Torthaí cuardaigh - Bergithe E Oftedal
- 1 - 9 toradh as 9 á dtaispeáint
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1
Clinical and Serologic Parallels to APS-I in Patients with Thymomas and Autoantigen Transcripts in Their Tumors de réir Anette S. B. Wolff, Jaanika Kärner, Jone Furlund Owe, Bergithe E Oftedal, Nils Erik Gilhus, Martina M. Erichsen, Olle Kämpe, Anthony Meager, Pärt Peterson, Kai Kisand, Nick Willcox, Eystein S. Husebye
Foilsithe / Cruthaithe 2014Artigo -
2
Expanding the Phenotypic and Genotypic Landscape of Autoimmune Polyendocrine Syndrome Type 1 de réir Elizaveta Orlova, Leila Sozaeva, Maria Kareva, Bergithe E Oftedal, Anette S. B. Wolff, Lars Breivik, Ekaterina Zakharova, О.Н. Иванова, Olle Kämpe, И. И. Дедов, Per M. Knappskog, Valentina Peterkova, Eystein S. Husebye
Foilsithe / Cruthaithe 2017Artigo -
3
Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and Proteomics de réir Zhiqiang Hu, Hamish S. Scott, Guangrong Qin, Guangyong Zheng, Xixia Chu, Lu Xie, David L. Adelson, Bergithe E Oftedal, Parvathy Venugopal, Milena Babic, Christopher N Hahn, Bing Zhang, Xiao‐Jing Wang, Nan Li, Chaochun Wei
Foilsithe / Cruthaithe 2015Artigo -
4
<i>ARMC5</i>Mutations Are Common in Familial Bilateral Macronodular Adrenal Hyperplasia de réir Lucia Gagliardi, Andreas Schreiber, Christopher N Hahn, Jinghua Feng, Treena Cranston, Hannah Boon, Cheri Hotu, Bergithe E Oftedal, Richard Cutfield, David L. Adelson, Wilton Braund, Richard D. Gordon, Aled Rees, Ashley Grossman, David J. Torpy, Hamish S. Scott
Foilsithe / Cruthaithe 2014Artigo -
5
A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1 de réir Øyvind Bruserud, Bergithe E Oftedal, Nils Landegren, Martina M. Erichsen, Eirik Bratland, Kari Lima, Anders Palmstrøm Jørgensen, Anne Grethe Myhre, Johan Svartberg, Kristian J. Fougner, A Bakke, Bjørn Gunnar Nedrebø, Bjarne Mella, Lars Breivik, Marte K. Viken, Per M. Knappskog, Mihaela Cuida Marthinussen, Kristian Løvås, Olle Kämpe, Anette S. B. Wolff, Eystein S. Husebye
Foilsithe / Cruthaithe 2016Artigo -
6
Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases de réir Bergithe E Oftedal, Alexander Hellesen, Martina M. Erichsen, Eirik Bratland, Ayelet Vardi, Jaakko Perheentupa, E. Helen Kemp, Torunn Fiskerstrand, Marte K. Viken, Anthony P. Weetman, Sarel J. Fleishman, Siddharth Banka, William G. Newman, William A. Sewell, Leila Sozaeva, Tetyana Zayats, Kristoffer Haugarvoll, Elizaveta Orlova, Jan Haavik, Stefan Johansson, Per M. Knappskog, Kristian Løvås, Anette S. B. Wolff, Jakub Abramson, Eystein S. Husebye
Foilsithe / Cruthaithe 2015Artigo -
7
Autoantibodies to Perilipin-1 Define a Subset of Acquired Generalized Lipodystrophy de réir Caleigh Mandel‐Brehm, Sara E. Vazquez, Christopher S. Liverman, Mickie Cheng, Zoe Quandt, Andrew F. Kung, Audrey V. Parent, Brenda Y. Miao, Emmanuel Disse, Christine Cugnet‐Anceau, Stéphane Dalle, Elizaveta Orlova, Elena Frolova, Diana Alba, Aaron W. Michels, Bergithe E Oftedal, Michail S. Lionakis, Eystein S. Husebye, Anil K. Agarwal, Xilong Li, Chengsong Zhu, Quan Li, Elif A Oral, Rebecca J. Brown, Mark S. Anderson, Abhimanyu Garg, Joseph L. DeRisi
