Induction of epigenetic variation in Arabidopsis by over-expression of DNA METHYLTRANSFERASE1 (MET1)

por Brocklehurst, Samuel, Watson, Michael, Carr, Ian M., Out, Suzan, Heidmann, Iris, Meyer, Peter
Publicado 2018

Genetic predisposition to fracture non-union: a case control study of a preliminary single nucleotide polymorphisms analysis of the BMP pathway

por Dimitriou, Rozalia, Carr, Ian M, West, Robert M, Markham, Alexander F, Giannoudis, Peter V
Publicado 2011

The proteomes of transcription factories containing RNA polymerases I, II or III

por Melnik, Svitlana, Deng, Binwei, Papantonis, Argyris, Baboo, Sabyasachi, Carr, Ian M., Cook, Peter R
Publicado 2011

Advantage from massive parallel sequencing of RYR1 and CACNA1S in diagnostics of malignant hyperthermia susceptibility

por Fiszer, Dorota, Fisher, Nickla A, Carr, Ian M, Shaw, Marie-Anne, Hopkins, Philip M
Publicado 2014

Sequence analysis and editing for bisulphite genomic sequencing projects

por Carr, Ian M., Valleley, Elizabeth M. A., Cordery, Sarah F., Markham, Alexander F., Bonthron, David T.
Publicado 2007

The Tudor SND1 protein is an m(6)A RNA reader essential for replication of Kaposi’s sarcoma-associated herpesvirus

por Baquero-Perez, Belinda, Antanaviciute, Agne, Yonchev, Ivaylo D, Carr, Ian M, Wilson, Stuart A, Whitehouse, Adrian
Publicado 2019

GeneTIER: prioritization of candidate disease genes using tissue-specific gene expression profiles

por Antanaviciute, Agne, Daly, Catherine, Crinnion, Laura A., Markham, Alexander F., Watson, Christopher M., Bonthron, David T., Carr, Ian M.
Publicado 2015

Cantú syndrome with coexisting familial pituitary adenoma

por Marques, Pedro, Spencer, Rupert, Morrison, Patrick J., Carr, Ian M., Dang, Mary N., Bonthron, David T., Hunter, Steven, Korbonits, Márta
Publicado 2018

MethylViewer: computational analysis and editing for bisulfite sequencing and methyltransferase accessibility protocol for individual templates (MAPit) projects

por Pardo, Carolina E., Carr, Ian M., Hoffman, Christopher J., Darst, Russell P., Markham, Alexander F., Bonthron, David T., Kladde, Michael P.
Publicado 2011

The use of high-frequency ultrasound imaging and biofluorescence for in vivo evaluation of gene therapy vectors

por Ingram, Nicola, Macnab, Stuart A, Marston, Gemma, Scott, Nigel, Carr, Ian M, Markham, Alexander F, Whitehouse, Adrian, Coletta, P Louise
Publicado 2013

OVA: integrating molecular and physical phenotype data from multiple biomedical domain ontologies with variant filtering for enhanced variant prioritization

por Antanaviciute, Agne, Watson, Christopher M., Harrison, Sally M., Lascelles, Carolina, Crinnion, Laura, Markham, Alexander F., Bonthron, David T., Carr, Ian M.
Publicado 2015

A Chromosome 7 Pericentric Inversion Defined at Single-Nucleotide Resolution Using Diagnostic Whole Genome Sequencing in a Patient with Hand-Foot-Genital Syndrome

por Watson, Christopher M., Crinnion, Laura A., Harrison, Sally M., Lascelles, Carolina, Antanaviciute, Agne, Carr, Ian M., Bonthron, David T., Sheridan, Eamonn
Publicado 2016

Cas9-based enrichment and single-molecule sequencing for precise characterization of genomic duplications

por Watson, Christopher M., Crinnion, Laura A., Hewitt, Sarah, Bates, Jennifer, Robinson, Rachel, Carr, Ian M., Sheridan, Eamonn, Adlard, Julian, Bonthron, David T.
Publicado 2019

Effects of EGFR Inhibitor on Helicobacter pylori Induced Gastric Epithelial Pathology in Vivo

por Crabtree, Jean E., Jeremy, Anthony H.T., Duval, Cedric, Dixon, Michael F., Danjo, Kazuma, Carr, Ian M., Pritchard, D. Mark, Robinson, Philip A.
Publicado 2013

An observational study on the expression levels of MDM2 and MDMX proteins, and associated effects on P53 in a series of human liposarcomas

por Touqan, Nader, Diggle, Christine P, Verghese, Edlo T, Perry, Sarah, Horgan, Kieran, Merchant, William, Anwar, Rashida, Markham, Alexander F, Carr, Ian M, Achuthan, Rajgopal
Publicado 2013

Translating Biomarkers of Cholangiocarcinoma for Theranosis: A Systematic Review

por Wijetunga, Imeshi, McVeigh, Laura E., Charalambous, Antonia, Antanaviciute, Agne, Carr, Ian M., Nair, Amit, Prasad, K. Raj, Ingram, Nicola, Coletta, P. Louise
Publicado 2020

Functionally impaired plasmacytoid dendritic cells and non-haematopoietic sources of type I interferon characterize human autoimmunity

por Psarras, Antonios, Alase, Adewonuola, Antanaviciute, Agne, Carr, Ian M., Md Yusof, Md Yuzaiful, Wittmann, Miriam, Emery, Paul, Tsokos, George C., Vital, Edward M.
Publicado 2020

Homozygosity for a missense mutation in the 67 kDa isoform of glutamate decarboxylase in a family with autosomal recessive spastic cerebral palsy: parallels with Stiff-Person Syndr...

por Lynex, Clare N, Carr, Ian M, Leek, Jack P, Achuthan, Rajgopal, Mitchell, Simon, Maher, Eamonn R, Woods, C Geoffrey, Bonthon, David T, Markham, Alex F
Publicado 2004

Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping

por Watson, Christopher M., Crinnion, Laura A., Berry, Ian R., Harrison, Sally M., Lascelles, Carolina, Antanaviciute, Agne, Charlton, Ruth S., Dobbie, Angus, Carr, Ian M., Bonthron, David T.
Publicado 2016

m6aViewer: software for the detection, analysis, and visualization of N(6)-methyladenosine peaks from m(6)A-seq/ME-RIP sequencing data

por Antanaviciute, Agne, Baquero-Perez, Belinda, Watson, Christopher M., Harrison, Sally M., Lascelles, Carolina, Crinnion, Laura, Markham, Alexander F., Bonthron, David T., Whitehouse, Adrian, Carr, Ian M.
Publicado 2017