نتائج البحث - "Barbosa I.A."

العلاقة: https://eprints.whiterose.ac.uk/191428/1/e202101284.full.pdfTest; Nolden, K.A., Egner, J.M., Collier, J.J. et al. (21 more authors) (2022) Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms. Life Science Alliance, 5 (12). ARTN e202101284.

الإتاحة: https://eprints.whiterose.ac.uk/191428Test/
https://eprints.whiterose.ac.uk/191428/1/e202101284.full.pdfTest

View record in BASE

4

Influ??ncia da tra????o nas caracter??sticas da fibra de carbono, de uso geral, produzida a partir de PAN t??xtil

المؤلفون: BELINELI BARBOSA, I.A., BERNARDI, H.H., BLANCO, G.C., SALES, R.C., BALDAN, M.R., MARCUZZO, J.S., CONGRESSO BRASILEIRO DE ENGENHARIA E CI??NCIA DOS MATERIAIS, 24.

العلاقة: http://repositorio.ipen.br/handle/123456789/33750Test

الإتاحة: http://repositorio.ipen.br/handle/123456789/33750Test

View record in BASE

5

دورية أكاديمية

Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onset

المؤلفون: Billingsley, K.J., Barbosa, I.A., Bandres-Ciga, S., Quinn, J.P., Bubb, V.J., Deshpande, C., Botia, J.A., Reynolds, R.H., Zhang, D., Simpson, M.A., Blauwendraat, C., Gan-Or, Z., Gibbs, J.R., Nalls, M.A., Singleton, A., Ryten, M., Koks, S., Noyce, A., Tucci, A., Middlehurst, B., Kia, D., Tan, M., Houlden, H., Morris, H.R., Plun-Favreau, H., Holmans, P., Hardy, J., Trabzuni, D., Bras, J., Mok, K., Kinghorn, K., Wood, N., Lewis, P., Guerreiro, R., Loverin, R., R'Bibo, L., Rizig, M., Escott-Price, V., Chelban, V., Foltynie, T., Williams, N., Brice, A., Danjou, F., Lesage, S., Martinez, M., Giri, A., Schulte, C., Brockmann, K., Simon-Sanchez, J., Heutink, P., Rizzu, P., Sharma, M., Gasser, T., Nicolas, A., Cookson, M., Faghri, F., Hernandez, D., Shulman, J., Robak, L., Lubbe, S., Finkbeiner, S., Mencacci, N., Lungu, C., Scholz, S., Reed, X., Leonard, H., Rouleau, G., Krohan, L., Hilten, J. van, Marinus, J., Adarmes-Gomez, A., Aguilar, M., Alvarez, I., Alvarez, V., Barrero, F.J., Yarza, J.B., Bernal-Bernal, I., Blazquez, M., Bernal, M.B.T., Boungiorne, M., Buiza-Rueda, D., Camara, A., Carcel, M., Carrillo, F., Carrion-Claro, M., Cerdan, D., Clarimon, J., Compta, Y., Diez-Fairen, M., Dols-Icardo, O., Duarte, J., Duran, R.I., Escamilla-Sevilla, F., Ezquerra, M., Fernandez, M., Fernandez-Santiago, R., Garcia, C., Garcia-Ruiz, P., Gomez-Garre, P., Heredia, M.G., Gonzalez-Aramburu, I., Pagola, A.G., Hoenicka, J., Infante, J., Jesus, S., Jimenez-Escrig, A., Kulisevsky, J., Labrador-Espinosa, M., Lopez-Sendon, J., Arregui, A.L.D., Macias, D., Torres, I.M., Marin, J., Marti, M.J., Martinez-Castrillo, J., Mendez-del-Barrio, C., Gonzalez, M.M., Minguez, A., Mir, P., Rezola, E.M., Munoz, E., Pagonabarraga, J., Pastor, P., Errazquin, F.P., Perinan-Tocino, T., Ruiz-Martinez, J., Ruz, C., Rodriguez, A.S., Sierra, M., Suarez-Sanmartin, E., Tabernero, C., Tartari, J.P., Tejera-Parrado, C., Tolosa, E., Valldeoriola, F., Vargas-Gonzalez, L., Vela, L., Vives, F., Zimprich, A., Pihlstrom, L., Taba, P., Majamaa, K., Siitonen, A., Okubadejo, N., Ojo, O., IPDGC

