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Mutations in the ATM gene lead to impaired overall and treatment-free survival that is independent of IGVH mutation status in patients with B-CLL. [electronic resource] by
- Austen, Belinda
- Powell, Judith E
- Alvi, Azra
- Edwards, Ian
- Hooper, Laura
- Starczynski, Jane
- Taylor, A Malcolm R
- Fegan, Christopher
- Moss, Paul
- Stankovic, Tatjana
Producer: 20051130
In:
Blood vol. 106
Availability: No items available.
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Variant ataxia telangiectasia: clinical and molecular findings and evaluation of radiosensitive phenotypes in a patient and relatives. [electronic resource] by
- Claes, Kathleen
- Depuydt, Julie
- Taylor, A Malcolm R
- Last, James I
- Baert, Annelot
- Schietecatte, Peter
- Vandersickel, Veerle
- Poppe, Bruce
- De Leeneer, Kim
- D'Hooghe, Marc
- Vral, Anne
Producer: 20140415
In:
Neuromolecular medicine vol. 15
Availability: No items available.
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Mutation status of the residual ATM allele is an important determinant of the cellular response to chemotherapy and survival in patients with chronic lymphocytic leukemia containing an 11q deletion. [electronic resource] by
- Austen, Belinda
- Skowronska, Anna
- Baker, Claire
- Powell, Judith E
- Gardiner, Anne
- Oscier, David
- Majid, Aneela
- Dyer, Martin
- Siebert, Reiner
- Taylor, A Malcolm
- Moss, Paul A
- Stankovic, Tatjana
Producer: 20071213
In:
Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 25
Availability: No items available.
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The ataxia-oculomotor apraxia 1 gene product has a role distinct from ATM and interacts with the DNA strand break repair proteins XRCC1 and XRCC4. [electronic resource] by
- Clements, Paula M
- Breslin, Claire
- Deeks, Emma D
- Byrd, Philip J
- Ju, Limei
- Bieganowski, Pawel
- Brenner, Charles
- Moreira, Maria-Céu
- Taylor, A Malcolm R
- Caldecott, Keith W
Producer: 20050322
In:
DNA repair vol. 3
Availability: No items available.
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Chromosome instability syndromes. [electronic resource] by
- Taylor, A Malcolm R
- Rothblum-Oviatt, Cynthia
- Ellis, Nathan A
- Hickson, Ian D
- Meyer, Stefan
- Crawford, Thomas O
- Smogorzewska, Agata
- Pietrucha, Barbara
- Weemaes, Corry
- Stewart, Grant S
Producer: 20200706
In:
Nature reviews. Disease primers vol. 5
Availability: No items available.
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RIDDLE immunodeficiency syndrome is linked to defects in 53BP1-mediated DNA damage signaling. [electronic resource] by
- Stewart, Grant S
- Stankovic, Tatjana
- Byrd, Philip J
- Wechsler, Thomas
- Miller, Edward S
- Huissoon, Aarn
- Drayson, Mark T
- West, Stephen C
- Elledge, Stephen J
- Taylor, A Malcolm R
Producer: 20071127
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 104
Availability: No items available.
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