BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome
Olley, Gabrielle, Ansari, Morad, Bengani, Hemant, Grimes, Graeme R, Rhodes, James, von Kriegsheim, Alex, Blatnik, Ana, Stewart, Fiona J, Wakeling, Emma, Carroll, Nicola, Ross, Alison, Park, Soo-Mi, Bickmore, Wendy A, Pradeepa, Madapura M, FitzPatrick, David R
Published in Nature genetics (01.03.2018)
Published in Nature genetics (01.03.2018)
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Journal Article
A short-sighted approach to high myopia—not just an eye problem
Burgess, Frederick R., Carroll, Nicola, Young, Su Ling, Schmoll, Conrad, Lampe, Anne Katrin, Chan, Jonathan
Published in Journal of AAPOS (01.08.2021)
Published in Journal of AAPOS (01.08.2021)
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Journal Article
Publisher Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome
Olley, Gabrielle, Ansari, Morad, Bengani, Hemant, Grimes, Graeme R, Rhodes, James, von Kriegsheim, Alex, Blatnik, Ana, Stewart, Fiona J, Wakeling, Emma, Carroll, Nicola, Ross, Alison, Park, Soo-Mi, Bickmore, Wendy A, Pradeepa, Madapura M, FitzPatrick, David R
Published in Nature genetics (01.07.2019)
Published in Nature genetics (01.07.2019)
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The Extent of Left Ventricular Scar Quantified by Late Gadolinium Enhancement MRI Is Associated With Spontaneous Ventricular Arrhythmias in Patients With Coronary Artery Disease and Implantable Cardioverter-Defibrillators
Scott, Paul A, Morgan, John M, Carroll, Nicola, Murday, David C, Roberts, Paul R, Peebles, Charles R, Harden, Stephen P, Curzen, Nick P
Published in Circulation. Arrhythmia and electrophysiology (01.06.2011)
Published in Circulation. Arrhythmia and electrophysiology (01.06.2011)
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Journal Article
Publisher Correction: BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange-like syndrome
Olley, Gabrielle, Ansari, Morad, Bengani, Hemant, Grimes, Graeme R, Rhodes, James, von Kriegsheim, Alex, Blatnik, Ana, Stewart, Fiona J, Wakeling, Emma, Carroll, Nicola, Ross, Alison, Park, Soo-Mi, Bickmore, Wendy A, Pradeepa, Madapura M, FitzPatrick, David R
Published in Nature genetics (01.05.2018)
Published in Nature genetics (01.05.2018)
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Journal Article
Simultaneous adult polycystic kidney disease and Alport syndrome
Phelan, Paul J, Fletcher, Elaine, Carroll, Nicola, Metcalfe, Wendy, Turner, A Neil
Published in Nephrology (Carlton, Vic.) (01.08.2016)
Published in Nephrology (Carlton, Vic.) (01.08.2016)
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Journal Article
Investigation of the molecular response to folate metabolism inhibition
Carroll, Nicola, Hughes, Linda, McEntee, Gráinne, Parle-McDermott, Anne
Published in The Journal of nutritional biochemistry (01.11.2012)
Published in The Journal of nutritional biochemistry (01.11.2012)
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Journal Article
Analysis of the MTHFD1 promoter and risk of neural tube defects
Carroll, Nicola, Pangilinan, Faith, Molloy, Anne M, Troendle, James, Mills, James L, Kirke, Peadar N, Brody, Lawrence C, Scott, John M, Parle-McDermott, Anne
Published in Human genetics (01.04.2009)
Published in Human genetics (01.04.2009)
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Journal Article
The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels
Parle-McDermott, Anne, Mills, James L., Molloy, Anne M., Carroll, Nicola, Kirke, Peadar N., Cox, Christopher, Conley, Mary R., Pangilinan, Faith J., Brody, Lawrence C., Scott, John M.
Published in Molecular genetics and metabolism (01.07.2006)
Published in Molecular genetics and metabolism (01.07.2006)
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Journal Article
A short-sighted approach to high myopia-not just an eye problem
Burgess, Frederick R, Carroll, Nicola, Young, Su Ling, Schmoll, Conrad, Lampe, Anne Katrin, Chan, Jonathan
Published in Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus (01.08.2021)
Published in Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus (01.08.2021)
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