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Results for
""Chromosomes, Human, Pair 14""[mesh_terms]

15 Results

Searching titles within these results

Guideline recommendations for diagnosis and clinical management of Ring14 syndrome-first report of an ad hoc task force.

Berardo Rinaldi, Alessandro Vaisfeld, Sergio Amarri, Chiara Baldo, Giuseppe Gobbi, Pamela Magini, Erto Melli, Giovanni Neri, Francesca Novara, Tommaso Pippucci, Romana Rizzi, Annarosa Soresina, Laura Zampini, Orsetta Zuffardi, Marco Crimi

Orphanet journal of rare diseases 2018;12(1):69

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Epilepsy in ring 14 chromosome syndrome.

Nicola Specchio, Marina Trivisano, Domenico Serino, Simona Cappelletti, Antonio Carotenuto, Dianela Claps, Carlo Efisio Marras, Lucia Fusco, Maurizio Elia, Federico Vigevano

Epilepsy & behavior : E&B 2013;25(4):585-92

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Genetic determinants of the humoral immune response in MS.

Christiane Gasperi, Till F M Andlauer, Ana Keating, Benjamin Knier, Ana Klein, Verena Pernpeintner, Peter Lichtner, Ralf Gold, Frauke Zipp, Florian Then Bergh, Martin Stangel, Hayrettin Tumani, Brigitte Wildemann, Heinz Wiendl, Antonios Bayas, Tania Kümpfel, Uwe K Zettl, Ralf A Linker, Ulf Ziemann, Matthias Knop, Clemens Warnke, Manuel A Friese, Friedemann Paul, Björn Tackenberg, Achim Berthele, Bernhard Hemmer

Neurology(R) neuroimmunology & neuroinflammation 2021;7(5):e827

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Determinants of the t(14;18) translocation and their role in t(14;18)-positive follicular lymphoma.

Rachel S Kelly, Sandrine Roulland, Ester Morgado, Stéphanie Sungalee, Nathalie Jouve, Rosario Tumino, Vittorio Krogh, Salvatore Panico, Silvia Polidoro, Giovanna Masala, María-José Sánchez, Maria-Dolores Chirlaque, Núria Sala, Aurelio Barricarte Gurrea, Miren Dorronsoro, Ruth C Travis, Elio Riboli, Marc Gunter, Neil Murphy, Roel Vermeulen, H B Bueno-de-Mesquita, Petra H Peeters, Antonia Trichopoulou, Dimitrios Trichopoulos, Pagona Lagiou, Alexandra Nieters, Federico Canzian, Rudolf Kaaks, Heiner Boeing, Elisabete Weiderpass, Tanja Stocks, Beatrice Melin, Kim Overvad, Anne Tjønneland, Anja Olsen, Paul Brennan, Mattias Johansson, Bertrand Nadel, Paolo Vineis

Cancer causes & control : CCC 2016;26(12):1845-55

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The t(9;14)(p13;q32) translocation in B-cell non-Hodgkin's lymphoma.

H Ohno, C Ueda, T Akasaka

Leukemia & lymphoma 2000;36(5-6):435-45

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Autosomal dominant dystonia-plus with cerebral calcifications.

Z K Wszolek, Y Baba, I R Mackenzie, R J Uitti, A J Strongosky, D F Broderick, M C Baker, S Melquist, M L Hutton, Y Tsuboi, J E Allanson, J Carr, A Kumar, S M Calne, J Miklossy, P L McGeer, D B Calne, A J Stoessl

Neurology 2006;67(4):620-5

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Formation of a G-quadruplex at the BCL2 major breakpoint region of the t(14;18) translocation in follicular lymphoma.

Mridula Nambiar, G Goldsmith, Balaji T Moorthy, Michael R Lieber, Mamata V Joshi, Bibha Choudhary, Ramakrishna V Hosur, Sathees C Raghavan

Nucleic acids research 2011;39(3):936-48

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Telomerase activity, apoptosis and cell cycle progression in ataxia telangiectasia lymphocytes expressing TCL1.

C Gabellini, A Antonelli, P Petrinelli, A Biroccio, L Marcucci, G Nigro, G Russo, G Zupi, R Elli

British journal of cancer 2003;89(6):1091-5

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Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.

