Pesquisas alternativas:
davies cara » davies sara (Expandir a Pesquisa), davies cary (Expandir a Pesquisa), davis cara (Expandir a Pesquisa)
c2 causes » ca2 causes (Expandir a Pesquisa), cd2 causes (Expandir a Pesquisa), co2 causes (Expandir a Pesquisa)
causes de » causales de (Expandir a Pesquisa), causes dna (Expandir a Pesquisa), causantes de (Expandir a Pesquisa)
nacl cacl » nacl kcl (Expandir a Pesquisa)
a davies » g davies (Expandir a Pesquisa), a davis (Expandir a Pesquisa), m davies (Expandir a Pesquisa)
cara can » carat can (Expandir a Pesquisa), cara con (Expandir a Pesquisa), cara ca (Expandir a Pesquisa)
cacl can » call can (Expandir a Pesquisa), cacl2 dan (Expandir a Pesquisa), al can (Expandir a Pesquisa)
can now » can non (Expandir a Pesquisa), can new (Expandir a Pesquisa), can ngoc (Expandir a Pesquisa)
3 nacl » _ nacl (Expandir a Pesquisa), m nacl (Expandir a Pesquisa), 3.5 nacl (Expandir a Pesquisa)
l c2 » l c (Expandir a Pesquisa), l cv (Expandir a Pesquisa), _ c2 (Expandir a Pesquisa)
davies cara » davies sara (Expandir a Pesquisa), davies cary (Expandir a Pesquisa), davis cara (Expandir a Pesquisa)
c2 causes » ca2 causes (Expandir a Pesquisa), cd2 causes (Expandir a Pesquisa), co2 causes (Expandir a Pesquisa)
causes de » causales de (Expandir a Pesquisa), causes dna (Expandir a Pesquisa), causantes de (Expandir a Pesquisa)
nacl cacl » nacl kcl (Expandir a Pesquisa)
a davies » g davies (Expandir a Pesquisa), a davis (Expandir a Pesquisa), m davies (Expandir a Pesquisa)
cara can » carat can (Expandir a Pesquisa), cara con (Expandir a Pesquisa), cara ca (Expandir a Pesquisa)
cacl can » call can (Expandir a Pesquisa), cacl2 dan (Expandir a Pesquisa), al can (Expandir a Pesquisa)
can now » can non (Expandir a Pesquisa), can new (Expandir a Pesquisa), can ngoc (Expandir a Pesquisa)
3 nacl » _ nacl (Expandir a Pesquisa), m nacl (Expandir a Pesquisa), 3.5 nacl (Expandir a Pesquisa)
l c2 » l c (Expandir a Pesquisa), l cv (Expandir a Pesquisa), _ c2 (Expandir a Pesquisa)
81
Por Colvin, L, Fyfe, S, Leonard, S, Schiavello, T, Ellaway, C, de Klerk, N, Christodoulou, J, Msall, M, Leonard, H
Publicado em 2003
“...Background: Mutations in the MECP2 gene have been recently identified as the cause of Rett syndrome...”Publicado em 2003
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82
“.... Hospital mortality rates for elective resections were 13% in 1955-1965, 8.4% in 1966-1973, and 4.2...”
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83
Por Subiza, J L, Rodriguez, C, Figueredo, A, Mateos, P, Alvarez, R, de la Concha, E G
Publicado em 1988
“... in HMMø raised from less than 2 +/- 1 u/ml to 19 +/- 12 u/ml and was similar to that found in stimulated...”Publicado em 1988
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84
Por Borirak, Orawan, de Koning, Leo J, van der Woude, Aniek D, Hoefsloot, Huub C J, Dekker, Henk L, Roseboom, Winfried, de Koster, Chris G, Hellingwerf, Klaas J
Publicado no Biotechnol Biofuels (2015)
“... in the initial stages of CO(2) fixation for cellular metabolism was detected. Also a general decrease...”Publicado no Biotechnol Biofuels (2015)
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85
Por Gerards, M, Sluiter, W, van den Bosch, B J C, de Wit, L E A, Calis, C M H, Frentzen, M, Akbari, H, Schoonderwoerd, K, Scholte, H R, Jongbloed, R J, Hendrickx, A T M, de Coo, I F M, Smeets, H J M
Publicado em 2009
“... (p.L159F) in C20orf7, a new complex I assembly factor. Parents were heterozygous and unaffected sibs...”Publicado em 2009
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86
Por Motes, M. L., DePaola, A., Cook, D. W., Veazey, J. E., Hunsucker, J. C., Garthright, W. E., Blodgett, R. J., Chirtel, S. J.
Publicado em 1998
“... of V. vulnificus: a consistently large number (median concentration, 2,300 organisms [most probable...”Publicado em 1998
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87
Por Foulkes, W. D., Thiffault, I., Gruber, S. B., Horwitz, M., Hamel, N., Lee, C., Shia, J., Markowitz, A., Figer, A., Friedman, E., Farber, D., Greenwood, C. M. T., Bonner, J. D., Nafa, K., Walsh, T., Marcus, V., Tomsho, L., Gebert, J., Macrae, F. A., Gaff, C. L., Paillerets, B. Bressac-de, Gregersen, P. K., Weitzel, J. N., Gordon, P. H., MacNamara, E., King, M.-C., Hampel, H., de la Chapelle, A., Boyd, J., Offit, K., Rennert, G., Chong, G., Ellis, N. A.
