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Nicolaas Jaspers
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24
Hoeijmakers, Jan
21
Raams, Anja
15
Vermeulen, Wim
14
Zdzienicka, Malgorzata
14
Kleijer, Wim
9
Appeldoorn, Esther
8
Lohman, Paul
8
Lehmann, Alan
6
Bootsma, Dirk
6
de Laat, Wouter
5
Garritsen, Victor
5
Shiloh, Yosef
5
Sijbers, AM
5
Stefanini, Miria
5
Ziv, Yehiel
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All Publications
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2009: Janssen Rolf J R J; Distelmaier Felix; Smeets Roel; Wijnhoven Tessa; Østergaard Elsebet; Jaspers Nicolaas G J; Raams Anja; Kemp Stephan; Rodenburg Richard J T; Willems Peter H M G; van den Heuvel Lambert P W J; Smeitink Jan A M; Nijtmans Leo G J
Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder.
Human molecular genetics 2009;18(18):3365-74.
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2009: Pothof Joris; Verkaik Nicole S; van IJcken Wilfred; Wiemer Erik A C; Ta Van T B; van der Horst Gijsbertus T J; Jaspers Nicolaas G J; van Gent Dik C; Hoeijmakers Jan H J; Persengiev Stephan P
MicroRNA-mediated gene silencing modulates the UV-induced DNA-damage response.
The EMBO journal 2009;28(14):2090-9.
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2008: Anttinen Anu; Koulu Leena; Nikoskelainen Eeva; Portin Raija; Kurki Timo; Erkinjuntti Matti; Jaspers Nicolaas G J; Raams Anja; Green Michael H L; Lehmann Alan R; Wing Jonathan F; Arlett Colin F; Marttila Reijo J
Neurological symptoms and natural course of xeroderma pigmentosum.
Brain : a journal of neurology 2008;131(Pt 8):1979-89.
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2008: Kleijer Wim J; Laugel Vincent; Berneburg Mark; Nardo Tiziana; Fawcett Heather; Gratchev Alexei; Jaspers Nicolaas G J; Sarasin Alain; Stefanini Miria; Lehmann Alan R
Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.
DNA repair 2008;7(5):744-50.
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2008: Das Devashish; Tripsianes Konstantinos; Jaspers Nicolaas G J; Hoeijmakers Jan H J; Kaptein Robert; Boelens Rolf; Folkers Gert E
The HhH domain of the human DNA repair protein XPF forms stable homodimers.
Proteins 2008;70(4):1551-63.
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2007: Kleijer Wim J; van der Sterre Marianne L T; Garritsen Victor H; Raams Anja; Jaspers Nicolaas G J
Prenatal diagnosis of xeroderma pigmentosum and trichothiodystrophy in 76 pregnancies at risk.
Prenatal diagnosis 2007;27(12):1133-7.
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2007: Bergink Steven; Jaspers Nicolaas G J; Vermeulen Wim
Regulation of UV-induced DNA damage response by ubiquitylation.
DNA repair 2007;6(9):1231-42.
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2007: Jaspers Nicolaas G J; Raams Anja; Silengo Margherita Cirillo; Wijgers Nils; Niedernhofer Laura J; Robinson Andria Rasile; Giglia-Mari Giuseppina; Hoogstraten Deborah; Kleijer Wim J; Hoeijmakers Jan H J; Vermeulen Wim
First reported patient with human ERCC1 deficiency has cerebro-oculo-facio-skeletal syndrome with a mild defect in nucleotide excision repair and severe developmental failure.
American journal of human genetics 2007;80(3):457-66.
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2007: Botta Elena; Offman Judith; Nardo Tiziana; Ricotti Roberta; Zambruno Giovanna; Sansone Daniela; Balestri Paolo; Raams Anja; Kleijer Wim J; Jaspers Nicolaas G J; Sarasin Alain; Lehmann Alan R; Stefanini Miria
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships.
