Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Ivan, Vogel"'
Publikováno v:
F1000Research, Vol 10 (2021)
Genotyping of single cells using single nucleotide polymorphism arrays is a cost-effective technology that provides good coverage and precision, but requires whole genome amplification (WGA) due to the low amount of genetic material. Since WGA introd
Externí odkaz:
https://doaj.org/article/4e99798a40ef45f0a70a9199ab57105c
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Folate deficiency is associated with a broad range of human disorders, including anemia, fetal neural tube defects, age-associated dementia and several types of cancer. It is well established that a subgroup of rare fragile sites (RFSs) containing ex
Externí odkaz:
https://doaj.org/article/e2e5ed400db84876a69da2b608443428
Autor:
Elena Albani, Matteo Figliuzzi, Marco Fabiani, Carmen Rubio, Maurizio Poli, Necati Findikli, Danilo Cimadomo, Cristina Patassini, Paolo E. Levi-Setti, Onder Coban, Alberto Vaiarelli, Antonio Capalbo, Filippo Maria Ubaldi, Laura Sacchi, Laura Rienzi, Alessio Farcomeni, Carlos Simón, Fazilet Kubra Boynukalin, Francesca Benini, Ivan Vogel, Claudia Livi, J. F. Cuzzi, Laura Girardi, Eva Hoffmann
Publikováno v:
AMERICAN JOURNAL OF HUMAN GENETICS
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
American Journal of Human Genetics
Capalbo, A, Poli, M, Rienzi, L, Girardi, L, Patassini, C, Fabiani, M, Cimadomo, D, Benini, F, Farcomeni, A, Cuzzi, J, Rubio, C, Albani, E, Sacchi, L, Vaiarelli, A, Figliuzzi, M, Findikli, N, Coban, O, Boynukalin, F K, Vogel, I, Hoffmann, E, Livi, C, Levi-Setti, P E, Ubaldi, F M & Simón, C 2021, ' Mosaic human preimplantation embryos and their developmental potential in a prospective, non-selection clinical trial ', American Journal of Human Genetics, vol. 108, no. 12, pp. 2238-2247 . https://doi.org/10.1016/j.ajhg.2021.11.002
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
American Journal of Human Genetics
Capalbo, A, Poli, M, Rienzi, L, Girardi, L, Patassini, C, Fabiani, M, Cimadomo, D, Benini, F, Farcomeni, A, Cuzzi, J, Rubio, C, Albani, E, Sacchi, L, Vaiarelli, A, Figliuzzi, M, Findikli, N, Coban, O, Boynukalin, F K, Vogel, I, Hoffmann, E, Livi, C, Levi-Setti, P E, Ubaldi, F M & Simón, C 2021, ' Mosaic human preimplantation embryos and their developmental potential in a prospective, non-selection clinical trial ', American Journal of Human Genetics, vol. 108, no. 12, pp. 2238-2247 . https://doi.org/10.1016/j.ajhg.2021.11.002
Summary Chromosome imbalance (aneuploidy) is the major cause of pregnancy loss and congenital disorders in humans. Analyses of small biopsies from human embryos suggest that aneuploidy commonly originates during early divisions, resulting in mosaicis
Autor:
Danilo Cimadomo, Ivan Vogel, Laura Girardi, Maurizio Poli, Eva Hoffmann, Levi-Setti P, Carmen Rubio, Carlos Simón, Alberto Vaiarelli, Benini F, Sacchi L, Alessio Farcomeni, Albani E, Filippo Maria Ubaldi, Livi C, Antonio Capalbo, Cuzzi J, Laura Rienzi
BackgroundNext generation sequencing (NGS) has increased detection sensitivity of intermediate chromosome copy number variations (CNV) consistent with chromosomal mosaicism. Recently, this methodology has found application in preimplantation genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ee218f8cc9517b62057c662dae00301
https://doi.org/10.1101/2021.02.07.21251201
https://doi.org/10.1101/2021.02.07.21251201
Publikováno v:
Garribba, L, Vogel, I, Lerdrup, M, Gonçalves Dinis, M M, Ren, L & Liu, Y 2021, ' Folate Deficiency Triggers the Abnormal Segregation of a Region With Large Cluster of CG-Rich Trinucleotide Repeats on Human Chromosome 2 ', Frontiers in Genetics, vol. 12, 695124 . https://doi.org/10.3389/fgene.2021.695124
Frontiers in genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Frontiers in genetics
Frontiers in Genetics, Vol 12 (2021)
Frontiers in Genetics
Folate deficiency is associated with a broad range of human disorders, including anemia, fetal neural tube defects, age-associated dementia and several types of cancer. It is well established that a subgroup of rare fragile sites (RFSs) containing ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fa0fce4b35d97485500b445c3c60632
