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M R Passos

Showing results (101-110 of 142) with videos related to

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American Journal of Human Genetics|November 1, 1992
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence riskM R Passos-Bueno, E Bakker, A L Kneppers, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Developmental Biology|February 8, 2018
Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teethE Kague, P E Witten, M Soenens, et al.
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
American Journal of Medical Genetics|May 29, 1998
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Human Mutation|October 3, 2000
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changesA Splendore, E O Silva, L G Alonso, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Arquivos De Neuro-Psiquiatria|June 16, 2001
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17R Nitrini, L S Teixeira da Silva, S Rosemberg, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Pageof 15

Showing results (101-110 of 142) with videos related to

Sort By:
Pageof 15
American Journal of Human Genetics|November 1, 1992
Different mosaicism frequencies for proximal and distal Duchenne muscular dystrophy (DMD) mutations indicate difference in etiology and recurrence riskM R Passos-Bueno, E Bakker, A L Kneppers, et al.
Molecular Psychiatry|October 17, 1998
The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's diseaseJ R Oliveira, R M Gallindo, L G Maia, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Developmental Biology|February 8, 2018
Zebrafish sp7 mutants show tooth cycling independent of attachment, eruption and poor differentiation of teethE Kague, P E Witten, M Soenens, et al.
Molecular and Cellular Probes|October 1, 1995
Molecular characterization of further dystrophin gene microsatellitesS C King, A L Roche, M R Passos-Bueno, et al.
American Journal of Medical Genetics|May 29, 1998
Analysis of a novel functional polymorphism within the promoter region of the serotonin transporter gene (5-HTT) in Brazilian patients affected by bipolar disorder and schizophreniaJ R Mendes de Oliveira, P A Otto, H Vallada, et al.
Human Mutation|October 3, 2000
High mutation detection rate in TCOF1 among Treacher Collins syndrome patients reveals clustering of mutations and 16 novel pathogenic changesA Splendore, E O Silva, L G Alonso, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1994
A Caucasian family with the 3271 mutation in mitochondrial DNAS K Marie, Y Goto, M R Passos-Bueno, et al.
Arquivos De Neuro-Psiquiatria|June 16, 2001
Prion disease resembling frontotemporal dementia and parkinsonism linked to chromosome 17R Nitrini, L S Teixeira da Silva, S Rosemberg, et al.
Human Molecular Genetics|May 1, 1993
No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy families (FSHD) with 4q markersM R Passos-Bueno, C Wijmenga, R E Takata, et al.
Pageof 15