Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Dobrawa Napierała"'
Autor:
Andrzej Pławski, M. Zając, Tomasz Banasiewicz, Dobrawa Napierała, Piotr Gronek, Katarzyna Nuc, Ryszard Słomski
Publikováno v:
Journal of Animal and Feed Sciences. 9:721-726
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2798f5c79f47bf607c2d745160b8792
https://doi.org/10.22358/jafs/68121/2000
https://doi.org/10.22358/jafs/68121/2000
Autor:
Jolanta Jura, Tomasz Banasiewicz, Andrzej Pławski, Jadwiga Sowinska, Jaroslaw Wronka, Ryszard Słomski, Robert Kalak, Dobrawa Napierała
Publikováno v:
Journal of Clinical Biochemistry and Nutrition. 28:113-127
Over the past decade geneticists have searched for rapid and efficient means of identification of genetic diseases. Nucleic acid techniques, such as restriction fragment length polymorphisms, polymerase chain reaction, and sequence analysis of amplif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::663cb05dc6b683e2c94f6f82a6569d94
https://doi.org/10.3164/jcbn.28.113
https://doi.org/10.3164/jcbn.28.113
Autor:
Ryszard Słomski, Andrzej Pławski, Tomasz Banasiewicz, A. Rosinski, Piotr Gronek, Dobrawa Napierała
Publikováno v:
Journal of Animal and Feed Sciences. 8:203-207
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77357a787426cfd739ed0b5f2d33fb0c
https://doi.org/10.22358/jafs/68839/1999
https://doi.org/10.22358/jafs/68839/1999
Autor:
Dobrawa Napierała, Ryszard Słomski, Jadwiga Wigowska-Sowińska, David J. Kwiatkowski, J. Kwiatkowska
Publikováno v:
New England Journal of Medicine. 340:703-707
Mosaicism is the phenomenon in which a fraction of, rather than all, germ-line and somatic cells contain a mutation or chromosomal abnormality. It occurs in all genetic disorders in which spontaneous mutations occur and has important clinical consequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::732c83fde187596ad2722f5e6d2c0894
https://doi.org/10.1056/nejm199903043400905
https://doi.org/10.1056/nejm199903043400905
Autor:
Mairobys Socorro, Priyanka Hoskere, Catherine Roberts, Lyudmila Lukashova, Kostas Verdelis, Elia Beniash, Dobrawa Napierala
Publikováno v:
Frontiers in Dental Medicine, Vol 3 (2022)
Dental caries is the most common chronic disease in children and adults worldwide. The complex etiology of dental caries includes environmental factors as well as host genetics, which together contribute to inter-individual variation in susceptibilit
Externí odkaz:
https://doaj.org/article/540f92f3b1e8419abf918e8d723b4ad3
Publikováno v:
Bone Reports, Vol 13, Iss , Pp 100435- (2020)
Externí odkaz:
https://doaj.org/article/378616974dc8426e933d6bd20ff30141
Autor:
Kah Yan Cho, Brian P. Kelley, Daisy Monier, Brendan Lee, Heather Szabo-Rogers, Dobrawa Napierala
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Trichorhinophalangeal syndrome (TRPS) is an autosomal dominant disorder resulting from heterozygous mutations of the TRPS1 gene. Common craniofacial abnormalities in TRPS patients include micrognathia, hypoplastic zygomatic arch, high-arched palate,
Externí odkaz:
https://doaj.org/article/8c279ea613be4ad3bcae0a2af31ab434
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0121568 (2015)
Osteosarcoma (OS) is a hyperproliferative malignant tumor that requires a high vascular density to maintain its large volume. Vascular Endothelial Growth Factor (VEGF) plays a crucial role in angiogenesis and acts as a paracrine and autocrine agent a
Externí odkaz:
https://doaj.org/article/5d5dec9047004fc5a26e0bf111b89ab3
Autor:
Erica P Homan, Caressa Lietman, Ingo Grafe, Jennifer Lennington, Roy Morello, Dobrawa Napierala, Ming-Ming Jiang, Elda M Munivez, Brian Dawson, Terry K Bertin, Yuqing Chen, Rhonald Lua, Olivier Lichtarge, John Hicks, Mary Ann Weis, David Eyre, Brendan H L Lee
Publikováno v:
PLoS Genetics, Vol 10, Iss 1, p e1004121 (2014)
Mutations in the genes encoding cartilage associated protein (CRTAP) and prolyl 3-hydroxylase 1 (P3H1 encoded by LEPRE1) were the first identified causes of recessive Osteogenesis Imperfecta (OI). These proteins, together with cyclophilin B (encoded
Externí odkaz:
https://doaj.org/article/37ae85070b0b4400b4a292992ff153e7