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Examining the homeostatic distribution of metals and Zn isotopes in Göttingen minipigs

Metallomics, 2018-09, Vol.10 (9), p.1264

2018

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MicroRNAs and Ascl1 facilitate direct conversion of porcine fibroblasts into induced neurons

Stem cell research, 2020-10, Vol.48, p.101984-101984, Article 101984

2020

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Transcriptomic profiling of porcine pluripotency identifies species-specific reprogramming requirements for culturing iPSCs

Stem cell research, 2019-12, Vol.41, p.101645-101645, Article 101645

2019

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Pig transgenesis by Sleeping Beauty DNA transposition

Transgenic research, 2011-06, Vol.20 (3), p.533-545

2011

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Regulatory mechanisms for 3'-end alternative splicing and polyadenylation of the Glial Fibrillary Acidic Protein, GFAP, transcript

Nucleic acids research, 2007-12, Vol.35 (22), p.7636

2007

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Directly Reprogrammed Neurons Express MAPT and APP Splice Variants Pertinent to Ageing and Neurodegeneration

Molecular neurobiology, 2021-05, Vol.58 (5), p.2075-2087

2021

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Expression of the Alzheimer's Disease Mutations AβPP695sw and PSEN1M146I in Double-Transgenic Göttingen Minipigs

Journal of Alzheimer's disease, 2016-07, Vol.53 (4), p.1617

2016

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Hemizygous minipigs produced by random gene insertion and handmade cloning express the Alzheimer's disease-causing dominant mutation APPsw

Transgenic research, 2009-08, Vol.18 (4), p.545-558

2009

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Identification and characterization of GFAPκ, a novel glial fibrillary acidic protein isoform

Glia, 2007-04, Vol.55 (5), p.497-507

2007

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Generation of minipigs with targeted transgene insertion by recombinase-mediated cassette exchange (RMCE) and somatic cell nuclear transfer (SCNT)

Transgenic research, 2013-08, Vol.22 (4), p.709-723

2013

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Structural and functional characterization of the zebrafish gene for glial fibrillary acidic protein, GFAP

Gene, 2003-05, Vol.310, p.123-132

2003

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Expression pattern of a single transgene cassette located in endogenous GLIS3 of cloned pigs; a nested situation

Gene, 2012-07, Vol.502 (2), p.94-98

2012

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Identification of the porcine homologous of human disease causing trinucleotide repeat sequences

Neurogenetics, 2007-08, Vol.8 (3), p.207-218

2007

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Self-assembly of the Cytoskeletal Glial Fibrillary Acidic Protein Is Inhibited by an Isoform-specific C Terminus

The Journal of biological chemistry, 2004-10, Vol.279 (40), p.41537-41545

2004

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Determination of Odor Detection Threshold in the Göttingen Minipig

Chemical senses, 2010-10, Vol.35 (8), p.727-734

2010

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Establishment of a pig fibroblast-derived cell line for locus-directed transgene expression in cell cultures and blastocysts

Molecular biology reports, 2011, Vol.38 (1), p.151-161

2011

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Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.924-930

1992

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A New Splice Variant of Glial Fibrillary Acidic Protein, GFAPε, Interacts with the Presenilin Proteins

The Journal of biological chemistry, 2002-08, Vol.277 (33), p.29983-29991

2002

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Identification and characterization of GFAPkappa, a novel glial fibrillary acidic protein isoform

Glia, 2007-04, Vol.55 (5), p.497-507

2007

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A presenilin-1 Thr116Asn substitution in a family with early-onset Alzheimerʼs disease

Neuroreport, 1999-08, Vol.10 (11), p.2255-2260

1999

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Variant Phenotypes of Incomplete Achromatopsia in Two Cousins with GNAT2 Gene Mutations

Investigative ophthalmology & visual science, 2004-12, Vol.45 (12), p.4256-4262

2004

Volltextzugriff (PDF)

Homologous Subfamilies of Human Alphoid Repetitive DNA on Different Nucleolus Organizing Chromosomes

Proceedings of the National Academy of Sciences - PNAS, 1987-02, Vol.84 (4), p.1075-1079

1987

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Familial Alzheimer's disease co-segregates with a Met 146 Ile substitution in presenilin-1

Clinical genetics, 1996-11, Vol.50 (5), p.281-286

1996

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Extreme variant of the short arm of chromosome 15

Human genetics, 1996-06, Vol.97 (6), p.710-713

1996

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X-inactivation pattern in carriers of X-linked retinitis pigmentosa : a valuable means of prognostic evaluation ?

Human genetics, 1993-10, Vol.92 (4), p.359-363

1993

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Examining the homeostatic distribution of metals and Zn isotopes in Göttingen minipigs

MicroRNAs and Ascl1 facilitate direct conversion of porcine fibroblasts into induced neurons

Transcriptomic profiling of porcine pluripotency identifies species-specific reprogramming requirements for culturing iPSCs

Pig transgenesis by Sleeping Beauty DNA transposition

Regulatory mechanisms for 3'-end alternative splicing and polyadenylation of the Glial Fibrillary Acidic Protein, GFAP, transcript

Directly Reprogrammed Neurons Express MAPT and APP Splice Variants Pertinent to Ageing and Neurodegeneration

Expression of the Alzheimer's Disease Mutations AβPP695sw and PSEN1M146I in Double-Transgenic Göttingen Minipigs

Hemizygous minipigs produced by random gene insertion and handmade cloning express the Alzheimer's disease-causing dominant mutation APPsw

Identification and characterization of GFAPκ, a novel glial fibrillary acidic protein isoform

Generation of minipigs with targeted transgene insertion by recombinase-mediated cassette exchange (RMCE) and somatic cell nuclear transfer (SCNT)

Structural and functional characterization of the zebrafish gene for glial fibrillary acidic protein, GFAP

Expression pattern of a single transgene cassette located in endogenous GLIS3 of cloned pigs; a nested situation

Identification of the porcine homologous of human disease causing trinucleotide repeat sequences

Self-assembly of the Cytoskeletal Glial Fibrillary Acidic Protein Is Inhibited by an Isoform-specific C Terminus

Determination of Odor Detection Threshold in the Göttingen Minipig

Establishment of a pig fibroblast-derived cell line for locus-directed transgene expression in cell cultures and blastocysts

Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization

A New Splice Variant of Glial Fibrillary Acidic Protein, GFAPε, Interacts with the Presenilin Proteins

Identification and characterization of GFAPkappa, a novel glial fibrillary acidic protein isoform

A presenilin-1 Thr116Asn substitution in a family with early-onset Alzheimerʼs disease

Variant Phenotypes of Incomplete Achromatopsia in Two Cousins with GNAT2 Gene Mutations

Homologous Subfamilies of Human Alphoid Repetitive DNA on Different Nucleolus Organizing Chromosomes

Familial Alzheimer's disease co-segregates with a Met 146 Ile substitution in presenilin-1

Extreme variant of the short arm of chromosome 15

X-inactivation pattern in carriers of X-linked retinitis pigmentosa : a valuable means of prognostic evaluation ?

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