Zobrazeno 1 - 10
of 30
pro vyhledávání: '"T. M. Neri"'
Publikováno v:
Journal of endocrinological investigation. 36(10)
The adiponectin gene has been identified as a susceptibility locus for metabolic syndrome, diabetes and cardiovascular disease.To examine the influence of two single nucleotide polymorphisms (SNPs) of this gene (+276GT and +45TG) on circulating adipo
Autor:
F, Riccardi, A, Tagliaferri, D, Martorana, G F, Rivolta, L, Valdrè, G, Rodorigo, C, Biasoli, M, D'Incà, M L, Serino, S, Macchi, D, Vincenzi, M, Arbasi, P, Pedrazzi, M, Volta, C, DI Perna, L, Ippolito, M, Savi, T M, Neri
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(5)
Haemophilia A (HA) is an X-linked recessive bleeding disorder caused by a lack or decrease of coagulation factor VIII activity. The molecular diagnosis of HA is challenging and a variety of different mutations have been identified throughout the F8 g
Autor:
Gianna Franca Rivolta, T. M. Neri, C. Pattacini, Mario Franchini, Annarita Tagliaferri, Federica Riccardi
Publikováno v:
Journal of Thrombosis and Haemostasis. 7:1234-1235
Publikováno v:
Leukemia. 8(6)
T-cell receptor TCR-beta gene expression is an early event during human ontogenesis since the majority of thymocytes express cytoplasmic beta chain as early as the 15th week of gestation, when a complete VDJ rearrangement and functional 1.3-kb beta g
Autor:
J. Stekrova, J. Reiterova, V. Elisakova, M. Merta, M. Kohoutova, V. Tesar, S. Suvakov, T. Damjanovic, N. Dimkovic, S. Pljesa, A. Savic-Radojevic, M. Pljesa-Ercegovac, M. Matic, T. Djukic, V. Coric, T. Simic, M. Gigante, M. d'Altilia, E. Montemurno, A. Schirinzi, F. Bruno, G. S. Netti, E. Ranieri, G. Stallone, B. Infante, G. Grandaliano, L. Gesualdo, F. Maritati, F. Alberici, F. Bonatti, E. Oliva, R. A. Sinico, G. Moroni, A. Leoni, G. Gregorini, G. Jeannin, S. Possenti, B. Tumiati, C. Grasselli, R. Brugnano, C. Salvarani, P. Fraticelli, L. Pavone, A. Pesci, G. Guida, T. M. Neri, C. Buzio, G. Malerba, D. Martorana, A. Vaglio, L. Santucci, G. Candiano, D. Cremasco, E. Tosetto, D. Del Prete, M. Bruschi, G. M. Ghiggeri, F. Anglani, F. Rainone, L. Soldati, A. Terranegra, T. Arcidiacono, A. Aloia, E. Dogliotti, G. Vezzoli, I. Maruniak-Chudek, M. Zenker, J. Chudek, L. Obeidova, P. Lnenicka, L. V. Iwanitskiy, T. N. Krasnova, L. M. Samokhodskaya, A. R. Bernasconi, L. Albarracin, A. A. Liste, J. M. Politei, R. M. Heguilen, H. Kaito, K. Nozu, K. Nakanishi, Y. Hashimura, Y. Shima, T. Ninchoji, N. Yoshikawa, K. Iijima, M. Matsuo, E. Hur, O. Gungor, D. Bozkurt, S. M. K. Bozgul, H. Caliskan, F. Dusunur, A. Basci, F. Akcicek, S. Duman, Y. Li, C. Wang, L. Nan, Z. Hruskova, I. Brabcova, V. Lanska, E. Honsova, V. Hanzal, V. Borovicka, R. Rysava, R. Zachoval, O. Viklicky, G. Miltenberger-Miltenyi, E. Almeida, J. Calado, F. Carvalho, S. Pereira, C. Teixeira, S. Jorge, H. Viana, A. Gomes da Costa, C.-S. Yang, M.-H. Tseng, S.-S. Yang, S.-H. Lin
Publikováno v:
Clinical Kidney Journal. 4:4.s2.28-4.s2.28
Publikováno v:
Blood. 79(6)
T-cell receptor (TCR) beta-chain proteins appear early (approximately 15th week of gestation) during human thymic ontogenesis. These beta-chain proteins, which appear before terminal deoxynucleotidyl transferase (TdT), could be an expression of a ful
Chromosome abnormalities in infertile males are not infrequent, ranging from 4% to about 1% for sex and autosomal chromosomes respectively. Autosomal abnormalities mainly consist of balanced translocations, mostly robertsonian. The Authors report a c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ed9f13416e3f84ebe5409d622388e6c3
http://hdl.handle.net/11379/35149
http://hdl.handle.net/11379/35149
Comparison of human and porcine insulin therapies in children with newly diagnosed diabetes mellitus
Publikováno v:
Diabetologia. 30:912-915
A multicenter, longitudinal study of children below the age of 16 years with newly diagnosed Type 1 (insulin-dependent) diabetes treated either with porcine monocomponent insulin (n = 26) or semisynthetic human monocomponent insulin (n = 26) was perf
Autor:
M. Savi, D. Adorno, E. Gandini, J. Martorell, S. Barocci, G. B. Ferrara, M. C. Mazzilli, A. Amoroso, T. M. Neri, A. Longo, J. Vives
Publikováno v:
Histocompatibility Testing 1984 ISBN: 9783642697722
At the 6th Workshop Aw33 was recognized as a single antigen in spite of some evidence for the existence of two specificities: the first Fe55 is present in Caucasian populations in linkage disequilibrium with B14; the second is present in the Malay po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99499ef51c245205c92f8bf16d0d4beb
https://doi.org/10.1007/978-3-642-69770-8_27
https://doi.org/10.1007/978-3-642-69770-8_27
Publikováno v:
Minerva nefrologica. 26(4)