Does Bacterial Elasticity Affect Adhesion to Polymer Fibers?
Tamayo, Laura, Melo, Francisco, Caballero, Leonardo, Hamm, Eugenio, Díaz, M, Leal, M. S, Guiliani, N, Urzúa, M. D
Published in ACS applied materials & interfaces (25.03.2020)
Published in ACS applied materials & interfaces (25.03.2020)
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Journal Article
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)
Ferguson, P J, Chen, S, Tayeh, M K, Ochoa, L, Leal, S M, Pelet, A, Munnich, A, Lyonnet, S, Majeed, H A, El-Shanti, H
Published in Journal of medical genetics (01.07.2005)
Published in Journal of medical genetics (01.07.2005)
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Long term measurements of aerosol optical properties at a primary forest site in Amazonia
Rizzo, L. V, Artaxo, P, Müller, T, Wiedensohler, A, Paixão, M, Cirino, G. G, Arana, A, Swietlicki, E, Roldin, P, Fors, E. O, Wiedemann, K. T, Leal, L. S. M, Kulmala, M
Published in Atmospheric chemistry and physics (01.03.2013)
Published in Atmospheric chemistry and physics (01.03.2013)
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Amino Acid-Functionalized Polyelectrolyte Films as Bioactive Surfaces for Cell Adhesion
Leal, M. S, Briones, X, Villalobos, V, Queneau, Y, Leiva, A, Ríos, H. E, Pavez, J, Silva, C. P, Carrasco, C, Neira-Carrillo, Andrónico, Roth, A. D, Tamayo, L, Urzúa, M. D
Published in ACS applied materials & interfaces (05.06.2019)
Published in ACS applied materials & interfaces (05.06.2019)
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Journal Article
Carcass, meat quality traits, and economic analysis of Nellore bulls fed with finishing feedlot diets containing mechanically processed corn silage
Costa, C., Baldassini, W. A., Leal, M. S., Meirelles, P. R. L., Castilhos, A. M., Nascimento Júnior, N. G., Silveira, J. P. F., Pariz, C. M., Roça, R. O., Factori, M. A., Silva, M. G. B.
Published in Tropical animal health and production (01.04.2023)
Published in Tropical animal health and production (01.04.2023)
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Hydraulic traits explain differential responses of Amazonian forests to the 2015 El Niño-induced drought
de V. Barros, Fernanda, Bittencourt, Paulo R. L., Brum, Mauro, Restrepo-Coupe, Natalia, Pereira, Luciano, Teodoro, Grazielle S., Saleska, Scott R., Borma, Laura S., Christoffersen, Bradley O., Penha, Deliane, Alves, Luciana F., Lima, Adriano J. N., Carneiro, Vilany M. C., Gentine, Pierre, Lee, Jung-Eun, Aragão, Luiz E. O. C., Ivanov, Valeriy, Leal, Leila S. M., Araujo, Alessandro C., Oliveira, Rafael S.
Published in The New phytologist (01.08.2019)
Published in The New phytologist (01.08.2019)
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Mutations in the γ-Actin Gene ( ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26)
Zhu, M., Yang, T., Wei, S., DeWan, A.T., Morell, R.J., Elfenbein, J.L., Fisher, R.A., Leal, S.M., Smith, R. J.H., Friderici, K.H.
Published in American journal of human genetics (01.11.2003)
Published in American journal of human genetics (01.11.2003)
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Journal Article
microsatellite-based, gene-rich linkage map for the AA genome of Arachis (Fabaceae)
Moretzsohn, M.C, Leoi, L, Proite, K, Guimaraes, P.M, Leal-Bertioli, S.C.M, Gimenes, M.A, Martins, W.S, Valls, J.F.M, Grattapaglia, D, Bertioli, D.J
Published in Theoretical and applied genetics (01.10.2005)
Published in Theoretical and applied genetics (01.10.2005)
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Journal Article
A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
Naeem, M, Wajid, M, Lee, K, Leal, S M, Ahmad, W
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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Journal Article
Pathogenic FBN1 variants in familial thoracic aortic aneurysms and dissections
Regalado, E.S., Guo, D.C., Santos-Cortez, R.L.P., Hostetler, E., Bensend, T.A., Pannu, H., Estrera, A., Safi, H., Mitchell, A.L., Evans, J.P., Leal, S.M., Bamshad, M., Shendure, J., Nickerson, D.A., Milewicz, D.M.
Published in Clinical genetics (01.06.2016)
Published in Clinical genetics (01.06.2016)
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Journal Article
Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene
Varga, R, Kelley, P M, Keats, B J, Starr, A, Leal, S M, Cohn, E, Kimberling, W J
Published in Journal of medical genetics (01.01.2003)
Published in Journal of medical genetics (01.01.2003)
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Journal Article
Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment
Lee, K, Khan, S, Islam, A, Ansar, M, Andrade, P B, Kim, S, Santos-Cortez, R L P, Ahmad, W, Leal, S M
Published in Clinical genetics (01.07.2012)
Published in Clinical genetics (01.07.2012)
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Journal Article
Guidelines for investigating causality of sequence variants in human disease
MacArthur, D. G., Manolio, T. A., Dimmock, D. P., Rehm, H. L., Shendure, J., Abecasis, G. R., Adams, D. R., Altman, R. B., Antonarakis, S. E., Ashley, E. A., Barrett, J. C., Biesecker, L. G., Conrad, D. F., Cooper, G. M., Cox, N. J., Daly, M. J., Gerstein, M. B., Goldstein, D. B., Hirschhorn, J. N., Leal, S. M., Pennacchio, L. A., Stamatoyannopoulos, J. A., Sunyaev, S. R., Valle, D., Voight, B. F., Winckler, W., Gunter, C.
Published in Nature (London) (24.04.2014)
Published in Nature (London) (24.04.2014)
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A novel g.-1258G>A mutation in a conserved putative regulatory element of PAX9 is associated with autosomal dominant molar hypodontia
Mendoza-Fandino, GA, Gee, JM, Ben-Dor, S, Gonzalez-Quevedo, C, Lee, K, Kobayashi, Y, Hartiala, J, Myers, RM, Leal, SM, Allayee, H, Patel, PI
Published in Clinical genetics (01.09.2011)
Published in Clinical genetics (01.09.2011)
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Journal Article
Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families
Lee, K, Chiu, I, Santos-Cortez, RLP, Basit, S, Khan, S, Azeem, Z, Andrade, PB, Kim, SS, Ahmad, W, Leal, SM
Published in Clinical genetics (01.09.2013)
Published in Clinical genetics (01.09.2013)
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Journal Article
Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment
Santos, RLP, Wajid, M, Pham, TL, Hussan, J, Ali, G, Ahmad, W, Leal, SM
Published in Clinical genetics (01.01.2005)
Published in Clinical genetics (01.01.2005)
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Analytical performance and potential clinical utility of the GenMark Dx ePlex® blood culture identification gram-positive panel
McCarty, T.P., White, C.M., Meeder, J., Moates, D., Pierce, H.M., Edwards, W.S., Hutchinson, J., Lee, R.A., Leal, S.M.
Published in Diagnostic microbiology and infectious disease (01.11.2022)
Published in Diagnostic microbiology and infectious disease (01.11.2022)
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