Regulating complement in the kidney: insights from CFHR5 nephropathy

por Gale, Daniel P., Pickering, Matthew C.
Publicado 2011

Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome

por Gibson, Joel T., Sadeghi-Alavijeh, Omid, Gale, Daniel P., Rothe, Hansjörg, Savige, Judy
Publicado 2022

End-stage renal failure associated with congenital deafness

por Annear, Nicholas M P, Gale, Daniel P, Loughlin, Sam, Dorkins, Huw R, Maxwell, Patrick H
Publicado 2008

Human decision making anticipates future performance in motor learning

por Moskowitz, Joshua B., Gale, Daniel J., Gallivan, Jason P., Wolpert, Daniel M., Flanagan, J. Randall
Publicado 2020

Delayed diagnosis of Townes-Brocks syndrome with multicystic kidneys and renal failure caused by a novel SALL1 nonsense mutation: A case report

por LIN, FU-JUN, LU, WEI, GALE, DANIEL, YAO, YAO, ZOU, REN, BIAN, FAN, JIANG, GENG-RU
Publicado 2016

Neural excursions from manifold structure explain patterns of learning during human sensorimotor adaptation

por Areshenkoff, Corson, Gale, Daniel J, Standage, Dominic, Nashed, Joseph Y, Flanagan, J Randall, Gallivan, Jason P
Publicado 2022

The association between patellar alignment on magnetic resonance imaging and radiographic manifestations of knee osteoarthritis

por Kalichman, Leonid, Zhang, Yuqing, Niu, Jingbo, Goggins, Joyce, Gale, Daniel, Zhu, Yanyan, Felson, David T, Hunter, David J
Publicado 2007

Genetic testing can resolve diagnostic confusion in Alport syndrome

por Adam, Jennifer, Connor, Thomas M. F., Wood, Katrina, Lewis, David, Naik, Ramesh, Gale, Daniel P., Sayer, John A.
Publicado 2014

Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney disease

por Lin, Fujun, Bian, Fan, Zou, Jun, Wu, Xiangru, Shan, Jianping, Lu, Wei, Yao, Yao, Jiang, Gengru, Gale, Daniel Philip
Publicado 2014

Incidence of End-Stage Renal Disease in the Turkish-Cypriot Population of Northern Cyprus: A Population Based Study

por Connor, Thomas M. F., Oygar, D. Deren, Gale, Daniel P., Steenkamp, Retha, Nitsch, Dorothea, Neild, Guy H., Maxwell, Patrick H.
Publicado 2013

Cascade Fumarate Hydratase mutation screening allows early detection of kidney tumour: a case report

por Chan, Melanie M. Y., Barnicoat, Angela, Mumtaz, Faiz, Aitchison, Michael, Side, Lucy, Brittain, Helen, Bates, Alan W. H., Gale, Daniel P.
Publicado 2017

Evidence for a Lack of a Direct Transcriptional Suppression of the Iron Regulatory Peptide Hepcidin by Hypoxia-Inducible Factors

por Volke, Melanie, Gale, Daniel P., Maegdefrau, Ulrike, Schley, Gunnar, Klanke, Bernd, Bosserhoff, Anja-Katrin, Maxwell, Patrick H., Eckardt, Kai-Uwe, Warnecke, Christina
Publicado 2009

Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies

por Levine, Adam P, Connor, Thomas M F, Oygar, D Deren, Neild, Guy H, Segal, Anthony W, Maxwell, Patrick H, Gale, Daniel P
Publicado 2015

Distinct patterns of cortical manifold expansion and contraction underlie human sensorimotor adaptation

por Gale, Daniel J., Areshenkoff, Corson N., Standage, Dominic I., Nashed, Joseph Y., Markello, Ross D., Flanagan, J. Randall, Smallwood, Jonathan, Gallivan, Jason P.
Publicado 2022

A novel COL4A1 frameshift mutation in familial kidney disease: the importance of the C-terminal NC1 domain of type IV collagen

por Gale, Daniel P., Oygar, D. Deren, Lin, Fujun, Oygar, P. Derin, Khan, Nadia, Connor, Thomas M.F., Lapsley, Marta, Maxwell, Patrick H., Neild, Guy H.
Publicado 2016

Clinical practice guideline monitoring children and young people with, or at risk of developing autosomal dominant polycystic kidney disease (ADPKD)

por Dudley, Jan, Winyard, Paul, Marlais, Matko, Cuthell, Oliver, Harris, Tess, Chong, Jiehan, Sayer, John, Gale, Daniel P., Moore, Lucy, Turner, Kay, Burrows, Sarah, Sandford, Richard
Publicado 2019

Biochemical markers of bone turnover and their association with bone marrow lesions

por Hunter, David J, LaValley, Michael, Li, Jiang, Bauer, Doug C, Nevitt, Michael, DeGroot, Jeroen, Poole, Robin, Eyre, David, Guermazi, Ali, Gale, Daniel, Totterman, Saara, Felson, David T
Publicado 2008

A novel LMX1B mutation in a family with end-stage renal disease of ‘unknown cause’

por Edwards, Noel, Rice, Sarah J., Raman, Shreya, Hynes, Ann Marie, Srivastava, Shalabh, Moore, Iain, Al-Hamed, Mohamed, Xu, Yaobo, Santibanez-Koref, Mauro, Thwaites, David T., Gale, Daniel P., Sayer, John A.
Publicado 2015

IgA Nephropathy Genetic Risk Score to Estimate the Prevalence of IgA Nephropathy in UK Biobank

por Sukcharoen, Kittiya, Sharp, Seth A., Thomas, Nicholas J., Kimmitt, Robert A., Harrison, Jamie, Bingham, Coralie, Mozere, Monika, Weedon, Michael N., Tyrrell, Jessica, Barratt, Jonathan, Gale, Daniel P., Oram, Richard A.
Publicado 2020

Genetic Modifiers of Mendelian Monogenic Collagen IV Nephropathies in Humans and Mice

por Deltas, Constantinos, Papagregoriou, Gregory, Louka, Stavroula F., Malatras, Apostolos, Flinter, Frances, Gale, Daniel P., Gear, Susie, Gross, Oliver, Hoefele, Julia, Lennon, Rachel, Miner, Jeffrey H., Renieri, Alessandra, Savige, Judy, Turner, A. Neil
Publicado 2023