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1
Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans
Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans
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Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans

Moore, Troy ; Shin-i, Tadasu ; Lee, Hongmei ; Doucette-Stamm, Lynn ; Jackson, Cindy ; Brasch, Michael A ; Temple, Gary F ; Vandenhaute, Jean ; Thierry-Mieg, Jean ; Reboul, Jérôme ; Thierry-Mieg, Nicolas ; Vaglio, Philippe ; Hartley, James L ; Hill, David E ; Hitti, Joseph ; Tzellas, Nia ; Vidal, Marc ; Kohara, Yuji ; Thierry-Mieg, Danielle ; Lamesch, Philippe E

Nature genetics, 2001-03, Vol.27 (3), p.332-336 [Periódico revisado por pares]

London: Nature Publishing Group

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2
The gene number dilemma: Direct evidence for at least 19,000 protein-encoding genes in C. elegans and implications for the human genome
The gene number dilemma: Direct evidence for at least 19,000 protein-encoding genes in C. elegans and implications for the human genome
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The gene number dilemma: Direct evidence for at least 19,000 protein-encoding genes in C. elegans and implications for the human genome

Reboul, J. ; Vaglio, P. ; Tzellas, N. ; Jackson, C. ; Moore, T. ; Kohara, Y. ; Thierry-Mieg, J. ; Thierry-Mieg, D. ; Hitti, J. ; Doucette-Stamm, L. ; Hartley, J. ; Temple, G. ; Brasch, M. ; Hill, D.E. ; Vidal, M.

Nature genetics, 2001-04, Vol.27 (S4), p.82-82 [Periódico revisado por pares]

New York: Nature Publishing Group

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3
The gene number dilemma: direct evidence for at least 19,000 protein-encoding genes in Caenorhabditis elegans and implications for the human genome
The gene number dilemma: direct evidence for at least 19,000 protein-encoding genes in Caenorhabditis elegans and implications for the human genome
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The gene number dilemma: direct evidence for at least 19,000 protein-encoding genes in Caenorhabditis elegans and implications for the human genome

Hill, David E. ; Reboul, J. ; Vaglio, P. ; Tzellas, N. ; Jackson, C. ; Moore, T. ; Kohara, Y. ; Thierry-Mieg, J. ; Thierry-Mieg, D. ; Hitti, J. ; Doucette-Stamm, L. ; Hartley, J. ; Temple, G. ; Brasch, M. ; Hill, D.E. ; Vidal, M.

Nature genetics, 2001-04, Vol.27 (S4), p.93-93 [Periódico revisado por pares]

New York: Nature Publishing Group

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4
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57
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Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57

Mackay, Deborah J G ; Callaway, Jonathan L A ; Marks, Sophie M ; White, Helen E ; Acerini, Carlo L ; Boonen, Susanne E ; Dayanikli, Pinar ; Firth, Helen V ; Goodship, Judith A ; Haemers, Andreas P ; Hahnemann, Johanne M D ; Kordonouri, Olga ; Masoud, Ahmed F ; Oestergaard, Elsebet ; Storr, John ; Ellard, Sian ; Hattersley, Andrew T ; Robinson, David O ; Temple, I Karen

Nature genetics, 2008-08, Vol.40 (8), p.949-951 [Periódico revisado por pares]

London: Nature Publishing Group

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5
Comparative analysis of the genome sequences of Bordetella pertussis , Bordetella parapertussis and Bordetella bronchiseptica
Comparative analysis of the genome sequences of Bordetella pertussis , Bordetella parapertussis and Bordetella bronchiseptica
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Comparative analysis of the genome sequences of Bordetella pertussis , Bordetella parapertussis and Bordetella bronchiseptica

Parkhill, Julian ; Maskell, Duncan J ; Sebaihia, Mohammed ; Preston, Andrew ; Murphy, Lee D ; Thomson, Nicholas ; Harris, David E ; Holden, Matthew T G ; Churcher, Carol M ; Bentley, Stephen D ; Mungall, Karen L ; Cerdeño-Tárraga, Ana M ; Temple, Louise ; James, Keith ; Harris, Barbara ; Quail, Michael A ; Achtman, Mark ; Atkin, Rebecca ; Baker, Steven ; Basham, David ; Bason, Nathalie ; Cherevach, Inna ; Chillingworth, Tracey ; Collins, Matthew ; Cronin, Anne ; Davis, Paul ; Doggett, Jonathan ; Feltwell, Theresa ; Goble, Arlette ; Hamlin, Nancy ; Hauser, Heidi ; Holroyd, Simon ; Jagels, Kay ; Leather, Sampsa ; Moule, Sharon ; Norberczak, Halina ; O'Neil, Susan ; Ormond, Doug ; Price, Claire ; Rabbinowitsch, Ester ; Rutter, Simon ; Sanders, Mandy ; Saunders, David ; Seeger, Katherine ; Sharp, Sarah ; Simmonds, Mark ; Skelton, Jason ; Squares, Robert ; Squares, Steven ; Stevens, Kim ; Unwin, Louise ; Whitehead, Sally ; Barrell, Bart G

Nature genetics, 2003-09, Vol.35 (1), p.32-40 [Periódico revisado por pares]

London: Nature Publishing Group

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6
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence
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Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequence

Vazquez, Marie-Paule ; Fantes, Judy A ; Vekemans, Michel ; Holder-Espinasse, Muriel ; Gordon, Christopher T ; Kilpatrick, Nicky ; Perry, Paul ; Heaney, Simon ; Thomas, Sophie ; Ayuso, Carmen ; Ramsay, Jacqueline ; Lees, Melissa M ; Crollius, Hugues Roest ; Farlie, Peter G ; Abadie, Véronique ; Temple, I Karen ; Lyonnet, Stanislas ; Amiel, Jeanne ; Fisher, Malcolm ; Thomas, Paul ; Kleinjan, Dirk-Jan ; Etchevers, Heather C ; Benko, Sabina ; Jamshidi, Negar ; Munnich, Arnold ; Pelet, Anna ; Essafi, Abdelkader ; McBride, David ; FitzPatrick, David R ; Golzio, Christelle ; Picard, Arnaud ; Hastie, Nicholas D

Nature genetics, 2009-03, Vol.41 (3), p.359-364 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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7
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene
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X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene

MacFarlane, John ; Stevenson, Roger ; Paterson, Joan ; Temple, Karen ; Ionasescu, Victor ; Kenwrick, Susan ; Armstrong, Giles ; Jouet, Monique ; Metzenberg, Aïda ; Rosenthal, André

Nature genetics, 1994-07, Vol.7 (3), p.402-407 [Periódico revisado por pares]

London: Nature Publishing Group

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