Որոնման արդյունքները - Melanie Chan
- Ցուցադրվում են 1 - 13 արդյունքները 13
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Efficacy and Safety of Exenatide Once Weekly Versus Metformin, Pioglitazone, and Sitagliptin Used as Monotherapy in Drug-Naive Patients With Type 2 Diabetes (DURATION-4) David Russell‐Jones, Robert Cuddihy, M Hanefeld, Ajay Kumar, José Gerardo González‐González, Melanie Chan, Anne M. Wolka, Marilyn K. Boardman
Հրապարակվել է 2011Artigo -
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Prevalence Estimates of Predicted Pathogenic COL4A3–COL4A5 Variants in a Population Sequencing Database and Their Implications for Alport Syndrome Joel T. Gibson, Rachel Fieldhouse, Melanie Chan, Omid Sadeghi‐Alavijeh, Leslie Burnett, Valerio Izzi, Anton V. Persikov, Daniel P. Gale, Helen Storey, Judy Savige
Հրապարակվել է 2021Artigo -
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Commentary: Tolvaptan for Autosomal Dominant Polycystic Kidney Disease (ADPKD) - an update Matthew Gittus, Helen Haley, Tess Harris, Sarah Borrows, Neal Padmanabhan, Danny Gale, Roslyn Simms, T. Franklin Williams, Aaron Acquaye, Alisa Wong, Melanie Chan, E J Lee, Albert Ong
Հրապարակվել է 2025Revisão -
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Tadalafil Therapy for Pulmonary Arterial Hypertension Nazzareno Galiè, Bruce H. Brundage, Hossein Ardeschir Ghofrani, Ronald J. Oudiz, Gérald Simonneau, Zeenat Safdar, Shelley Shapiro, R. James White, Melanie Chan, Anthony Beardsworth, Lyn R. Frumkin, Robyn J. Barst
Հրապարակվել է 2009Artigo -
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Emotion-Dependent Functional Connectivity of the Default Mode Network in Adolescent Depression Tiffany C. Ho, Colm G. Connolly, Eva Henje, Kaja Z. LeWinn, Irina A. Strigo, Martin P. Paulus, Guido Frank, Jeffrey E. Max, Jing Wu, Melanie Chan, Susan F. Tapert, Alan N. Simmons, Tony T. Yang
Հրապարակվել է 2014Artigo -
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Functional connectivity of negative emotional processing in adolescent depression Tiffany C. Ho, Guang Yang, Jing Wu, Pete Cassey, Scott Brown, Napoleon Hoang, Melanie Chan, Colm G. Connolly, Eva Henje-Blom, Larissa G. Duncan, Margaret A. Chesney, Martin P. Paulus, Jeffrey E. Max, Ronak Patel, Alan N. Simmons, Tony T. Yang
Հրապարակվել է 2013Artigo -
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Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy Adam P. Levine, Melanie Chan, Omid Sadeghi‐Alavijeh, Edwin Wong, H. Terence Cook, Sofie Ashford, Keren Carss, Martin Christian, Matthew Hall, Claire L. Harris, Paul McAlinden, Kevin J. Marchbank, Stephen D. Marks, Heather Maxwell, Karyn Mégy, Christopher J. Penkett, Monika Mozere, Kathleen Stirrups, Salih Tuna, Julie Wessels, Deborah Whitehorn, Sally Johnson, Daniel P. Gale
Հրապարակվել է 2020Artigo -
