Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Teresa Płatek"'
Autor:
Teresa Płatek, Anna Polus, Joanna Góralska, Urszula Raźny, Anna Gruca, Beata Kieć-Wilk, Piotr Zabielski, Maria Kapusta, Krystyna Słowińska-Solnica, Bogdan Solnica, Małgorzata Malczewska-Malec, Aldona Dembińska-Kieć
Publikováno v:
Molecular Medicine, Vol 26, Iss 1, Pp 1-12 (2020)
Abstract Background Epigenetics can contribute to lipid disorders in obesity. The DNA methylation pattern can be the cause or consequence of high blood lipids. The aim of the study was to investigate the DNA methylation profile in peripheral leukocyt
Externí odkaz:
https://doaj.org/article/a4f5a162150249cba0d9abe94b54f9e0
Autor:
Małgorzata Malczewska-Malec, Agnieszka Dziewońska, Teresa Płatek, Urszula Raźny, Joanna Góralska, Anna Polus, Bogdan Solnica, Aldona Dembinska-Kiec, Agnieszka Micek
Publikováno v:
Genes, Vol 12, Iss 307, p 307 (2021)
Genes
Volume 12
Issue 2
Genes
Volume 12
Issue 2
We hypothesised that epigenetics may play an important role in mediating fibroblast growth factor 21 (FGF21) resistance in obesity. We aimed to evaluate DNA methylation changes and miRNA pattern in obese subjects associated with high serum FGF21 leve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48f73f6c01417d05f44ecc207df0c3b
https://www.mdpi.com/2073-4425/12/2/307
https://www.mdpi.com/2073-4425/12/2/307
Autor:
Anna Gruca, Krystyna Slowinska-Solnica, Maria Kapusta, Teresa Płatek, Beata Kieć-Wilk, Urszula Raźny, Małgorzata Malczewska-Malec, Joanna Góralska, Piotr Zabielski, Bogdan Solnica, Anna Polus, Aldona Dembinska-Kiec
Publikováno v:
Molecular Medicine
Molecular Medicine, Vol 26, Iss 1, Pp 1-12 (2020)
Molecular Medicine, Vol 26, Iss 1, Pp 1-12 (2020)
Background Epigenetics can contribute to lipid disorders in obesity. The DNA methylation pattern can be the cause or consequence of high blood lipids. The aim of the study was to investigate the DNA methylation profile in peripheral leukocytes associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a363b8696799c990f7e08f9203fd2b75
https://ruj.uj.edu.pl/xmlui/handle/item/264474
https://ruj.uj.edu.pl/xmlui/handle/item/264474
Autor:
Magdalena Szopa, Sandra Mrozinska, Barbara Zapała, Teresa Płatek, Jerzy Hohendorff, Beata Kieć-Wilk, T. Parpan, Tomasz Klupa, Wojciech Glodzik, Maria Kapusta, Maciej T. Malecki, Jan Skupien, Agnieszka Ludwig-Gałęzowska
Publikováno v:
Endocrine
Aims SGLT2 inhibitors are a new class of oral hypoglycemic agents used in type 2 diabetes (T2DM). Their effectiveness in maturity onset diabetes of the young (MODY) is unknown. We aimed to assess the response to a single dose of 10 mg dapagliflozin i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c6117c1e03715ab4820e371470d890a
http://europepmc.org/articles/PMC5511327
http://europepmc.org/articles/PMC5511327
Autor:
Iwona Solecka, Maciej T. Malecki, Cyrus M Sani, Bartłomiej Matejko, Damian Ucieklak, Barbara Zapała, Teresa Płatek, Wojciech Glodzik, Magdalena Szopa, Jerzy Hohendorff, Sandra Mrozinska, Agata Uchman
Aim The impact of maturity onset diabetes of the young (MODY) on quality of life (QoL) has never been examined. We assessed disease impact on QoL among patients with HNF1A-MODY and GCK mutation carrier status. Methods The study included 80 patients w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62bbf176b48032e785edb2804160d68b
https://ruj.uj.edu.pl/xmlui/handle/item/114597
https://ruj.uj.edu.pl/xmlui/handle/item/114597
Autor:
Urszula Ciałowicz, Monika Chojnacka, Anna Polus, Gerd Schmitz, Barbara Zapała, Teresa Płatek, Beata Kieć-Wilk, Evelyn Orsó, Małgorzata Malczewska-Malec, Aldona Dembinska-Kiec, Bogdan Solnica, Monika Piwowar
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
Rationale: X-linked adrenoleukodystrophy (X-ALD) is a rare disorder caused by mutations in the ABCD1 gene, coding for peroxisomal membrane transporter adrenoleukodystrophy (ALD) protein. The
Rationale: X-linked adrenoleukodystrophy (X-ALD) is a rare disorder caused by mutations in the ABCD1 gene, coding for peroxisomal membrane transporter adrenoleukodystrophy (ALD) protein. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1719e1e3778cdf93caf8651d57a2e3a
https://ruj.uj.edu.pl/xmlui/handle/item/144885
https://ruj.uj.edu.pl/xmlui/handle/item/144885
Publikováno v:
Annals of Human Genetics
Barth syndrome (BTHS) is an X-linked recessive disease primarily affecting males. Clinically, the disease is characterized by hypertrophic or dilated cardiomyopathy, skeletal myopathy, chronic/cyclic neutropenia, 3-methylglutaconic aciduria, growth r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5293730feb2aeff1cbecfb88516d4b2b
https://ruj.uj.edu.pl/xmlui/handle/item/126533
https://ruj.uj.edu.pl/xmlui/handle/item/126533
Autor:
Teresa Płatek, Piotr Radkowski, Tomasz Klupa, Agnieszka Ludwig-Gałęzowska, Barbara Zapała, Paweł Wołkow, Maciej T. Malecki, Magdalena Szopa, Wojciech Młynarski, Maciej Borowiec, Beata Kieć-Wilk, Jan Skupien
Introduction Molecular diagnosis of monogenic diabetes mellitus is important for individualized patient care. Next-generation sequencing (NGS) enables a simultaneous analysis of multiple genes in a single test. Objectives We aimed to assess the feasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fa49fae4fdcc28f504f12616e5bb3ff
https://ruj.uj.edu.pl/xmlui/handle/item/102619
https://ruj.uj.edu.pl/xmlui/handle/item/102619