Human mutation 2007;28(1):92-6.
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2006: Niedernhofer Laura J; Garinis George A; Raams Anja; Lalai Astrid S; Robinson Andria Rasile; Appeldoorn Esther; Odijk Hanny; Oostendorp Roos; Ahmad Anwaar; van Leeuwen Wibeke; Theil Arjan F; Vermeulen Wim; van der Horst Gijsbertus T J; Meinecke Peter; Kleijer Wim J; Vijg Jan; Jaspers Nicolaas G J; Hoeijmakers Jan H J
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis.
Nature 2006;444(7122):1038-43.
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2006: Oh Kyu-Seon; Khan Sikandar G; Jaspers N G J; Raams Anja; Ueda Takahiro; Lehmann Alan; Friedmann Peter S; Emmert Steffen; Gratchev Alexi; Lachlan Katherine; Lucassan Anneke; Baker Carl C; Kraemer Kenneth H
Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
Human mutation 2006;27(11):1092-103.
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2006: Kleijer Wim J; van der Sterre Marianne L T; Garritsen Victor H; Raams Anja; Jaspers Nicolaas G J
Prenatal diagnosis of the Cockayne syndrome: survey of 15 years experience.
Prenatal diagnosis 2006;26(10):980-4.
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2006: Godthelp Barbara C; van Buul Paul P W; Jaspers Nicolaas G J; Elghalbzouri-Maghrani Elhaam; van Duijn-Goedhart Annemarie; Arwert Fré; Joenje Hans; Zdzienicka Malgorzata Z
Cellular characterization of cells from the Fanconi anemia complementation group, FA-D1/BRCA2.
Mutation research 2006;601(1-2):191-201.
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2006: Andressoo Jaan-Olle; Mitchell James R; de Wit Jan; Hoogstraten Deborah; Volker Marcel; Toussaint Wendy; Speksnijder Ewoud; Beems Rudolph B; van Steeg Harry; Jans Judith; de Zeeuw Chris I; Jaspers Nicolaas G J; Raams Anja; Lehmann Alan R; Vermeulen Wim; Hoeijmakers Jan H J; van der Horst Gijsbertus T J
An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria.
Cancer cell 2006;10(2):121-32.
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2006: van der Burg Mirjam; van Veelen Lieneke R; Verkaik Nicole S; Wiegant Wouter W; Hartwig Nico G; Barendregt Barbara H; Brugmans Linda; Raams Anja; Jaspers Nicolaas G J; Zdzienicka Malgorzata Z; van Dongen Jacques J M; van Gent Dik C
A new type of radiosensitive T-B-NK+ severe combined immunodeficiency caused by a LIG4 mutation.
The Journal of clinical investigation 2006;116(1):137-45.
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2006: Jaspers Nicolaas G J; Zdzienicka Malgorzata Z
Inhibition of DNA synthesis by ionizing radiation: a marker for an S-phase checkpoint.
Methods in molecular biology (Clifton, N.J.) 2006;314():51-9.
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2005: Tripsianes Konstantinos; Folkers Gert; Ab Eiso; Das Devashish; Odijk Hanny; Jaspers Nicolaas G J; Hoeijmakers Jan H J; Kaptein Robert; Boelens Rolf
The structure of the human ERCC1/XPF interaction domains reveals a complementary role for the two proteins in nucleotide excision repair.
Structure (London, England : 1993) 2005;13(12):1849-58.
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2005: Theron Therina; Fousteri Maria I; Volker Marcel; Harries Lorna W; Botta Elena; Stefanini Miria; Fujimoto Mitsuo; Andressoo Jaan-Olle; Mitchell Jay; Jaspers Nicolaas G J; McDaniel Lisa D; Mullenders Leon H; Lehmann Alan R
Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndrome.
Molecular and cellular biology 2005;25(18):8368-78.
