromatin: A Bottom-Up Approach to Angelman Syndrome

Imprinting centers, chromatin structure, and disease

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

Genomic Organization of theUBE3A/E6-AP Gene and Related Pseudogenes

A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus

Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene

Effects of a low dose of melatonin on sleep in children with Angelman syndrome

Genetics beyond Mendel: Understanding nontraditional inheritance patterns

Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans

Meiosis in Haploid Yeast

Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABA A receptor β 3 -subunit gene

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region: Carlton VEH, Knisely AS, Freimer NB. Hum Mol Genet 1995; 4: 1049–1053

FISH ordering of reference markers and of the gene for the α5 subunit of the γ-aminobutyric acid receptor (GABRA5) within the Angelman and Prader–Willi syndrome chromosomal regions

High-resolution mapping of the γ-aminobutyric acid receptor subunit β3 and α5 gene cluster on chromosome 15q11-q13, and localization of breakpoints in two Angelman syndrome patients

Income Tax Consciousness under Withholding

Closing in on a “familial cholestasis gene”

Neurologic complications in galactosemia

Evidence for two pathways of meiotic intrachromosomal recombination in yeast

Severe folate deficiency and pancytopenia in a nutritionally deprived infant with homocystinuria caused by cystathionine beta-synthase deficiency

A cluster of three GABA sub(A) receptor subunit genes is deleted in a neurological mutant of the mouse p locus

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