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Fré Arwert
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48
Joenje, Hans
23
Rooimans, Martin
16
Waisfisz, Quinten
15
Pronk, Jan
15
de Winter, Johan
11
Pals, Gerard
10
Oostra, Anneke
10
Mathew, Christopher
9
van de Vrugt, Henri
9
van Berkel, Carola
9
Eriksson, Aldur
9
Hoatlin, Maureen
8
Zdzienicka, Malgorzata
7
Westerveld, Andries
7
Kruyt, Frank
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All Publications
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2008: Sii-Felice Karine; Etienne Olivier; Hoffschir Françoise; Mathieu Céline; Riou Lydia; Barroca Vilma; Haton Céline; Arwert Fré; Fouchet Pierre; Boussin François D; Mouthon Marc-André
Fanconi DNA repair pathway is required for survival and long-term maintenance of neural progenitors.
The EMBO journal 2008;27(5):770-81.
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2007: Dorsman Josephine C; Levitus Marieke; Rockx Davy; Rooimans Martin A; Oostra Anneke B; Haitjema Anneke; Bakker Sietske T; Steltenpool Jûrgen; Schuler Dezsö; Mohan Sheila; Schindler Detlev; Arwert Fré; Pals Gerard; Mathew Christopher G; Waisfisz Quinten; de Winter Johan P; Joenje Hans
Identification of the Fanconi anemia complementation group I gene, FANCI.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2007;29(3):211-8.
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2006: Si Yue; Ciccone Samantha; Yang Feng-Chun; Yuan Jin; Zeng Daisy; Chen Shi; van de Vrugt Henri J; Critser John; Arwert Fre; Haneline Laura S; Clapp D Wade
Continuous in vivo infusion of interferon-gamma (IFN-gamma) enhances engraftment of syngeneic wild-type cells in Fanca-/- and Fancg-/- mice.
Blood 2006;108(13):4283-7.
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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: Godthelp Barbara C; Wiegant Wouter W; Waisfisz Quinten; Medhurst Annette L; Arwert Fré; Joenje Hans; Zdzienicka Malgorzata Z
Inducibility of nuclear Rad51 foci after DNA damage distinguishes all Fanconi anemia complementation groups from D1/BRCA2.
Mutation research 2006;594(1-2):39-48.
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2005: Levitus Marieke; Waisfisz Quinten; Godthelp Barbara C; de Vries Yne; Hussain Shobbir; Wiegant Wouter W; Elghalbzouri-Maghrani Elhaam; Steltenpool Jûrgen; Rooimans Martin A; Pals Gerard; Arwert Fré; Mathew Christopher G; Zdzienicka Malgorzata Z; Hiom Kevin; De Winter Johan P; Joenje Hans
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Nature genetics 2005;37(9):934-5.
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2004: Franco Sonia; van de Vrugt Henri J; Fernández Piedad; Aracil Miguel; Arwert Fre; Blasco María A
Telomere dynamics in Fancg-deficient mouse and human cells.
Blood 2004;104(13):3927-35.
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2004: Chen F; Medhurst A L; de Winter J P; Waisfisz Q; Rooimans M A; Oostra A B; Meyer S; Zhang K J; Xia B; Pals G; Arwert F; Zwaan C M; Joenje H
Apparent absence of BRCA2 protein in a proportion of acute myeloid leukemia cell lines.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2004;18(11):1918-20.
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2004: Léveillé France; Blom Eric; Medhurst Annette L; Bier Patrick; Laghmani El Houari; Johnson Mark; Rooimans Martin A; Sobeck Alexandra; Waisfisz Quinten; Arwert Fré; Patel K J; Hoatlin Maureen E; Joenje Hans; de Winter Johan P
The Fanconi anemia gene product FANCF is a flexible adaptor protein.
The Journal of biological chemistry 2004;279(38):39421-30.
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2004: Levitus Marieke; Rooimans Martin A; Steltenpool Jûrgen; Cool Nicolle F C; Oostra Anneke B; Mathew Christopher G; Hoatlin Maureen E; Waisfisz Quinten; Arwert Fré; de Winter Johan P; Joenje Hans
Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.
Blood 2004;103(7):2498-503.
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2004: Blom Eric; van de Vrugt Henri J; de Vries Yne; de Winter Johan P; Arwert Fré; Joenje Hans
Multiple TPR motifs characterize the Fanconi anemia FANCG protein.
DNA repair 2004;3(1):77-84.
