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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 22q11
R 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 diseases
J 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 condition
A 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 individuals
N R Harvey, S Voisin, P J Dunn, et al.
Translational Psychiatry
|
February 13, 2026
Electrophysiological effects of psilocybin co-administered with midazolam
Michael 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 chromosomes
T L McDowell, R J Gibbons, H Sutherland, et al.
Circulation
|
June 2, 2005
From stem cells to viable autologous semilunar heart valve
Fraser 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 alkaptonuria
B 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 study
M 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 Inflammation
Clément Triaille, Neha Mohan Rao, Gillian I Rice, et al.
Page
of 29
Search research articles
Search
Showing results (271-280 of 282) with videos related to
Sort By:
Page
of 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 22q11
R 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 diseases
J 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 condition
A 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 individuals
N R Harvey, S Voisin, P J Dunn, et al.
Translational Psychiatry
|
February 13, 2026
Electrophysiological effects of psilocybin co-administered with midazolam
Michael 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 chromosomes
T L McDowell, R J Gibbons, H Sutherland, et al.
Circulation
|
June 2, 2005
From stem cells to viable autologous semilunar heart valve
Fraser 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 alkaptonuria
B 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 study
M 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 Inflammation
Clément Triaille, Neha Mohan Rao, Gillian I Rice, et al.
Page
of 29