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2005: Nakabayashi Kazuhiko; Amann Daniela; Ren Yan; Saarialho-Kere Ulpu; Avidan Nili; Gentles Simone; MacDonald Jeffrey R; Puffenberger Erik G; Christiano Angela M; Martinez-Mir Amalia; Salas-Alanis Julio C; Rizzo Renata; Vamos Esther; Raams Anja; Les Clifford; Seboun Eric; Jaspers Nicolaas G J; Beckmann Jacques S; Jackson Charles E; Scherer Stephen W
Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy.
American journal of human genetics 2005;76(3):510-6.
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2005: Essers Jeroen; van Cappellen Wiggert A; Theil Arjan F; van Drunen Ellen; Jaspers Nicolaas G J; Hoeijmakers Jan H J; Wyman Claire; Vermeulen Wim; Kanaar Roland
Dynamics of relative chromosome position during the cell cycle.
Molecular biology of the cell 2005;16(2):769-75.
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2004: Thorel Fabrizio; Constantinou Angelos; Dunand-Sauthier Isabelle; Nouspikel Thierry; Lalle Philippe; Raams Anja; Jaspers Nicolaas G J; Vermeulen Wim; Shivji Mahmud K K; Wood Richard D; Clarkson Stuart G
Definition of a short region of XPG necessary for TFIIH interaction and stable recruitment to sites of UV damage.
Molecular and cellular biology 2004;24(24):10670-80.
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2004: Horibata Katsuyoshi; Iwamoto Yuka; Kuraoka Isao; Jaspers Nicolaas G J; Kurimasa Akihiro; Oshimura Mitsuo; Ichihashi Masamitsu; Tanaka Kiyoji
Complete absence of Cockayne syndrome group B gene product gives rise to UV-sensitive syndrome but not Cockayne syndrome.
Proceedings of the National Academy of Sciences of the United States of America 2004;101(43):15410-5.
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2004: Giglia-Mari Giuseppina; Coin Frederic; Ranish Jeffrey A; Hoogstraten Deborah; Theil Arjan; Wijgers Nils; Jaspers Nicolaas G J; Raams Anja; Argentini Manuela; van der Spek P J; Botta Elena; Stefanini Miria; Egly Jean-Marc; Aebersold Ruedi; Hoeijmakers Jan H J; Vermeulen Wim
A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group A.
Nature genetics 2004;36(7):714-9.
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2004: Niedernhofer Laura J; Odijk Hanny; Budzowska Magda; van Drunen Ellen; Maas Alex; Theil Arjan F; de Wit Jan; Jaspers N G J; Beverloo H Berna; Hoeijmakers Jan H J; Kanaar Roland
The structure-specific endonuclease Ercc1-Xpf is required to resolve DNA interstrand cross-link-induced double-strand breaks.
Molecular and cellular biology 2004;24(13):5776-87.
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2003: Bosma Peter T; van Eert Simone J; Jaspers Nicolaas G J; Stoter Gerrit; Nooter Kees
Functional cloning of drug resistance genes from retroviral cDNA libraries.
Biochemical and biophysical research communications 2003;309(3):605-11.
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2002: Jaspers Nicolaas G J; Raams Anja; Kelner Michael J; Ng Jessica M Y; Yamashita Yukiko M; Takeda Shiunichi; McMorris Trevor C; Hoeijmakers Jan H J
Anti-tumour compounds illudin S and Irofulven induce DNA lesions ignored by global repair and exclusively processed by transcription- and replication-coupled repair pathways.
DNA repair 2002;1(12):1027-38.
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2002: van den Boom Vincent; Jaspers Nicolaas G J; Vermeulen Wim
When machines get stuck--obstructed RNA polymerase II: displacement, degradation or suicide.
BioEssays : news and reviews in molecular, cellular and developmental biology 2002;24(9):780-4.
