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Showing results (411-420 of 551) with videos related to

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The American Journal of Pathology|January 7, 2000
Intraneuronal Abeta42 accumulation in human brainG K Gouras, J Tsai, J Naslund, et al.
Psychiatric Genetics|November 4, 2015
Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disabilityNasim Vasli, Iltaf Ahmed, Kirti Mittal, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 23, 2014
Findings in patients from Benin with osteomyelitis and polymerase chain reaction-confirmed Mycobacterium ulcerans infectionVirginie Pommelet, Quentin B Vincent, Marie-Françoise Ardant, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 17, 2008
Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18qJohn B Vincent, Abdul Noor, Christian Windpassinger, et al.
Journal of Inorganic Biochemistry|April 27, 2010
Urinary chromium loss associated with diabetes is offset by increases in absorptionNicholas R Rhodes, DeAna McAdory, Sharifa Love, et al.
Schizophrenia Research|July 24, 2007
Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong KongAlbert K Mensah, Vincenzo De Luca, Beata Stachowiak, et al.
Psychiatric Genetics|November 11, 2024
Association of NTRK2 gene with suicidality: a meta-analysisWenzhu Ye, Ruo Su Zhang, Georgina M Hosang, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 2, 2016
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkageAziz Belkadi, Vincent Pedergnana, Aurélie Cobat, et al.
American Journal of Human Genetics|April 5, 2008
CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosaAbdul Noor, Christian Windpassinger, Megha Patel, et al.
Molecular Psychiatry|June 8, 2011
A multi-tissue analysis identifies HLA complex group 9 gene methylation differences in bipolar disorderZ Kaminsky, M Tochigi, P Jia, et al.
Pageof 56

Showing results (411-420 of 551) with videos related to

Sort By:
Pageof 56
The American Journal of Pathology|January 7, 2000
Intraneuronal Abeta42 accumulation in human brainG K Gouras, J Tsai, J Naslund, et al.
Psychiatric Genetics|November 4, 2015
Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disabilityNasim Vasli, Iltaf Ahmed, Kirti Mittal, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 23, 2014
Findings in patients from Benin with osteomyelitis and polymerase chain reaction-confirmed Mycobacterium ulcerans infectionVirginie Pommelet, Quentin B Vincent, Marie-Françoise Ardant, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 17, 2008
Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18qJohn B Vincent, Abdul Noor, Christian Windpassinger, et al.
Journal of Inorganic Biochemistry|April 27, 2010
Urinary chromium loss associated with diabetes is offset by increases in absorptionNicholas R Rhodes, DeAna McAdory, Sharifa Love, et al.
Schizophrenia Research|July 24, 2007
Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong KongAlbert K Mensah, Vincenzo De Luca, Beata Stachowiak, et al.
Psychiatric Genetics|November 11, 2024
Association of NTRK2 gene with suicidality: a meta-analysisWenzhu Ye, Ruo Su Zhang, Georgina M Hosang, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 2, 2016
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkageAziz Belkadi, Vincent Pedergnana, Aurélie Cobat, et al.
American Journal of Human Genetics|April 5, 2008
CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosaAbdul Noor, Christian Windpassinger, Megha Patel, et al.
Molecular Psychiatry|June 8, 2011
A multi-tissue analysis identifies HLA complex group 9 gene methylation differences in bipolar disorderZ Kaminsky, M Tochigi, P Jia, et al.
Pageof 56