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P Monaco

Showing results (541-550 of 719) with videos related to

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Journal of Medical Genetics|November 3, 2004
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UKT S Scerri, S E Fisher, C Francks, et al.
Genomics|May 1, 1993
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YACM T Geraghty, L C Brody, L S Martin, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 24, 2005
Preemptive plasmapheresis and recurrence of FSGS in high-risk renal transplant recipientsR Y Gohh, A F Yango, P E Morrissey, et al.
Archives of Neurology|October 12, 2011
Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindredAntonio Velayos-Baeza, Elke Holinski-Feder, Birgit Neitzel, et al.
American Journal of Clinical Pathology|November 1, 1987
An unusual case of splenic abscess and sepsis in an immunocompromised hostM E Sherman, M Albrecht, P C DeGirolami, et al.
Journal of Cell Science|June 12, 2008
Oxidised LDL internalisation by the LOX-1 scavenger receptor is dependent on a novel cytoplasmic motif and is regulated by dynamin-2Jane E Murphy, Ravinder S Vohra, Sarah Dunn, et al.
Clinical Nephrology|February 1, 1986
Vitamin E supplementation in hemodialysis patients: effects on peripheral blood mononuclear cells lipid peroxidation and immune responseM Taccone-Gallucci, O Giardini, C Ausiello, et al.
Genes, Brain, and Behavior|November 17, 2007
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairmentM Falcaro, A Pickles, D F Newbury, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
DNA linkage analysis of X chromosome-linked chronic granulomatous diseaseR L Baehner, L M Kunkel, A P Monaco, et al.
American Journal of Human Genetics|February 1, 1992
Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21M F Ho, A P Monaco, L A Blonden, et al.
Pageof 72

Showing results (541-550 of 719) with videos related to

Sort By:
Pageof 72
Journal of Medical Genetics|November 3, 2004
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UKT S Scerri, S E Fisher, C Francks, et al.
Genomics|May 1, 1993
The isolation of cDNAs from OATL1 at Xp 11.2 using a 480-kb YACM T Geraghty, L C Brody, L S Martin, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 24, 2005
Preemptive plasmapheresis and recurrence of FSGS in high-risk renal transplant recipientsR Y Gohh, A F Yango, P E Morrissey, et al.
Archives of Neurology|October 12, 2011
Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindredAntonio Velayos-Baeza, Elke Holinski-Feder, Birgit Neitzel, et al.
American Journal of Clinical Pathology|November 1, 1987
An unusual case of splenic abscess and sepsis in an immunocompromised hostM E Sherman, M Albrecht, P C DeGirolami, et al.
Journal of Cell Science|June 12, 2008
Oxidised LDL internalisation by the LOX-1 scavenger receptor is dependent on a novel cytoplasmic motif and is regulated by dynamin-2Jane E Murphy, Ravinder S Vohra, Sarah Dunn, et al.
Clinical Nephrology|February 1, 1986
Vitamin E supplementation in hemodialysis patients: effects on peripheral blood mononuclear cells lipid peroxidation and immune responseM Taccone-Gallucci, O Giardini, C Ausiello, et al.
Genes, Brain, and Behavior|November 17, 2007
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairmentM Falcaro, A Pickles, D F Newbury, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
DNA linkage analysis of X chromosome-linked chronic granulomatous diseaseR L Baehner, L M Kunkel, A P Monaco, et al.
American Journal of Human Genetics|February 1, 1992
Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21M F Ho, A P Monaco, L A Blonden, et al.
Pageof 72