Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Kininogen 1"'
Autor:
Hilary Longhurst, Aaqib Zaffar Banday, Jyoti Sharma, Amit Rawat, Ankur Kumar Jindal, Surjit Singh, Anit Kaur
Publikováno v:
Clinical Reviews in Allergy & Immunology. 60:305-315
Hereditary Angioedema (HAE) is an autosomal dominant disorder characterized clinically by recurrent episodes of swelling involving subcutaneous tissues, gastrointestinal tract, and oro-pharyngeal area. Gene mutations are the most common genetic cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24daaead632bceabbc15c96ee6471f9b
https://doi.org/10.1007/s12016-021-08835-8
https://doi.org/10.1007/s12016-021-08835-8
Autor:
Luisa Brussino, Stefania Loffredo, Alessandra Zoli, Angelica Petraroli, Stefano Del Giacco, Maurizio Margaglione, Davide Firinu, Chiara Suffritti, Anna Radice, Tiziana De Pasquale, Giorgia Cordisco, Vincenzo Montinaro, Marco Cicardi, Andrea Zanichelli, Maria Bova, Valeria Bafunno
Publikováno v:
Allergy. 75:1394-1403
Background Hereditary angioedema (HAE) comprises HAE with C1-inhibitor deficiency (C1-INH-HAE) and HAE with normal C1-INH activity (nl-C1-INH-HAE), due to mutations in factor XII (FXII-HAE), plasminogen (PLG-HAE), angiopoietin 1 (ANGPT1-HAE), kininog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5522d792e8be2b59236e860d87cbfaf1
https://doi.org/10.1111/all.14160
https://doi.org/10.1111/all.14160
Publikováno v:
Frontiers in Endocrinology
Frontiers in Endocrinology, Vol 12 (2021)
Frontiers in Endocrinology, Vol 12 (2021)
Globally, nearly 40 percent of all diabetic patients develop serious diabetic kidney disease (DKD). The identification of the potential early-stage biomarkers and elucidation of their underlying molecular mechanisms in DKD are required. In this study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff12fab2d5aefa03a19c70c845c5079
https://doi.org/10.3389/fendo.2021.721202
https://doi.org/10.3389/fendo.2021.721202
Autor:
Giovanna D'Andrea, Rosa Santacroce, Maria D'Apolito, Maurizio Margaglione, Angela Bruna Maffione
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 2023, p 2023 (2021)
Journal of Clinical Medicine
Journal of Clinical Medicine
Hereditary angioedema is a rare inherited disorder characterized by recurrent episodes of the accumulation of fluids outside of the blood vessels, causing rapid swelling of tissues in the hands, feet, limbs, face, intestinal tract, or airway. Mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cba3878a897a77eea7db9a3fc8da8dd
https://www.mdpi.com/2077-0383/10/9/2023
https://www.mdpi.com/2077-0383/10/9/2023
Autor:
Yuya Nakamura, Chisako Fujiwara, Tomoya Hirose, Takeo Yamaguchi, Osamu Ishikawa, Isao Ohsawa, Daisuke Honda, Masahiro Ieko, Junichi Maehara, Shinya Imamura, Akio Tanaka, Hiromichi Gotoh, Kouhei Yamashita, Kazumasa Iwamoto, Atsushi Fukunaga, Michihiro Hide, Kunihiko Umekita
Publikováno v:
World Allergy Organization Journal, Vol 14, Iss 2, Pp 100511-(2021)
The World Allergy Organization Journal
The World Allergy Organization Journal
Background: Hereditary angioedema (HAE) is a rare but life-threatening condition. HAE types I and II (HAE-1/2) result from C1-inhibitor (C1–INH) deficiency. However, recent genetic analysis has established a new type of HAE with normal C1–INH (HA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::058fab494d95449674a674a69089e9ae
http://www.sciencedirect.com/science/article/pii/S1939455121000053
http://www.sciencedirect.com/science/article/pii/S1939455121000053
Autor:
Meriç Kocatürk, Richard Burchmore, José J. Cerón, Zeki Yilmaz, Damián Escribano, Vladimir Mrljak, Luis Pardo-Marín, Anita Horvatić, Silvia Martínez-Subiela
