41
TÍTULO: NO* Binds Human Cystathionine  -Synthase Quickly and Tightly
AUTORES: Vicente, JB; Colaco, HG; Mendes, MIS; Sarti, P; Leandro, P ; Giuffre, A;
PUBLICAÇÃO: 2014, FONTE: Journal of Biological Chemistry, VOLUME: 289, NÚMERO: 12
INDEXADO EM: CrossRef
42
TÍTULO: Phenylalanine iminoboronates as new phenylalanine hydroxylase modulators
AUTORES: Francesco Montalbano; Joao Leandro; Goncalo D V F Farias; Paulo R Lino; Rita C Guedes; Joao B Vicente; Paula Leandro ; Pedro M P Gois;
PUBLICAÇÃO: 2014, FONTE: RSC ADVANCES, VOLUME: 4, NÚMERO: 105
INDEXADO EM: Scopus WOS CrossRef
43
TÍTULO: Reduced response of Cystathionine Beta-Synthase (CBS) to S-Adenosylmethionine (SAM): Identification and functional analysis of CBS gene mutations in Homocystinuria patients  Full Text
AUTORES: Mendes, MIS; Colaco, HG; Smith, DEC; Ramos, RJJF; Pop, A; van Dooren, SJM; de Almeida, IT; Kluijtmans, LAJ; Janssen, MCH; Rivera, I ; Salomons, GS; Leandro, P ; Blom, HJ;
PUBLICAÇÃO: 2014, FONTE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 37, NÚMERO: 2
INDEXADO EM: Scopus WOS
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TÍTULO: A new approach on protein folding correction: rescue of arginine to cysteine mutations using thiol compounds  Full Text
AUTORES: Mendes, M; Smith, D; Colaco, H; Santos, S; Rivera, I; Ben Omran, T; Salomons, G; Blom, H; Leandro, P ;
PUBLICAÇÃO: 2013, FONTE: 38th Congress of the Federation-of-European-Biochemical-Societies (FEBS) in FEBS JOURNAL, VOLUME: 280
INDEXADO EM: WOS
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TÍTULO: High molecular weight forms of human phenylalanine hydroxylase: the role of the ACT domain in the balance between a fully functional protein and the large inactive aggregates  Full Text
AUTORES: Leandro, J; Amaro, MP; Lino, PR; Flatmark, T; Leandro, P ;
PUBLICAÇÃO: 2013, FONTE: 38th Congress of the Federation-of-European-Biochemical-Societies (FEBS) in FEBS JOURNAL, VOLUME: 280
INDEXADO EM: WOS
48
TÍTULO: Reduced response of Cystathionine Beta-Synthase (CBS) to S-Adenosylmethionine (SAM): Identification and functional analysis of CBS gene mutations in Homocystinuria patients  Full Text
AUTORES: Mendes, MIS; Colaco, HG; Smith, DEC; Ramos, RJJF; Pop, A; van Dooren, SJM; Tavares de Almeida, I; Kluijtmans, LAJ; Janssen, MCH; Rivera, I ; Salomons, GS; Leandro, P ; Blom, HJ;
PUBLICAÇÃO: 2013, FONTE: Journal of Inherited Metabolic Disease, VOLUME: 37, NÚMERO: 2
INDEXADO EM: Scopus CrossRef
49
TÍTULO: Retrospective study of the medium-chain acyl-CoA dehydrogenase deficiency in Portugal
AUTORES: Ventura, F; Leandro, P ; Luz, A; Rivera, I; Silva, M ; Ramos, R; Rocha, H; Lopes, A; Fonseca, H; Gaspar, A; Diogo, L; Martins, E; Leao Teles, E; Vilarinho, L; Tavares de Almeida, I;
PUBLICAÇÃO: 2013, FONTE: Clinical Genetics
INDEXADO EM: Scopus
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TÍTULO: Deciphering Protein Arginine Methylation in Mammals
AUTORES: Ruben Esse; Paula Leandro ; Isabel Rivera ; Isabel Tavares de Almeida; Henk J; Rita Castro;
PUBLICAÇÃO: 2012, FONTE: Methylation - From DNA, RNA and Histones to Diseases and Treatment
INDEXADO EM: CrossRef: 1 Openlibrary
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