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H Sutherland

Showing results (271-280 of 282) with videos related to

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American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
European Journal of Cancer & Clinical Oncology|July 1, 1982
A clinical assessment of fluorescence polarisation changes in lymphocytes stimulated by phytohaemagglutinin (PHA) in malignant and benign diseasesJ A Pritchard, W H Sutherland, J E Siddall, et al.
Osteoarthritis and Cartilage|May 1, 2012
Ochronosis in a murine model of alkaptonuria is synonymous to that in the human conditionA M Taylor, A J Preston, N K Paulk, et al.
Molecular Genetics and Genomics : MGG|January 4, 2020
Genetic variants associated with exercise performance in both moderately trained and highly trained individualsN R Harvey, S Voisin, P J Dunn, et al.
Translational Psychiatry|February 13, 2026
Electrophysiological effects of psilocybin co-administered with midazolamMichael H Sutherland, Christopher R Nicholas, Richard C Lennertz, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1999
Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomesT L McDowell, R J Gibbons, H Sutherland, et al.
Circulation|June 2, 2005
From stem cells to viable autologous semilunar heart valveFraser W H Sutherland, Tjorvi E Perry, Ying Yu, et al.
Journal of Inherited Metabolic Disease|March 15, 2024
Hepatobiliary circulation and dominant urinary excretion of homogentisic acid in a mouse model of alkaptonuriaB P Norman, H Sutherland, P J M Wilson, et al.
Bone Marrow Transplantation|November 3, 2010
Long-term follow-up of patients undergoing auto-SCT for advanced germ cell tumour: a multicentre cohort studyM D Seftel, K Paulson, R Doocey, et al.
Journal of Clinical Immunology|August 28, 2024
Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.
Pageof 29

Showing results (271-280 of 282) with videos related to

Sort By:
Pageof 29
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
European Journal of Cancer & Clinical Oncology|July 1, 1982
A clinical assessment of fluorescence polarisation changes in lymphocytes stimulated by phytohaemagglutinin (PHA) in malignant and benign diseasesJ A Pritchard, W H Sutherland, J E Siddall, et al.
Osteoarthritis and Cartilage|May 1, 2012
Ochronosis in a murine model of alkaptonuria is synonymous to that in the human conditionA M Taylor, A J Preston, N K Paulk, et al.
Molecular Genetics and Genomics : MGG|January 4, 2020
Genetic variants associated with exercise performance in both moderately trained and highly trained individualsN R Harvey, S Voisin, P J Dunn, et al.
Translational Psychiatry|February 13, 2026
Electrophysiological effects of psilocybin co-administered with midazolamMichael H Sutherland, Christopher R Nicholas, Richard C Lennertz, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1999
Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomesT L McDowell, R J Gibbons, H Sutherland, et al.
Circulation|June 2, 2005
From stem cells to viable autologous semilunar heart valveFraser W H Sutherland, Tjorvi E Perry, Ying Yu, et al.
Journal of Inherited Metabolic Disease|March 15, 2024
Hepatobiliary circulation and dominant urinary excretion of homogentisic acid in a mouse model of alkaptonuriaB P Norman, H Sutherland, P J M Wilson, et al.
Bone Marrow Transplantation|November 3, 2010
Long-term follow-up of patients undergoing auto-SCT for advanced germ cell tumour: a multicentre cohort studyM D Seftel, K Paulson, R Doocey, et al.
Journal of Clinical Immunology|August 28, 2024
Hereditary C1q Deficiency is Associated with Type 1 Interferon-Pathway Activation and a High Risk of Central Nervous System InflammationClément Triaille, Neha Mohan Rao, Gillian I Rice, et al.
Pageof 29