T. Nouspikel

发表

Attenuated nucleotide excision repair leads to mutagenesis in cancer cells.

T. Nouspikel, 2011, Future oncology.

DNA Repair in Mammalian Cells

T. Nouspikel, 2009, Cellular and Molecular Life Sciences.

Transcription Domain-Associated Repair in Human Cells

P. Hanawalt, T. Nouspikel, Nevila Hyka-Nouspikel, 2006, Molecular and Cellular Biology.

Regulation of nucleotide excision repair in bacteria and mammalian cells.

P. Hanawalt, J. Ford, S. Tornaletti, 2000, Cold Spring Harbor symposia on quantitative biology.

DNA repair in terminally differentiated cells.

P. Hanawalt, T. Nouspikel, 2002, DNA repair.

Definition of a Short Region of XPG Necessary for TFIIH Interaction and Stable Recruitment to Sites of UV Damage

R. Wood, A. Constantinou, W. Vermeulen, 2004, Molecular and Cellular Biology.

A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function.

S. A. Leadon, S. Clarkson, T. Nouspikel, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Transcriptional induction of glucokinase gene by insulin in cultured liver cells and its repression by the glucagon-cAMP system.

T. Nouspikel, P. Iynedjian, D. Jotterand, 1989, The Journal of biological chemistry.

When parsimony backfires: neglecting DNA repair may doom neurons in Alzheimer's disease.

P. Hanawalt, T. Nouspikel, 2003, BioEssays : news and reviews in molecular, cellular and developmental biology.

Insulin signalling and regulation of glucokinase gene expression in cultured hepatocytes.

T. Nouspikel, P. Iynedjian, 1992, European journal of biochemistry.

Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndrome.

S. Clarkson, A. Ellison, D. Gruenert, 1998, Experimental cell research.

Mutations that disable the DNA repair gene XPG in a xeroderma pigmentosum group G patient.

S. Clarkson, T. Nouspikel, 1994, Human molecular genetics.

Unimpaired effect of insulin on glucokinase gene expression in hepatocytes challenged with amylin

T. Nouspikel, P. Iynedjian, A. Gjinovci, 1992, FEBS letters.

Differential expression and regulation of the glucokinase gene in liver and islets of Langerhans.

C. Ucla, C. Newgard, T. Nouspikel, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Genetic instability in human embryonic stem cells: prospects and caveats.

T. Nouspikel, 2013, Future oncology.

Deficient DNA Damage Response and Cell Cycle Checkpoints Lead to Accumulation of Point Mutations in Human Embryonic Stem Cells

P. Andrews, M. Meuth, P. Gokhale, 2012, Stem cells.

Nucleotide excision repair and B lymphoma: Somatic hypermutation is not the only culprit

T. Nouspikel, Nevila Hyka-Nouspikel, 2011, Cell cycle.

Circulating human B lymphocytes are deficient in nucleotide excision repair and accumulate mutations upon proliferation.

T. Nouspikel, Nevila Hyka-Nouspikel, Wei-Ting Lu, 2011, Blood.

Terminally Differentiated Human Neurons Repair Transcribed Genes but Display Attenuated Global DNA Repair and Modulation of Repair Gene Expression

P. Hanawalt, T. Nouspikel, 2000, Molecular and Cellular Biology.

Nucleotide excision repair : variations on versatility

T. Nouspikel, 2009 .

Severe and Early Hepatic Failure in A Neonate: A New CFTR Mutation Associated with Medium-Chain Acyl-CoA Deficiency

A. Rougemont, T. Nouspikel, C. Barazzone-Argiroffo, 2021, Frontiers in Medical Case Reports.

Nucleotide excision repair phenotype of human acute myeloid leukemia cell lines at various stages of differentiation.

P. Hanawalt, T. Nouspikel, Pei-hsin Hsu, 2007, Mutation research.

Defective Transcription-Coupled Repair of Oxidative Base Damage in Cockayne Syndrome Patients from XP Group G

S. Clarkson, T. Nouspikel, P. Cooper, 1997, Science.

Nucleotide excision repair and neurological diseases.

T. Nouspikel, 2008, DNA repair.

DNA repair in differentiated cells: Some new answers to old questions

T. Nouspikel, 2007, Neuroscience.

Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2

A. Bairoch, C. Ucla, D. Scherly, 1993, Nature.

Multiple roles of ubiquitination in the control of nucleotide excision repair

T. Nouspikel, 2011, Mechanisms of Ageing and Development.

Impaired nucleotide excision repair upon macrophage differentiation is corrected by E1 ubiquitin-activating enzyme

P. Hanawalt, T. Nouspikel, 2006, Proceedings of the National Academy of Sciences.

DNA Repair in Mammalian Cells

T. Nouspikel, 2009, Cellular and Molecular Life Sciences.

The founding members of xeroderma pigmentosum group G produce XPG protein with severely impaired endonuclease activity.

A. Constantinou, S. Clarkson, T. Nouspikel, 2002, The Journal of investigative dermatology.

The Fanconi anemia pathway is downregulated upon macrophage differentiation through two distinct mechanisms

T. Nouspikel, Wei-Ting Lu, R. Drayton, 2011, Cell cycle.

Nucleotide excision repair : variations on versatility

T. Nouspikel, 2009 .

Circulating human B lymphocytes are deficient in nucleotide excision repair and accumulate mutations upon proliferation.

T. Nouspikel, Nevila Hyka-Nouspikel, Wei-Ting Lu, 2011, Blood.

Retraction

S. Clarkson, T. Nouspikel, Priscilla K. Cooper, 2005, Science.