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2003: Yamada Kaoru; Ramezani Ali; Hawley Robert G; Ebell Wolfram; Arwert Fre; Arnold Larry W; Walsh Christopher E
Phenotype correction of Fanconi anemia group A hematopoietic stem cells using lentiviral vector.
Molecular therapy : the journal of the American Society of Gene Therapy 2003;8(4):600-10.
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2002: Zdzienicka Malgorzata Z; Arwert Fré
Breast cancer and Fanconi anemia: what are the connections?
Trends in molecular medicine 2002;8(10):458-60.
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2002: Río Paula; Segovia José Carlos; Hanenberg Helmut; Casado José Antonio; Martínez Jesús; Göttsche Kerstin; Cheng Ngan Ching; Van de Vrugt Henri J; Arwert Fré; Joenje Hans; Bueren Juan A
In vitro phenotypic correction of hematopoietic progenitors from Fanconi anemia group A knockout mice.
Blood 2002;100(6):2032-9.
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2002: van de Vrugt Henri J; Koomen Mireille; Berns Mariska A D; de Vries Yne; Rooimans Martin A; van der Weel Laura; Blom Eric; de Groot Jan; Schepers Rik J; Stone Stacie; Hoatlin Maureen E; Cheng Ngan Ching; Joenje Hans; Arwert Fré
Characterization, expression and complex formation of the murine Fanconi anaemia gene product Fancg.
Genes to cells : devoted to molecular & cellular mechanisms 2002;7(3):333-42.
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2002: Koomen Mireille; Cheng Ngan C; van de Vrugt Henri J; Godthelp Barbara C; van der Valk Martin A; Oostra Anneke B; Zdzienicka Malgorzata Z; Joenje Hans; Arwert Fré
Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice.
Human molecular genetics 2002;11(3):273-81.
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2002: Blom Eric; van de Vrugt Henri J; de Winter Johan P; Arwert Fré; Joenje Hans
Evolutionary clues to the molecular function of fanconi anemia genes.
Acta haematologica 2002;108(4):231-6.
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2001: Geldof A A; Versteegh LRT; van Mourik J C; Rooimans M A; Arwert F; Hermsen M A; Schadee-Eestermans I L; van Dongen G A; van der Valk P; van der Clement EHP; Lips P; Teule G J
Clonally related but phenotypically divergent human cancer cell lines derived from a single follicular thyroid cancer recurrence (TT2609).
Thyroid : official journal of the American Thyroid Association 2001;11(10):909-17.
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2001: Hermsen M A; Xie Y; Rooimans M A; Meijer G A; Baak J P; Plukker J T; Arwert F; Joenje H
Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemia.
Familial cancer 2001;1(1):39-43.
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2001: van den Berg J S; Limburg M; Pals G; Arwert F; Westerveld A
Type III collagen deficiency in a family with intracranial aneurysms.
Cerebrovascular diseases (Basel, Switzerland) 2001;11(2):92-4.
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2000: Xie Y; de Winter J P; Waisfisz Q; Nieuwint A W; Scheper R J; Arwert F; Hoatlin M E; Ossenkoppele G J; Schuurhuis G J; Joenje H
Aberrant Fanconi anaemia protein profiles in acute myeloid leukaemia cells.
British journal of haematology 2000;111(4):1057-64.
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2000: de Winter J P; van der Weel L; de Groot J; Stone S; Waisfisz Q; Arwert F; Scheper R J; Kruyt F A; Hoatlin M E; Joenje H
The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG.
Human molecular genetics 2000;9(18):2665-74.
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2000: de Winter J P; Léveillé F; van Berkel C G; Rooimans M A; van Der Weel L; Steltenpool J; Demuth I; Morgan N V; Alon N; Bosnoyan-Collins L; Lightfoot J; Leegwater P A; Waisfisz Q; Komatsu K; Arwert F; Pronk J C; Mathew C G; Digweed M; Buchwald M; Joenje H
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
American journal of human genetics 2000;67(5):1306-8.
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2000: Joenje H; Levitus M; Waisfisz Q; D'Andrea A; Garcia-Higuera I; Pearson T; van Berkel C G; Rooimans M A; Morgan N; Mathew C G; Arwert F
Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.
American journal of human genetics 2000;67(3):759-62.
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2000: Cheng N C; van de Vrugt H J; van der Valk M A; Oostra A B; Krimpenfort P; de Vries Y; Joenje H; Berns A; Arwert F
Mice with a targeted disruption of the Fanconi anemia homolog Fanca.