Dieter Kotzot

Annales de genetique 2004;47(3):251-60

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Frequency of bcl-2/IgH translocation in patients with non-Hodgkin's lymphoma and chronic hepatitis C virus infection.

M Libra, V De Re, A Gloghini, D Callari, G Malaponte, S Travali, M C Mazzarino, F Stivala, M Boiocchi, A Carbone

Minerva gastroenterologica e dietologica 2005;51(2):165-70

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Niemann-Pick disease type C.

M T Vanier, G Millat

Clinical genetics 2004;64(4):269-81

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Epigenetic silencing of genes and microRNAs within the imprinted Dlk1-Dio3 region at human chromosome 14.32 in giant cell tumor of bone.

Burkhard Lehner, Pierre Kunz, Heiner Saehr, Joerg Fellenberg

BMC cancer 2015;14():495

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Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.

Anath C Lionel, Andrea K Vaags, Daisuke Sato, Matthew J Gazzellone, Elyse B Mitchell, Hong Yang Chen, Gregory Costain, Susan Walker, Gerald Egger, Bhooma Thiruvahindrapuram, Daniele Merico, Aparna Prasad, Evdokia Anagnostou, Eric Fombonne, Lonnie Zwaigenbaum, Wendy Roberts, Peter Szatmari, Bridget A Fernandez, Lyudmila Georgieva, Linda M Brzustowicz, Katharina Roetzer, Wolfgang Kaschnitz, John B Vincent, Christian Windpassinger, Christian R Marshall, Rosario R Trifiletti, Salman Kirmani, George Kirov, Erwin Petek, Jennelle C Hodge, Anne S Bassett, Stephen W Scherer

Human molecular genetics 2013;22(10):2055-66

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Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: results from a multicenter study in Italy.

Valentina Silvestri, Piera Rizzolo, Marco Scarnò, Giovanni Chillemi, Anna Sara Navazio, Virginia Valentini, Veronica Zelli, Ines Zanna, Calogero Saieva, Giovanna Masala, Simonetta Bianchi, Siranoush Manoukian, Monica Barile, Valeria Pensotti, Paolo Peterlongo, Liliana Varesco, Stefania Tommasi, Antonio Russo, Giuseppe Giannini, Laura Cortesi, Alessandra Viel, Marco Montagna, Paolo Radice, Domenico Palli, Laura Ottini

European journal of cancer (Oxford, England : 1990) 2016;51(16):2289-95

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Candidate genes for nonsyndromic cleft lip and palate.

A R Vieira, I M Orioli

ASDC journal of dentistry for children 2002;68(4):272-9, 229

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Results: 1 – 15 / 15

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Results for ""Chromosomes, Human, Pair 14""[mesh_terms]

Guideline recommendations for diagnosis and clinical management of Ring14 syndrome-first report of an ad hoc task force.

Epilepsy in ring 14 chromosome syndrome.

Genetic determinants of the humoral immune response in MS.

Determinants of the t(14;18) translocation and their role in t(14;18)-positive follicular lymphoma.

The t(9;14)(p13;q32) translocation in B-cell non-Hodgkin's lymphoma.

Autosomal dominant dystonia-plus with cerebral calcifications.

Formation of a G-quadruplex at the BCL2 major breakpoint region of the t(14;18) translocation in follicular lymphoma.

Telomerase activity, apoptosis and cell cycle progression in ataxia telangiectasia lymphocytes expressing TCL1.

Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting.

Frequency of bcl-2/IgH translocation in patients with non-Hodgkin's lymphoma and chronic hepatitis C virus infection.

Niemann-Pick disease type C.

Epigenetic silencing of genes and microRNAs within the imprinted Dlk1-Dio3 region at human chromosome 14.32 in giant cell tumor of bone.

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.

Novel and known genetic variants for male breast cancer risk at 8q24.21, 9p21.3, 11q13.3 and 14q24.1: results from a multicenter study in Italy.

Candidate genes for nonsyndromic cleft lip and palate.

Results for
""Chromosomes, Human, Pair 14""[mesh_terms]