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C Wallace

Showing results (891-900 of 1,458) with videos related to

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Journal of Acquired Immune Deficiency Syndromes (1999)|January 26, 2010
Mitochondrial haplogroups are associated with risk of neuroretinal disorder in HIV-positive patientsSher L Hendrickson, Douglas A Jabs, Mark Van Natta, et al.
Communications Biology|April 9, 2024
Visualizing subcellular changes in the NAD(H) pool size versus redox state using fluorescence lifetime imaging microscopy of NADHAngela Song, Nicole Zhao, Diana C Hilpert, et al.
Clinical Anatomy (New York, N.Y.)|June 29, 2000
Anatomic variations of anterior cerebral artery cortical branchesM A Stefani, F L Schneider, A C Marrone, et al.
Growth Factors (Chur, Switzerland)|January 29, 2002
Contribution of residues A54 and L55 of the human insulin-like growth factor-II (IGF-II) A domain to Type 2 IGF receptor binding specificityB E Forbe, K A McNeil, C D Scott, et al.
The Journal of Endocrinology|August 1, 1995
Long R3 insulin-like growth factor-I (IGF-I) infusion stimulates organ growth but reduces plasma IGF-I, IGF-II and IGF binding protein concentrations in the guinea pigM A Conlon, F M Tomas, P C Owens, et al.
Journal of Clinical Neuro-Ophthalmology|March 1, 1992
Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutationE M Stone, N J Newman, N R Miller, et al.
Biochimica Et Biophysica Acta|April 30, 2008
Microbial biotin protein ligases aid in understanding holocarboxylase synthetase deficiencyNicole R Pendini, Lisa M Bailey, Grant W Booker, et al.
JCI Insight|March 4, 2025
Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutationCheng Ai, Huiying Li, Chunyan Wang, et al.
Journal of Dietary Supplements|May 18, 2013
An industry perspective: dietary supplements and mortality rates in older womenTaylor C Wallace, Douglas MacKay, Barry W Ritz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutationR G Ortiz, N J Newman, J M Shoffner, et al.
Pageof 146

Showing results (891-900 of 1,458) with videos related to

Sort By:
Pageof 146
Journal of Acquired Immune Deficiency Syndromes (1999)|January 26, 2010
Mitochondrial haplogroups are associated with risk of neuroretinal disorder in HIV-positive patientsSher L Hendrickson, Douglas A Jabs, Mark Van Natta, et al.
Communications Biology|April 9, 2024
Visualizing subcellular changes in the NAD(H) pool size versus redox state using fluorescence lifetime imaging microscopy of NADHAngela Song, Nicole Zhao, Diana C Hilpert, et al.
Clinical Anatomy (New York, N.Y.)|June 29, 2000
Anatomic variations of anterior cerebral artery cortical branchesM A Stefani, F L Schneider, A C Marrone, et al.
Growth Factors (Chur, Switzerland)|January 29, 2002
Contribution of residues A54 and L55 of the human insulin-like growth factor-II (IGF-II) A domain to Type 2 IGF receptor binding specificityB E Forbe, K A McNeil, C D Scott, et al.
The Journal of Endocrinology|August 1, 1995
Long R3 insulin-like growth factor-I (IGF-I) infusion stimulates organ growth but reduces plasma IGF-I, IGF-II and IGF binding protein concentrations in the guinea pigM A Conlon, F M Tomas, P C Owens, et al.
Journal of Clinical Neuro-Ophthalmology|March 1, 1992
Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutationE M Stone, N J Newman, N R Miller, et al.
Biochimica Et Biophysica Acta|April 30, 2008
Microbial biotin protein ligases aid in understanding holocarboxylase synthetase deficiencyNicole R Pendini, Lisa M Bailey, Grant W Booker, et al.
JCI Insight|March 4, 2025
Vitamin A treatment restores vision failures arising from Leber's hereditary optic neuropathy-linked mtDNA mutationCheng Ai, Huiying Li, Chunyan Wang, et al.
Journal of Dietary Supplements|May 18, 2013
An industry perspective: dietary supplements and mortality rates in older womenTaylor C Wallace, Douglas MacKay, Barry W Ritz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutationR G Ortiz, N J Newman, J M Shoffner, et al.
Pageof 146