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2002: Broughton Bernard C; Cordonnier Agnes; Kleijer Wim J; Jaspers Nicolaas G J; Fawcett Heather; Raams Anja; Garritsen Victor H; Stary Anne; Avril Marie-Françoise; Boudsocq Francois; Masutani Chikahide; Hanaoka Fumio; Fuchs Robert P; Sarasin Alain; Lehmann Alan R
Molecular analysis of mutations in DNA polymerase eta in xeroderma pigmentosum-variant patients.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(2):815-20.
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2002: Kraakman-van der Zwet Maria; Overkamp Wilhelmina J I; van Lange Rebecca E E; Essers Jeroen; van Duijn-Goedhart Annemarie; Wiggers Ingrid; Swaminathan Srividya; van Buul Paul P W; Errami Abdellatif; Tan Raoul T L; Jaspers Nicolaas G J; Sharan Shyam K; Kanaar Roland; Zdzienicka Malgorzata Z
Brca2 (XRCC11) deficiency results in radioresistant DNA synthesis and a higher frequency of spontaneous deletions.
Molecular and cellular biology 2002;22(2):669-79.
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2001: Graham J M; Anyane-Yeboa K; Raams A; Appeldoorn E; Kleijer W J; Garritsen V H; Busch D; Edersheim T G; Jaspers N G
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
American journal of human genetics 2001;69(2):291-300.
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2001: Kraakman-van der Zwet M; Overkamp W J; Jaspers N G; Natarajan A T; Lohman P H; Zdzienicka M Z
Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells.
Mutation research 2001;485(3):177-85.
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2001: Vermeulen W; Rademakers S; Jaspers N G; Appeldoorn E; Raams A; Klein B; Kleijer W J; Hansen L K; Hoeijmakers J H
A temperature-sensitive disorder in basal transcription and DNA repair in humans.
Nature genetics 2001;27(3):299-303.
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2001: Zafeiriou D I; Thorel F; Andreou A; Kleijer W J; Raams A; Garritsen V H; Gombakis N; Jaspers N G; Clarkson S G
Xeroderma pigmentosum group G with severe neurological involvement and features of Cockayne syndrome in infancy.
Pediatric research 2001;49(3):407-12.
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2000: Petit-Frère C; Capulas E; Lowe J E; Koulu L; Marttila R J; Jaspers N G; Clingen P H; Green M H; Arlett C F
Ultraviolet-B-induced apoptosis and cytokine release in xeroderma pigmentosum keratinocytes.
The Journal of investigative dermatology 2000;115(4):687-93.
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1999: Stewart G S; Maser R S; Stankovic T; Bressan D A; Kaplan M I; Jaspers N G; Raams A; Byrd P J; Petrini J H; Taylor A M
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.
Cell 1999;99(6):577-87.
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1999: Kraakman-van der Zwet M; Overkamp W J; Friedl A A; Klein B; Verhaegh G W; Jaspers N G; Midro A T; Eckardt-Schupp F; Lohman P H; Zdzienicka M Z
Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts.
Mutation research 1999;434(1):17-27.
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1999: de Laat W L; Jaspers N G; Hoeijmakers J H
Molecular mechanism of nucleotide excision repair.
Genes & development 1999;13(7):768-85.
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1999: Jaspers N G; Zdzienicka M Z
Inhibition of DNA synthesis by ionizing radiation.
Methods in molecular biology (Clifton, N.J.) 1999;113():535-42.
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1998: de Laat W L; Sijbers A M; Odijk H; Jaspers N G; Hoeijmakers J H
Mapping of interaction domains between human repair proteins ERCC1 and XPF.
Nucleic acids research 1998;26(18):4146-52.
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1998: Ellison A R; Nouspikel T; Jaspers N G; Clarkson S G; Gruenert D C
Complementation of transformed fibroblasts from patients with combined xeroderma pigmentosum-Cockayne syndrome.
Experimental cell research 1998;243(1):22-8.
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1998: de Laat W L; Appeldoorn E; Sugasawa K; Weterings E; Jaspers N G; Hoeijmakers J H
DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair.
