M. Rasmussen

发表

IPEC-J2 rMdr1a, a New Cell Line with Functional Expression of Rat P-glycoprotein Encoded by Rat Mdr1a for Drug Screening Purposes

B. Brodin, L. Saaby, B. Holst, 2020, Pharmaceutics.

An advanced pluripotent stem cell test for developmental toxicity

A. Vinggaard, A. K. Rosenmai, C. Taxvig, 2021 .

Derivation and characterization of sleeping beauty transposon-mediated porcine induced pluripotent stem cells.

T. Buchholz, H. Niemann, Z. Ivics, 2013, Stem cells and development.

Paternal breed effects on expression of IGF-II, BAK1 and BCL2-L1 in bovine preimplantation embryos

M. Joupari, H. Dehghani, P. Hyttel, 2014, Zygote.

Scalable expansion of iPSC and their derivatives across multiple lineages.

C. Verfaillie, H. Zimmermann, A. Ebneth, 2022, Reproductive toxicology.

Combination effects of epidermal growth factor and glial cell line-derived neurotrophic factor on the in vitro developmental potential of porcine oocytes

P. Hyttel, M. Rasmussen, M. V. Valleh, 2015, Zygote.

Insulin-like growth factor 2: a modulator of anti-apoptosis related genes (HSP70, BCL2-L1) in bovine preimplantation embryos.

P. Hyttel, L. Strøbech, M. Rasmussen, 2014, Theriogenology.

Human iPSC-derived hepatocytes in 2D and 3D suspension culture for cryopreservation and in vitro toxicity studies.

B. Nielsen, A. Vinggaard, H. Zimmermann, 2022, Reproductive toxicology.

BioZoom INDUCED PLURIPOTENT STEM CELLS ( IPSC ) FOR MODELING OF ALZHEIMER ’ S DISEASE

G. Waldemar, T. Nielsen, J. Nielsen, 2015 .

Generation of two gene edited iPSC-lines carrying a DOX-inducible NGN2 expression cassette with and without GFP in the AAVS1 locus.

U. Mau-Holzmann, A. Ebneth, Rachel Steeg, 2021, Stem cell research.

Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein tau (MAPT) gene.

U. Mau-Holzmann, T. Nielsen, J. Nielsen, 2016, Stem cell research.

Generation of an isogenic, gene-corrected iPSC line from a symptomatic 59-year-old female patient with frontotemporal dementia caused by an R406W mutation in the microtubule associated protein tau (MAPT) gene.

U. Mau-Holzmann, T. Nielsen, J. Nielsen, 2016, Stem cell research.

59-year-old female patient with frontotemporal dementia caused by a R 406 W mutation in microtubule associated protein tau ( MAPT )

U. Mau-Holzmann, T. Nielsen, J. Nielsen, 2016 .

A novel human pluripotent stem cell-based assay to predict developmental toxicity

A. Vinggaard, C. Taxvig, I. Meiser, 2020, Archives of Toxicology.

Ultrastructural and molecular distinctions between the porcine inner cell mass and epiblast reveal unique pluripotent cell states

P. Hyttel, V. Hall, M. Rasmussen, 2010, Developmental dynamics : an official publication of the American Association of Anatomists.

Directed differentiation of porcine epiblast-derived neural progenitor cells into neurons and glia.

T. Carter, P. Hyttel, V. Hall, 2011, Stem cell research.

Structural Analysis of Three-dimensional Human Neural Tissue derived from Induced Pluripotent Stem Cells

P. Hyttel, M. Rasmussen, P. T. Brooks, 2016 .

Neurosphere Based Differentiation of Human iPSC Improves Astrocyte Differentiation

S. Cirera, Anna Ochałek, A. Dinnyés, 2015, Stem cells international.

Isolation and culture of porcine neural progenitor cells from embryos and pluripotent stem cells.

P. Hyttel, V. Hall, M. Rasmussen, 2013, Methods in molecular biology.

OCT4 expression in outgrowth colonies derived from porcine inner cell masses and epiblasts.

