Maria Celeste Bastos Cabrita de Sousa Lechner
AuthID: R-000-AQ4
11
TITLE: The correlation of genotype and phenotype in Portuguese hyperphenylalaninemic patients Full Text
AUTHORS: Rivera, I ; Cabral, A; Almeida, M; Leandro, P ; Carmona, C; Eusebio, F; Tasso, T; Vilarinho, L; Martins, E ; Lechner, MC; de Almeida, IT ; Konecki, DS; Lichter Konecki, U;
PUBLISHED: 2000, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 69, ISSUE: 3
AUTHORS: Rivera, I ; Cabral, A; Almeida, M; Leandro, P ; Carmona, C; Eusebio, F; Tasso, T; Vilarinho, L; Martins, E ; Lechner, MC; de Almeida, IT ; Konecki, DS; Lichter Konecki, U;
PUBLISHED: 2000, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 69, ISSUE: 3
12
TITLE: The V388M mutation results in a kinetic variant form of phenylalanine hydroxylase Full Text
AUTHORS: Leandro, P ; Rivera, I ; Lechner, MC; de Almeida, IT ; Konecki, D;
PUBLISHED: 2000, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 69, ISSUE: 3
AUTHORS: Leandro, P ; Rivera, I ; Lechner, MC; de Almeida, IT ; Konecki, D;
PUBLISHED: 2000, SOURCE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 69, ISSUE: 3
13
TITLE: Cerebral hemorrhage and apoE Full Text
AUTHORS: Garcia, C; Melo, TP; Rocha, L; Lechner, MC;
PUBLISHED: 1999, SOURCE: JOURNAL OF NEUROLOGY, VOLUME: 246, ISSUE: 9
AUTHORS: Garcia, C; Melo, TP; Rocha, L; Lechner, MC;
PUBLISHED: 1999, SOURCE: JOURNAL OF NEUROLOGY, VOLUME: 246, ISSUE: 9
14
TITLE: N-acetyltransferase (NAT2) genotype and susceptibility to sporadic Alzheimer's disease
AUTHORS: Rocha, L; Garcia, C; de Mendonca, A ; Gil, JP ; Bishop, DT; Lechner, MC;
PUBLISHED: 1999, SOURCE: PHARMACOGENETICS, VOLUME: 9, ISSUE: 1
AUTHORS: Rocha, L; Garcia, C; de Mendonca, A ; Gil, JP ; Bishop, DT; Lechner, MC;
PUBLISHED: 1999, SOURCE: PHARMACOGENETICS, VOLUME: 9, ISSUE: 1
INDEXED IN: Scopus WOS
15
TITLE: Absence of stimulation of poly(ADP-ribose) polymerase activity in patients predisposed to colon cancer
AUTHORS: Cristovao, L; Lechner, MC; Fidalgo, P; Leitao, CN; Mira, FC; Rueff, J ;
PUBLISHED: 1998, SOURCE: BRITISH JOURNAL OF CANCER, VOLUME: 77, ISSUE: 10
AUTHORS: Cristovao, L; Lechner, MC; Fidalgo, P; Leitao, CN; Mira, FC; Rueff, J ;
PUBLISHED: 1998, SOURCE: BRITISH JOURNAL OF CANCER, VOLUME: 77, ISSUE: 10
INDEXED IN: Scopus WOS
16
TITLE: Population genetics of hyperphenylalaninaemia resulting from phenylalanine hydroxylase deficiency in Portugal
AUTHORS: Rivera, I ; Leandro, P ; Lichter Konecki, U; de Almeida, IT ; Lechner, MC;
PUBLISHED: 1998, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 35, ISSUE: 4
AUTHORS: Rivera, I ; Leandro, P ; Lichter Konecki, U; de Almeida, IT ; Lechner, MC;
PUBLISHED: 1998, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 35, ISSUE: 4
17
TITLE: Increased frequency of wild-type arylamine-N-acetyltransferase allele NAT2*4 homozygotes in Portuguese patients with colorectal cancer
AUTHORS: Gil, JP; Lechner, MC;
PUBLISHED: 1998, SOURCE: CARCINOGENESIS, VOLUME: 19, ISSUE: 1
AUTHORS: Gil, JP; Lechner, MC;
PUBLISHED: 1998, SOURCE: CARCINOGENESIS, VOLUME: 19, ISSUE: 1
18
TITLE: Identification of a Functional Glucocorticoid Response Element in the CYP3A1/IGC2 Gene
AUTHORS: TERESA M PEREIRA; JAN CARLSTEDT-DUKE; CELESTE C LECHNER; JAN-ÅKE GUSTAFSSON;
PUBLISHED: 1998, SOURCE: DNA and Cell Biology, VOLUME: 17, ISSUE: 1
AUTHORS: TERESA M PEREIRA; JAN CARLSTEDT-DUKE; CELESTE C LECHNER; JAN-ÅKE GUSTAFSSON;
PUBLISHED: 1998, SOURCE: DNA and Cell Biology, VOLUME: 17, ISSUE: 1
INDEXED IN: CrossRef
19
TITLE: Developmental changes in the constitutive and inducible expression of cytochrome P450 3A2 Full Text
AUTHORS: Wright, MC; Edwards, RJ; Pimenta, M; Ribeiro, V ; Ratra, GS; Lechner, MC; Paine, AJ;
PUBLISHED: 1997, SOURCE: BIOCHEMICAL PHARMACOLOGY, VOLUME: 54, ISSUE: 7
AUTHORS: Wright, MC; Edwards, RJ; Pimenta, M; Ribeiro, V ; Ratra, GS; Lechner, MC; Paine, AJ;
PUBLISHED: 1997, SOURCE: BIOCHEMICAL PHARMACOLOGY, VOLUME: 54, ISSUE: 7
20
TITLE: Allele frequency of CYP2C19 in a Portuguese population
AUTHORS: Ruas, JL; Lechner, MC;
PUBLISHED: 1997, SOURCE: PHARMACOGENETICS, VOLUME: 7, ISSUE: 4
AUTHORS: Ruas, JL; Lechner, MC;
PUBLISHED: 1997, SOURCE: PHARMACOGENETICS, VOLUME: 7, ISSUE: 4