skip to main content
Idioma:
Resultados 1 2 3 4 5 next page
Mostrar Somente
Result Number Material Type Add to My Shelf Action Record Details and Options
1
The Exometabolome of Xylella fastidiosa in contact with Paraburkholderia phytofirmans supernatant reveals changes in nicotinamide, amino acids, biotin, and plant hormones
The Exometabolome of Xylella fastidiosa in contact with Paraburkholderia phytofirmans supernatant reveals changes in nicotinamide, amino acids, biotin, and plant hormones
Material Type:
Artigo 		Adicionar ao Meu Espaço

The Exometabolome of Xylella fastidiosa in contact with Paraburkholderia phytofirmans supernatant reveals changes in nicotinamide, amino acids, biotin, and plant hormones

Oséias Rodrigues Feitosa Junior Andrea Lubbe; Suzanne M Kosina; Joaquim Martins Junior; Deibs Barbosa; Clelia Baccari; Paulo Adriano Zaini; Benjamin P Bowen; Trent R Northen; Steven E Lindow; Aline Maria Da Silva

Metabolites Basel v. 14, p. 1-26 art. 82, 2024

Basel 2024

Item não circula. Consulte sua biblioteca.(Acessar)

2
Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk
Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk
Material Type:
Artigo 		Adicionar ao Meu Espaço

Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk

Lubbe, Steven J ; Bustos, Bernabe I ; Hu, Jing ; Krainc, Dimitri ; Joseph, Theresita ; Hehir, Jason ; Tan, Manuela ; Zhang, Weijia ; Escott-Price, Valentina ; Williams, Nigel M ; Blauwendraat, Cornelis ; Singleton, Andrew B ; Morris, Huw R

Human molecular genetics, 2021-03, Vol.30 (1), p.78-86 [Periódico revisado por pares]

England: Oxford University Press

Texto completo disponível

Citações Citado por
3
Mid51/Fis1 mitochondrial oligomerization complex drives lysosomal untethering and network dynamics
Mid51/Fis1 mitochondrial oligomerization complex drives lysosomal untethering and network dynamics
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mid51/Fis1 mitochondrial oligomerization complex drives lysosomal untethering and network dynamics

Wong, Yvette C ; Kim, Soojin ; Cisneros, Jasmine ; Molakal, Catherine G ; Song, Pingping ; Lubbe, Steven J ; Krainc, Dimitri

The Journal of cell biology, 2022-10, Vol.221 (10), p.1 [Periódico revisado por pares]

United States: Rockefeller University Press

Texto completo disponível

Citações Citado por
4
Recessive mutations in >VPS13D cause childhood onset movement disorders
Recessive mutations in >VPS13D cause childhood onset movement disorders
Material Type:
Artigo 		Adicionar ao Meu Espaço

Recessive mutations in >VPS13D cause childhood onset movement disorders

Gauthier, Julie ; Meijer, Inge A. ; Lessel, Davor ; Mencacci, Niccolò E. ; Krainc, Dimitri ; Hempel, Maja ; Tsiakas, Konstantinos ; Prokisch, Holger ; Rossignol, Elsa ; Helm, Margaret H. ; Rodan, Lance H. ; Karamchandani, Jason ; Carecchio, Miryam ; Lubbe, Steven J. ; Telegrafi, Aida ; Henderson, Lindsay B. ; Lorenzo, Kerry ; Wallace, Stephanie E. ; Glass, Ian A. ; Hamdan, Fadi F. ; Michaud, Jacques L. ; Rouleau, Guy A. ; Campeau, Philippe M.

Annals of neurology, 2018-06, Vol.83 (6), p.1089-1095 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

Texto completo disponível

Citações Citado por
5
Nuclear aggregates of NONO/SFPQ and A-to-I-edited RNA in Parkinson’s disease and dementia with Lewy bodies
Nuclear aggregates of NONO/SFPQ and A-to-I-edited RNA in Parkinson’s disease and dementia with Lewy bodies
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nuclear aggregates of NONO/SFPQ and A-to-I-edited RNA in Parkinson’s disease and dementia with Lewy bodies

Belur, Nandkishore R. ; Bustos, Bernabe I. ; Lubbe, Steven J. ; Mazzulli, Joseph R.