Human molecular genetics 2000;9(12):1805-11.
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2000: van de Vrugt H J; Cheng N C; de Vries Y; Rooimans M A; de Groot J; Scheper R J; Zhi Y; Hoatlin M E; Joenje H; Arwert F
Cloning and characterization of murine fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(4):326-31.
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2000: de Winter J P; Rooimans M A; van Der Weel L; van Berkel C G; Alon N; Bosnoyan-Collins L; de Groot J; Zhi Y; Waisfisz Q; Pronk J C; Arwert F; Mathew C G; Scheper R J; Hoatlin M E; Buchwald M; Joenje H
The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM.
Nature genetics 2000;24(1):15-6.
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1999: Waisfisz Q; de Winter J P; Kruyt F A; de Groot J; van der Weel L; Dijkmans L M; Zhi Y; Arwert F; Scheper R J; Youssoufian H; Hoatlin M E; Joenje H
A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(18):10320-5.
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1999: van den Berg J S; Pals G; Arwert F; Hennekam R C; Albrecht K W; Westerveld A; Limburg M
Type III collagen deficiency in saccular intracranial aneurysms. Defect in gene regulation?
Stroke; a journal of cerebral circulation 1999;30(8):1628-31.
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1999: Waisfisz Q; Morgan N V; Savino M; de Winter J P; van Berkel C G; Hoatlin M E; Ianzano L; Gibson R A; Arwert F; Savoia A; Mathew C G; Pronk J C; Joenje H
Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.
Nature genetics 1999;22(4):379-83.
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1999: Cloos J; Nieuwenhuis E J; Boomsma D I; Kuik D J; van der Sterre M L; Arwert F; Snow G B; Braakhuis B J
Inherited susceptibility to bleomycin-induced chromatid breaks in cultured peripheral blood lymphocytes.
Journal of the National Cancer Institute 1999;91(13):1125-30.
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1999: Waisfisz Q; Saar K; Morgan N V; Altay C; Leegwater P A; de Winter J P; Komatsu K; Evans G R; Wegner R D; Reis A; Joenje H; Arwert F; Mathew C G; Pronk J C; Digweed M
The Fanconi anemia group E gene, FANCE, maps to chromosome 6p.
American journal of human genetics 1999;64(5):1400-5.
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1998: de Winter J P; Waisfisz Q; Rooimans M A; van Berkel C G; Bosnoyan-Collins L; Alon N; Carreau M; Bender O; Demuth I; Schindler D; Pronk J C; Arwert F; Hoehn H; Digweed M; Buchwald M; Joenje H
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
Nature genetics 1998;20(3):281-3.
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1998: Joenje H; Arwert F; Kwee M L; Madan K; Hoehn H
Confounding factors in the diagnosis of Fanconi anaemia.
American journal of medical genetics 1998;79(5):403-5.
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1998: van den Berg J S; Limburg M; Kappelle L J; Pals G; Arwert F; Westerveld A
The role of type III collagen in spontaneous cervical arterial dissections.
Annals of neurology 1998;43(4):494-8.
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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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1998: Lo Ten Foe J R; Kruyt F A; Zweekhorst M B; Pals G; Gibson R A; Mathew C G; Joenje H; Arwert F
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstream.
Human mutation 1998;Suppl 1():S25-7.
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1997: van den Berg J S; Limburg M; Pals G; Arwert F; Westerveld A; Hennekam R C; Albrecht K W
Some patients with intracranial aneurysms have a reduced type III/type I collagen ratio. A case-control study.
Neurology 1997;49(6):1546-51.
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1997: Hermsen M A; Joenje H; Arwert F; Braakhuis B J; Baak J P; Westerveld A; Slater R
Assessment of chromosomal gains and losses in oral squamous cell carcinoma by comparative genomic hybridisation.
Oral oncology 1997;33(6):414-8.
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1997: Kruyt F A; Waisfisz Q; Dijkmans L M; Hermsen M A; Youssoufian H; Arwert F; Joenje H
Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cells.
Blood 1997;90(9):3288-95.
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1997: Joenje H; Oostra A B; Wijker M; di Summa F M; van Berkel C G; Rooimans M A; Ebell W; van Weel M; Pronk J C; Buchwald M; Arwert F
Evidence for at least eight Fanconi anemia genes.
American journal of human genetics 1997;61(4):940-4.
