Zobrazeno 1 - 10
of 117
pro vyhledávání: '"Angelica Beate Winter Boldt"'
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/b436b1d46c8c41529585232b390af8b6
Autor:
David Lemke Dück, Marco Antonio Takashi Utiumi, Angelica Beate Winter Boldt, Elcio Juliato Piovesan
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 09, Pp 795-802 (2023)
Background Genetic variants play a pathophysiological role in headaches, especially in migraine. The Mennonite group (MG) has been geographically and genetically isolated throughout its history, harboring a distinctive distribution of diseases.
Externí odkaz:
https://doaj.org/article/31e1c5d5837f44b9a1891343809bcb09
Autor:
Maiara Sulzbach Denardin, Valéria Bumiller-Bini Hoch, Amanda Salviano-Silva, Sara Cristina Lobo-Alves, Gabriel Adelman Cipolla, Danielle Malheiros, Danillo G. Augusto, Michael Wittig, Andre Franke, Claudia Pföhler, Margitta Worm, Nina van Beek, Matthias Goebeler, Miklós Sárdy, Saleh Ibrahim, Hauke Busch, Enno Schmidt, Jennifer Elisabeth Hundt, Maria Luiza Petzl-Erler, Angelica Beate Winter Boldt
Publikováno v:
Life, Vol 14, Iss 1, p 60 (2023)
Pemphigus foliaceus (PF) is an autoimmune skin blistering disease characterized by antidesmoglein-1 IgG production, with an endemic form (EPF) in Brazil. Genetic and epigenetic factors have been associated with EPF, but its etiology is still not full
Externí odkaz:
https://doaj.org/article/57d564500a92445f8b440b7dc151d1c6
Autor:
Kathleen Liedtke Kolb, Ana Luiza Sprotte Mira, Eduardo Delabio Auer, Isabela Dall’Oglio Bucco, Carla Eduarda de Lima e Silva, Priscila Ianzen dos Santos, Valéria Bumiller-Bini Hoch, Luana Caroline Oliveira, Aline Borsato Hauser, Jennifer Elisabeth Hundt, Alan R. Shuldiner, Fabiana Leão Lopes, Teide-Jens Boysen, Andre Franke, Luis Felipe Ribeiro Pinto, Sheila Coelho Soares-Lima, Gabriela Canalli Kretzschmar, Angelica Beate Winter Boldt
Publikováno v:
Genes, Vol 14, Iss 9, p 1805 (2023)
The regulation of the hypothalamic-pituitary-adrenal (HPA) axis is associated with polymorphisms and the methylation degree of the glucocorticoid receptor gene (NR3C1) and is potentially involved in the development of metabolic syndrome (MetS). In or
Externí odkaz:
https://doaj.org/article/0d794d3907654b76ba7f833aa6692391
Autor:
Gabriel Adelman Cipolla, Ticiana D. -J. Farias, Angelica Beate Winter Boldt, Amanda Salviano-Silva
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/0f81c274b59f49259f7aa68114a42916
Autor:
Luana Caroline Oliveira, Amanda Coelho Dornelles, Renato Mitsunori Nisihara, Estevan Rafael Dutra Bruginski, Priscila Ianzen dos Santos, Gabriel Adelman Cipolla, Stefanie Epp Boschmann, Iara José de Messias-Reason, Francinete Ramos Campos, Maria Luiza Petzl-Erler, Angelica Beate Winter Boldt
Publikováno v:
Genes, Vol 14, Iss 5, p 1026 (2023)
Celiac disease (CD), despite its high morbidity, is an often-underdiagnosed autoimmune enteropathy. Using a modified version of the Brazilian questionnaire of the 2013 National Health Survey, we interviewed 604 Mennonites of Frisian/Flemish origin th
Externí odkaz:
https://doaj.org/article/4194c4e1358540388c29434c96151b77
Autor:
João Paulo Kazmierczak de Camargo, Giovanna Nazaré de Barros Prezia, Naoye Shiokawa, Mario Teruo Sato, Roberto Rosati, Angelica Beate Winter Boldt
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Central areolar choroidal dystrophy (CACD) is a rare hereditary disease that mainly affects the macula, resulting in progressive and usually profound visual loss. Being part of congenital retinal dystrophies, it may have an autosomal dominant or rece
Externí odkaz:
https://doaj.org/article/e7a5ba4d6d1d4c27a812a1cd8370741c
Autor:
Gabriela Canalli Kretzschmar, Adriano D. S. Targa, Sheila Coelho Soares-Lima, Priscila Ianzen dos Santos, Lais S. Rodrigues, Daniel A. Macedo, Luis Felipe Ribeiro Pinto, Marcelo M. S. Lima, Angelica Beate Winter Boldt
Publikováno v:
Genes, Vol 13, Iss 12, p 2397 (2022)
Parkinson’s disease (PD) is characterized by a range of motor signs, but cognitive dysfunction is also observed. Supplementation with folic acid and vitamin B12 is expected to prevent cognitive impairment. To test this in PD, we promoted a lesion w
Externí odkaz:
https://doaj.org/article/dc8019cd0f114df3b6604af4834639dc
Autor:
Luana Caroline Oliveira, Andrey Lucas Dias Barros, Angelica Beate Winter Boldt, Gabriel Adelman Cipolla
Publikováno v:
Lifestyle Genomics, Vol 13, Iss 4, Pp 129-133 (2020)
Background/Aims: Polymorphisms in the enhancer of the lactase gene (LCT) are strongly associated with lactase persistence, but not always predictive of the phenotype. We investigated a possible association between the regulatory rs140433552*CA>del va
Externí odkaz:
https://doaj.org/article/46ddf2db833f49478ea57237647f2817
Autor:
Eduardo Delabio Auer, Hoang Van Tong, Leonardo Maldaner Amorim, Danielle Malheiros, Nghiem Xuan Hoan, Hellen Caroline Issler, Maria Luiza Petzl-Erler, Márcia Holsbach Beltrame, Angelica Beate Winter Boldt, Nguyen Linh Toan, Le Huu Song, Thirumalaisamy P. Velavan, Danillo G. Augusto
Publikováno v:
International Journal of Infectious Diseases, Vol 96, Iss , Pp 541-547 (2020)
Objectives: Genes of host immunity play an important role in disease pathogenesis and are determinants of clinical courses of infections, including hepatitis B virus (HBV). Killer-cell immunoglobulin-like receptor (KIR), expressed on the surface of n
Externí odkaz:
https://doaj.org/article/8b23abe6fbb04bcdb423d8a602fca1bf