Filter paper blood spot enzyme linked immunoassay for adiponectin and application in the evaluation of determinants of child insulin sensitivity.

Autor: Richard M Martin, Rita Patel, Emily Oken, Jennifer Thompson, Alexander Zinovik, Michael S Kramer, Konstantin Vilchuck, Natalia Bogdanovich, Natalia Sergeichick, Ying Foo, Nina Gusina

Publikováno v: PLoS ONE, Vol 8, Iss 8, p e71315 (2013)

Adiponectin is an adipocyte-derived hormone that acts as a marker of insulin sensitivity. Bloodspot sampling by fingerstick onto filter paper may increase the feasibility of large-scale studies of the determinants of insulin sensitivity. We first des

Externí odkaz: https://doaj.org/article/ce4c56f7f412427bb7df3a1038f270aa

Associations of prenatal and postnatal growth with insulin-like growth factor-I levels in pre-adolescence

Autor: Michael S. Kramer, Nina Gusina, Richard M. Martin, N Bogdanovich, Ryan Arathimos, Caroline J. Bull, Jeffrey M P Holly, Emily Oken, Kate Tilling, Konstantin Vilchuck, Rita Patel, Macdonald-Wallis C

Publikováno v: Arathimos, R, Macdonald-Wallis, C, Bull, C, Holly, J M P, Oken, E, Kramer, M S, Gusina, N, Bogdanovich, N, Vilchuck, K, Patel, R, Martin, R & Tilling, K 2017, ' Associations Of Prenatal And Postnatal Growth With Insulin-Like Growth Factor-I Levels In Pre-Adolescence ', bioRxiv .

BackgroundRapid pre - and postnatal growth have been associated with later life adverse health outcomes, which could implicate (as a mediator) circulating insulin-like-growth-factor I (IGF-I), an important regulator of growth. We investigated associa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f2e37c918d2cb3fbc75adb7a001d9e1

Molecular analysis of mucopolysaccharidosis type VI in Poland, Belarus, Lithuania and Estonia

Autor: Loreta Cimbalistiene, Agnieszka Sobczyńska, Kamila Czerska, Ewa Piotrowska, Katrin Õunap, Anna Tylki-Szymańska, Grzegorz Węgrzyn, Nina Gusina, Barbara Czartoryska, Agnieszka Jurecka

Publikováno v: Molecular Genetics and Metabolism. 105:237-243

Mucopolysaccharidosis VI (MPS VI) is a rare autosomal recessive disorder caused by a deficiency of N-acetylgalactosamine-4-sulfatase (ARSB). Over 130 ARSB gene mutations have been identified thus far and most mutations are unique to individual famili

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::790eab33faf1f3c788d9aee99f43329b
https://doi.org/10.1016/j.ymgme.2011.11.003

Mucopolysaccharidosis type VI in Russia, Kazakhstan, and Central and Eastern Europe

Autor: Agnieszka, Jurecka, Ekaterina, Zakharova, Loreta, Cimbalistiene, Nina, Gusina, Vera, Malinova, Agnieszka, Różdżyńska-Świątkowska, Adam, Golda, Anna, Kulpanovich, Gulnara, Kaldenovna Abdilova, Elena, Voskoboeva, Anna, Tylki-Szymańska

Publikováno v: Pediatrics international : official journal of the Japan Pediatric Society. 56(4)

The aim of this study was to describe the natural clinical course, incidence and prevalence of mucopolysaccharidosis type VI (MPS VI) in Russia, Kazakhstan, and Central and Eastern Europe.Patients (n = 49) were identified by retrieving the data from

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fba0faa54d6d0ab7253dea34cb8840e8
https://pubmed.ncbi.nlm.nih.gov/24373060

Mucopolysaccharidosis type VI: a predominantly cardiac phenotype associated with homozygosity for p.R152W mutation in the ARSB gene

Autor: Ewa Piotrowska, Violetta Opoka-Winiarska, Elena Voskoboeva, Adam Golda, Loreta Cimbalistiene, Anna Tylki-Szymańska, Anna Kulpanovich, Agnieszka Jurecka, Ekaterina Zakharova, Nina Gusina

Publikováno v: American journal of medical genetics. Part A. (6)

Mucopolysaccharidosis type VI (MPS VI) is a rare lysosomal, autosomal recessive storage disorder caused by deficient activity of N-acetylgalactosamine-4-sulfatase (ARSB). Approximately, 140 ARSB gene mutations have been identified; however, most are

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31ef93e0030738409ee8ad2ecf483701
https://pubmed.ncbi.nlm.nih.gov/23633437