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Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA Daan H.H.M. Viering, Karl P. Schlingmann, Marguerite Hureaux, Tom Nijenhuis, Andrew Mallett, Melanie Chan, André P. van Beek, Albertien M. van Eerde, Jean-Marie Coulibaly, Marion Vallet, Stéphane Decramer, Sandra Pelletier, Günter Klaus, Martin Kömhoff, Rolf Beetz, Chirag Patel, Mohan Shenoy, Eric J. Steenbergen, Glenn Anderson, Ernie M.H.F. Bongers, Carsten Bergmann, Daan M. Panneman, Richard J. Rodenburg, Robert Kleta, Pascal Houillier, Martin Konrad, Rosa Vargas‐Poussou, Nine V.A.M. Knoers, Detlef Böckenhauer, Jeroen H. F. de Baaij
Հրապարակվել է 2021Artigo -
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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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Genotype–phenotype correlations for COL4A3–COL4A5 variants resulting in Gly substitutions in Alport syndrome Joel T. Gibson, Mary Huang, Marina Shenelli Croos Dabrera, Krushnam Shukla, H. Rothe, Pascale Hilbert, Constantinos Deltas, Helen Storey, Beata S. Lipska‐Ziętkiewicz, Melanie Chan, Omid Sadeghi‐Alavijeh, Daniel P. Gale, J. C. Ambrose, P. Arumugam, E. L. Baple, Marta Bleda, F. Boardman-Pretty, J. M. Boissiere, C. R. Boustred, Helen Brittain, Mark J. Caulfield, G. C. Chan, C. E. H. Craig, Louise C. Daugherty, Anna de Burca, A. Devereau, Greg Elgar, R. E. Foulger, Tom Fowler, Pedro Furió‐Tarí, A. Giess, J. M. Hackett, Dina Halai, Angela Hamblin, S. A. Henderson, J. E. Holman, Tim Hubbard, Kristina Ibáñez, R. Jackson, L. J. Jones, D. Kasperaviciute, Melis Kayikci, A. Kousathanas, L. Lahnstein, Kim Lawson, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Joanne Mason, Ellen M. McDonagh, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Chris A. Odhams, Andrea Orioli, Christine Patch, D. Perez-Gil, Mariana Buongermino Pereira, Dimitris Polychronopoulos, J. Pullinger, T. Rahim, Augusto Rendon, Pablo Riesgo-Ferreiro, T. Rogers, Mina Ryten, K. Savage, K. Sawant, Richard H. Scott, A. Siddiq, A. Sieghart, D. Smedley, K. R. Smith, S. C. Smith, Alona Sosinsky, W. Spooner, H. E. Stevens, Alexander Stuckey, Razia Sultana Mohammad, M. Tanguy, Elaine Thomas, S. R. Thompson, Carolyn Tregidgo, Arianna Tucci, Edward E. Walsh, S. A. Watters, M. J. Welland, Eric O. Williams, Kate Witkowska, S. M. Wood, Magdalena Zarowiecki, Agnė Čerkauskaitė, Judy Savige
Հրապարակվել է 2022Artigo -
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GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements Peter H. Dixon, Adam P. Levine, Inês Cebola, Melanie Chan, Aliya S. Amin, Anshul Aich, Monika Mozere, Hannah Maude, Alice Mitchell, Jun Zhang, Julian Adlard, Munaza Ahmed, Timothy J. Aitman, Hana Alachkar, David Allsup, J. P. Almeida, Philip Ancliff, Richard Antrobus, Ruth Armstrong, Gavin Arno, Sofie Ashford, William J. Astle, Anthony Attwood, Chris Babbs, Tamam Bakchoul, Tadbir K. Bariana, Julian Barwell, David Bennett, David Bentley, Agnieszka Bierżyńska, Tina Biss, Marta Bleda, Harm Jan Bogaard, Christian Bourne, Sara Boyce, John Bradley, Gerome Breen, Paul Brennan, Carole Brewer, Matthew A. Brown, Michael J. Browning, Rachel Buchan, Matthew Buckland, Teofila Bueser, Siobhán O. Burns, Oliver S. Burren, Paul Calleja, Gerald Carr‐White, Keren Carss, Ruth Casey, Mark J. Caulfield, John C. Chambers, Jennifer Chambers, Floria Cheng, Patrick F. Chinnery, Martin