UB Paderborn / Katalog / Suche / in CDI

Oxygen is a critical parameter for chondrogenic differentiation of human umbilical cord blood mesenchymal stem cell in 3D-cultures

Osteoarthritis and cartilage, 2014-04, Vol.22, p.S486-S486

2014

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Specific UV-Induced Mutation Spectrum in the p53 Gene of Skin Tumors from DNA-Repair-Deficient Xeroderma Pigmentosum Patients

Proceedings of the National Academy of Sciences - PNAS, 1993-11, Vol.90 (22), p.10529-10533

1993

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Redifferentiation of human dedifferentiated chondrocytes : an innovative combination for the cell therapy of articular cartilage

Osteoarthritis and cartilage, 2012-04, Vol.20, p.S132-S132

2012

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Differentiation of human adult mesenchymal stem cells in chondrocytes for cartilage engineering

Osteoarthritis and cartilage, 2012-04, Vol.20, p.S278-S278

2012

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Facteurs influençant la longue survie chez les patients atteints de mésothéliome pleural malin. Étude sur 182 cas du registre Mésonat et du Programme national de surveillance du mésothéliome

Annales de pathologie, 2011-11, Vol.31 (5), p.S133-S133

2011

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P.317Rimeporide, a repositioned NHE-1 inhibitor for DMD: a preclinical trial in GRMD dogs

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S159-S159

2019

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P.288Multi-exon skipping by CRISPR/Cas9-mediated genome editing in GRMD dog

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S151-S151

2019

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BMP-2, hypoxia, and COL1A1/HtrA1 siRNAs favor neo-cartilage hyaline matrix formation in chondrocytes

Tissue engineering. Part C, Methods, 2015-02, Vol.21 (2), p.133

2015

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G.P.1.15 Clinical description and molecular analysis of a promising model of DMD, the LRMD dog

Neuromuscular disorders : NMD, 2007, Vol.17 (9), p.776-776

2007

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High Levels of Patched Gene Mutations in Basal-Cell Carcinomas from Patients with Xeroderma Pigmentosum

Proceedings of the National Academy of Sciences - PNAS, 1999-04, Vol.96 (9), p.5117-5122

1999

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Effects of XPD Mutations on Ultraviolet-Induced Apoptosis in Relation to Skin Cancer-Proneness in Repair-Deficient Syndromes

Journal of investigative dermatology, 2001-11, Vol.117 (5), p.1162-1170

2001

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p53 mutations in skin and internal tumors of xeroderma pigmentosum patients belonging to the complementation group C

Cancer research (Chicago, Ill.), 1998-10, Vol.58 (19), p.4402-4409

1998

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Relationship between posttranslational modification of transaldolase and catalase deficiency in UV-sensitive repair-deficient xeroderma pigmentosum fibroblasts and SV40-transformed human cells

Free radical biology & medicine, 2001-06, Vol.30 (12), p.1365-1373

2001

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High mutation frequency in ras genes of skin tumors isolated from DNA repair deficient xeroderma pigmentosum patients

Cancer research (Chicago, Ill.), 1993-04, Vol.53 (7), p.1625-1629

1993

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Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes

Molecular carcinogenesis, 1997-12, Vol.20 (4), p.340-347

1997

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Recovery of the normal p53 response after UV treatment in DNA repair-deficient fibroblasts by retroviral-mediated correction with the XPD gene

Carcinogenesis (New York), 1998-09, Vol.19 (9), p.1701-1704

1998

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p53 mutations in cutaneous lesions induced in the hairless mouse by a solar ultraviolet light simulator

Molecular carcinogenesis, 1998-07, Vol.22 (3), p.167-174

1998

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CARACTERISATION D'ONCOGENES ACTIVES DANS LES TUMEURS DE XERODERMA PIGMENTOSUM

Reproduction, nutrition, development, 1989, Vol.29 (Suppl), p.34-34

1989

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Utilisation de tests salivaires dans l'investigation d'une épidémie d'hépatite A, Auvergne, décembre 2004: Numéro thématique. Risques infectieux : approches méthodologiques de la veille et de l'aide à la décision en santé publique

Bulletin epidémiologique hebdomadaire (Paris, France), 2006 (2-3), p.13-15

2006

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An immortalized xeroderma pigmentosum, group C, cell line which replicates SV40 shuttle vectors

