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Identification of tissue-specific cell death using methylation patterns of circulating DNA

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (13), p.E1826-E1834

2016

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Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains

Proceedings of the National Academy of Sciences - PNAS, 2012-05, Vol.109 (19), p.7403-7408

2012

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MeCP2 Deficiency in the Brain Decreases BDNF Levels by REST/CoREST-Mediated Repression and Increases TRKB Production

Epigenetics, 2007-10, Vol.2 (4), p.214-222

2007

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Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation

PloS one, 2015-10, Vol.10 (10), p.e0138807-e0138807

2015

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IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation

PloS one, 2014-04, Vol.9 (4), p.e94612-e94612

2014

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Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain

Proceedings of the National Academy of Sciences - PNAS, 2009-06, Vol.106 (25), p.10242-10247

2009

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Annotating the genome by DNA methylation

The International journal of developmental biology, 2017, Vol.61 (3-4-5), p.137

2017

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Structure of the Imprinted Mouse Snrpn Gene and Establishment of its Parental-Specific Methylation Pattern

Proceedings of the National Academy of Sciences - PNAS, 1997-09, Vol.94 (19), p.10267-10272

1997

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Establishing the epigenetic status of the Prader–Willi/Angelman imprinting center in the gametes and embryo

Human molecular genetics, 2004-11, Vol.13 (22), p.2767-2779

2004

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CpG methylation, chromatin structure and gene silencing-a three-way connection

The EMBO journal, 1998-09, Vol.17 (17), p.4905-4908

Razin, Aharon

1998

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The imprinting box of the Prader-Willi/Angelman syndrome domain

Nature genetics, 2000-12, Vol.26 (4), p.440-443

2000

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Islet cells share promoter hypomethylation independently of expression, but exhibit cell-type–specific methylation in enhancers

Proceedings of the National Academy of Sciences - PNAS, 2017-12, Vol.114 (51), p.13525-13530

2017

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Expression and localization of components of the histone deacetylases multiprotein repressory complexes in the mouse preimplantation embryo

Gene Expression Patterns, 2003-12, Vol.3 (6), p.697-702

2003

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MeCP2 involvement in the regulation of neuronal α-tubulin production

Human molecular genetics, 2009-04, Vol.18 (8), p.1415-1423

2009

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MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

Human molecular genetics, 2005-04, Vol.14 (8), p.1049-1058

2005

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IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia

Human molecular genetics, 2011-04, Vol.20 (8), p.1585-1594

2011

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Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study

Journal of molecular neuroscience, 2016-07, Vol.59 (3), p.382-391

2016

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DNA methylation in epigenetic control of gene expression

Progress in molecular and subcellular biology, 2005, Vol.38, p.151

2005

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IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination

Human molecular genetics, 2007-09, Vol.16 (17), p.2097-2104

2007

Volltextzugriff (PDF)

DNA methylation and genomic imprinting

Cell, 1994-05, Vol.77 (4), p.473-476

1994

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DNA Methylation and Gene Function

Science (American Association for the Advancement of Science), 1980-11, Vol.210 (4470), p.604-610

1980

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Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patients

Autonomic neuroscience, 2014-02, Vol.180, p.59-65

2014

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DNA methylation in early development

Human molecular genetics, 1995-01, Vol.4 (suppl_1), p.1751-1755

1995

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Familial Dysautonomia

PloS one, 2015-10, Vol.10 (10)

2015

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Sequence specificity of methylation in higher plant DNA

Nature (London), 1981-08, Vol.292 (5826), p.860-862

1981

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Identification of tissue-specific cell death using methylation patterns of circulating DNA

Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains

MeCP2 Deficiency in the Brain Decreases BDNF Levels by REST/CoREST-Mediated Repression and Increases TRKB Production

Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation

Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain

Annotating the genome by DNA methylation

Structure of the Imprinted Mouse Snrpn Gene and Establishment of its Parental-Specific Methylation Pattern

Establishing the epigenetic status of the Prader–Willi/Angelman imprinting center in the gametes and embryo

CpG methylation, chromatin structure and gene silencing-a three-way connection

The imprinting box of the Prader-Willi/Angelman syndrome domain

Islet cells share promoter hypomethylation independently of expression, but exhibit cell-type–specific methylation in enhancers

Expression and localization of components of the histone deacetylases multiprotein repressory complexes in the mouse preimplantation embryo

MeCP2 involvement in the regulation of neuronal α-tubulin production

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia

Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study

DNA methylation in epigenetic control of gene expression

IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination

DNA methylation and genomic imprinting

DNA Methylation and Gene Function

Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patients

DNA methylation in early development

Familial Dysautonomia

Sequence specificity of methylation in higher plant DNA

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