Publikováno v:
Veterinary Immunology and Immunopathology. 191:60-67
The objective of this study was to use the Tandem Mass Tag (TMT) isobaric label-based proteomic approach, in order to identify new potential biomarkers for the treatment monitoring of canine leishmaniosis that could not be identified by the use of ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f77b808e47bd8200fb6ca385fde058e
https://doi.org/10.1016/j.vetimm.2017.08.004
https://doi.org/10.1016/j.vetimm.2017.08.004
Autor:
Camila Lopes Veronez, Farrukh R. Sheikh, Bruce L. Zuraw, Henriette Farkas, Dorottya Csuka, Konrad Bork
Publikováno v:
The journal of allergy and clinical immunology. In practice. 9(6)
The evolution in the knowledge of rare genetic diseases such as hereditary angioedema (HAE) has increased at a parallel pace with the development of new molecular tools. The deficiency of C1 inhibitor (C1-INH) has been recognized as the main cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb732ffd8e3696893d121a7ef660da20
https://pubmed.ncbi.nlm.nih.gov/33746090
https://pubmed.ncbi.nlm.nih.gov/33746090
Cerebrospinal Fluid Levels of Kininogen‐1 Indicate Early Cognitive Impairment in Parkinson's Disease
Autor:
Anna Månberg, Wassilios G. Meissner, Kimmo Sorjonen, Julia Remnestål, Stephanie Carvalho, Wojciech Paslawski, Peter Nilsson, Mathias Uhlén, Eloi Magnin, Ioanna Markaki, Sofia Bergström, Ellen Hertz, Graziella Mangone, Olivier Rascol, Jean-Christophe Corvol, Ullrich Wüllner, Panagiota Tsitsi, Per Svenningsson
Publikováno v:
Movement Disorders
Movement Disorders, Wiley, 2020, 35 (11), pp.2101-2106. ⟨10.1002/mds.28192⟩
Movement Disorders, 2020, 35 (11), pp.2101-2106. ⟨10.1002/mds.28192⟩
Movement disorders 35(11), 2101-2106 (2020). doi:10.1002/mds.28192
Movement Disorders, Wiley, 2020, 35 (11), pp.2101-2106. ⟨10.1002/mds.28192⟩
Movement Disorders, 2020, 35 (11), pp.2101-2106. ⟨10.1002/mds.28192⟩
Movement disorders 35(11), 2101-2106 (2020). doi:10.1002/mds.28192
International audience; Background: Cognitive impairment is common in patients with PD. Core markers of Alzheimer's dementia have been related also to PD dementia, but no disease-specific signature to predict PD dementia exists to date.Objectives: Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca87125631698dfc42776a74647577ff
https://hal.sorbonne-universite.fr/hal-03212590/document
https://hal.sorbonne-universite.fr/hal-03212590/document
Publikováno v:
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research
BACKGROUND Immune-related genes (IRGs) are closely related to the incidence and progression of tumors, potentially indicating that IRGs play an important role in laryngeal squamous cell carcinoma (LSCC). MATERIAL AND METHODS An RNA sequencing dataset
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::338ee91c6cfc20e18cacb701a2f22bec
https://doi.org/10.12659/msm.928185
https://doi.org/10.12659/msm.928185
Autor:
Venkatesh Chanukuppa, Ravindra Taware, Khushman Taunk, Tathagat Chatterjee, Sanjeevan Sharma, Venkatesan Somasundaram, Faraz Rashid, Dipankar Malakar, Manas K. Santra, Srikanth Rapole
Publikováno v:
Frontiers in Oncology
Frontiers in Oncology, Vol 10 (2021)
Frontiers in Oncology, Vol 10 (2021)
Multiple myeloma (MM) is a plasma cell-associated cancer and exists as the second most common hematological malignancy worldwide. Although researchers have been working on MM, a comprehensive quantitative Bone Marrow Interstitial Fluid (BMIF) and ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfa313760a5b4610483f7fa9ee4bc1c8
https://pubmed.ncbi.nlm.nih.gov/33585190
https://pubmed.ncbi.nlm.nih.gov/33585190