Items where Subject is "QM0001 General"

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Number of items at this level: 13.

B

Bignami, M, O'Driscoll, M, Aquilina, G and Karran, P (2000) Unmasking a killer: DNA O(6)-methylguanine and the cytotoxicity of methylating agents. Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 462 (2-3). pp. 71-82. ISSN 0027-5107

Brenner, Erich, Chirculescu, Andy R M, Reblet, Concepción and Smith, Claire (2015) Assessment in anatomy. European Journal of Anatomy, 19 (1). pp. 105-124. ISSN 1136‐4890

D

Dyment, David A, Smith, Amanda C, Alcantara, Diana, Schwartzentruber, Jeremy A, Basel-Vanagaite, Lina, Curry, Cynthia J, Temple, I Karen, Reardon, William, Mansour, Sahar, Haq, Mushfequr R, Gilbert, Rodney, Lehmann, Ordan J, Vanstone, Megan R, Beaulieu, Chandree L, FORGE Canada Consortium, , Majewski, Jacek, Bulman, Dennis E, O'Driscoll, Mark, Boycott, Kym M and Inness, A Micheil (2013) Mutations in PIK3R1 cause SHORT syndrome. American Journal of Human Genetics, 93 (1). pp. 158-166. ISSN 0002-9297

F

Fouquet, M, Pisanski, K, Mathevon, N and Reby, D (2016) Individual differences in male voice fundamental frequency emerge before puberty and remain stable throughout adulthood. Royal Society Open Science (manuscript RSOS-160395) -- Dataset accompanying research article. [Dataset] (Accepted)

L

Lawrance-Owen, Adam J, Bargary, Gary, Bosten, Jenny M, Goodbourn, Patrick T, Hogg, Ruth E and Mollon, J D (2013) Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio. Human Genetics, 132 (4). pp. 415-421. ISSN 0340-6717

M

McDonell, Laura M, Mirzaa, Ghayda M, Alcantara, Diana, Schwartzentruber, Jeremy, Carter, Melissa T, Lee, Leo J, Clericuzio, Carol L, Graham, John M, Morris-Rosendahl, Deborah J, Polster, Tilman, Acsadi, Gyula, Townshend, Sharron, Williams, Simon, Halbert, Anne, Isidor, Bertrand, David, Albert, Smyser, Christopher D, Paciorkowski, Alex R, Willing, Marcia, Woulfe, John, Das, Soma, Beaulieu, Chandree L, Marcadier, Janet, FORGE Canada Consortium, , Geraghty, Michael T, Frey, Brendan J, Majewski, Jacek, Bulman, Dennis E, Dobyns, William B, O'Driscoll, Mark and Boycott, Kym M (2013) Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome. Nature genetics, 45 (5). pp. 556-562. ISSN 1546-1718

O

O'Driscoll, M, Macpherson, P, Xu, Y Z and Karran, P (1999) The cytotoxicity of DNA carboxymethylation and methylation by the model carboxymethylating agent azaserine in human cells. Carcinogenesis, 20 (9). pp. 1855-1862. ISSN 0143-3334

O'Driscoll, M, Martinelli, S, Ciotta, C and Karran, P (1999) Combined mismatch and nucleotide excision repair defects in a human cell line: mismatch repair processes methylation but not UV- or ionizing radiation-induced DNA damage. Carcinogenesis, 20 (5). pp. 799-804. ISSN 0143-3334

O'Driscoll, Mark (2013) INK4a/ARF-dependent senescence upon persistent replication stress. Cell Cycle, 12 (13). pp. 1997-1998. ISSN 1538-4101

O'Driscoll, Mark (2017) The pathological consequences of impaired genome integrity in humans; disorders of the DNA replication machinery. Journal of Pathology, 241 (2). pp. 192-207. ISSN 0022-3417

P

Payne, Felicity, Colnaghi, Rita, Rocha, Nuno, Seth, Asha, Harris, Julie, Carpenter, Gillian, Bottomley, William E, Wheeler, Eleanor, Wong, Stephen, Saudek, Vladimir, Savage, David, O'Rahilly, Stephen, Carel, Jean-Claude, Barroso, Inês, O'Driscoll, Mark and Semple, Robert (2014) Hypomorphism in human NSMCE2 linked to primordial dwarfism and insulin resistance. The Journal of Clinical Investigation, 124 (9). pp. 4028-4038. ISSN 0021-9738

S

Smith, Claire F, Hall, Samuel, Border, Scott, Adds, Philip J and Finn, Gabrielle M (2015) Interprofessional anatomy education in the United Kingdom and Ireland: perspectives from students and teachers. Anatomical Sciences Education, 8 (4). pp. 360-370. ISSN 1935-9772

Stiff, Tom, Alagoz, Meryem, Alcantara, Diana, Outwin, Emily, Brunner, Han G, Bongers, Ernie M H F, O'Driscoll, Mark and Jeggo, Penny A (2013) Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of meier-gorlin syndrome. PLoS Genetics, 9 (3). e1003360. ISSN 1553-7404

This list was generated on Wed Oct 16 15:13:47 2019 BST.