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1
Electromagnetically induced transparency with tunable single-photon pulses
Electromagnetically induced transparency with tunable single-photon pulses
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Electromagnetically induced transparency with tunable single-photon pulses

Zibrov, A. S ; Massou, F ; Fleischhauer, M ; Lukin, M. D ; Eisaman, M. D ; André, A

Nature, 2005-12, Vol.438 (7069), p.837-841 [Periódico revisado por pares]

London: Nature Publishing

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2
Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain
Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain
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Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain

Iourov, Ivan Y. ; Vorsanova, Svetlana G. ; Liehr, Thomas ; Kolotii, Alexei D. ; Yurov, Yuri B.

Human molecular genetics, 2009-07, Vol.18 (14), p.2656-2669 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Mycobacterial Dissemination and Cellular Responses after 1-Lobe Restricted Tuberculosis Infection of Genetically Susceptible and Resistant Mice
Mycobacterial Dissemination and Cellular Responses after 1-Lobe Restricted Tuberculosis Infection of Genetically Susceptible and Resistant Mice
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Mycobacterial Dissemination and Cellular Responses after 1-Lobe Restricted Tuberculosis Infection of Genetically Susceptible and Resistant Mice

Mischenko, Vladimir V. ; Kapina, Marina A. ; Eruslanov, Evgenyi B. ; Kondratieva, Elena V. ; Lyadova, Irina V. ; Young, Douglas B. ; Apt, Alexander S.

The Journal of infectious diseases, 2004-12, Vol.190 (12), p.2137-2145 [Periódico revisado por pares]

Chicago, IL: The University of Chicago Press

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4
Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells
Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells
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Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells

Kolesnikova, Olga A. ; Entelis, Nina S. ; Jacquin-Becker, Clarisse ; Goltzene, Francine ; Chrzanowska-Lightowlers, Zofia M. ; Lightowlers, Robert N. ; Martin, Robert P. ; Tarassov, Ivan

Human molecular genetics, 2004-10, Vol.13 (20), p.2519-2534 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
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Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis

Johansson, Åsa ; Marroni, Fabio ; Hayward, Caroline ; Franklin, Christopher S. ; Kirichenko, Anatoly V. ; Jonasson, Inger ; Hicks, Andrew A. ; Vitart, Veronique ; Isaacs, Aaron ; Axenovich, Tatiana ; Campbell, Susan ; Dunlop, Malcolm G. ; Floyd, Jamie ; Hastie, Nick ; Hofman, Albert ; Knott, Sara ; Kolcic, Ivana ; Pichler, Irene ; Polasek, Ozren ; Rivadeneira, Fernando ; Tenesa, Albert ; Uitterlinden, André G. ; Wild, Sarah H. ; Zorkoltseva, Irina V. ; Meitinger, Thomas ; Wilson, James F. ; Rudan, Igor ; Campbell, Harry ; Pattaro, Cristian ; Pramstaller, Peter ; Oostra, Ben A. ; Wright, Alan F. ; van Duijn, Cornelia M. ; Aulchenko, Yurii S. ; Gyllensten, Ulf

Human molecular genetics, 2009-01, Vol.18 (2), p.373-380 [Periódico revisado por pares]

Oxford: Oxford University Press

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6
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma
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The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma

Han, Summer S ; Yeager, Meredith ; Moore, Lee E ; Wei, Ming-Hui ; Pfeiffer, Ruth ; Toure, Ousmane ; Purdue, Mark P ; Johansson, Mattias ; Scelo, Ghislaine ; Chung, Charles C ; Gaborieau, Valerie ; Zaridze, David ; Schwartz, Kendra ; Szeszenia-Dabrowska, Neonilia ; Davis, Faith ; Bencko, Vladimir ; Colt, Joanne S ; Janout, Vladimir ; Matveev, Vsevolod ; Foretova, Lenka ; Mates, Dana ; Navratilova, M ; Boffetta, Paolo ; Berg, Christine D ; Grubb, Robert L ; Stevens, Victoria L ; Thun, Michael J ; Diver, W. Ryan ; Gapstur, Susan M ; Albanes, Demetrius ; Weinstein, Stephanie J ; Virtamo, Jarmo ; Burdett, Laurie ; Brisuda, Antonin ; McKay, James D ; Fraumeni, Joseph F ; Chatterjee, Nilanjan ; Rosenberg, Philip S ; Rothman, Nathaniel ; Brennan, Paul ; Chow, Wong-Ho ; Tucker, Margaret A ; Chanock, Stephen J ; Toro, Jorge R