P. Hyttel, M. Rasmussen, M. Schmidt, 2011, Reproduction in domestic animals = Zuchthygiene.

Impaired APP activity and altered Tau splicing in embryonic stem cell-derived astrocytes obtained from an APPsw transgenic minipig

D. Volke, P. Hyttel, T. Zuchner, 2015, Disease Models & Mechanisms.

Epigenetic regulation of gene expression in porcine epiblast, hypoblast, trophectoderm and epiblast-derived neural progenitor cells

H. Jammes, N. Beaujean, P. Hyttel, 2011, Epigenetics.

Transient p53 Suppression Increases Reprogramming of Human Fibroblasts without Affecting Apoptosis and DNA Damage

Z. Tümer, M. G. Johnsen, P. Hyttel, 2014, Stem cell reports.

The positional identity of iPSC-derived neural progenitor cells along the anterior-posterior axis is controlled in a dosage-dependent manner by bFGF and EGF.

Andras Dinnyes, Susanna Cirera, Bjørn Holst, 2016, Differentiation; research in biological diversity.

Lab resource: Stem cell lineGeneration of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1

G. Waldemar, T. Nielsen, J. Nielsen, 2016 .

Temporal repression of endogenous pluripotency genes during reprogramming of porcine induced pluripotent stem cells.

A. Dinnyés, O. Ujhelly, P. Hyttel, 2012, Cellular reprogramming.

Optimal doses of EGF and GDNF act as biological response modifiers to improve porcine oocyte maturation and quality

P. Hyttel, M. Rasmussen, M. V. Valleh, 2017, Zygote.

Patient iPSC-Derived Neurons for Disease Modeling of Frontotemporal Dementia with Mutation in CHMP2B

L. Bolund, Xin Liu, Fengping Xu, 2022 .

Generation of a set of isogenic, gene-edited iPSC lines homozygous for all main APOE variants and an APOE knock-out line.

U. Mau-Holzmann, A. Ebneth, Ravi S Muddashetty, 2019, Stem cell research.

Induced pluripotent stem cell - derived neurons for the study of spinocerebellar ataxia type 3.

Z. Tümer, T. Nielsen, J. Nielsen, 2016, Stem cell research.

Creating a human-induced pluripotent stem cell-based NKX2.5 reporter gene assay for developmental toxicity testing

A. Vinggaard, C. Taxvig, Andreas Frederik Treschow, 2021, Archives of Toxicology.

Patient iPSC-Derived Neurons for Disease Modeling of Frontotemporal Dementia with Mutation in CHMP2B

L. Bolund, Fengping Xu, Yonglun Luo, 2017, Stem cell reports.

Generation of induced pluripotent stem cells derived from a 77-year-old healthy woman as control for age related diseases.

T. Gasser, U. Mau-Holzmann, T. Kluba, 2016, Stem cell research.

Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11.

Z. Tümer, T. Nielsen, J. Nielsen, 2016, Stem cell research.

Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a P301L mutation in microtubule-associated protein tau (MAPT).

G. Waldemar, J. Nielsen, L. Hasholt, 2016, Stem cell research.

Lab resource: Stem cell lineGeneration of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1

G. Waldemar, T. Nielsen, J. Nielsen, 2016 .

Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11.

Z. Tümer, T. Nielsen, J. Nielsen, 2016, Stem cell research.

Induced pluripotent stem cells (iPSCs) derived from a pre-symptomatic carrier of a R406W mutation in microtubule-associated protein tau (MAPT) causing frontotemporal dementia.

G. Waldemar, J. Nielsen, L. Hasholt, 2016, Stem cell research.

Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT).

G. Waldemar, J. Nielsen, L. Hasholt, 2016, Stem cell research.

Lab resource : Stem cell line Induced pluripotent stem cells ( iPSCs ) derived from a patient with frontotemporal dementia caused by a R 406 W mutation in microtubule-associated protein tau ( MAPT )

G. Waldemar, J. Nielsen, L. Hasholt, 2015 .