Resultados de búsqueda - Darren Fowler
- Mostrando 1 - 6 Resultados de 6
-
1
-
2
N‐methyl‐D‐aspartate receptor antibody production from germinal center reactions: Therapeutic implications por Mateusz Makuch, R. Wilson, Adam Al‐Diwani, James Varley, Anne‐Kathrin Kienzler, Jennifer Taylor, Antonio Berretta, Darren Fowler, Belinda Lennox, Maria Isabel Leite, Patrick Waters, Sarosh R. Irani
Publicado 2018Artigo -
3
Spatiotemporal analysis of human intestinal development at single-cell resolution por David Fawkner-Corbett, Agne Antanaviciute, Kaushal Parikh, Marta Jagielowicz, Ana Sousa Gerós, Tarun Gupta, Neil Ashley, Doran Khamis, Darren Fowler, Edward Morrissey, Chris Cunningham, P. V. Johnson, Hashem Koohy, Alison Simmons
Publicado 2021Artigo -
4
Cervical lymph nodes and ovarian teratomas as germinal centres in NMDA receptor-antibody encephalitis por Adam Al‐Diwani, Jakob Theorell, Valentina Damato, Joshua A. Bull, Nicholas McGlashan, Edward Green, Anne‐Kathrin Kienzler, Ruby Harrison, Tasneem Hassanali, Leticia Campo, Molly Browne, Alistair Easton, Hooman Soleymani majd, Keiko Tenaka, Raffaele Iorio, Russell C. Dale, Paul J. Harrison, John Geddes, Digby Quested, David Sharp, Soon‐Tae Lee, David W. Nauen, Mateusz Makuch, Belinda Lennox, Darren Fowler, Fintan Sheerin, Patrick Waters, Maria Isabel Leite, Adam E. Handel, Sarosh R. Irani
Publicado 2022Artigo -
5
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations por Veerle Rc Eggens, P. G. Barth, Jikke-Mien F. Niermeijer, Jonathan Berg, Niklas Darín, Abhijit Dixit, Joël Fluss, Nicola Foulds, Darren Fowler, Tibor Hortobágyi, Thomas S. Jacques, Mary D. King, Periklis Makrythanasis, Adrienn Máté, James A. R. Nicoll, Declan O’Rourke, Sue Price, Andrew N. Williams, Louise C. Wilson, Mohnish Suri, László Sztriha, Marit B Dijns-de Wissel, Mia T van Meegen, Fred van Ruissen, Eleonora Aronica, Dirk Troost, Charles B.L.M. Majoie, Henk A. Marquering, Bwee Tien Poll‐The, Frank Baas
Publicado 2014Artigo -
6
The impact of inversions across 33,924 families with rare disease from a national genome sequencing project por Alistair T. Pagnamenta, Jing Yu, Susan Walker, Alexandra Noble, Jenny Lord, Prasun Dutta, Mona Hashim, Carlos Camps, Hannah Green, Smrithi Devaiah, Lina Nashef, Jason Parr, Carl Fratter, Rana Hussein, Sarah Lindsay, Fiona Lalloo, Benito Banos‐Pinero, David M. Evans, Lucy Mallin, Adrian J. Waite, Julie Evans, Andrew G. Newman, Zoe Allen, Cristina Perez‐Becerril, Gavin Ryan, Rachel Hart, John‐Stephen Taylor, Tina Bedenham, Emma Clement, Ed Blair, Eleanor Hay, Francesca Forzano, Jenny Higgs, Natalie Canham, Anirban Majumdar, Meriel McEntagart, Nayana Lahiri, Helen Stewart, Sarah Smithson, Eduardo Calpena, Adam Jackson, Siddharth Banka, Hannah Titheradge, Ruth McGowan, Julia Rankin, Charles Shaw‐Smith, D. Gareth Evans, George J. Burghel, Miriam J. Smith, Emily E. Anderson, Rajesh Madhu, Helen V. Firth, Sian Ellard, Paul Brennan, Claire Anderson, Doug Taupin, Mark T. Rogers, Jackie A. Cook, Miranda Durkie, James E. East, Darren Fowler, Louise C. Wilson, Rebecca Igbokwe, Alice Gardham, Ian Tomlinson, Diana Baralle, Holm H. Uhlig, Jenny C. Taylor
Publicado 2024Artigo
Herramientas de búsqueda:
Materias Relacionadas
Biology
Medicine
Endocrinology
Genetics
Antibody
B cell
Computational biology
Gene
Germinal center
Immunology
Ovarian Teratoma
Pathology
Allele
Anatomy
Anovulation
Artificial intelligence
Atrophy
Autoantibody
Biochemistry
Cell biology
Cerebellar hypoplasia (non-human)
Cerebellum
Compound heterozygosity
Computer science
Decidualization
Degenerative disease
Disease
Endometrium
Fetus
Genome