Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mikhail Gylling"'
Autor:
Aaro Miettinen, Jaakko Perheentupa, Heli Tuovinen, Nora Pöntynen, Mikhail Gylling, Eliisa Kekäläinen, T. Petteri Arstila
Publikováno v:
Cellular Immunology. 257:5-12
Mutations in the transcriptional regulator Aire disrupt thymic alphabeta T cell selection, causing in humans Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). However, it is not known whether Aire is needed for normal gammadelt
Autor:
Eva Åström, Harry Holthöfer, Johanna Rinta-Valkama, Mikhail Gylling, Heikki Ahola, T. Timonen, Aaro Miettinen
Publikováno v:
Cellular and Molecular Life Sciences CMLS. 63:498-504
When nephrin, the protein product of NPHS1, was cloned, it was proposed to be specific for the kidney glomerular podocytes. Recently, however, new reports have emerged verifying additional nephrin expression sites, particularly the insulin-producing
Autor:
Eeva Juvonen, Mikhail Gylling, Dontscho Kerjaschki, Riitta Alitalo, Laura Kerosuo, Aaro Miettinen
Publikováno v:
British Journal of Haematology. 124:809-818
Podocalyxin-like protein (PCLP) is a sialomucin-type membrane protein structurally related to CD34 and endoglycan. It was first described in glomerular podocytes and endothelial cells. In mice, PCLP is present in haemangioblasts, and in both chicken
Autor:
Olle Kämpe, Petra Eskelin, Gennet Gebre-Medhin, Michael P. Manns, Annika Söderbergh, Eva Landgren, Thomas Nilsson, Anne Grethe Myhre, Tiinamaija Tuomi, Jaakko Perheentupa, Maria Halonen, Olov Ekwall, Håkan Hedstrand, Eystein S. Husebye, Jan Gustafsson, Fredrik Rorsman, Mikhail Gylling, Aaro Miettinen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 89:557-562
The prevalence of autoantibodies against nine intracellular enzyme autoantigens, namely 21-hydroxylase, side-chain cleavage enzyme (SCC), 17 alpha-hydroxylase, glutamic acid decarboxylase 65, aromatic L-amino acid decarboxylase, tyrosine phosphatase-
Autor:
Mikhail Gylling, Petra Björses, Mikael Knip, Sirkka Kontiainen, Jukka Partanen, Aaro Miettinen, Michael R. Christie, Jaakko Perheentupa, Tiinamaija Tuomi
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 85:4434-4440
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is caused by lack of functional products of the autoimmune regulator gene located on chromosome 21q22.3. The patients are at high risk of developing insulin-dependent (type 1) di
Autor:
Heli Tuovinen, Nora Pöntynen, Mikhail Gylling, Eliisa Kekäläinen, Jaakko Perheentupa, Aaro Miettinen, Petteri Arstila
Publikováno v:
University of Helsinki
Mutations in the transcriptional regulator Aire disrupt thymic alphabeta T cell selection, causing in humans Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED). However, it is not known whether Aire is needed for normal gammadelt
Autor:
Laura, Kerosuo, Eeva, Juvonen, Riitta, Alitalo, Mikhail, Gylling, Dontscho, Kerjaschki, Aaro, Miettinen
Publikováno v:
British journal of haematology. 124(6)
Podocalyxin-like protein (PCLP) is a sialomucin-type membrane protein structurally related to CD34 and endoglycan. It was first described in glomerular podocytes and endothelial cells. In mice, PCLP is present in haemangioblasts, and in both chicken
Autor:
Riitta Väisänen, Laura Kerosuo, Mikhail Gylling, Essi Kääriäinen, Aaro Miettinen, Marja-Liisa Solin, Leena Halme, Maria Halonen, Seppo Saari, Olle Kämpe, Jaakko Perheentupa
Publikováno v:
The Journal of clinical endocrinology and metabolism. 88(10)
In autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy, hypoparathyroidism (HP) is the most common endocrine component. It occurs in most (but not all) patients. Determinants of its occurrence are unknown, and there is no proof for its aut
Autor:
Heli Tuovinen, Aaro Miettinen, Mikhail Gylling, Nora Pöntynen, Jaakko Perheentupa, Kimmo Talvensaari, T. Petteri Arstila, Rauli Franssila, Joonas Joensuu, Eliisa Kekäläinen
Publikováno v:
University of Helsinki
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), a monogenic recessive disease characterized by autoimmunity against multiple tissues, offers a unique possibility to study the breakdown of self-tolerance in humans. It is cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c0f280f38492433a5272204f49c313
https://researchportal.helsinki.fi/en/publications/bbbe4acc-01a5-4789-b0d8-6d77a6264d21
https://researchportal.helsinki.fi/en/publications/bbbe4acc-01a5-4789-b0d8-6d77a6264d21