Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Intissar, Anan"'
Publikováno v:
Annals of Medicine, Vol 55, Iss 2 (2023)
AbstractIntroduction In hereditary transthyretin amyloidosis (ATTRv), two different fibrillar forms causing the amyloid deposition, have been identified, displaying substantially cardiac or neuropathic symptoms. Neuropathic symptoms are more frequent
Externí odkaz:
https://doaj.org/article/74b86dae988044bab2f46ab7a7bb3133
Autor:
Irina Iakovleva, Michael Hall, Melanie Oelker, Linda Sandblad, Intissar Anan, A. Elisabeth Sauer-Eriksson
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Systemic ATTR amyloidosis causes the abnormal accumulation of ATTR fibrils formed from the human plasma protein transthyretin (TTR) in multiple organs including the eye. Here, the authors present a 3.2 Å cryo-EM structure of an ATTR fibril isolated
Externí odkaz:
https://doaj.org/article/205058912dca45fe996644a0164ffb89
Autor:
Hedvig Paulsson Rokke, Nima Sadat Gousheh, Per Westermark, Ole B. Suhr, Intissar Anan, Elisabet Ihse, Björn Pilebro, Jonas Wixner
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-10 (2020)
Abstract Background The diagnostic accuracy of histopathological detection of transthyretin amyloid (ATTR) by Congo red staining of abdominal fat samples has been questioned since low sensitivity has been reported, especially for patients with ATTR c
Externí odkaz:
https://doaj.org/article/c40549b432104364b8d7c4ba08cf13ff
Autor:
Erica Irene Uneus, Christer Wilhelmsson, David Bäckström, Intissar Anan, Jonas Wixner, Björn Pilebro, Katrine Riklund, Mattias Ögren, Margareta Ögreen, Jan Axelsson, Ole B. Suhr, Torbjörn Sundström
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionHereditary transthyretin (ATTRv) amyloidosis caused by the V30M (p. V50M) mutation is a fatal, neuropathic systemic amyloidosis. Liver transplantation has prolonged the survival of patients and central nervous system (CNS) complications,
Externí odkaz:
https://doaj.org/article/4f2230cb46d24ac39ec5c0e1062d9eaf
Autor:
Intissar Anan, Ole B Suhr, Katarzyna Liszewska, Jorge Mejia Baranda, Björn Pilebro, Jonas Wixner, Elisabet Ihse
Publikováno v:
PLoS ONE, Vol 17, Iss 3, p e0266092 (2022)
BackgroundWe have previously shown that transthyretin (TTR) amyloidosis patients have amyloid fibrils of either of two compositions; type A fibrils consisting of large amounts of C-terminal TTR fragments in addition to full-length TTR, or type B fibr
Externí odkaz:
https://doaj.org/article/19b9341c1bbd41899b9f9234cdf69edf
Autor:
Violaine Planté-Bordeneuve, Farida Gorram, Malin Olsson, Intissar Anan, Anna Mazzeo, Luca Gentile, Eugenia Cisneros-Barroso, Juan Gonzalez-Moreno, Ines Losada, Marcia Waddington-Cruz, Luiz Felipe Pinto, Yeşim Parman, Pascale Fanen, Flora Alarcon, Gregory Nuel
Publikováno v:
Amyloid. :1-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f290c0dc782c64a4e3acda80ed527cf
https://doi.org/10.1080/13506129.2023.2178891
https://doi.org/10.1080/13506129.2023.2178891
Publikováno v:
Biomolecules, Vol 12, Iss 3, p 446 (2022)
Amyloid formation is a pathological process associated with a wide range of degenerative disorders, including Alzheimer’s disease, Parkinson’s disease, and diabetes mellitus type 2. During disease progression, abnormal accumulation and deposition
Externí odkaz:
https://doaj.org/article/7703cc0dc6d1447a8bfe02d82a32ec87
Autor:
Sanduni Wasana Jayaweera, Solmaz Surano, Nina Pettersson, Elvira Oskarsson, Lovisa Lettius, Anna L. Gharibyan, Intissar Anan, Anders Olofsson
Publikováno v:
Biomolecules, Vol 11, Iss 3, p 411 (2021)
Amyloid-formation by the islet amyloid polypeptide (IAPP), produced by the β-cells in the human pancreas, has been associated with the development of type II diabetes mellitus (T2DM). The human plasma-protein transthyretin (TTR), a well-known amyloi
Externí odkaz:
https://doaj.org/article/7d771b7b050a4884afb38f3f461d4a04
Autor:
Kristin, Samuelsson, Ana, Jovanovic, Karl, Egervall, Intissar, Anan, Jonas, Wixner, Rayomand, Press
Publikováno v:
Amyloid. 29:220-227
Hereditary transthyretin amyloidosis (ATTRv) is endemic in northern Sweden (Västerbotten). The awareness of ATTRv amyloidosis is lower in Stockholm, a non-endemic region in Sweden. The aim of this study was to compare the possible differences in dia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9074af4d10184adac3421ace26242656
https://doi.org/10.1080/13506129.2022.2065191
https://doi.org/10.1080/13506129.2022.2065191
Autor:
Ole Bernt Suhr, Jonas Wixner, Intissar Anan, Hans-Erik Lundgren, Priyantha Wijayatunga, Per Westermark, Elisabet Ihse
Publikováno v:
PLoS ONE, Vol 14, Iss 2, p e0211983 (2019)
BACKGROUND:The amyloid fibril in hereditary transthyretin (TTR) Val30Met (pVal50Met) amyloid (ATTR Val30Met) amyloidosis is composed of either a mixture of full-length and TTR fragments (Type A) or of only full-length TTR (Type B). The type of amyloi
Externí odkaz:
https://doaj.org/article/fc1362f9554241cd81fb87d00e511bfc