Zobrazeno 1 - 10
of 190
pro vyhledávání: '"V. Pecile"'
Autor:
L. Fontana, M. F. Bedeschi, S. Maitz, A. Cereda, C. Faré, S. Motta, A. Seresini, P. D’Ursi, A. Orro, V. Pecile, M. Calvello, A. Selicorni, F. Lalatta, D. Milani, S. M. Sirchia, M. Miozzo, S. Tabano
Publikováno v:
Epigenetics, Vol 13, Iss 9, Pp 897-909 (2018)
The identification of multilocus imprinting disturbances (MLID) appears fundamental to uncover molecular pathways underlying imprinting disorders (IDs) and to complete clinical diagnosis of patients. However, MLID genetic associated mechanisms remain
Externí odkaz:
https://doaj.org/article/636a1de7037f49c083e24d8c49ec7ca6
Autor:
N. Villa, D. Conconi, D. Gambel Benussi, G. Tornese, F. Crosti, E. Sala, L. Dalprà, V. Pecile
Publikováno v:
Molecular Cytogenetics, Vol 10, Iss 1, Pp 1-7 (2017)
Abstract Background Neocentromeres are rare and considered chromosomal aberrations, because a non-centromeric region evolves in an active centromere by mutation. The literature reported several structural anomalies of X chromosome and they influence
Externí odkaz:
https://doaj.org/article/45cf410ef07f4b23bd8f5cabe16cb592
Publikováno v:
Case Reports in Pediatrics, Vol 2011 (2011)
Prader-Willi syndrome in the newborn is essentially characterized by marked hypotonia, feeding difficulties, hypogonadism, and possible characteristic facial features. However, diagnosis at this age may be particularly difficult, and dysmorphic featu
Externí odkaz:
https://doaj.org/article/ed16242fb76f4909972cf21a0c68c056
Autor:
S. Salman, M. Fan, H. Tünnermann, P. Balla, J. Darvill, D. Laumer, V. Pecile, J. Fellinger, V. Shumakova, C. Mahnke, Y. Ma, C. Mohr, O. H. Heckl, C. M. Heyl, I. Hartl
Publikováno v:
Conference on Lasers and Electro-Optics.
We demonstrate an all-PM high power ultrafast Yb-fiber laser utilizing digital controls for frequency comb stabilization and femtosecond pulse shaping.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4123a6a5543f4dfb310b09a07989af46
https://doi.org/10.1364/cleo_si.2022.sf2m.1
https://doi.org/10.1364/cleo_si.2022.sf2m.1
Akademický článek
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Autor:
M. Candolini, Ilaria Fantasia, Caterina Cortivo, V. De Angelis, V. Pecile, Donatella Londero, C. Dreossi, Tamara Stampalija, D. Bolzicco, E. Castro Silva
Objective This study aimed to validate non-invasive RHD genotyping of cell-free fetal DNA (cff-DNA) using different DNA extraction methods and of fresh and frozen extracted cff-DNA. Background Non-invasive RHD genotyping of cff-DNA predicts fetal RhD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25ed568e4bc8b8708bbb33f41a724e93
https://hdl.handle.net/11368/2955382
https://hdl.handle.net/11368/2955382
Autor:
L. Bensefa-Colas, K. Ivanova, Paul P. Tak, K. Glatz, M.N. Crépy, Druck Reinhardt Druck Basel, Marjan de Groot, G. Chaby, B. Cortés, I. Berti, V. Pecile, Annamaria Mazzotta, E. Alberini, C. Lok, Satz Mengensatzproduktion, A. Dadban, Eyal Kalish, Dan Ben-Amitai, A. Zippelius, Longfeng Cai, Katarina Steen Carlsson, Andrea Chiricozzi, Zhiming Yu, F. Dhaille, Maria Esposito, Shlomit Halachmi, S. Cazzaniga, L. Naldi, L. Cleva, L. Borradori, Marcus Schmitt-Egenolf, Eyal Raveh, Alex Zvulunov, Maria Sole Chimenti, Arianna Zangrilli, Florian C. Beikert, Matthias Augustin, Ines Schäfer, M.M. Tang, M. Jourdan, Ulf Persson, H. Tang, Aurélie Sarah Clottu, B. Bouquiaux, L. Clivaz, A. Caudron, S. Billon, Daisy I. Picavet, Roberto Perricone, Emmanuel Laffitte, Rosita Saraceno, Katharina Herberger, Jan D. Bos, Christine Blome, T. Kornek, J.H. Saurat, Johanna Mihály, Javier Garcia, Menno A. de Rie, Hongxiao Chen, Marcel B. M. Teunissen, F. Faletra, H. Assier, Graziella Babino, Jenny M. Norlin, Steven Paul Nisticò, Alessandro Giunta, B. Halioua, Maria Vittoria Cannizzaro, Michael Reusch, Gamze Aydemir, F. Schibler, Rune Blomhoff, Carlo Chizzolini, Arno W.R. van Kuijk, Moshe Lapidoth, Xiaoling Zhu, Christa Prins, Kathrin Weiss, O. Chosidow, Limin Cai, P. Gasparini, N. Pelivani, N. Yawalkar, L. Meziane, G. Nicolas, Sergio Chimenti, E. Khelifa, Harald Carlsen, Mauro Bavetta, Janine Gericke, P. Itin, A. Tommasini, Z. Spanou, Ralph Rühl, I. Bruno
Publikováno v:
Dermatology. 225:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82ebcfe696c9a66175540f803861cd16
https://doi.org/10.1159/000348800
https://doi.org/10.1159/000348800
Akademický článek
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Autor:
S. Crovella, M. Del Pero, N. Marziliano, S. Garagna, V. Pecile, M. Morgutti, M. Boniotto, A. Amoroso, D. Montagnon, C. Carlà Campa, L. Lamberti, M.P. Bigatti, G. Ardito
Publikováno v:
Genome. 42:1066-1070
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a96e647c127c5648d2181430a709656
https://doi.org/10.1139/gen-42-6-1066
https://doi.org/10.1139/gen-42-6-1066
Autor:
L. Fischer-Tamaro, G. Conoscenti, V. Pecile, G. D'Ottauio, R. Natale, Mariangela Rustico, Y. J. Meir, G. P. Mandruzzato
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 10:375-380
A prospective study of screening for fetal abnormalities and chromosomal defects was carried out by ultrasound examination at 13–l5 weeks of gestation and 20–22 weeks; the first scan was performed transvaginally and the second transabdominally. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9546e00a58cc69c68125fefb5434b90
https://doi.org/10.1046/j.1469-0705.1997.10060375.x
https://doi.org/10.1046/j.1469-0705.1997.10060375.x