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1997: Kruyt F A; Dijkmans L M; Arwert F; Joenje H
Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase.
Cancer research 1997;57(11):2244-51.
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1997: Lo Ten Foe J R; Kwee M L; Rooimans M A; Oostra A B; Veerman A J; van Weel M; Pauli R M; Shahidi N T; Dokal I; Roberts I; Altay C; Gluckman E; Gibson R A; Mathew C G; Arwert F; Joenje H
Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.
European journal of human genetics : EJHG 1997;5(3):137-48.
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1997: Kwee M L; van der Kleij J M; van Essen A J; Begeer J H; Joenje H; Arwert F; ten Kate L P
An atypical case of Fanconi anemia in elderly sibs.
American journal of medical genetics 1997;68(3):362-6.
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1997: Savoia A; Piemontese M R; Savino M; Zatterale A; Pronk J; Arwert F; Joenje H; Ramenghi U; Dagna-Bricarelli F; Dallapiccola B; Zelante L
Linkage analysis of Fanconi anaemia in Italy and mapping of the complementation group A gene.
Human genetics 1997;99(1):93-7.
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1996: Kishore A; Wszolek Z K; Snow B J; de la Fuente-Fernandez R; Arwert F; Wijker M; Schulzer M; Calne D B; Vingerhoets F J
Presynaptic nigrostriatal function in genetically tested asymptomatic relatives from the pallido-ponto-nigral degeneration family.
Neurology 1996;47(6):1588-90.
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1996: Foe J R; Rooimans M A; Bosnoyan-Collins L; Alon N; Wijker M; Parker L; Lightfoot J; Carreau M; Callen D F; Savoia A; Cheng N C; van Berkel C G; Strunk M H; Gille J J; Pals G; Kruyt F A; Pronk J C; Arwert F; Buchwald M; Joenje H
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Nature genetics 1996;14(4):488.
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1996: Lo Ten Foe J R; Rooimans M A; Bosnoyan-Collins L; Alon N; Wijker M; Parker L; Lightfoot J; Carreau M; Callen D F; Savoia A; Cheng N C; van Berkel C G; Strunk M H; Gille J J; Pals G; Kruyt F A; Pronk J C; Arwert F; Buchwald M; Joenje H
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Nature genetics 1996;14(3):320-3.
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1996: Lo ten Foe J R; Barel M T; Thuss P; Digweed M; Arwert F; Joenje H
Sequence variations in the Fanconi anaemia gene, FAC: pathogenicity of 1806insA and R548X and recognition of D195V as a polymorphic variant.
Human genetics 1996;98(5):522-3.
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1996: Abrahams P J; Houweling A; Cornelissen-Steijger D M; Arwert F; Menko F H; Pinedo H M; Terleth C; van der Eb A J
Inheritance of abnormal expression of SOS-like response in xeroderma pigmentosum and hereditary cancer-prone syndromes.
Cancer research 1996;56(11):2621-5.
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1996: Kwee M L; Lo Ten Foe J R; Arwert F; Pals G; Madan K; Nieuwint A; In't Veld P A; Van der Horst A R; Van Vugt J M; Ten Kate L P
Early prenatal diagnosis of Fanconi anaemia in a twin pregnancy, using DNA analysis.
Prenatal diagnosis 1996;16(4):345-8.
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1996: Hermsen M A; Joenje H; Arwert F; Welters M J; Braakhuis B J; Bagnay M; Westerveld A; Slater R
Centromeric breakage as a major cause of cytogenetic abnormalities in oral squamous cell carcinoma.
Genes, chromosomes & cancer 1996;15(1):1-9.
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1996: Wijker M; Wszolek Z K; Wolters E C; Rooimans M A; Pals G; Pfeiffer R F; Lynch T; Rodnitzky R L; Wilhelmsen K C; Arwert F
Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21.
Human molecular genetics 1996;5(1):151-4.
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1996: Lo Ten Foe J R; Rooimans M A; Joenje H; Arwert F
Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia C gene, FAC.
Human mutation 1996;7(3):264-5.
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1995: Steenbergen R D; Hermsen M A; Walboomers J M; Joenje H; Arwert F; Meijer C J; Snijders P J
Integrated human papillomavirus type 16 and loss of heterozygosity at 11q22 and 18q21 in an oral carcinoma and its derivative cell line.
Cancer research 1995;55(22):5465-71.