Human molecular genetics, 2012-03, Vol.21 (5), p.1190-1200 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
The Δccr5 Mutation Conferring Protection Against HIV-1 in Caucasian Populations Has a Single and Recent Origin in Northeastern Europe
The Δccr5 Mutation Conferring Protection Against HIV-1 in Caucasian Populations Has a Single and Recent Origin in Northeastern Europe
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The Δccr5 Mutation Conferring Protection Against HIV-1 in Caucasian Populations Has a Single and Recent Origin in Northeastern Europe

Libert, Frédérick ; Cochaux, Pascale ; Beckman, Gunhild ; Samson, Michel ; Aksenova, Marina ; Cao, Antonio ; Czeizel, Andrew ; Claustres, Mireille ; de la Rúa, Concepción ; Ferrari, Maurizio ; Ferrec, Claude ; Glover, Guillermo ; Grinde, Bjorn ; Güran, Sefik ; Kucinskas, Vaidutis ; Lavinha, Joao ; Mercier, Bernard ; Ogur, Gönül ; Peltonen, Leena ; Rosatelli, Cristina ; Schwartz, Marianne ; Spitsyn, Victor ; Timar, Laszlo ; Beckman, Lars ; Parmentier, Marc ; Vassart, Gilbert

Human molecular genetics, 1998-03, Vol.7 (3), p.399-406 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder
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Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder

Cichon, Sven ; Winge, Ingeborg ; Mattheisen, Manuel ; Georgi, Alexander ; Karpushova, Anna ; Freudenberg, Jan ; Freudenberg-Hua, Yun ; Babadjanova, Gulia ; Van Den Bogaert, Ann ; Abramova, Lilia I. ; Kapiletti, Sofia ; Knappskog, Per M. ; McKinney, Jeffrey ; Maier, Wolfgang ; Abou Jamra, Rami ; Schulze, Thomas G. ; Schumacher, Johannes ; Propping, Peter ; Rietschel, Marcella ; Haavik, Jan ; Nöthen, Markus M.

Human molecular genetics, 2008-01, Vol.17 (1), p.87-97 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation
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A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation

Estrada, Karol ; Krawczak, Michael ; Schreiber, Stefan ; van Duijn, Kate ; Stolk, Lisette ; van Meurs, Joyce B.J. ; Liu, Fan ; Penninx, Brenda W.J.H. ; Smit, Jan H. ; Vogelzangs, Nicole ; Hottenga, Jouke Jan ; Willemsen, Gonneke ; de Geus, Eco J.C. ; Lorentzon, Mattias ; von Eller-Eberstein, Huberta ; Lips, Paul ; Schoor, Natascha ; Pop, Victor ; de Keijzer, Jules ; Hofman, Albert ; Aulchenko, Yurii S. ; Oostra, Ben A. ; Ohlsson, Claes ; Boomsma, Dorret I. ; Uitterlinden, Andre G. ; van Duijn, Cornelia M. ; Rivadeneira, Fernando ; Kayser, Manfred

Human molecular genetics, 2009-09, Vol.18 (18), p.3516-3524 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
Transcript-Assisted Transcriptional Proofreading
Transcript-Assisted Transcriptional Proofreading
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Transcript-Assisted Transcriptional Proofreading

Zenkin, Nikolay ; Yuzenkova, Yulia ; Severinov, Konstantin

Science (American Association for the Advancement of Science), 2006-07, Vol.313 (5786), p.518-520 [Periódico revisado por pares]

Washington, DC: American Association for the Advancement of Science

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