Christian, Colin Church, Naomi Clements Brod, Gerry Coghlan, Elizabeth Colby, Trevor Cole, Janine Collins, Peter Collins, Camilla Colombo, Robin Condliffe, Stuart A. Cook, Terry Cook, Nichola Cooper, Paul A. Corris, Abigail Crisp-Hihn, Nicola Curry, Cesare Danesino, Matthew J. Daniels, Louise C. Daugherty, John B. Davis, Sri V. V. Deevi, Timothy Dent, Eleanor Dewhurst, Peter H. Dixon, Kate Downes, Anna M. Drazyk, Elizabeth Drewe, Tina Dutt, David Edgar, Karen L. Edwards, William Egner, Wendy N. Erber, Marie Erwood, Maria C. Estiú, Gillian Evans, D. Gareth Evans, Tamara Everington, Mélanie Eyries, Rémi Favier, Debra Fletcher, James Fox, Amy Frary, Courtney E. French, Kathleen Freson, Mattia Frontini
Հրապարակվել է 2022Revisão -
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Effects of rare kidney diseases on kidney failure: a longitudinal analysis of the UK National Registry of Rare Kidney Diseases (RaDaR) cohort Katie Wong, David Pitcher, Fiona Braddon, Lewis Downward, Retha Steenkamp, Nicholas M. P. Annear, Jonathan Barratt, Coralie Bingham, Constantina Chrysochou, Richard J. Coward, David Game, Siân Griffin, Matt Hall, Sally Johnson, Durga Kanigicherla, Fiona Karet Frankl, David Kavanagh, Larissa Kerecuk, Eamonn R. Maher, Shabbir H. Moochhala, Jenny Pinney, John A. Sayer, Roslyn Simms, Smeeta Sinha, Shalabh Srivastava, Frederick W.K. Tam, Andrew Neil Turner, Stephen B. Walsh, Aoife Waters, Patricia D. Wilson, Edwin Wong, C. Mark Taylor, Dorothea Nitsch, Moin A. Saleem, Detlef Böckenhauer, Kate Bramham, Daniel P. Gale, Sharirose Abat, Shazia Adalat, Joy O. Agbonmwandolor, Zubaidah Ahmad, Abdulfattah Alejmi, Rashid Almasarwah, Nicholas M. P. Annear, Ellie Asgari, Amanda Ayers, Jyoti Baharani, Gowrie Balasubramaniam, Felix Kpodo, Tarun Bansal, Alison Barratt, Jonathan Barratt, Megan Bates, N K Bayne, Janet Bendle, Sarah Benyon, Carsten Bergmann, Sunil Bhandari, Coralie Bingham, Preetham Boddana, Sally L. Bond, Fiona Braddon, Kate Bramham, Angela Branson, Stephen Brearey, Vicky Brocklebank, Sharanjit Budwal, Conor Byrne, Hugh Cairns, Brian Camilleri, Gary Campbell, A. Capell, Margaret Carmody, Marion Carson, Tracy Cathcart, Christine Catley, Karine Cesar, Melanie Chan, Houda Chea, James Chess, Chee Kay Cheung, Katy-Jane Chick, Nihil Chitalia, Martin Christian, Constantina Chrysochou, Katherine Clark, Christopher L. Clayton, Rhian Clissold, Helen Cockerill, Joshua Coelho, Elizabeth Colby, Viv Colclough, Eileen Conway, H. Terence Cook, Wendy L. Cook, Theresa Cooper, Richard J. Coward, Sarah Crosbie, Gabor Cserep, Anjali Date
Հրապարակվել է 2024Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Medicine
Internal medicine
Biology
Gene
Genetics
Endocrinology
Kidney
Kidney disease
Alternative medicine
Compound heterozygosity
Genotype
Glomerulonephritis
Pathology
Placebo
Receptor
Adverse effect
Alport syndrome
Anesthesia
Anterior cingulate cortex
Bosentan
Cognition
Cohort
Computational biology
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Endothelin receptor
Environmental health
Functional magnetic resonance imaging
Genome-wide association study
Major depressive disorder
Neuroscience