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1995: Joenje H; Lo ten Foe J R; Oostra A B; van Berkel C G; Rooimans M A; Schroeder-Kurth T; Wegner R D; Gille J J; Buchwald M; Arwert F
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.
Blood 1995;86(6):2156-60.
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1995: Pals G; Meijerink P H; Defize J; Bebelman J P; Strunk M; Arwert F; Timmerman A; Mager W H
Transcription regulation of human and porcine pepsinogen A.
Advances in experimental medicine and biology 1995;362():67-75.
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1994: Joenje H; Lo Ten Foe J R; Arwert F; ten Kate L P
Complementation testing and genetic classification of Fanconi's anaemia.
Lancet 1994;343(8901):862.
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1993: Overkamp W J; Rooimans M A; Neuteboom I; Telleman P; Arwert F; Zdzienicka M Z
Genetic diversity of mitomycin C-hypersensitive Chinese hamster cell mutants: a new complementation group with chromosomal instability.
Somatic cell and molecular genetics 1993;19(5):431-7.
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1992: Wszolek Z K; Pfeiffer R F; Bhatt M H; Schelper R L; Cordes M; Snow B J; Rodnitzky R L; Wolters E C; Arwert F; Calne D B
Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration.
Annals of neurology 1992;32(3):312-20.
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1992: Bank R A; Hettema E H; Muijs M A; Pals G; Arwert F; Boomsma D I; Pronk J C
Variation in gene copy number and polymorphism of the human salivary amylase isoenzyme system in Caucasians.
Human genetics 1992;89(2):213-22.
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1991: Bank R A; Hettema E H; Arwert F; Amerongen A V; Pronk J C
Electrophoretic characterization of posttranslational modifications of human parotid salivary alpha-amylase.
Electrophoresis 1991;12(1):74-9.
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1991: Arwert F; Rooimans M A; Westerveld A; Simons J W; Zdzienicka M Z
The Chinese hamster cell mutant V-H4 is homologous to Fanconi anemia (complementation group A).
Cytogenetics and cell genetics 1991;56(1):23-6.
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1991: Meijerink P H; Bebelman J P; Pals G; Arwert F; Planta R J; Eriksson A W; Mager W H
Analysis of the promoter of a human pepsinogen A gene.
Advances in experimental medicine and biology 1991;306():87-90.
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1990: Zdzienicka M Z; Arwert F; Neuteboom I; Rooimans M; Simons J W
The Chinese hamster V79 cell mutant V-H4 is phenotypically like Fanconi anemia cells.
Somatic cell and molecular genetics 1990;16(6):575-81.
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1990: Groot P C; Mager W H; Henriquez N V; Pronk J C; Arwert F; Planta R J; Eriksson A W; Frants R R
Evolution of the human alpha-amylase multigene family through unequal, homologous, and inter- and intrachromosomal crossovers.
Genomics 1990;8(1):97-105.
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1989: Groot P C; Bleeker M J; Pronk J C; Arwert F; Mager W H; Planta R J; Eriksson A W; Frants R R
The human alpha-amylase multigene family consists of haplotypes with variable numbers of genes.
Genomics 1989;5(1):29-42.
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1989: Gille J J; Mullaart E; Vijg J; Leyva A L; Arwert F; Joenje H
Chromosomal instability in an oxygen-tolerant variant of Chinese hamster ovary cells.
Mutation research 1989;219(1):17-28.
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1988: Bank R A; Crusius B C; Zwiers T; Meuwissen S G; Arwert F; Pronk J C
Identification of a Glu greater than Lys substitution in the activation segment of human pepsinogen A-3 and -5 isozymogens by peptide mapping using endoproteinase Lys-C.
FEBS letters 1988;238(1):105-8.
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1988: Groot P C; Bleeker M J; Pronk J C; Arwert F; Mager W H; Planta R J; Eriksson A W; Frants R R
Human pancreatic amylase is encoded by two different genes.
Nucleic acids research 1988;16(10):4724.
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1987: Joenje H; Nieuwint A W; Oostra A B; Arwert F; de Koning H; Roozendaal K J
Cytogenetic toxicity of paraquat and streptonigrin in Fanconi's anemia.
Cancer genetics and cytogenetics 1987;25(1):37-45.
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1987: Lafleur M V; Nieuwint A W; Aubry J M; Kortbeek H; Arwert F; Joenje H
DNA damage by chemically generated singlet oxygen.
Free radical research communications 1987;2(4-6):343-50.