Foilsithe / Cruthaithe 2022Artigo -
8
Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes de réir Bergithe E Oftedal, Kristian Assing, Safa Barış, Stephanie L. Safgren, Işık Somuncu Johansen, Marianne Antonius Jakobsen, Dusica Babovic‐Vuksanovic, Katherine Agre, Eric W. Klee, Emina Majcic, Elise M. N. Ferré, Monica M. Schmitt, Tom DiMaggio, Lindsey B. Rosen, Muhammad Obaidur Rahman, Dionisios Chrysis, Aristeidis Giannakopoulos, Maria Tallon Garcia, Luis Ignacio González‐Granado, Katherine Stanley, Jessica Galant-Swafford, Pim Suwannarat, Isabelle Meyts, Michail S. Lionakis, Eystein S. Husebye
Foilsithe / Cruthaithe 2023Artigo -
9
GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility de réir Daniel Eriksson, Ellen C. Røyrvik, Maribel Aranda‐Guillén, Amund Holte Berger, Nils Landegren, Haydeé Artaza, Åsa Hallgren, Marianne Aardal Grytaas, Sara S. Strom, Eirik Bratland, Ileana Ruxandra Botusan, Bergithe E Oftedal, Lars Breivik, Marc Vaudel, Øyvind Helgeland, Alberto Falorni, Anders Palmstrøm Jørgensen, Anna‐Lena Hulting, Johan Svartberg, Olov Ekwall, Kristian J. Fougner, Jeanette Wahlberg, Bjørn Gunnar Nedrebø, Per Dahlqvist, Helge Ræder, Nevena Jovanovic, Sigfrid Christine Reisegg, Geir Hølleland, Siri Carlsen, Tore Julsrud Berg, Jan Bertil Eggesbø, Thomas Svendsen, Kari Lima, Ingrid Nermoen, Rolf Whitfield, Stina Therese Sollid, Dagfinn Aarskog, Elin Korsgaard, Solveig Sæta, Trine Finnes, Susanna F Valland, Caroline Fossum, Eli Brevik, Ragnar Bekkhus Moe, Margrethe Svendsen, Aleksandra Dębowska, Petya Milova, Synnøve Emblem Holte, Aneta Eva Tomkowicz, Dag Eirik Sørmo, Anders Svare, Marthe Landsverk Rensvik, Randi Revheim, T. Haug, Ivar Blix, Lars Petter Jensen, Anna‐Karin Åkerman, Anna‐Lena Hulting, Bengt Lindberg, Berit Kriström, Erik Waldenström, Gudmundur Johannsson, Jakob Skov, Jeanette Wahlberg, Karel Duchén, Magnus Isaksson, Maria Elfving, Maria Halldin Stenlid, Ola Nilsson, Olle Kämpe, Olov Ekwall, Per Dahlqvist, Ragnhildur Bergthorsdottir, Ricard Nergårdh, Sigríður Björnsdóttir, Sophie Bensing, Tommy Olsson, Per M. Knappskog, Anette S. B. Wolff, Sophie Bensing, Stefan Johansson, Olle Kämpe, Eystein S. Husebye
Foilsithe / Cruthaithe 2021Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Antibody
Immunology
Medicine
Autoimmune regulator
Biology
Gene
Genetics
Autoantibody
Autoimmunity
Internal medicine
Autoimmune disease
Disease
Immune system
Mutation
Allele
Chronic mucocutaneous candidiasis
Genotype
Hypoparathyroidism
Pathology
Phenotype
Sanger sequencing
Adipocyte
Adipose tissue
Adrenal insufficiency
Alternative splicing
Antiretroviral therapy
Compound heterozygosity
Computational biology
Endocrinology
Enteropathy