Genes & development 1998;12(16):2598-609.
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1998: Sijbers A M; van Voorst Vader P C; Snoek J W; Raams A; Jaspers N G; Kleijer W J
Homozygous R788W point mutation in the XPF gene of a patient with xeroderma pigmentosum and late-onset neurologic disease.
The Journal of investigative dermatology 1998;110(5):832-6.
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1998: de Laat W L; Appeldoorn E; Jaspers N G; Hoeijmakers J H
DNA structural elements required for ERCC1-XPF endonuclease activity.
The Journal of biological chemistry 1998;273(14):7835-42.
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1998: Abrahams P J; Houweling A; Cornelissen-Steijger P D; Jaspers N G; Darroudi F; Meijers C M; Mullenders L H; Filon R; Arwert F; Pinedo H M; Natarajan A P; Terleth C; Van Zeeland A A; van der Eb A J
Impaired DNA repair capacity in skin fibroblasts from various hereditary cancer-prone syndromes.
Mutation research 1998;407(2):189-201.
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1997: Taylor E M; Broughton B C; Botta E; Stefanini M; Sarasin A; Jaspers N G; Fawcett H; Harcourt S A; Arlett C F; Lehmann A R
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(16):8658-63.
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1997: Vermeulen W; de Boer J; Citterio E; van Gool A J; van der Horst G T; Jaspers N G; de Laat W L; Sijbers A M; van der Spek P J; Sugasawa K; Weeda G; Winkler G S; Bootsma D; Egly J M; Hoeijmakers J H
Mammalian nucleotide excision repair and syndromes.
Biochemical Society transactions 1997;25(1):309-15.
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1997: Jaspers N G
DNA repair genes, enzymes, patients, and mouse models.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1997;143():329-35.
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1996: Jongmans W; Verhaegh G W; Jaspers N G; Demant P; Natarajan A T; Shiloh Y; Oshimura M; Stanbridge E J; Athwal R S; Cuthbert A P; Newbold R F; Lohman P H; Zdzienicka M Z
The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes.
Mutation research 1996;364(2):91-102.
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1996: Sijbers A M; van der Spek P J; Odijk H; van den Berg J; van Duin M; Westerveld A; Jaspers N G; Bootsma D; Hoeijmakers J H
Mutational analysis of the human nucleotide excision repair gene ERCC1.
Nucleic acids research 1996;24(17):3370-80.
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1996: Sijbers A M; de Laat W L; Ariza R R; Biggerstaff M; Wei Y F; Moggs J G; Carter K C; Shell B K; Evans E; de Jong M C; Rademakers S; de Rooij J; Jaspers N G; Hoeijmakers J H; Wood R D
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease.
Cell 1996;86(5):811-22.
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1996: Hamel B C; Raams A; Schuitema-Dijkstra A R; Simons P; van der Burgt I; Jaspers N G; Kleijer W J
Xeroderma pigmentosum--Cockayne syndrome complex: a further case.
Journal of medical genetics 1996;33(7):607-10.
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1996: Jaspers N G
Multiple involvement of nucleotide excision repair enzymes: clinical manifestations of molecular intricacies.
Cytokines and molecular therapy 1996;2(2):115-9.
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1996: Gilad S; Khosravi R; Shkedy D; Uziel T; Ziv Y; Savitsky K; Rotman G; Smith S; Chessa L; Jorgensen T J; Harnik R; Frydman M; Sanal O; Portnoi S; Goldwicz Z; Jaspers N G; Gatti R A; Lenoir G; Lavin M F; Tatsumi K; Wegner R D; Shiloh Y; Bar-Shira A
Predominance of null mutations in ataxia-telangiectasia.
Human molecular genetics 1996;5(4):433-9.
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1995: Verhaegh G W; Jongmans W; Jaspers N G; Natarajan A T; Oshimura M; Lohman P H; Zdzienicka M Z
A gene that regulates DNA replication in response to DNA damage is located on human chromosome 4q.
