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Refined human artificial chromosome vectors for gene therapy and animal transgenesis

Gene therapy, 2011-04, Vol.18 (4), p.384-393

2011

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Correction of a genetic defect in multipotent germline stem cells using a human artificial chromosome

Gene therapy, 2008-04, Vol.15 (8), p.617-624

2008

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Carvedilol Suppresses Apoptosis and Ion Channel Remodelling of HL-1 Cardiac Myocytes Expressing E334K cMyBPC

Drug research, 2016-03, Vol.66 (3), p.126

2016

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Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)-1 stabilizes K(v) 1.5 channels in HL-1 cells

British journal of pharmacology, 2011-04, Vol.162 (8), p.1832-1842

2011

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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

Human molecular genetics, 2000-09, Vol.9 (14), p.2075-2083

2000

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Simultaneous treatment with azelnidipine and olmesartan inhibits apoptosis of Hl-1 cardiac myocytes expressing E334k cMyBPC

Drug research (Stuttgart), 2013-10, Vol.63 (10), p.515

2013

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Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)‐1 stabilizes Kv1.5 channels in HL‐1 cells

British journal of pharmacology, 2011-04, Vol.162 (8), p.1832-1842

2011

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Functional requirement of gp130-mediated signaling for growth and survival of mouse primordial germ cells in vitro and derivation of embryonic germ (EG) cells

Development (Cambridge), 1996-04, Vol.122 (4), p.1235-1242

1996

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Proteomic signatures and aberrations of mouse embryonic stem cells containing a single human chromosome 21 in neuronal differentiation: An in vitro model of down syndrome

Neuroscience, 2004, Vol.129 (2), p.325-335

2004

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Proteomics-based identification of differentially expressed genes in human gliomas: down-regulation of SIRT2 gene

Biochemical and biophysical research communications, 2003-09, Vol.309 (3), p.558-566

2003

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Ubiquitin-Proteasome System Impairment Caused by a Missense Cardiac Myosin-binding Protein C Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy

Journal of molecular biology, 2008-12, Vol.384 (4), p.896-907

2008

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Proto‐oncogene of int‐3, a mouse Notch homologue, is expressed in endothelial cells during early embryogenesis

Genes to cells : devoted to molecular & cellular mechanisms, 1997-03, Vol.2 (3), p.213-224

1997

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ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

Nucleic acids research, 2005, Vol.33 (8), p.2650

2005

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Construction of a novel human artificial chromosome vector for gene delivery

Biochemical and biophysical research communications, 2004-08, Vol.321 (2), p.280-290

2004

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Instability of KCNE1-D85N that Causes Long QT Syndrome: Stabilization by Verapamil

Pacing and clinical electrophysiology, 2014-07, Vol.37 (7), p.853-863

2014

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Cloning of inv , a gene that controls left/right asymmetry and kidney development

Nature (London), 1998-09, Vol.395 (6698), p.177-181

1998

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Regulation of mouse CYP1A1 gene expression by dioxin: requirement of two cis-acting elements during induction

Molecular and Cellular Biology, 1989-06, Vol.9 (6), p.2378-2386

1989

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Binding of multiple nuclear factors to the 5' upstream regulatory element of the murine major histocompatibility class I gene

Molecular and Cellular Biology, 1987-12, Vol.7 (12), p.4542-4548

1987

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A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly

Science (American Association for the Advancement of Science), 1992-02, Vol.255 (5048), p.1132-1134

1992

Volltextzugriff (PDF)

Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)‐1 stabilizes K v 1.5 channels in HL‐1 cells

British journal of pharmacology, 2011-04, Vol.162 (8), p.1832-1842

2011

Volltextzugriff (PDF)

Tumour invasion and metastasis are promoted in mice deficient in tenascin‐X

Genes to cells : devoted to molecular & cellular mechanisms, 2001-12, Vol.6 (12), p.1101-1111

2001

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Elevated apoptosis in pre-mature neurons differentiated from mouse ES cells containing a single human chromosome 21

Biochemical and biophysical research communications, 2002-12, Vol.299 (4), p.599-605

2002

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Developmental and tissue-specific expression of nuclear proteins that bind the regulatory element of the major histocompatibility complex class I gene

The Journal of experimental medicine, 1989-04, Vol.169 (4), p.1309-1321

1989

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Cadherin cell adhesion molecules with distinct binding specificities share a common structure

The EMBO journal, 1986-10, Vol.5 (10), p.2485-2488

1986

Volltextzugriff (PDF)

Negative Regulation of the Major Histocompatibility Complex Class I Promoter in Embryonal Carcinoma Cells

Proceedings of the National Academy of Sciences - PNAS, 1991-04, Vol.88 (8), p.3145-3149

1991

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Refined human artificial chromosome vectors for gene therapy and animal transgenesis

Correction of a genetic defect in multipotent germline stem cells using a human artificial chromosome

Carvedilol Suppresses Apoptosis and Ion Channel Remodelling of HL-1 Cardiac Myocytes Expressing E334K cMyBPC

Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)-1 stabilizes K(v) 1.5 channels in HL-1 cells

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

Simultaneous treatment with azelnidipine and olmesartan inhibits apoptosis of Hl-1 cardiac myocytes expressing E334k cMyBPC

Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)‐1 stabilizes Kv1.5 channels in HL‐1 cells

Functional requirement of gp130-mediated signaling for growth and survival of mouse primordial germ cells in vitro and derivation of embryonic germ (EG) cells

Proteomic signatures and aberrations of mouse embryonic stem cells containing a single human chromosome 21 in neuronal differentiation: An in vitro model of down syndrome

Proteomics-based identification of differentially expressed genes in human gliomas: down-regulation of SIRT2 gene

Ubiquitin-Proteasome System Impairment Caused by a Missense Cardiac Myosin-binding Protein C Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy

Proto‐oncogene of int‐3, a mouse Notch homologue, is expressed in endothelial cells during early embryogenesis

ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome

Construction of a novel human artificial chromosome vector for gene delivery

Instability of KCNE1-D85N that Causes Long QT Syndrome: Stabilization by Verapamil

Cloning of inv , a gene that controls left/right asymmetry and kidney development

Regulation of mouse CYP1A1 gene expression by dioxin: requirement of two cis-acting elements during induction

Binding of multiple nuclear factors to the 5' upstream regulatory element of the murine major histocompatibility class I gene

A Human Gene Responsible for Zellweger Syndrome That Affects Peroxisome Assembly

Transcriptional activation of the anchoring protein SAP97 by heat shock factor (HSF)‐1 stabilizes K v 1.5 channels in HL‐1 cells

Tumour invasion and metastasis are promoted in mice deficient in tenascin‐X

Elevated apoptosis in pre-mature neurons differentiated from mouse ES cells containing a single human chromosome 21

Developmental and tissue-specific expression of nuclear proteins that bind the regulatory element of the major histocompatibility complex class I gene

Cadherin cell adhesion molecules with distinct binding specificities share a common structure

Negative Regulation of the Major Histocompatibility Complex Class I Promoter in Embryonal Carcinoma Cells

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