https://curis.ku.dk/ws/files/275822445/fgene_12_695124.pdf
https://curis.ku.dk/ws/files/275822445/fgene_12_695124.pdf
Autor:
Wei Wu, Chunhui Li, Zihui Liu, Liqun Ren, Lorenza Garribba, Long Chen, Ying Liu, Ian D. Hickson, Huanna Tian, Ivan Vogel
Publikováno v:
Oncotarget
Ren, L, Chen, L, Wu, W, Garribba, L, Tian, H, Liu, Z, Ivan, V, Li, C, Hickson, I D & Liu, Y 2017, ' Potential biomarkers of DNA replication stress in cancer ', OncoTarget, vol. 8, no. 23, pp. 36996-37008 . https://doi.org/10.18632/oncotarget.16940
Ren, L, Chen, L, Wu, W, Garribba, L, Tian, H, Liu, Z, Ivan, V, Li, C, Hickson, I D & Liu, Y 2017, ' Potential biomarkers of DNA replication stress in cancer ', OncoTarget, vol. 8, no. 23, pp. 36996-37008 . https://doi.org/10.18632/oncotarget.16940
Oncogene activation is an established driver of tumorigenesis. An apparently inevitable consequence of oncogene activation is the generation of DNA replication stress (RS), a feature common to most cancer cells. RS, in turn, is a causal factor in the
Autor:
Claus Andersen, Anne Mette Bay Bjørn, Agata P. Zielinska, Robert Blanshard, Lotte Berdiin Colmorn, Deborah M. Taylor, Geraldine M. Hartshorne, Joanna Liss, Louise Newnham, Eva Hoffmann, Marie Louise Grøndahl, Junping Cheng, Dmitry Nikiforov, Ivan Vogel, Jennifer R. Gruhn, Stine Gry Kristensen, Martyn Blayney, Danilo Cimadomo, Andrew Chi-Ho Chan, Vallari Shukla, Rajiv C. McCoy, Melina Schuh, Catello Scarica, Marta Krapchev, Antonio Capalbo, Krzysztof Lukaszuk, Filippo Ubaldi, Erik Ernst, Kay Elder, Laura Rienzi
Publikováno v:
Science
Gruhn, J R, Zielinska, A P, Shukla, V, Blanshard, R, Capalbo, A, Cimadomo, D, Nikiforov, D, Chan, A C H, Newnham, L J, Vogel, I, Scarica, C, Krapchev, M, Taylor, D, Kristensen, S G, Cheng, J, Ernst, E, Bjørn, A M B, Colmorn, L B, Blayney, M, Elder, K, Liss, J, Hartshorne, G, Grøndahl, M L, Rienzi, L, Ubaldi, F, McCoy, R, Lukaszuk, K, Andersen, C Y, Schuh, M & Hoffmann, E R 2019, ' Chromosome errors in human eggs shape natural fertility over reproductive life span ', Science, vol. 365, no. 6460, pp. 1466-1469 . https://doi.org/10.1126/science.aav7321
Gruhn, J R, Zielinska, A P, Shukla, V, Blanshard, R, Capalbo, A, Cimadomo, D, Nikiforov, D, Chan, A C H, Newnham, L J, Vogel, I, Scarica, C, Krapchev, M, Taylor, D, Kristensen, S G, Cheng, J, Ernst, E, Bjørn, A M B, Colmorn, L B, Blayney, M, Elder, K, Liss, J, Hartshorne, G, Grøndahl, M L, Rienzi, L, Ubaldi, F, McCoy, R, Lukaszuk, K, Andersen, C Y, Schuh, M & Hoffmann, E R 2019, ' Chromosome errors in human eggs shape natural fertility over reproductive life span ', Science, vol. 365, no. 6460, pp. 1466-1469 . https://doi.org/10.1126/science.aav7321
Understanding fertility in young and old Fertility in humans follows a U-curve, with low rates in both teenagers and women of advancing maternal age (mid-30s and above). Gruhn et al. found that this distinct shape originates from chromosomal errors i
Autor:
Radim Cegan, Boris Vyskot, Zdenek Kubat, Ivan Vogel, Roman Hobza, Jitka Zluvova, Viera Kovacova, Tomas Cermak, Eduard Kejnovsky
Publikováno v:
New Phytologist. 202:662-678
Some transposable elements (TEs) show extraordinary variance in abundance along sex chromosomes but the mechanisms responsible for this variance are unknown. Here, we studied Ogre long terminal repeat (LTR) retrotransposons in Silene latifolia, a dio
Autor:
Jana Čížková, Boris Vyskot, Radim Cegan, Eva Nevrtalova, Roman Hobza, Magda Soukupova, Ivan Vogel
Publikováno v:
Cytogenetic and Genome Research. 143:96-103
Silene latifolia (or white campion) possesses a well-established sex determination system with a dominant Y chromosome in males (the mammalian type). The heteromorphic sex chromosomes X and Y in S. latifolia largely stopped recombination; thus, we ca
Autor:
Zdenek Kubat, Eduard Kejnovsky, Ivan Vogel, Roman Hobza, Boris Vyskot, Tereza Králová, Radim Cegan, Jan Vrána
Publikováno v:
Cytogenetic and Genome Research. 143:87-95
Silene latifolia is a dioecious plant species with chromosomal sex determination. Although the evolution of sex chromosomes in S. latifolia has been the subject of numerous studies, a global view of X chromosome structure in this species is still mis