American journal of human genetics 1995;57(5):1095-103.
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1995: Verhaegh G W; Jongmans W; Morolli B; Jaspers N G; van der Schans G P; Lohman P H; Zdzienicka M Z
A novel type of X-ray-sensitive Chinese hamster cell mutant with radioresistant DNA synthesis and hampered DNA double-strand break repair.
Mutation research 1995;337(2):119-29.
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1995: van Vuuren A J; Appeldoorn E; Odijk H; Humbert S; Moncollin V; Eker A P; Jaspers N G; Egly J M; Hoeijmakers J H
Partial characterization of the DNA repair protein complex, containing the ERCC1, ERCC4, ERCC11 and XPF correcting activities.
Mutation research 1995;337(1):25-39.
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1995: Savitsky K; Bar-Shira A; Gilad S; Rotman G; Ziv Y; Vanagaite L; Tagle D A; Smith S; Uziel T; Sfez S; Ashkenazi M; Pecker I; Frydman M; Harnik R; Patanjali S R; Simmons A; Clines G A; Sartiel A; Gatti R A; Chessa L; Sanal O; Lavin M F; Jaspers N G; Taylor A M; Arlett C F; Miki T; Weissman S M; Lovett M; Collins F S; Shiloh Y
A single ataxia telangiectasia gene with a product similar to PI-3 kinase.
Science (New York, N.Y.) 1995;268(5218):1749-53.
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1995: Jongmans W; Verhaegh G W; Jaspers N G; Oshimura M; Stanbridge E J; Lohman P H; Zdzienicka M Z
Studies on phenotypic complementation of ataxia-telangiectasia cells by chromosome transfer.
American journal of human genetics 1995;56(2):438-43.
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1994: Zdzienicka M Z; Verhaegh G W; Jongmans W; Morolli B; Jaspers N G; Oshimura M
Functional complementation studies with X-ray-sensitive mutants of Chinese hamster cells closely resembling ataxia-telangiectasia cells.
International journal of radiation biology 1994;66(6 Suppl):S189-95.
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1994: Kleijer W J; van der Kraan M; Los F J; Jaspers N G
Prenatal diagnosis of ataxia-telangiectasia and Nijmegen Breakage syndrome by the assay of radioresistant DNA synthesis.
International journal of radiation biology 1994;66(6 Suppl):S167-74.
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1994: van Vuuren A J; Vermeulen W; Ma L; Weeda G; Appeldoorn E; Jaspers N G; van der Eb A J; Bootsma D; Hoeijmakers J H; Humbert S
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).
The EMBO journal 1994;13(7):1645-53.
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1994: Vermeulen W; van Vuuren A J; Chipoulet M; Schaeffer L; Appeldoorn E; Weeda G; Jaspers N G; Priestley A; Arlett C F; Lehmann A R
Three unusual repair deficiencies associated with transcription factor BTF2(TFIIH): evidence for the existence of a transcription syndrome.
Cold Spring Harbor symposia on quantitative biology 1994;59():317-29.
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1993: van Vuuren A J; Appeldoorn E; Odijk H; Yasui A; Jaspers N G; Bootsma D; Hoeijmakers J H
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group F.
The EMBO journal 1993;12(9):3693-701.
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1993: Vermeulen W; Jaeken J; Jaspers N G; Bootsma D; Hoeijmakers J H
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome.
American journal of human genetics 1993;53(1):185-92.
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1993: Taylor A M; Jaspers N G; Gatti R A
Fifth International Workshop on Ataxia-Telangiectasia.
Cancer research 1993;53(2):438-41.
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1993: Verhaegh G W; Jaspers N G; Lohman P H; Zdzienicka M Z
Co-dominance of radioresistant DNA synthesis in a group of AT-like Chinese hamster cell mutants.
Cytogenetics and cell genetics 1993;63(3):176-80.
