Zobrazeno 1 - 10
of 296
pro vyhledávání: '"I, Mikula"'
Autor:
L. Palkova, A. Tomova, G. Repiska, K. Babinska, B. Bokor, I. Mikula, G. Minarik, D. Ostatnikova, K. Soltys
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Abstract intestinal microbiota is becoming a significant marker that reflects differences between health and disease status also in terms of gut-brain axis communication. Studies show that children with autism spectrum disorder (ASD) often h
Externí odkaz:
https://doaj.org/article/013366bbfc27401ba8c6f2b47c70265a
Autor:
Benjamin N. Fogel, Deepa Saravana, Mary Lewis, Nicole M. Hackman, Barbara E Ostrov, Jennifer R. Miller, Tammy E. Corr, Margaret I. Mikula, Carrie Daymont, Erich K. Batra
Publikováno v:
Pediatrics. 148
BACKGROUND AND OBJECTIVES Sudden unexpected infant death often results from unsafe sleep environments and is the leading cause of postneonatal mortality in the United States. Standardization of infant sleep environment education has been revealed to
Akademický článek
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Autor:
Gabriela Repiská, Lenka Pálková, Katarína Šoltys, I. Mikula, Katarina Babinska, Aleksandra Tomova, Boris Bokor, G. Minarik, Daniela Ostatníková
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract intestinal microbiota is becoming a significant marker that reflects differences between health and disease status also in terms of gut-brain axis communication. Studies show that children with autism spectrum disorder (ASD) often have a mix
Publikováno v:
Вісник проблем біології і медицини, Iss 3, Pp 170-173 (2020)
The purpose of the study. To investigate the relationship of gender, age, karyotype, chronic diseases of spouses with reproductive losses, caused by different chromosomal abnormalities in abortions/fetuses. Object and methods. Clinical examination an
Publikováno v:
Biopolymers and Cell, Vol 29, Iss 5, Pp 413-417 (2013)
Aim. Analyze the distribution of allelic polymorphism of HLA-DRB1, DQA1, DQB1 genes and HLA-G 14-bp insertion/deletion polymorphism in women with RPL. Methods. DNA extraction, PCR, agarose gel electrophoresis. Results. A comprehensive analysis of the
Publikováno v:
Folia biologica. 61(6)
Porphyrias are metabolic disorders resulting from mutations in haem biosynthetic pathway genes. Hepatoerythropoietic porphyria (HEP) is a rare type of porphyria caused by the deficiency of the fifth enzyme (uroporphyrinogen decarboxylase, UROD) in th
Publikováno v:
Veterinary Immunology and Immunopathology. 138:51-59
Toll-like receptors (TLRs) 2, 3, 4, 7, 8 and 9 play a crucial role in the recognition of viral entities and modulation of the innate immune system. This work presents sequence analysis of ovine TLR7 and TLR8 genes, depicts novel mutations and describ
Publikováno v:
Veterinary Immunology and Immunopathology. 128:381-388
Toll like receptors (TLRs) are a class of pattern recognition receptors belonging to the innate immune system. Mutations in the protein coding region of TLRs are associated with altered responsiveness to pathogen-associated molecular patterns (PAMPs)