Neuron (Cambridge, Mass.), 2024-08, Vol.112 (15), p.2558-2580.e13 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
6
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single‐center cohort study
Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single‐center cohort study
Material Type:
Artigo 		Adicionar ao Meu Espaço

Frequency and phenotypic spectrum of KMT2B dystonia in childhood: A single‐center cohort study

Carecchio, Miryam ; Invernizzi, Federica ; Gonzàlez‐Latapi, Paulina ; Panteghini, Celeste ; Zorzi, Giovanna ; Romito, Luigi ; Leuzzi, Vincenzo ; Galosi, Serena ; Reale, Chiara ; Zibordi, Federica ; Joseph, Agnel P. ; Topf, Maya ; Piano, Carla ; Bentivoglio, Anna Rita ; Girotti, Floriano ; Morana, Paolo ; Morana, Benedetto ; Kurian, Manju A. ; Garavaglia, Barbara ; Mencacci, Niccolò E. ; Lubbe, Steven J. ; Nardocci, Nardo

Movement disorders, 2019-10, Vol.34 (10), p.1516-1527 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

Texto completo disponível

Citações Citado por
7
Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation
Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical Implications of the Colorectal Cancer Risk Associated With MUTYH Mutation

LUBBE, Steven J ; CHIARA DI BERNARDO, Maria ; CHANDLER, Ian P ; HOULSTON, Richard S

Journal of clinical oncology, 2009-08, Vol.27 (24), p.3975-3980 [Periódico revisado por pares]

Alexandria, VA: American Society of Clinical Oncology

Texto completo disponível

Citações Citado por
8
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk

Bustos, Bernabe I ; Billingsley, Kimberley ; Blauwendraat, Cornelis ; Gibbs, J Raphael ; Gan-Or, Ziv ; Krainc, Dimitri ; Singleton, Andrew B ; Lubbe, Steven J

Brain (London, England : 1878), 2023-01, Vol.146 (1), p.65-74 [Periódico revisado por pares]

England: Oxford University Press

Texto completo disponível

Citações Citado por
9
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets
Material Type:
Artigo 		Adicionar ao Meu Espaço

Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets

Kia, Demis A ; Zhang, David ; Guelfi, Sebastian ; Manzoni, Claudia ; Hubbard, Leon ; Reynolds, Regina H ; Botía, Juan ; Ryten, Mina ; Ferrari, Raffaele ; Lewis, Patrick A ; Williams, Nigel ; Trabzuni, Daniah ; Hardy, John ; Wood, Nicholas W

Archives of neurology (Chicago), 2021-04, Vol.78 (4), p.464-472 [Periódico revisado por pares]

United States: American Medical Association

Texto completo disponível

Citações Citado por
10
Melanin and Neuromelanin: Linking Skin Pigmentation and Parkinson's Disease
Melanin and Neuromelanin: Linking Skin Pigmentation and Parkinson's Disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Melanin and Neuromelanin: Linking Skin Pigmentation and Parkinson's Disease

Krainc, Talia ; Monje, Mariana H.G. ; Kinsinger, Morgan ; Bustos, Bernabe I. ; Lubbe, Steven J.

Movement disorders, 2023-02, Vol.38 (2), p.185-195 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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 (150)
  2. Revistas revisadas por pares (138)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (163)
  2. Reports  (4)
  3. Conjunto de Dados  (3)
  4. Imagens  (1)
  5. Dissertações  (1)
  6. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de2008  (10)
  2. 2008Até2011  (31)
  3. 2012Até2015  (21)
  4. 2016Até2020  (50)
  5. Após 2020  (61)
  6. Mais opções open sub menu

Idioma 

  1. Inglês  (170)
  2. Japonês  (21)
  3. Holandês  (1)
  4. Francês  (1)
  5. Mais opções open sub menu

Novas Pesquisas Sugeridas

Ignorar minha busca e procurar por tudo

Deste Autor:

  1. Lindow, S
  2. Martins Junior, J
  3. Zaini, P
  4. Northen, T
  5. Lubbe, A

Neste Assunto:

  1. Science & Technology
  2. Humans
  3. Life Sciences & Biomedicine
  4. Neurosciences & Neurology
  5. Female

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

Buscando em bases de dados remotas. Favor aguardar.