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1992: Eker A P; Vermeulen W; Miura N; Tanaka K; Jaspers N G; Hoeijmakers J H; Bootsma D
Xeroderma pigmentosum group A correcting protein from calf thymus.
Mutation research 1992;274(3):211-24.
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1992: Sobel E; Lange E; Jaspers N G; Chessa L; Sanal O; Shiloh Y; Taylor A M; Weemaes C M; Lange K; Gatti R A
Ataxia-telangiectasia: linkage evidence for genetic heterogeneity.
American journal of human genetics 1992;50(6):1343-8.
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1992: Ziv Y; Frydman M; Lange E; Zelnik N; Rotman G; Julier C; Jaspers N G; Dagan Y; Abeliovicz D; Dar H; Borochowitz Z; Lathrop M; Gatti R A; Shiloh Y
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome.
Human genetics 1992;88(6):619-26.
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1990: Jaspers N G; van der Kraan M; Linssen P C; Maçek M; Seemanová E; Kleijer W J
First-trimester prenatal diagnosis of the Nijmegen breakage syndrome and ataxia telangiectasia using an assay of radioresistant DNA synthesis.
Prenatal diagnosis 1990;10(10):667-74.
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1990: Roza L; Vermeulen W; Bergen Henegouwen J B; Eker A P; Jaspers N G; Lohman P H; Hoeijmakers J H
Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblasts.
Cancer research 1990;50(6):1905-10.
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1989: Ziv Y; Jaspers N G; Etkin S; Danieli T; Trakhtenbrot L; Amiel A; Ravia Y; Shiloh Y
Cellular and molecular characteristics of an immortalized ataxia-telangiectasia (group AB) cell line.
Cancer research 1989;49(9):2495-501.
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1989: Zdzienicka M Z; Jaspers N G; van der Schans G P; Natarajan A T; Simons J W
Ataxia-telangiectasia-like Chinese hamster V79 cell mutants with radioresistant DNA synthesis, chromosomal instability, and normal DNA strand break repair.
Cancer research 1989;49(6):1481-5.
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1989: Ziv Y; Amiel A; Jaspers N G; Berkel A I; Shiloh Y
Ataxia-telangiectasia: a variant with altered in vitro phenotype of fibroblast cells.
Mutation research 1989;210(2):211-9.
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1988: Jaspers N G; Taalman R D; Baan C
Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia.
American journal of human genetics 1988;42(1):66-73.
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1988: Wegner R D; Metzger M; Hanefeld F; Jaspers N G; Baan C; Magdorf K; Kunze J; Sperling K
A new chromosomal instability disorder confirmed by complementation studies.
Clinical genetics 1988;33(1):20-32.
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1988: Jaspers N G; Gatti R A; Baan C; Linssen P C; Bootsma D
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients.
Cytogenetics and cell genetics 1988;49(4):259-63.
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1984: van Voorst Vader P C; Jaspers N G; van der Kamp A W
Retinoic acid and defective UV light induced DNA excision repair in xeroderma pigmentosum: absence of ameliorating effect.
Archives of dermatological research 1984;276(3):201-2.
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1983: Taalman R D; Jaspers N G; Scheres J M; de Wit J; Hustinx T W
Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage Syndrome.
Mutation research 1983;112(1):23-32.
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1982: Jaspers N G; de Wit J; Regulski M R; Bootsma D
Abnormal regulation of DNA replication and increased lethality in ataxia telangiectasia cells exposed to carcinogenic agents.
Cancer research 1982;42(1):335-41.
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1981: Jaspers N G; Scheres J M; De Wit J; Bootsma D
Rapid diagnostic test for ataxia telangiectasia.
Lancet 1981;2(8244):473.
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1981: de Wit J; Jaspers N G; Bootsma D
The rate of DNA synthesis in normal human and ataxia telangiectasia cells after exposure to X-irradiation.
Mutation research 1981;80(1):221-6.
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