Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Alina Wojda"'
Autor:
Małgorzata Kurkowiak, Ewa Ziętkiewicz, Agnieszka Greber, Katarzyna Voelkel, Alina Wojda, Andrzej Pogorzelski, Michał Witt
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0148067 (2016)
Primary ciliary dyskinesia (PCD) is a rare recessive disease with a prevalence of 1/10,000; its symptoms are caused by a kinetic dysfunction of motile cilia in the respiratory epithelium, flagella in spermatozoids, and primary cilia in the embryonic
Externí odkaz:
https://doaj.org/article/c999534674cf4332ac952ee1bafec959
Autor:
Zuzanna, Bukowy-Bieryllo, Alicja, Rabiasz, Maciej, Dabrowski, Andrzej, Pogorzelski, Alina, Wojda, Hanna, Dmenska, Katarzyna, Grzela, Jakub, Sroczynski, Michal, Witt, Ewa, Zietkiewicz
Publikováno v:
Journal of medical genetics. 56(11)
Primary ciliary dyskinesia (PCD) is a motile ciliopathy, whose symptoms include airway infections, male infertility andTo elucidate the role of motile cilia defects in the respiratory phenotype of PCD patients with C-terminal OFD1 mutations.Whole-exo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d9cf8d11121c8ee15a07c1f9ae619eba
https://pubmed.ncbi.nlm.nih.gov/31366608
https://pubmed.ncbi.nlm.nih.gov/31366608
Publikováno v:
Journal of Applied Genetics. 50:261-273
Analysis of relationships between the ageing cell phenotype and the age of cell donors is one of the ways towards understanding the link between cellular and organismal ageing. Cytogenetically, ageing is associated with a number of gross cellular cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ee3d73a74be4c7b069b093975cc43a9
https://doi.org/10.1007/bf03195682
https://doi.org/10.1007/bf03195682
Autor:
Agnieszka Greber, Małgorzata Kurkowiak, Michał Witt, Andrzej Pogorzelski, Alina Wojda, Katarzyna Voelkel, Ewa Ziętkiewicz
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 1, p e0148067 (2016)
PLoS ONE, Vol 11, Iss 1, p e0148067 (2016)
Primary ciliary dyskinesia (PCD) is a rare recessive disease with a prevalence of 1/10,000; its symptoms are caused by a kinetic dysfunction of motile cilia in the respiratory epithelium, flagella in spermatozoids, and primary cilia in the embryonic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a18b77dbce3d983e6ff6bf0c3f26835
https://pubmed.ncbi.nlm.nih.gov/26824761
https://pubmed.ncbi.nlm.nih.gov/26824761
Autor:
Alina Wojda, Leszek Pawelczyk, David C. Page, Aleksandra Korcz, Jadwiga Jaruzelska, Tatiana Surmacz, Maciej Kotecki, Piotr Jedrzejczak, Joanna Bierla
Publikováno v:
Journal of Medical Genetics. 38:798-802
Editor—Over the past 10 years, several authors have reported microdeletions in the long arm of the Y chromosome (Yq) in men with idiopathic, non-obstructive azoospermia or severe oligospermia. These microdeletions were clustered on the Yq fragment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2de33b8fb1bc579bb450eb95f9d3c8c
https://doi.org/10.1136/jmg.38.11.798
https://doi.org/10.1136/jmg.38.11.798
Autor:
Jolanta Andrzejewska, Katarzyna Lacka, Maciej R Krawczyński, Adam Czyzyk, Alina Wojda, Anna Latos-Bielenska, Joanna Skołożdrzy
Publikováno v:
The Endocrinologist. 20:283-285
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5d3a625c784d6262a211e9b5d48d40a
https://doi.org/10.1097/ten.0b013e3181fcfeba
https://doi.org/10.1097/ten.0b013e3181fcfeba
Publikováno v:
Mutagenesis. 22(3)
Studies have shown a significant increase in chromosome aneuploidy with age. The aim of this study was to elucidate whether the age-related changes in the level of hypoploidy correlate with the occurrence of micronuclei (MN) and chromosome nondisjunc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d93273bfb7202b2124a7a9c4a3d35f2
https://pubmed.ncbi.nlm.nih.gov/17284771
https://pubmed.ncbi.nlm.nih.gov/17284771
Autor:
Alina Wojda, Krzysztof Skrzypczak, Włodzimierz Pawłowski, Małgorzata Mossakowska, Michał Witt, Ewa Ziętkiewicz
Publikováno v:
The journals of gerontology. Series A, Biological sciences and medical sciences. 61(8)
To answer whether the age-related accumulation of chromosomal damage differs in men and women, and whether the aberration level in centenarians is proportional to their age, cytogenetic aberrations in dividing cells were analyzed. G-band karyotyping
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c8ff0b15ea18cbb2e4dd818c7daa98
https://pubmed.ncbi.nlm.nih.gov/16912092
https://pubmed.ncbi.nlm.nih.gov/16912092
Publikováno v:
Journal of applied genetics. 44(3)
In this study we present a 102-year old woman carrying a (7;12)(q11.3;q14) translocation. A woman displays a normal phenotype and infertility in anamnesis. This is the first report linking t(7;12) and infertility.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d809fcbfbd6d7e96a31afc8e93a7fbe6
https://pubmed.ncbi.nlm.nih.gov/12923318
https://pubmed.ncbi.nlm.nih.gov/12923318
Publikováno v:
Medical science monitor : international medical journal of experimental and clinical research. 8(5)
The possibility of a link between altered sperm morphology and functional ability, possibly reflected on the genetic level, is still a matter of controversy.60 infertile males with pathological spermiogram and 14 healthy individuals with confirmed in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::45b5e9fd2f482f360b31bf2279d91076
https://pubmed.ncbi.nlm.nih.gov/12016421
https://pubmed.ncbi.nlm.nih.gov/12016421