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1986: Arwert F; Porck H J; Fràter-Schröder M; Brahe C; Geurts van Kessel A; Westerveld A; Meera Khan P; Zang K; Frants R R; Kortbeek H T
Assignment of human transcobalamin II (TC2) to chromosome 22 using somatic cell hybrids and monosomic meningioma cells.
Human genetics 1986;74(4):378-81.
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1986: Brahe C; Bannetta P; Meera Khan P; Arwert F; Serra A
Assignment of the catechol-O-methyltransferase gene to human chromosome 22 in somatic cell hybrids.
Human genetics 1986;74(3):230-4.
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1986: Brahe C; Bannetta P; Serra A; Arwert F
The increased COMT activity in Down syndrome patients is not a consequence of dosage effect owing to location of the gene on chromosome 21: further evidence.
American journal of medical genetics 1986;24(1):203-4.
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1986: Starink T M; van der Veen J P; Arwert F; de Waal L P; de Lange G G; Gille J J; Eriksson A W
The Cowden syndrome: a clinical and genetic study in 21 patients.
Clinical genetics 1986;29(3):222-33.
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1986: Claassen E; Kortbeek H; Arwert F
Effects of mitomycin C on the rate of DNA synthesis in normal and Fanconi anaemia cells.
Mutation research 1986;165(1):15-9.
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1985: Fràter-Schröder M; Porck H J; Erten J; Müller M R; Steinmann B; Kierat L; Arwert F
Synthesis and secretion of the human vitamin B12-binding protein, transcobalamin II, by cultured skin fibroblasts and by bone marrow cells.
Biochimica et biophysica acta 1985;845(3):421-7.
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1985: Fràter-Schröder M; Prochazka M; Haller O; Arwert F; Porck H J; Skow L C; Lundin L G; Hilkens J; Hilgers J
Localization of the gene for the vitamin B12 binding protein, transcobalamin II, near the centromere on mouse chromosome 11, linked with the hemoglobin alpha-chain locus.
Biochemical genetics 1985;23(1-2):139-53.
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1985: Poll E H; Arwert F
Differential response to mitomycin-C- and cis-diamminedichloroplatinum(II)-induced damage in normal human fibroblasts during confluent holding.
Mutation research 1985;145(1-2):77-80.
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1985: Poll E H; Arwert F; Joenje H; Wanamarta A H
Differential sensitivity of Fanconi anaemia lymphocytes to the clastogenic action of cis-diamminedichloroplatinum (II) and trans-diamminedichloroplatinum (II).
Human genetics 1985;71(3):206-10.
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1985: Nieuwint A W; Aubry J M; Arwert F; Kortbeek H; Herzberg S; Joenje H
Inability of chemically generated singlet oxygen to break the DNA backbone.
Free radical research communications 1985;1(1):1-9.
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1985: Zelle B; Geurts van Kessel A; de Wit J; Evers P; Arwert F; Pronk J C; Mager W H; Planta R J; Eriksson A W; Frants R R
Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11.
Human genetics 1985;70(4):337-40.
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1985: Defize J; Arwert F; Kortbeek H; Frants R R; Meuwissen S G; Eriksson A W
Pepsinogen synthesis in monolayer culture of human and rabbit gastric mucosal cells.
Virchows Archiv. B, Cell pathology including molecular pathology 1985;49(3):225-30.
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1984: Poll E H; Abrahams P J; Arwert F; Eriksson A W
Host-cell reactivation of cis-diamminedichloroplatinum(II)-treated SV40 DNA in normal human, Fanconi anaemia and xeroderma pigmentosum fibroblasts.
Mutation research 1984;132(5-6):181-7.
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1984: Kwee M L; Barth P G; Arwert F; Madan K
Mosaic tetrasomy 21 in a male child.
Clinical genetics 1984;26(2):150-5.
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1984: Poll E H; Arwert F; Kortbeek H T; Eriksson A W
Fanconi anaemia cells are not uniformly deficient in unhooking of DNA interstrand crosslinks, induced by mitomycin C or 8-methoxypsoralen plus UVA.
Human genetics 1984;68(3):228-34.
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1982: Poll E H; Arwert F; Joenje H; Eriksson A W
Cytogenetic toxicity of antitumor platinum compounds in Fanconi's anemia.
Human genetics 1982;61(3):228-30.
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1981: Joenje H; Arwert F; Eriksson A W; de Koning H; Oostra A B
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia.
Nature 1981;290(5802):142-3.
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