skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Base de dados/Biblioteca: HighWire Press (Free Journals) remover assunto: Molecular And Cellular Biology remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
A pilot open label, single dose trial of fenobam in adults with fragile X syndrome
A pilot open label, single dose trial of fenobam in adults with fragile X syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome

Berry-Kravis, E ; Hessl, D ; Coffey, S ; Hervey, C ; Schneider, A ; Yuhas, J ; Hutchison, J ; Snape, M ; Tranfaglia, M ; Nguyen, D V ; Hagerman, R

Journal of medical genetics, 2009-04, Vol.46 (4), p.266-271 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

Texto completo disponível

Citações Citado por
2
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder

Dempster, Emma L ; Pidsley, Ruth ; Schalkwyk, Leonard C ; Owens, Sheena ; Georgiades, Anna ; Kane, Fergus ; Kalidindi, Sridevi ; Picchioni, Marco ; Kravariti, Eugenia ; Toulopoulou, Timothea ; Murray, Robin M ; Mill, Jonathan

Human molecular genetics, 2011-12, Vol.20 (24), p.4786-4796 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
3
The genetics of panic disorder
The genetics of panic disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

The genetics of panic disorder

Schumacher, Johannes ; Kristensen, Ann Suhl ; Wendland, Jens R ; Nöthen, Markus M ; Mors, Ole ; McMahon, Francis J

Journal of Medical Genetics, 2011-06, Vol.48 (6), p.361-368 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

Texto completo disponível

Citações Citado por
4
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

Kirov, George ; Grozeva, Detelina ; Norton, Nadine ; Ivanov, Dobril ; Mantripragada, Kiran K. ; Holmans, Peter ; Craddock, Nick ; Owen, Michael J. ; O'Donovan, Michael C.

Human molecular genetics, 2009-04, Vol.18 (8), p.1497-1503 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
5
Altered serotonin receptor expression is associated with depression-related behavior in the R6/1 transgenic mouse model of Huntington's disease
Altered serotonin receptor expression is associated with depression-related behavior in the R6/1 transgenic mouse model of Huntington's disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Altered serotonin receptor expression is associated with depression-related behavior in the R6/1 transgenic mouse model of Huntington's disease

Pang, Terence Y.C. ; Du, Xin ; Zajac, Michelle S. ; Howard, Monique L. ; Hannan, Anthony J.

Human molecular genetics, 2009-02, Vol.18 (4), p.753-766 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
6
Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing
Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing
Material Type:
Artigo 		Adicionar ao Meu Espaço

Direct contact in inviting high-risk members of hereditary colon cancer families to genetic counselling and DNA testing

Aktan-Collan, K ; Haukkala, A ; Pylvänäinen, K ; Järvinen, H J ; Aaltonen, L A ; Peltomäki, P ; Rantanen, E ; Kääriäinen, H ; Mecklin, J-P

Journal of medical genetics, 2007-11, Vol.44 (11), p.732-738 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

Texto completo disponível

Citações Citado por
7
Recurrent 16p11.2 microdeletions in autism
Recurrent 16p11.2 microdeletions in autism
Material Type:
Artigo 		Adicionar ao Meu Espaço

Recurrent 16p11.2 microdeletions in autism

Kumar, Ravinesh A. ; KaraMohamed, Samer ; Sudi, Jyotsna ; Conrad, Donald F. ; Brune, Camille ; Badner, Judith A. ; Gilliam, T. Conrad ; Nowak, Norma J. ; Cook, Edwin H. ; Dobyns, William B. ; Christian, Susan L.

Human molecular genetics, 2008-02, Vol.17 (4), p.628-638 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
8
Disruption of the neurexin 1 gene is associated with schizophrenia
Disruption of the neurexin 1 gene is associated with schizophrenia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Disruption of the neurexin 1 gene is associated with schizophrenia

Rujescu, Dan ; Ingason, Andres ; Cichon, Sven ; Pietiläinen, Olli P.H. ; Barnes, Michael R. ; Toulopoulou, Timothea ; Picchioni, Marco ; Vassos, Evangelos ; Ettinger, Ulrich ; Bramon, Elvira ; Murray, Robin ; Ruggeri, Mirella ; Tosato, Sarah ; Bonetto, Chiara ; Steinberg, Stacy ; Sigurdsson, Engilbert ; Sigmundsson, Thordur ; Petursson, Hannes ; Gylfason, Arnaldur ; Olason, Pall I. ; Hardarsson, Gudmundur ; Jonsdottir, Gudrun A. ; Gustafsson, Omar ; Fossdal, Ragnheidur ; Giegling, Ina ; Möller, Hans-Jürgen ; Hartmann, Annette M. ; Hoffmann, Per ; Crombie, Caroline ; Fraser, Gillian ; Walker, Nicholas ; Lonnqvist, Jouko ; Suvisaari, Jaana ; Tuulio-Henriksson, Annamari ; Djurovic, Srdjan ; Melle, Ingrid ; Andreassen, Ole A. ; Hansen, Thomas ; Werge, Thomas ; Kiemeney, Lambertus A. ; Franke, Barbara ; Veltman, Joris ; Buizer-Voskamp, Jacobine E. ; Sabatti, Chiara ; Ophoff, Roel A. ; Rietschel, Marcella ; Nöthen, Markus M. ; Stefansson, Kari ; Peltonen, Leena ; St Clair, David ; Stefansson, Hreinn ; Collier, David A.

Human molecular genetics, 2009-03, Vol.18 (5), p.988-996 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
9
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression
Material Type:
Artigo 		Adicionar ao Meu Espaço

Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression

Daoud, Fatma ; Angeard, Nathalie ; Demerre, Bénédicte ; Martie, Itxaso ; Benyaou, Rabah ; Leturcq, France ; Cossée, Mireille ; Deburgrave, Nathalie ; Saillour, Yoann ; Tuffery, Sylvie ; Urtizberea, Andoni ; Toutain, Annick ; Echenne, Bernard ; Frischman, Martine ; Mayer, Michèle ; Desguerre, Isabelle ; Estournet, Brigitte ; Réveillère, Christian ; Penisson-Besnier ; Cuisset, Jean Marie ; Kaplan, Jean Claude ; Héron, Delphine ; Rivier, François ; Chelly, Jamel

Human molecular genetics, 2009-10, Vol.18 (20), p.3779-3794 [Periódico revisado por pares]

Oxford: Oxford University Press

Texto completo disponível

Citações Citado por
10
Transposable Elements, Epigenetics, and Genome Evolution
Transposable Elements, Epigenetics, and Genome Evolution
Material Type:
Artigo 		Adicionar ao Meu Espaço

Transposable Elements, Epigenetics, and Genome Evolution

Fedoroff, Nina V.

Science (American Association for the Advancement of Science), 2012-11, Vol.338 (6108), p.758-767 [Periódico revisado por pares]

Washington, DC: American Association for the Advancement of Science

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (65.678)
  2. Revistas revisadas por pares (66.840)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (66.913)
  2. Anais de Congresso  (77)
  3. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1987  (10.150)
  2. 1987Até1992  (29.166)
  3. 1993Até1998  (13.864)
  4. 1999Até2005  (7.510)
  5. Após 2005  (6.301)
  6. Mais opções open sub menu

Idioma 

  1. Japonês  (17.007)
  2. Latim  (9)
  3. Catalão  (1)
  4. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.