Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nardo, Tiziana"'
Autor:
Perucca P; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy., Mocchi R; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy., Guardamagna I; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy., Bassi E; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy., Sommatis S; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy., Nardo T; Istituto di Genetica Molecolare (IGM) del CNR, Pavia, Italy., Prosperi E; Istituto di Genetica Molecolare (IGM) del CNR, Pavia, Italy. Electronic address: prosperi@igm.cnr.it., Stivala LA; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy. Electronic address: luciaanna.stivala@unipv.it., Cazzalini O; Dipartimento di Medicina Molecolare, Unità di Immunologia e Patologia generale, Università degli Studi di Pavia, Pavia, Italy. Electronic address: ornella.cazzalini@unipv.it.
Publikováno v:
Biochimica et biophysica acta. Molecular cell research [Biochim Biophys Acta Mol Cell Res] 2018 Jun; Vol. 1865 (6), pp. 898-907. Date of Electronic Publication: 2018 Mar 28.
Autor:
Corbett MA; Neurogenetics Research Program, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia., Dudding-Byth T; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia University of Newcastle, Newcastle, Australia., Crock PA; Department of Paediatric Endocrinology and Diabetes, John Hunter Children's Hospital, University of Newcastle, Newcastle, Australia., Botta E; Istituto di Genetica Molecolare CNR, Pavia, Italy., Christie LM; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia., Nardo T; Istituto di Genetica Molecolare CNR, Pavia, Italy., Caligiuri G; Istituto di Genetica Molecolare CNR, Pavia, Italy., Hobson L; Molecular Genetics, Department of Genetic Medicine, SA Pathology at Women's and Children's Hospital, North Adelaide, Australia., Boyle J; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia., Mansour A; The Children's Hospital at Westmead, Westmead, Australia., Friend KL; Molecular Genetics, Department of Genetic Medicine, SA Pathology at Women's and Children's Hospital, North Adelaide, Australia., Crawford J; Neurogenetics Research Program, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia., Jackson G; Brain Research Institute, Florey Neurosciences Institutes, West Heidelberg, Australia., Vandeleur L; Neurogenetics Research Program, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia., Hackett A; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia., Tarpey P; The Wellcome Trust Sanger Institute, Hinxton, UK., Stratton MR; The Wellcome Trust Sanger Institute, Hinxton, UK., Turner G; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia., Gécz J; Neurogenetics Research Program, School of Paediatrics and Reproductive Health, University of Adelaide, Adelaide, Australia School of Molecular and Biomedical Science, The University of Adelaide, Adelaide, Australia Robinson Research Institute, The University of Adelaide, Adelaide, Australia., Field M; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Australia.
Publikováno v:
Journal of medical genetics [J Med Genet] 2015 Apr; Vol. 52 (4), pp. 269-74. Date of Electronic Publication: 2015 Jan 22.
Autor:
Kashiyama K; Department of Plastic and Reconstructive Surgery, Graduate School of Biomedical Sciences, Nagasaki University, 1-7-1 Sakamoto, Nagasaki 852-8501, Japan., Nakazawa Y, Pilz DT, Guo C, Shimada M, Sasaki K, Fawcett H, Wing JF, Lewin SO, Carr L, Li TS, Yoshiura K, Utani A, Hirano A, Yamashita S, Greenblatt D, Nardo T, Stefanini M, McGibbon D, Sarkany R, Fassihi H, Takahashi Y, Nagayama Y, Mitsutake N, Lehmann AR, Ogi T
Publikováno v:
American journal of human genetics [Am J Hum Genet] 2013 May 02; Vol. 92 (5), pp. 807-19. Date of Electronic Publication: 2013 Apr 25.
Autor:
Soltys DT; Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, São Paulo, SP, Brazil., Rocha CR, Lerner LK, de Souza TA, Munford V, Cabral F, Nardo T, Stefanini M, Sarasin A, Cabral-Neto JB, Menck CF
Publikováno v:
Human mutation [Hum Mutat] 2013 Mar; Vol. 34 (3), pp. 481-9. Date of Electronic Publication: 2013 Jan 17.
Autor:
Tillhon M; Istituto di Genetica Molecolare (IGM) del CNR, Pavia, Italy., Cazzalini O, Nardo T, Necchi D, Sommatis S, Stivala LA, Scovassi AI, Prosperi E
Publikováno v:
DNA repair [DNA Repair (Amst)] 2012 Oct 01; Vol. 11 (10), pp. 844-52. Date of Electronic Publication: 2012 Sep 03.
Autor:
Rapić-Otrin V; Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA., Navazza V, Nardo T, Botta E, McLenigan M, Bisi DC, Levine AS, Stefanini M
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2003 Jul 01; Vol. 12 (13), pp. 1507-22.