Mutation research, 1987-03, Vol.183 (2), p.185-196

1987

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Comparative study of Epstein—Barr virus and SV40-based shuttle-expression vectors in human repair-deficient cells

Mutation research, 1989-03, Vol.220 (2), p.169-185

1989

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S09 03 MA - ONCOGENE ACTIVATION IN ULTRAVIOLET-INDUCED SKIN TUMORS FROM NORMAL INDIVIDUALS AND XERODERMA PIGMENTOSUM PATIENTS

Radiation Research: A Twentieth-Century Perspective: Congress Abstracts, 1991, p.42-42

1991

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N-acetylaspartate catabolism determines cytosolic acetyl-CoA levels and histone acetylation in brown adipocytes

Scientific reports, 2016-04, Vol.6 (1), p.23723-23723, Article 23723

2016

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Towards Mixed-Initiative Human-Robot Interaction: Assessment of Discriminative Physiological and Behavioral Features for Performance Prediction

Sensors (Basel, Switzerland), 2020-01, Vol.20 (1), p.296

2020

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Activation of oncogenesis in skin tumors from a repair-deficient syndrome, xeroderma pigmentosum

Mutation Research/Environmental Mutagenesis and Related Subjects, 1990-12, Vol.234 (6), p.425-425

1990

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Oxygen is a critical parameter for chondrogenic differentiation of human umbilical cord blood mesenchymal stem cell in 3D-cultures

Specific UV-Induced Mutation Spectrum in the p53 Gene of Skin Tumors from DNA-Repair-Deficient Xeroderma Pigmentosum Patients

Redifferentiation of human dedifferentiated chondrocytes : an innovative combination for the cell therapy of articular cartilage

Differentiation of human adult mesenchymal stem cells in chondrocytes for cartilage engineering

Facteurs influençant la longue survie chez les patients atteints de mésothéliome pleural malin. Étude sur 182 cas du registre Mésonat et du Programme national de surveillance du mésothéliome

P.317Rimeporide, a repositioned NHE-1 inhibitor for DMD: a preclinical trial in GRMD dogs

P.288Multi-exon skipping by CRISPR/Cas9-mediated genome editing in GRMD dog

BMP-2, hypoxia, and COL1A1/HtrA1 siRNAs favor neo-cartilage hyaline matrix formation in chondrocytes

G.P.1.15 Clinical description and molecular analysis of a promising model of DMD, the LRMD dog

High Levels of Patched Gene Mutations in Basal-Cell Carcinomas from Patients with Xeroderma Pigmentosum

Effects of XPD Mutations on Ultraviolet-Induced Apoptosis in Relation to Skin Cancer-Proneness in Repair-Deficient Syndromes

p53 mutations in skin and internal tumors of xeroderma pigmentosum patients belonging to the complementation group C

Relationship between posttranslational modification of transaldolase and catalase deficiency in UV-sensitive repair-deficient xeroderma pigmentosum fibroblasts and SV40-transformed human cells

High mutation frequency in ras genes of skin tumors isolated from DNA repair deficient xeroderma pigmentosum patients

Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes

Recovery of the normal p53 response after UV treatment in DNA repair-deficient fibroblasts by retroviral-mediated correction with the XPD gene

p53 mutations in cutaneous lesions induced in the hairless mouse by a solar ultraviolet light simulator

CARACTERISATION D'ONCOGENES ACTIVES DANS LES TUMEURS DE XERODERMA PIGMENTOSUM

Utilisation de tests salivaires dans l'investigation d'une épidémie d'hépatite A, Auvergne, décembre 2004: Numéro thématique. Risques infectieux : approches méthodologiques de la veille et de l'aide à la décision en santé publique

An immortalized xeroderma pigmentosum, group C, cell line which replicates SV40 shuttle vectors

Comparative study of Epstein—Barr virus and SV40-based shuttle-expression vectors in human repair-deficient cells

S09 03 MA - ONCOGENE ACTIVATION IN ULTRAVIOLET-INDUCED SKIN TUMORS FROM NORMAL INDIVIDUALS AND XERODERMA PIGMENTOSUM PATIENTS

N-acetylaspartate catabolism determines cytosolic acetyl-CoA levels and histone acetylation in brown adipocytes

Towards Mixed-Initiative Human-Robot Interaction: Assessment of Discriminative Physiological and Behavioral Features for Performance Prediction

Activation of oncogenesis in skin tumors from a repair-deficient syndrome, xeroderma pigmentosum

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