Zobrazeno 1 - 10
of 276
pro vyhledávání: '"PSMB8"'
Autor:
Yong Zhong, Fan Yu, Ling Yang, Yu Wang, Lin Liu, Chengyou Jia, Haidong Cai, Jianshe Yang, Shiyang Sheng, Zhongwei Lv, Li Weng, Bo Wu, Xiaoping Zhang
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-23 (2023)
Abstract Anaplastic thyroid carcinoma (ATC) is a deadly disease with a poor prognosis. Thus, there is a pressing need to determine the mechanism of ATC progression. The homeobox D9 (HOXD9) transcription factor has been associated with numerous malign
Externí odkaz:
https://doaj.org/article/e9d7c4a5f8c548efa72469976c6585bd
Autor:
Agnieszka Terlikowska-Brzósko, Ryszard Galus, Piotr Murawski, Justyna Niderla-Bielińska, Izabela Młynarczuk-Biały, Elwira Paluchowska, Witold Owczarek
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 17, p 9192 (2024)
(1): Atopic dermatitis and psoriasis vulgaris are chronic, inflammatory diseases. Clinical presentation usually leads to a proper diagnosis, but sometimes neither clinical examination nor histopathological evaluation can be conclusive. Therefore, we
Externí odkaz:
https://doaj.org/article/405ce0795d7e4ed2b08bac180acb070a
Autor:
Jonas Johannes Papendorf, Frédéric Ebstein, Sara Alehashemi, Daniela Gerent Petry Piotto, Anna Kozlova, Maria Teresa Terreri, Anna Shcherbina, Andre Rastegar, Marta Rodrigues, Renan Pereira, Sophia Park, Bin Lin, Kat Uss, Sophie Möller, Ana Flávia da Silva Pina, Flavio Sztajnbok, Sofia Torreggiani, Julie Niemela, Jennifer Stoddard, Sergio D. Rosenzweig, Andrew J. Oler, Colton McNinch, Marietta M. de Guzman, Adriana Fonseca, Nicole Micheloni, Melissa Mariti Fraga, Sandro Félix Perazzio, Raphaela Goldbach-Mansky, Adriana A. de Jesus, Elke Krüger
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Mutations in genes coding for proteasome subunits and/or proteasome assembly helpers typically cause recurring autoinflammation referred to as chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperatures (CANDLE) or proteasom
Externí odkaz:
https://doaj.org/article/797414f038e44fa0bb0b536c59ac957d
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Natasha Salame, Jean-Pierre Bikorimana, Nehme El-Hachem, Wael Saad, Mazen Kurdi, Jing Zhao, Nicoletta Eliopoulos, Riam Shammaa, Moutih Rafei
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-15 (2022)
Abstract Background Mesenchymal stromal cells (MSCs) have been extensively used in the clinic due to their exquisite tissue repair capacity. However, they also hold promise in the field of cellular vaccination as they can behave as conditional antige
Externí odkaz:
https://doaj.org/article/fffee480623141a1968e76cc81908d9e
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 36, Iss 7, Pp 494-500 (2020)
Abstract Abnormal expression of microRNAs (miRNAs) is frequently occurred in prostate cancer (PCa). This study was aimed to investigate the biological roles of miR‐451a in PCa. Quantitative real‐time PCR (qRT‐PCR) and Western blot were employed
Externí odkaz:
https://doaj.org/article/e162ba85d2bc42b3af57cfb0c44243d0
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Background Nakajo-Nishimura syndrome (NNS) is an autosomal recessive heredity disorder, one of a spectrum of autoinflammatory diseases named proteasome-associated autoinflammatory syndrome (PRAAS) caused by mutations of PSMB8 gene. NNS is ch
Externí odkaz:
https://doaj.org/article/6d9f0d2b14de47dc9a69bad696acce7d
Autor:
Ohmura K
Publikováno v:
Journal of Inflammation Research, Vol Volume 12, Pp 259-265 (2019)
Koichiro Ohmura Department of Rheumatology and Clinical Immunology, Kyoto University Graduate School of Medicine, Kyoto 606-8507, JapanCorrespondence: Koichiro OhmuraDepartment of Rheumatology and Clinical Immunology, Kyoto University Graduate School
Externí odkaz:
https://doaj.org/article/682483f0780b4f649139417e9c0f95e2
Publikováno v:
Inflammation and Regeneration, Vol 39, Iss 1, Pp 1-8 (2019)
Abstract Nakajo-Nishimura syndrome is a proteasome-associated autoinflammatory syndrome with a distinct homozygous mutation in the PSMB8 gene encoding an inducible β5i subunit of the immunoproteasome. Although it is considered that immunoproteasome
Externí odkaz:
https://doaj.org/article/2ea82fdf34084182ab8af4c58321ae06