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M KOENIG

Showing results (361-370 of 524) with videos related to

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American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Leukemia|September 20, 2011
Early recipient chimerism testing in the T- and NK-cell lineages for risk assessment of graft rejection in pediatric patients undergoing allogeneic stem cell transplantationS Breuer, S Preuner, G Fritsch, et al.
The Journal of Clinical Investigation|January 1, 1989
Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasiaE R McCabe, J Towbin, J Chamberlain, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 10, 2012
Targeting TIM-1 on CD4 T cells depresses macrophage activation and overcomes ischemia-reperfusion injury in mouse orthotopic liver transplantationY Zhang, H Ji, X Shen, et al.
Journal of the American Chemical Society|August 25, 2020
Fullertubes: Cylindrical Carbon with Half-Fullerene End-Caps and Tubular Graphene Belts, Their Chemical Enrichment, Crystallography of Pristine C<sub>90</sub>-<i>D</i><sub></sub>(1) and C<sub>100</sub>-<i>D</i><sub></sub>(1) Fullertubes, and Isolation of C<sub>108</sub>, C<sub>120</sub>, C<sub>132</sub>, and C<sub>156</sub> Cages of Unknown StructuresRyan M Koenig, Han-Rui Tian, Tiffany L Seeler, et al.
Neurology|November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.
Human Mutation|March 26, 2003
Identification of seven novel mutations in the GAN geneP Bomont, C Ioos, C Yalcinkaya, et al.
Blood|June 1, 1980
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H diseaseJ A Phillips, T A Vik, A F Scott, et al.
Scandinavian Journal of Rheumatology|August 5, 2014
Left heart disease: a frequent cause of early pulmonary hypertension in systemic sclerosis, unrelated to elevated NT-proBNP levels or overt cardiac fibrosis but associated with increased levels of MR-proANP and MR-proADM: retrospective analysis of a French Canadian cohortL Miller, S Chartrand, M Koenig, et al.
Plos One|March 6, 2018
The technical reliability and biotemporal stability of cerebrospinal fluid biomarkers for profiling multiple pathophysiologies in Alzheimer's diseaseBianca A Trombetta, Becky C Carlyle, Aaron M Koenig, et al.
Pageof 53

Showing results (361-370 of 524) with videos related to

Sort By:
Pageof 53
American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Leukemia|September 20, 2011
Early recipient chimerism testing in the T- and NK-cell lineages for risk assessment of graft rejection in pediatric patients undergoing allogeneic stem cell transplantationS Breuer, S Preuner, G Fritsch, et al.
The Journal of Clinical Investigation|January 1, 1989
Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasiaE R McCabe, J Towbin, J Chamberlain, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 10, 2012
Targeting TIM-1 on CD4 T cells depresses macrophage activation and overcomes ischemia-reperfusion injury in mouse orthotopic liver transplantationY Zhang, H Ji, X Shen, et al.
Journal of the American Chemical Society|August 25, 2020
Fullertubes: Cylindrical Carbon with Half-Fullerene End-Caps and Tubular Graphene Belts, Their Chemical Enrichment, Crystallography of Pristine C<sub>90</sub>-<i>D</i><sub></sub>(1) and C<sub>100</sub>-<i>D</i><sub></sub>(1) Fullertubes, and Isolation of C<sub>108</sub>, C<sub>120</sub>, C<sub>132</sub>, and C<sub>156</sub> Cages of Unknown StructuresRyan M Koenig, Han-Rui Tian, Tiffany L Seeler, et al.
Neurology|November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.
Human Mutation|March 26, 2003
Identification of seven novel mutations in the GAN geneP Bomont, C Ioos, C Yalcinkaya, et al.
Blood|June 1, 1980
Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H diseaseJ A Phillips, T A Vik, A F Scott, et al.
Scandinavian Journal of Rheumatology|August 5, 2014
Left heart disease: a frequent cause of early pulmonary hypertension in systemic sclerosis, unrelated to elevated NT-proBNP levels or overt cardiac fibrosis but associated with increased levels of MR-proANP and MR-proADM: retrospective analysis of a French Canadian cohortL Miller, S Chartrand, M Koenig, et al.
Plos One|March 6, 2018
The technical reliability and biotemporal stability of cerebrospinal fluid biomarkers for profiling multiple pathophysiologies in Alzheimer's diseaseBianca A Trombetta, Becky C Carlyle, Aaron M Koenig, et al.
Pageof 53