Zobrazeno 1 - 6
of 6
pro vyhledávání: '"David Konvalinka"'
Autor:
Zuzana Zděblová Čermáková, Pavel Hurník, David Konvalinka, Jan Štembírek, Tereza Paračková, Kamila Resová, Jakub Cvek, Tomáš Blažek, Lukáš Knybel, Martin Formánek, Mariam Gachechiladze, Markus Joerger, Alex Soltermann, Jozef Škarda, Oldřich Motyka, Jana Janoutová
Publikováno v:
Medicina, Vol 59, Iss 2, p 361 (2023)
Introduction: The incidence of advanced oral cavity and oropharyngeal cancers is generally high. Treatment outcomes for patients, especially those unfit for comprehensive cancer treatment, are unsatisfactory. Therefore, the search for factors to pred
Externí odkaz:
https://doaj.org/article/dc3fbdc18cc242049c3c14b69da5670d
Autor:
Magdalena Uvírová, Radek Mech, Lenka Jezova, Irena Urbanovska, Jirina Janoscova, David Konvalinka, Alena Kocarkova, Jarmila Simova, Sylva Hlavacova, Katerina Tvrdonova, Iveta Zebrakova
Publikováno v:
Reproductive BioMedicine Online. 38:e60
Introduction Embryonic mosaicism is described as a presence of 2 or more distinct cell lines in embryo. This phenomenon is common and more prevalent in human preimplantation embryos than in later prenatal samples, affecting 15-90% of cleavage stage e
Autor:
Radek Vrtel, Ishraq Dhaifalah, Arvind Rup Singh, Jiri Santavy, David Konvalinka, Radek Vodicka
Publikováno v:
International Journal of Human Genetics. 6:209-217
The human Y chromosome harbours genes that are essential for spermatogenesis. Most of these genes lie in the male-specific region (MSY) of Y chromosome. Microdeletions of AZF within the MSY have been reported in infertile men. Widely different freque
Autor:
Radek Vrtel, Arvind Rup Singh, Radek Vodicka, Jiri Santavy, Ishraq Dhaifalah, David Konvalinka
Publikováno v:
International Journal of Human Genetics. 6:163-169
Infertility in 20% of involuntary childless couples is attributable to purely male factors. In about 30% of such males the underlying cause is genetic. Male infertility problems tend to aggregate in the families and a decline of ~ 50% in the sperm co
Autor:
Arvind Rup Singh, Radek Vrtel, Radek Vodicka, Ishraq Dhaifalah, David Konvalinka, Maria Janikova, Jiri Santavy
Publikováno v:
International Journal of Human Genetics. 5:225-235
KEYWORDS Y chromosome; male infertility; microdeletions; SRY; TSPY; AZF; DAZ; CDY1; BPY2; PRY; TTY2 ABSTRACT The Y chromosome though representing only 2-3% of the haploid genome harbours about 107 genes and pseudogenes. Many of these are responsible
Autor:
Hans F. A. Vasen, Juul T. Wijnen, Martijn H. Breuning, Frederik J. Hes, David Konvalinka, Egbert Bakker, Maartje Nielsen, Carli M. J. Tops, Elsa C. Bik
BACKGROUND: The patient with 10 or more adenomas in the colon poses a diagnostic challenge. Beside germline mutations in the APC and MUTYH genes, only four cases of mosaic APC mutations have been reported. AIM: Given the relatively high frequency of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7cb30aa5bf59d7c0d0f2640c576cf82
https://biblio.vub.ac.be/vubir/(ba939981-ef5f-400e-9632-9fa6380070aa).html
https://biblio.vub.ac.be/vubir/(ba939981-ef5f-400e-9632-9fa6380070aa).html