المصدر: npj Parkinson's Disease

العلاقة: lumc-id: 111401154; https://hdl.handle.net/1887/3195223Test

الإتاحة: https://doi.org/10.1038/s41531-019-0080-xTest
https://hdl.handle.net/1887/3195223Test

View record in BASE

6

Mitochondria function associated genes contribute to Parkinson’s Disease risk and later age at onset

المؤلفون: Billingsley K.J., Barbosa I.A., Bandrés-Ciga S., Quinn J.P., Bubb V.J., Deshpande C., Botia J.A., Reynolds R.H., Zhang D., Simpson M.A., Blauwendraat C., Gan-Or Z., Gibbs J.R., Nalls M.A., Singleton A., Noyce A., Tucci A., Middlehurst B., Kia D., Tan M., Houlden H., Morris H.R., Plun-Favreau H., Holmans P., Hardy J., Trabzuni D., Bras J., Mok K., Kinghorn K., Wood N., Lewis P., Guerreiro R., Lovering R., R’Bibo L., Rizig M., Escott-Price V., Chelban V., Foltynie T., Williams N., Brice A., Danjou F., Lesage S., Martinez M., Giri A., Schulte C., Brockmann K., Simón-Sánchez J., Heutink P., Rizzu P., Sharma M., Gasser T., Nicolas A., Cookson M., Faghri F., Hernandez D., Shulman J., Robak L., Lubbe S., Finkbeiner S., Mencacci N., Lungu C., Scholz S., Reed X., Leonard H., Rouleau G., Krohan L., van Hilten J., Marinus J., Adarmes-Gómez A., Aguilar M., Alvarez I., Alvarez V., Javier Barrero F., Bergareche Yarza J., Bernal-Bernal I., Blazquez M., Bernal M.B.-T., Boungiorno M., Buiza-Rueda D., Cámara A., Carcel M., Carrillo F., Carrión-Claro M., Cerdan D., Clarimón J., Compta Y., Diez-Fairen M., Dols-Icardo O., Duarte J., Duran R., Escamilla-Sevilla F., Ezquerra M., Fernández M., Fernández-Santiago R., Garcia C., García-Ruiz P., Gómez-Garre P., Heredia M.G., Gonzalez-Aramburu I., Pagola A.G., Hoenicka J., Infante J., Jesús S., Jimenez-Escrig A., Kulisevsky J., Labrador-Espinosa M., Lopez-Sendon J., de Munain Arregui A.L., Macias D., Torres I.M., Marín J., Marti M.J., Martínez-Castrillo J., Méndez-del-Barrio C., Menéndez González M., Mínguez A., Mir P., Rezola E.M., Muñoz E., Pagonabarraga J., Pastor P., Errazquin F.P., Periñán-Tocino T., Ruiz-Martínez J., Ruz C., Rodriguez A.S., Sierra M., Suarez-Sanmartin E., Tabernero C., Tartari J.P., Tejera-Parrado C., Tolosa E., Valldeoriola F., Vargas-González L., Vela L., Vives F., Zimprich A., Pihlstrom L., Taba P., Majamaa K., Siitonen A., Okubadejo N., Ojo O., Ryten M., Koks S.

المصدر: npj Parkinsons Disease
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::9375763f2b9ae8b0fc7b9fdef2856c1fTest
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10173Test

7

دورية أكاديمية

Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk

المؤلفون: Billingsley, K.J., Barbosa, I.A., Bandrés-Ciga, S., Quinn, J.P., Bubb, V.J., Deshpande, C., Botia, J.A., Reynolds, R.H., Simpson, M.A., Blauwendraat, C., Gan-Or, Z., Gibbs, J.R., Nalls, M.A., Singleton, A., Ryten, M., Kõks, S.

