Ngā hua rapu kaituhi :: APM

1

Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia mā Martin Digweed

I whakaputaina 2002

Whiwhi kuputuhi katoa
Artigo

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2

Nijmegen breakage syndrome (NBS) mā Krystyńa Chrzańowska, Hanna Gregorek, Bożenna Dembowska‐Bagińska, Maria Kalina, Martin Digweed

I whakaputaina 2012

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Revisão

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3

Cancer Risk of Heterozygotes With the NBN Founder Mutation mā E Seemanová, Petr Jarolı́m, Pavel Seeman, Raymonda Varon, Martin Digweed, M Swift, Karl Sperling

I whakaputaina 2007

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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4

Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita mā Tom Vulliamy, Richard Beswick, Michael Kirwan, Anna Marrone, Martin Digweed, Amanda J. Walne, Inderjeet Dokal

I whakaputaina 2008

Whiwhi kuputuhi katoa
Artigo

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5

Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair mā Koji Nakanishi, Yun‐Gui Yang, Andrew J. Pierce, Toshiyasu Taniguchi, Martin Digweed, Alan D. D’Andrea, Zhao‐Qi Wang, Maria Jasin

I whakaputaina 2005

Whiwhi kuputuhi katoa
Artigo

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6

Nibrin functions in Ig class-switch recombination mā Sven Kracker, Yvonne Bergmann, Ilja Demuth, Pierre‐Olivier Frappart, Gabriele Hildebrand, Rainer Christine, Zhao‐Qi Wang, Karl Sperling, Martin Digweed, Andreas Radbruch

I whakaputaina 2005

Whiwhi kuputuhi katoa
Artigo

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7

The Fanconi anemia group A protein modulates homologous repair of DNA double-strand breaks in mammalian cells mā Yun‐Gui Yang, Zdenko Herceg, Koji Nakanishi, Ilja Demuth, C. Piccoli, Jocelyne Michelon, Gabriele Hildebrand, Maria Jasin, Martin Digweed, Zhao‐Qi Wang

I whakaputaina 2005

Whiwhi kuputuhi katoa
Artigo

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8

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome mā Raymonda Varon, Christine Vissinga, Matthias Platzer, Karen Cerosaletti, Krystyńa Chrzańowska, Kathrin Saar, Georg Beckmann, E Seemanová, Paul R. Cooper, Norma J. Nowak, Markus Stümm, Corry M.R. Weemaes, Richard A. Gatti, Richard K. Wilson, Martin Digweed, André Rosenthal, Karl Sperling, Patrick Concannon, André Reis

I whakaputaina 1998

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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9

Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene mā Johan P. de Winter, France Léveillé, Carola G.M. van Berkel, Martin A. Rooimans, Laura van der Weel, Jûrgen Steltenpool, Ilja Demuth, Neil V. Morgan, Noa Alon, Lucine Bosnoyan-Collins, Jeff Lightfoot, Peter A. J. Leegwater, Quinten Waisfisz, Kenshi Komatsu, Fré Arwert, Jan C. Pronk, Christopher G. Mathew, Martin Digweed, Manuel Buchwald, Hans Joenje

I whakaputaina 2000

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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10

Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans mā Federica Buonocore, Peter Kühnen, Jenifer P. Suntharalingham, Ignacio del Valle, Martin Digweed, Harald Stachelscheid, Noushafarin Khajavi, Mohammed Didi, Angela F. Brady, Oliver Blankenstein, Annie Procter, Paul Dimitri, J K Wales, Paolo Ghirri, Dieter Knöbl, Brigitte Strahm, Miriam Erlacher, Marcin W. Włodarski, Wei Chen, George Kokai, Glenn Anderson, Deborah Morrogh, Dale Moulding, Shane McKee, Charlotte M. Niemeyer, Annette Grüters, John C. Achermann

I whakaputaina 2017

Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
Artigo

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