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I Henry

Showing results (121-130 of 135) with videos related to

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Human Genetics|January 1, 1985
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19F Tata, I Henry, A F Markham, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1989
Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinomaI Henry, S Grandjouan, P Couillin, et al.
Physical Review. E|March 18, 2016
Nonconservative dynamics of optically trapped high-aspect-ratio nanowiresWen Jun Toe, Ignacio Ortega-Piwonka, Christopher N Angstmann, et al.
Human Genetics|May 1, 1989
Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex regionP Couillin, M Azoulay, I Henry, et al.
Nature|July 26, 2013
Reactivating head regrowth in a regeneration-deficient planarian speciesS-Y Liu, C Selck, B Friedrich, et al.
Annals of Human Genetics|May 1, 1987
The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.
Genomics|July 1, 1988
Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1I Henry, A Bernheim, M Bernard, et al.
Autophagy|October 27, 2021
Lysosomal targetomics of <i>ghr KO</i> mice shows chaperone-mediated autophagy degrades nucleocytosolic acetyl-coA enzymesS Joseph Endicott, Alexander C Monovich, Eric L Huang, et al.
American Journal of Human Genetics|June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseC Jeanpierre, E Denamur, I Henry, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 3, 2021
The French multicentre elevated bone mass study: prevalence and causesJ Paccou, R-M Javier, I Henry-Desailly, et al.
Pageof 14

Showing results (121-130 of 135) with videos related to

Sort By:
Pageof 14
Human Genetics|January 1, 1985
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19F Tata, I Henry, A F Markham, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1989
Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinomaI Henry, S Grandjouan, P Couillin, et al.
Physical Review. E|March 18, 2016
Nonconservative dynamics of optically trapped high-aspect-ratio nanowiresWen Jun Toe, Ignacio Ortega-Piwonka, Christopher N Angstmann, et al.
Human Genetics|May 1, 1989
Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex regionP Couillin, M Azoulay, I Henry, et al.
Nature|July 26, 2013
Reactivating head regrowth in a regeneration-deficient planarian speciesS-Y Liu, C Selck, B Friedrich, et al.
Annals of Human Genetics|May 1, 1987
The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22M Azoulay, I Henry, F Tata, et al.
Genomics|July 1, 1988
Mapping of a human fibrillar collagen gene, pro alpha 1 (XI) (COL11A1), to the p21 region of chromosome 1I Henry, A Bernheim, M Bernard, et al.
Autophagy|October 27, 2021
Lysosomal targetomics of <i>ghr KO</i> mice shows chaperone-mediated autophagy degrades nucleocytosolic acetyl-coA enzymesS Joseph Endicott, Alexander C Monovich, Eric L Huang, et al.
American Journal of Human Genetics|June 13, 1998
Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation databaseC Jeanpierre, E Denamur, I Henry, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 3, 2021
The French multicentre elevated bone mass study: prevalence and causesJ Paccou, R-M Javier, I Henry-Desailly, et al.
Pageof 14