المصدر: Billingsley, K.J., Barbosa, I.A., Bandrés-Ciga, S., Quinn, J.P., Bubb, V.J., Deshpande, C., Botia, J.A., Reynolds, R.H., Simpson, M.A., Blauwendraat, C., Gan-Or, Z., Gibbs, J.R., Nalls, M.A., Singleton, A., Ryten, M. and Kõks, S. (2018) Genetic variation within genes associated with mitochondrial function is significantly associated with later age at onset of Parkinson disease and contributes to disease risk. bioRxiv .

العلاقة: https://researchrepository.murdoch.edu.au/id/eprint/51018Test/; full_text_status:public

الإتاحة: https://researchrepository.murdoch.edu.au/id/eprint/51018Test/

View record in BASE

8

دورية أكاديمية

Senescence-associated reprogramming promotes cancer stemness

مصطلحات موضوعية: Cancer Research, Technology Platforms

وصف الملف: application/pdf; other

العلاقة: http://edoc.mdc-berlin.de/16986/3/16986oa.pdfTest; http://edoc.mdc-berlin.de/16986/2/16986suppl.zipTest; Senescence-associated reprogramming promotes cancer stemness. Milanovic, M. and Fan, D.N.Y. and Belenki, D. and Däbritz, J.H.M. and Zhao, Z. and Yu, Y. and Dörr, J.R. and Dimitrova, L. and Lenze, D. and Monteiro Barbosa, I.A. and Mendoza-Parra, M.A. and Kanashova, T. and Metzner, M. and Pardon, K. and Reimann, M. and Trumpp, A. and Dörken, B. and Zuber, J. and Gronemeyer, H. and Hummel, M. and Dittmar, G. and Lee, S. and Schmitt, C.A. Nature 553 (7686): 96-100. 4 January 2018

الإتاحة: https://doi.org/10.1038/nature25167Test
http://edoc.mdc-berlin.de/16986Test/
https://edoc.mdc-berlin.de/16986Test/
http://edoc.mdc-berlin.de/16986/3/16986oa.pdfTest
http://edoc.mdc-berlin.de/16986/2/16986suppl.zipTest

View record in BASE

9

دورية أكاديمية

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits.

المؤلفون: Glasgow, R.I.C., Thompson, K., Barbosa, I.A., He, L., Alston, C.L., Deshpande, C., Simpson, M.A., Morris, A.A.M., Neu, A., Löbel, U., Hall, J., Prokisch, H., Haack, T.B., Hempel, M., McFarland, R., Taylor, R.W.

المصدر: Neurogenetics 18, 1-9 (2017)

مصطلحات موضوعية: Developmental Delay, Gfm2, Mitochondrial Disease, Mitochondrial Translation, Wes

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29075935; info:eu-repo/semantics/altIdentifier/wos/WOS:000416416000006; info:eu-repo/semantics/altIdentifier/isbn/1364-6745; info:eu-repo/semantics/; https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52264Test; urn:isbn:1364-6745; urn:issn:1364-6745; urn:issn:1364-6753

الإتاحة: https://doi.org/10.1007/s10048-017-0526-4Test
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=52264Test

View record in BASE

10

دورية أكاديمية

Novel GFM2 variants identified in two cases of early-onset mitochondrial disease cause impaired expression of mtDNA encoded OXPHOS subunits

المؤلفون: Glasgow, R.I.C., Thompson, K., He, L., Alston, C.L., Barbosa, I.A., Deshpande, C., Simpson, M.A., Neu, A., Löbel, U., Prokisch, H., Haack, T.B., Hempel, M., McFarland, R., Taylor, R.W.

المصدر: Neuromuscular Disorders ; volume 27, page S22 ; ISSN 0960-8966

مصطلحات موضوعية: Genetics (clinical), Neurology (clinical), Neurology, Pediatrics, Perinatology and Child Health

الإتاحة: https://doi.org/10.1016/s0960-8966Test(17)30283-3
https://api.elsevier.com/content/article/PII:S0960896617302833?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0960896617302833?httpAccept=text/plainTest

View record in BASE

تنقيح النتائج