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Results: 1-25 | 26-43
Results: 1-25/43
SIMULTANEOUS TRANSFER OF MITOCHONDRIAL-DNA AND SINGLE CHROMOSOMES IN SOMATIC-CELLS - A NOVEL-APPROACH FOR THE STUDY OF DEFECTS IN NUCLEAR-MITOCHONDRIAL COMMUNICATION
Authors: BARRIENTOS A MORAES CT
Citation: A. Barrientos et Ct. Moraes, SIMULTANEOUS TRANSFER OF MITOCHONDRIAL-DNA AND SINGLE CHROMOSOMES IN SOMATIC-CELLS - A NOVEL-APPROACH FOR THE STUDY OF DEFECTS IN NUCLEAR-MITOCHONDRIAL COMMUNICATION, Human molecular genetics (Print), 7(11), 1998, pp. 1801-1808
DUPLICATION AND TRIPLICATION WITH STAGGERED BREAKPOINTS IN HUMAN MITOCHONDRIAL-DNA
Authors: TENGAN CH MORAES CT
Citation: Ch. Tengan et Ct. Moraes, DUPLICATION AND TRIPLICATION WITH STAGGERED BREAKPOINTS IN HUMAN MITOCHONDRIAL-DNA, Biochimica et biophysica acta. Molecular basis of disease, 1406(1), 1998, pp. 73-80
STRUCTURE OF HEPARAN-SULFATE - IDENTIFICATION OF VARIABLE AND CONSTANT OLIGOSACCHARIDE DOMAINS IN 8 HEPARAN SULFATES OF DIFFERENT ORIGINS
Authors: DIETRICH CP TERSARIOL ILS TOMA L MORAES CT PORCIONATTO MA OLIVEIRA FW NADER HB
Citation: Cp. Dietrich et al., STRUCTURE OF HEPARAN-SULFATE - IDENTIFICATION OF VARIABLE AND CONSTANT OLIGOSACCHARIDE DOMAINS IN 8 HEPARAN SULFATES OF DIFFERENT ORIGINS, Cellular and molecular biology, 44(3), 1998, pp. 417-429
CYBRIDS IN ALZHEIMERS-DISEASE - A CELLULAR-MODEL OF THE DISEASE
Authors: SCHON EA SHOUBRIDGE EA MORAES CT
Citation: Ea. Schon et al., CYBRIDS IN ALZHEIMERS-DISEASE - A CELLULAR-MODEL OF THE DISEASE, Neurology, 51(1), 1998, pp. 326-326
CHRONIC INTESTINAL PSEUDOOBSTRUCTION AS A PRESENTING FEATURE IN MITOCHONDRIAL ENCEPHALOMYOPATHIES
Authors: VERMA A BERRY GT PICCOLI DA MORAES CT
Citation: A. Verma et al., CHRONIC INTESTINAL PSEUDOOBSTRUCTION AS A PRESENTING FEATURE IN MITOCHONDRIAL ENCEPHALOMYOPATHIES, Neurology, 50(4), 1998, pp. 3003-3003
MITOCHONDRIAL ENCEPHALOMYOPATHY AND HYPOPARATHYROIDISM ASSOCIATED WITH A DUPLICATION AND A DELETION OF MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID
Authors: TENGAN CH KIYOMOTO BH ROCHA MS TAVARES VLS GABBAI AA MORAES CT
Citation: Ch. Tengan et al., MITOCHONDRIAL ENCEPHALOMYOPATHY AND HYPOPARATHYROIDISM ASSOCIATED WITH A DUPLICATION AND A DELETION OF MITOCHONDRIAL DEOXYRIBONUCLEIC-ACID, The Journal of clinical endocrinology and metabolism, 83(1), 1998, pp. 125-129
HUMAN XENOMITOCHONDRIAL CYBRIDS - CELLULAR-MODELS OF MITOCHONDRIAL COMPLEX-I DEFICIENCY
Authors: BARRIENTOS A KENYON L MORAES CT
Citation: A. Barrientos et al., HUMAN XENOMITOCHONDRIAL CYBRIDS - CELLULAR-MODELS OF MITOCHONDRIAL COMPLEX-I DEFICIENCY, The Journal of biological chemistry, 273(23), 1998, pp. 14210-14217
A DISEASE-ASSOCIATED G5703A MUTATION IN HUMAN MITOCHONDRIAL-DNA CAUSES A CONFORMATIONAL CHANGE AND A MARKED DECREASE IN STEADY-STATE LEVELSOF MITOCHONDRIAL TRNA(ASN)
Authors: HAO HL MORAES CT
Citation: Hl. Hao et Ct. Moraes, A DISEASE-ASSOCIATED G5703A MUTATION IN HUMAN MITOCHONDRIAL-DNA CAUSES A CONFORMATIONAL CHANGE AND A MARKED DECREASE IN STEADY-STATE LEVELSOF MITOCHONDRIAL TRNA(ASN), Molecular and cellular biology, 17(12), 1997, pp. 6831-6837
