UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 76

Sortiert nach

Mechanisms of imprinting of the Prader-Willi/Angelman region

American journal of medical genetics. Part A, 2008-08, Vol.146A (16), p.2041-2052

2008

Volltextzugriff (PDF)

Angelman syndrome 2005: Updated consensus for diagnostic criteria

American journal of medical genetics. Part A, 2006-03, Vol.140A (5), p.413-418

2006

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Sleep disturbances in Ube3a maternal-deficient mice modeling Angelman syndrome

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

2005

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

UBE3A/E6-AP mutations cause Angelman syndrome

Nature genetics, 1997-01, Vol.15 (1), p.70-73

1997

Volltextzugriff (PDF)

Imprinting centers, chromatin structure, and disease

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

2005

Volltextzugriff (PDF)

Neurobehavioral and electroencephalographic abnormalities in Ube3a maternal-deficient mice

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

2002

Volltextzugriff (PDF)

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

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

1998

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Parent-Specific Complementary Patterns of Histone H3 Lysine 9 and H3 Lysine 4 Methylation at the Prader-Willi Syndrome Imprinting Center

American journal of human genetics, 2001-12, Vol.69 (6), p.1389-1394

2001

Volltextzugriff (PDF)

Neurobehavioral and Electroencephalographic Abnormalities in Ube3aMaternal-Deficient Mice

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

2002

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Journal of pediatric endocrinology & metabolism : JPEM, 1999-01, Vol.12 (1), p.57

1999

Volltextzugriff (PDF)

Mutation Analysis of UBE3A in Angelman Syndrome Patients

American journal of human genetics, 1998-06, Vol.62 (6), p.1353-1360

1998

Volltextzugriff (PDF)

Genomic organization of the UBE3A/E6-AP gene and related pseudogenes

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

1998

Volltextzugriff (PDF)

Genetics beyond Mendel: Understanding nontraditional inheritance patterns

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

Wagstaff, Joseph

2000

Volltextzugriff (PDF)

Clinical outcome of infants with confined placental mosaicism and intrauterine growth restriction of unknown cause

American journal of medical genetics. Part A, 2006-09, Vol.140A (17), p.1827-1833

2006

Volltextzugriff (PDF)

A familial balanced 3:9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings

American journal of human genetics, 1995, Vol.56 (1), p.302-309

1995

Volltextzugriff (PDF)

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

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

2005

Volltextzugriff (PDF)

Meiosis in Haploid Yeast

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

1982

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

1 – 25 von 76

Suche als RSS-Feed

Aktive Filter

KollektionSpringerLINK Contemporary (Konsortium Baden-Württemberg)

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(58)
Mit Volltextzugriff
(71)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mechanisms of imprinting of the Prader-Willi/Angelman region

Angelman syndrome 2005: Updated consensus for diagnostic criteria

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

UBE3A/E6-AP mutations cause 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

Parent-Specific Complementary Patterns of Histone H3 Lysine 9 and H3 Lysine 4 Methylation at the Prader-Willi Syndrome Imprinting Center

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

Mutation Analysis of UBE3A in Angelman Syndrome Patients

Genomic organization of the UBE3A/E6-AP gene and related pseudogenes

Genetics beyond Mendel: Understanding nontraditional inheritance patterns

Clinical outcome of infants with confined placental mosaicism and intrauterine growth restriction of unknown cause

A familial balanced 3:9 translocation with cryptic 8q insertion leading to deletion and duplication of 9p23 loci in siblings

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

Aktive Filter

Suchergebnisse filtern