Publicado em 2002
“... in the Ashkenazi Jewish population. We identified a nucleotide substitution, MSH2*1906G→C, which results in a...”Publicado em 2002
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88
Por Beysen, D., Raes, J., Leroy, B. P., Lucassen, A., Yates, J. R. W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J. P., Kim, J. R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L. M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R. A., De Paepe, A., De Baere, E.
Publicado em 2005
“... upstream of FOXL2 in patients with BPES suggested a position effect. Here, we identified novel...”Publicado em 2005
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89
Por Elfring, L K, Daniel, C, Papoulas, O, Deuring, R, Sarte, M, Moseley, S, Beek, S J, Waldrip, W R, Daubresse, G, DePace, A, Kennison, J A, Tamkun, J W
Publicado em 1998
“... and causes defects in the peripheral nervous system of the adult. A dominant-negative brm mutation...”Publicado em 1998
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90
Por PESSATTI M. L., RESGALLA JR. C., REIS Fo. R. W., KUEHN J., SALOMÃO L. C., FONTANA J. D.
Publicado em 2002-01-01
“... filtration rates (1.04 and 2.3 and L.h-1.g-1; p < 0.05) and lower assimilation rates (71.96% and 54.1...”Publicado em 2002-01-01
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91
“...-CoA were equal, indicating that H2O2 production is a reliable index for the release of acetyl units...”
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92
Por Oud, M S, Okutman, Ö, Hendricks, L A J, de Vries, P F, Houston, B J, Vissers, L E L M, O’Bryan, M K, Ramos, L, Chemes, H E, Viville, S, Veltman, J A
Publicado no Hum Reprod (2020)
“...STUDY QUESTION: Can exome sequencing identify new genetic causes of globozoospermia? SUMMARY ANSWER...”Publicado no Hum Reprod (2020)
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93
Por Talley, Jennell M., DeZwaan, Diane C., Maness, Leslie D., Freeman, Brian C., Friedman, Katherine L.
Publicado em 2011
“... of Est3p disrupt this interaction with Est2p, reduce assembly of Est3p with telomerase in vivo, and cause...”Publicado em 2011
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94
Por De Schepper, H U, De Winter, B Y, Van Nassauw, L, Timmermans, J-P, Herman, A G, Pelckmans, P A, De Man, J G
Publicado em 2008
“... staining of TRPV1 and NF200, a marker for A-fibre neurons, was performed in the dorsal root ganglia L6–S1...”Publicado em 2008
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95
Por de Kok, I M C M, Polder, J J, Habbema, J D F, Berkers, L-M, Meerding, W J, Rebolj, M, van Ballegooijen, M
Publicado em 2009
“..., nursing homes, and mortality data for 2.1 million inhabitants in the Netherlands in 1998–1999. Costs...”Publicado em 2009
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96
Por Hermans, M. P. J., Eindhoven, D. C., van Winden, L. A. M., de Grooth, G. J., Blauw, G. J., Muller, M., Schalij, M. J.
Publicado no Neth Heart J (2019)
“...OBJECTIVE: Consistent with the aging population in the Western world, there is a growing number...”Publicado no Neth Heart J (2019)
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97
Por Blikkendaal, M. D., Twijnstra, A. R. H., Pacquee, S. C. L., Rhemrev, J. P. T., Smeets, M. J. G. H., de Kroon, C. D., Jansen, F. W.
Publicado em 2012
“... (3.3 %) after laparoscopic interrupted suturing and four (2.4 %) after a laparoscopic running suture...”Publicado em 2012
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98
Por Marthey, L., Mateus, C., Mussini, C., Nachury, M., Nancey, S., Grange, F., Zallot, C., Peyrin-Biroulet, L., Rahier, J. F., Bourdier de Beauregard, M., Mortier, L., Coutzac, C., Soularue, E., Lanoy, E., Kapel, N., Planchard, D., Chaput, N., Robert, C., Carbonnel, F.
Publicado no J Crohns Colitis (2016)
“...) antibodies are associated with immune-mediated enterocolitis. The aim of this study was to provide a detailed...”Publicado no J Crohns Colitis (2016)
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99
“...PURPOSE: Femoral osteochondritis dissecans (OCD) is a disorder of unknown aetiology and variable...”
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100
Por Antoniou, A.C., Casadei, S., Heikkinen, T., Barrowdale, D., Pylkäs, K., Roberts, J., Lee, A., Subramanian, D., De Leeneer, K., Fostira, F., Tomiak, E., Neuhausen, S.L., Teo, Z.L., Khan, S., Aittomäki, K., Moilanen, J.S., Turnbull, C., Seal, S., Mannermaa, A., Kallioniemi, A., Lindeman, G.J., Buys, S.S., Andrulis, I.L., Radice, P., Tondini, C., Manoukian, S., Toland, A.E., Miron, P., Weitzel, J.N., Domchek, S.M., Poppe, B., Claes, K.B.M., Yannoukakos, D., Concannon, P., Bernstein, J.L., James, P.A., Easton, D.F., Goldgar, D.E., Hopper, J.L., Rahman, N., Peterlongo, P., Nevanlinna, H., King, M.-C., Couch, F.J., Southey, M.C., Winqvist, R., Foulkes, W.D., Tischkowitz, M.
Publicado em 2014
“...BACKGROUND: Germline loss-of-function mutations in PALB2 are known to confer a predisposition...”Publicado em 2014
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Artigo