UP-REGULATION OF D-3 DOPAMINE-RECEPTOR MESSENGER-RNA IN THE NUCLEUS-ACCUMBENS OF HUMAN COCAINE FATALITIES
Authors: SEGAL DM MORAES CT MASH DC
Citation: Dm. Segal et al., UP-REGULATION OF D-3 DOPAMINE-RECEPTOR MESSENGER-RNA IN THE NUCLEUS-ACCUMBENS OF HUMAN COCAINE FATALITIES, Molecular brain research, 45(2), 1997, pp. 335-339
A NOVEL MITOCHONDRIAL G8313A MUTATION ASSOCIATED WITH PROMINENT INITIAL GASTROINTESTINAL SYMPTOMS AND PROGRESSIVE ENCEPHALONEUROPATHY
Authors: VERMA A PICCOLI DA BONILLA E BERRY GT DIMAURO S MORAES CT
Citation: A. Verma et al., A NOVEL MITOCHONDRIAL G8313A MUTATION ASSOCIATED WITH PROMINENT INITIAL GASTROINTESTINAL SYMPTOMS AND PROGRESSIVE ENCEPHALONEUROPATHY, Pediatric research, 42(4), 1997, pp. 448-454
HYPOPARATHYROIDISM WITH 2 TYPES OF REARRANGEMENTS OF MTDNA
Authors: KIYOMOTO BH TENGAN CH GABBAI AA ROCHA MS TAVARES VLS MORAES CT
Citation: Bh. Kiyomoto et al., HYPOPARATHYROIDISM WITH 2 TYPES OF REARRANGEMENTS OF MTDNA, Neurology, 48(3), 1997, pp. 6141-6141
MUTATIONS IN THE MITOCHONDRIAL TRNALEU(UUR) GENE CAUSE A PREFERENTIALDECREASE IN THE MITOCHONDRIALLY SYNTHESIZED POLYPEPTIDES
Authors: VERMA A HAO HL SHANSKE S DIMAURO S MORAES CT
Citation: A. Verma et al., MUTATIONS IN THE MITOCHONDRIAL TRNALEU(UUR) GENE CAUSE A PREFERENTIALDECREASE IN THE MITOCHONDRIALLY SYNTHESIZED POLYPEPTIDES, Neurology, 48(3), 1997, pp. 51004-51004
EXPANDING THE FUNCTIONAL HUMAN MITOCHONDRIAL-DNA DATABASE BY THE ESTABLISHMENT OF PRIMATE XENOMITOCHONDRIAL CYBRIDS
Authors: KENYON L MORAES CT
Citation: L. Kenyon et Ct. Moraes, EXPANDING THE FUNCTIONAL HUMAN MITOCHONDRIAL-DNA DATABASE BY THE ESTABLISHMENT OF PRIMATE XENOMITOCHONDRIAL CYBRIDS, Proceedings of the National Academy of Sciences of the United Statesof America, 94(17), 1997, pp. 9131-9135
OXIDATIVE-PHOSPHORYLATION DYSFUNCTION DOES NOT INCREASE THE RATE OF ACCUMULATION OF AGE-RELATED MTDNA DELETIONS IN SKELETAL-MUSCLE
Authors: TENGAN CH GABBAI AA SHANSKE S ZEVIANI M MORAES CT
Citation: Ch. Tengan et al., OXIDATIVE-PHOSPHORYLATION DYSFUNCTION DOES NOT INCREASE THE RATE OF ACCUMULATION OF AGE-RELATED MTDNA DELETIONS IN SKELETAL-MUSCLE, Mutation research, 379(1), 1997, pp. 1-11
MITOCHONDRIAL-DNA DEFECTS IN BRAZILIAN PATIENTS WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
Authors: KIYOMOTO BH TENGAN CH MORAES CT OLIVEIRA ASB GABBAI AA
Citation: Bh. Kiyomoto et al., MITOCHONDRIAL-DNA DEFECTS IN BRAZILIAN PATIENTS WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, Journal of the neurological sciences, 152(2), 1997, pp. 160-165
INTERGENUS MTDNA TRANSFER TO HUMAN-CELLS - NEW MODELS FOR THE STUDY OF NUCLEAR-MITOCHONDRIAL INTERACTIONS AND OXIDATIVE-PHOSPHORYLATION DEFICIENCIES
Authors: BARRIENTOS A KENYON L MORAES CT
Citation: A. Barrientos et al., INTERGENUS MTDNA TRANSFER TO HUMAN-CELLS - NEW MODELS FOR THE STUDY OF NUCLEAR-MITOCHONDRIAL INTERACTIONS AND OXIDATIVE-PHOSPHORYLATION DEFICIENCIES, American journal of human genetics, 61(4), 1997, pp. 1773-1773
A DISEASE-ASSOCIATED G5703A MUTATION IN THE HUMAN MITOCHONDRIAL-DNA CAUSES A CONFORMATIONAL CHANGE AND A MARKED DISEASE IN STEADY-STATE LEVELS OF THE MITOCHONDRIAL TRNA(ASN)
