Որոնման արդյունքները - Sarah Howles
- Ցուցադրվում են 1 - 12 արդյունքները 12
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Use of Temporally Validated Machine Learning Models To Predict Outcomes of Percutaneous Nephrolithotomy Using Data from the British Association of Urological Surgeons Percutaneous... Robert Geraghty, Anshul Thakur, Sarah Howles, William Finch, Sarah Fowler, Alistair Rogers, Seshadri Sriprasad, Daron Smith, Andrew Dickinson, Zara Gall, Bhaskar Somani
Հրապարակվել է 2024Artigo -
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Mutations Affecting G-Protein Subunit α<sub>11</sub>in Hypercalcemia and Hypocalcemia M. Andrew Nesbit, Fadil Hannan, Sarah Howles, Valerie Babinsky, Rosie Head, Treena Cranston, Nigel Rust, Maurine R. Hobbs, Hunter Heath, Rajesh V. Thakker
Հրապարակվել է 2013Artigo -
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Cinacalcet for Symptomatic Hypercalcemia Caused by <i>AP2S1</i> Mutations Sarah Howles, Fadil Hannan, Valerie Babinsky, Ralph Rogers, Caroline M. Gorvin, Nigel Rust, Tristan Richardson, Malachi J. McKenna, M. Andrew Nesbit, Rajesh V. Thakker
Հրապարակվել է 2016Carta -
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Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2) Siân E. Piret, Caroline M. Gorvin, Alistair T. Pagnamenta, Sarah Howles, Treena Cranston, Nigel Rust, M. Andrew Nesbit, Ben Glaser, Jenny C. Taylor, Andreas Buchs, Fadil Hannan, Rajesh V. Thakker
Հրապարակվել է 2016Artigo -
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Genetic variants of calcium and vitamin D metabolism in kidney stone disease Sarah Howles, Akira Wiberg, Michelle Goldsworthy, Asha L. Bayliss, Anna Gluck, Michael Ng, Emily Grout, Chizu Tanikawa, Yoichiro Kamatani, Chikashi Terao, Atsushi Takahashi, Michiaki Kubo, Koichi Matsuda, Rajesh V. Thakker, Benjamin W. Turney, Dominic Furniss
Հրապարակվել է 2019Revisão -
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Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 M. Andrew Nesbit, Fadil Hannan, Sarah Howles, Adam J. Reed, Treena Cranston, Clare Thakker, Lorna Gregory, Andrew J. Rimmer, Nigel Rust, Una Graham, Patrick J. Morrison, Steven Hunter, Michael P. Whyte, Gil McVean, David Buck, Rajesh V. Thakker
Հրապարակվել է 2012Artigo -
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Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy Caroline M. Gorvin, Fadil Hannan, Sarah Howles, Valerie Babinsky, Siân E. Piret, Angela Rogers, Andrew Freidin, Michelle Stewart, Anju Paudyal, Tertius Hough, M. Andrew Nesbit, Sara Wells, Tonia L. Vincent, S.D.M. Brown, Roger Cox, Rajesh V. Thakker
Հրապարակվել է 2017Artigo -
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Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations Catherine Lovegrove, Jelena Bešević, Akira Wiberg, Ben Lacey, Thomas J. Littlejohns, Naomi E. Allen, Michelle Goldsworthy, Jihye Kim, Fadil Hannan, Gary C. Curhan, Benjamin W. Turney, Mark I. McCarthy, Anubha Mahajan, Rajesh V. Thakker, Michael V. Holmes, Dominic Furniss, Sarah Howles
Հրապարակվել է 2023Artigo -
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Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype–phenotype correlations, codon bias and dominant-negative... Fadil Hannan, Sarah Howles, Angela Rogers, Treena Cranston, Caroline M. Gorvin, Valerie Babinsky, Adam J. Reed, Clare E. Thakker, Detlef Böckenhauer, Rosalind S. Brown, John Connell, Jacqueline Cook, Ken Darzy, Sarah Ehtisham, Una Graham, Tony Hulse, Steven Hunter, Louise Izatt, Dhavendra Kumar, Malachi J. McKenna, John McKnight, Patrick J. Morrison, M. Zulf Mughal, Domhnall O’Halloran, Simon H. S. Pearce, Mary Porteous, Mushtaqur Rahman, Tristan Richardson, Robert Robinson, Isabelle Scheers, Haroon Siddique, William G. van’t Hoff, Timothy C. Wang, Michael P. Whyte, M. Andrew Nesbit, Rajesh V. Thakker
Հրապարակվել է 2015Artigo -
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Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease Omid Sadeghi‐Alavijeh, Melanie Chan, Shabbir H. Moochhala, Sarah Howles, Daniel P. Gale, Detlef Böckenhauer, John C. Ambrose, Prabhu Arumugam, R. Bevers, Marta Bleda, F. Boardman-Pretty, C. R. Boustred, Helen Brittain, Mark J. Caulfield, G. C. Chan, Greg Elgar, Tom Fowler, Adam Giess, Angela Hamblin, Bingyang Shi, Tim Hubbard, R. Jackson, J. Louise Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, S. E. A. Leigh, I. U. S. Leong, Javier F. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A. Odhams, Christine Patch, Mariana Buongermino Pereira, D. Perez-Gil, J. Pullinger, T. Rahim, Augusto Rendon, Tim Rogers, K. Savage, Kushmita Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Samuel C. Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Ellen Thomas, Simon R. Thompson, Arianna Tucci, M. J. Welland, Eleanor Williams, Katarzyna Witkowska, S. M. Wood
Հրապարակվել է 2023Artigo -
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Rare disease gene association discovery in the 100,000 Genomes Project Valentina Cipriani, Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr, Katherine A. Benson, Marta Bértoli, Detlef Böckenhauer, Michael R. Bowl, Kate Burley, Li Chan, Patrick F. Chinnery, Peter J. Conlon, Marcos Abreu Costa, Alice E. Davidson, Sally J. Dawson, Elhussein A. Elhassan, Sarah E. Flanagan, Marta Futema, Daniel P. Gale, Sonia García-Ruiz, M. Cecilia Gonzalez Corcia, Helen Griffin, Sophie Hambleton, Amy R. Hicks, Henry Houlden, Richard S. Houlston, Sarah Howles, Robert Kleta, Iris Lekkerkerker, Siying Lin, Petra Lišková, Hannah M. Mitchison, Heba Morsy, Andrew Mumford, William G. Newman, Ruxandra Neatu, Edel A. O’Toole, Albert Ong, Alistair T. Pagnamenta, Shamima Rahman, Neil Rajan, Peter N. Robinson, Mina Ryten, Omid Sadeghi‐Alavijeh, John A. Sayer, Claire L. Shovlin, Jenny C. Taylor, Omri Teltsh, Ian Tomlinson, Arianna Tucci, Clare Turnbull, Albertien M. van Eerde, James S. Ware, Laura Watts, Andrew R. Webster, Sarah K. Westbury, Sean L. Zheng, Mark J. Caulfield, Damian Smedley
Հրապարակվել է 2025Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Medicine
Biology
Gene
Genetics
Internal medicine
Calcium
Endocrinology
Mutation
Calcium-sensing receptor
Genotype
Calcium metabolism
Disease
Bioinformatics
Genome-wide association study
Parathyroid hormone
Receptor
Single-nucleotide polymorphism
Chemistry
Cinacalcet
Economics
Genetic association
Genetic variants
Kidney disease
Kidney stone disease
Kidney stones
Mendelian inheritance
Mendelian randomization
Missense mutation
Pathology
Secondary hyperparathyroidism