Authors: HAO H MORAES CT
Citation: H. Hao et Ct. Moraes, A DISEASE-ASSOCIATED G5703A MUTATION IN THE HUMAN MITOCHONDRIAL-DNA CAUSES A CONFORMATIONAL CHANGE AND A MARKED DISEASE IN STEADY-STATE LEVELS OF THE MITOCHONDRIAL TRNA(ASN), American journal of human genetics, 61(4), 1997, pp. 1811-1811
FUNCTIONAL AND STRUCTURAL FEATURES OF A TANDEM DUPLICATION OF THE HUMAN MTDNA PROMOTER REGION
Authors: HAO HL MANFREDI G MORAES CT
Citation: Hl. Hao et al., FUNCTIONAL AND STRUCTURAL FEATURES OF A TANDEM DUPLICATION OF THE HUMAN MTDNA PROMOTER REGION, American journal of human genetics, 60(6), 1997, pp. 1363-1372
MITOCHONDRIAL DISORDERS
Authors: MORAES CT
Citation: Ct. Moraes, MITOCHONDRIAL DISORDERS, Current opinion in neurology, 9(5), 1996, pp. 369-374
DETECTION AND ANALYSIS OF MITOCHONDRIAL-DNA DELETIONS BY WHOLE GENOMEPCR
Authors: TENGAN CH MORAES CT
Citation: Ch. Tengan et Ct. Moraes, DETECTION AND ANALYSIS OF MITOCHONDRIAL-DNA DELETIONS BY WHOLE GENOMEPCR, Biochemical and molecular medicine, 58(1), 1996, pp. 130-134
IDENTIFICATION OF A MUTATION IN THE MITOCHONDRIAL TRNA(CYS) GENE ASSOCIATED WITH MITOCHONDRIAL ENCEPHALOPATHY
Authors: MANFREDI G SCHON EA BONILLA E MORAES CT SHANSKE S DIMAURO S
Citation: G. Manfredi et al., IDENTIFICATION OF A MUTATION IN THE MITOCHONDRIAL TRNA(CYS) GENE ASSOCIATED WITH MITOCHONDRIAL ENCEPHALOPATHY, Human mutation, 7(2), 1996, pp. 158-163
A NOVEL MITOCHONDRIAL-DNA G8313A MUTATION ASSOCIATED WITH SEVERE CHILDHOOD ENCEPHALOMYOPATHY
Authors: VERMA A MORAES CT PICCOLI DA BERRY GT
Citation: A. Verma et al., A NOVEL MITOCHONDRIAL-DNA G8313A MUTATION ASSOCIATED WITH SEVERE CHILDHOOD ENCEPHALOMYOPATHY, Annals of neurology, 40(3), 1996, pp. 204-204
A MERRF PEO OVERLAP SYNDROME-ASSOCIATED WITH THE MITOCHONDRIAL-DNA-3243 MUTATION/
Authors: VERMA A MORAES CT SHEBERT RT BRADLEY WG
Citation: A. Verma et al., A MERRF PEO OVERLAP SYNDROME-ASSOCIATED WITH THE MITOCHONDRIAL-DNA-3243 MUTATION/, Neurology, 46(5), 1996, pp. 1334-1336
A SIMPLE ENDONUCLEASE-SINGLE-STRAND CONFORMATIONAL POLYMORPHISM TECHNIQUE TO SEARCH FOR PATHOGENIC MUTATIONS IN HUMAN MITOCHONDRIAL GENOME
Authors: VERMA A MORAES CT
Citation: A. Verma et Ct. Moraes, A SIMPLE ENDONUCLEASE-SINGLE-STRAND CONFORMATIONAL POLYMORPHISM TECHNIQUE TO SEARCH FOR PATHOGENIC MUTATIONS IN HUMAN MITOCHONDRIAL GENOME, Neurology, 46(2), 1996, pp. 3004-3004
FUNCTIONAL AND MOLECULAR MITOCHONDRIAL ABNORMALITIES ASSOCIATED WITH A C-]T TRANSITION AT POSITION-3256 OF THE HUMAN MITOCHONDRIAL GENOME -THE EFFECTS OF A PATHOGENIC MITOCHONDRIAL TRANSFER-RNA POINT MUTATIONIN ORGANELLE TRANSLATION AND RNA PROCESSING
Authors: HAO HL MORAES CT
Citation: Hl. Hao et Ct. Moraes, FUNCTIONAL AND MOLECULAR MITOCHONDRIAL ABNORMALITIES ASSOCIATED WITH A C-]T TRANSITION AT POSITION-3256 OF THE HUMAN MITOCHONDRIAL GENOME -THE EFFECTS OF A PATHOGENIC MITOCHONDRIAL TRANSFER-RNA POINT MUTATIONIN ORGANELLE TRANSLATION AND RNA PROCESSING, The Journal of biological chemistry, 271(4), 1996, pp. 2347-2352
Risultati: 1-25 | 26-43