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M Doss

Showing results (131-140 of 180) with videos related to

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Neuroscience|January 5, 2025
Correlation of repetitive behaviors in deer mice with striatal mRNA expression of endogenous opioids and mu, delta, kappa, and dopamine receptors: A preliminary reportFarhan Augustine, Shawn M Doss, Justin Pellicciotti, et al.
Deutsche Medizinische Wochenschrift (1946)|May 25, 1990
[The coincidence of acute intermittent porphyria and Crohn's disease]K Beckh, I Sieg, M Stellwaag, et al.
Klinische Wochenschrift|June 1, 1989
Multiple nodular foci in the liver associated with chronic hepatic porphyria after previous treatment of breast cancerW K Lelbach, T R Müller, W Kersjes, et al.
Cardiovascular Surgery (London, England)|March 29, 2003
Do surface modifying additives (SMA) influence blood loss and thrombogenicity in conventional cardiopulmonary bypass for coronary artery bypass grafting?S Martens, G Matheis, G Wimmer-Greinecker, et al.
Health Science Reports|April 20, 2026
Racial Disparities in Time to Treatment of Pancreatic Adenocarcinoma During the COVID-19 Era: A Retrospective Database AnalysisArchana Venkatesan, Raag Patel, Shawn M Doss, et al.
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|November 1, 1971
[Chronic hepatic porphyrias (author's transl)]M Doss, D Look, H Henning, et al.
Transactions of the Association of American Physicians|January 1, 1992
Cloning and expression of the defective genes in delta-aminolevulinate dehydratase porphyria: compound heterozygosity in this hereditary liver diseaseS Sassa, N Ishida, H Fujita, et al.
The New England Journal of Medicine|June 15, 1972
Intermittent acute porphyria--demonstration of a genetic defect in porphobilinogen metabolismU A Meyer, L J Strand, M Doss, et al.
Journal of the American Chemical Society|July 13, 2006
Programmable oligomers for minor groove DNA recognitionRaymond M Doss, Michael A Marques, Shane Foister, et al.
European Journal of Clinical Investigation|April 1, 1991
Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytesS Sassa, H Fujita, M Doss, et al.
Pageof 18

Showing results (131-140 of 180) with videos related to

Sort By:
Pageof 18
Neuroscience|January 5, 2025
Correlation of repetitive behaviors in deer mice with striatal mRNA expression of endogenous opioids and mu, delta, kappa, and dopamine receptors: A preliminary reportFarhan Augustine, Shawn M Doss, Justin Pellicciotti, et al.
Deutsche Medizinische Wochenschrift (1946)|May 25, 1990
[The coincidence of acute intermittent porphyria and Crohn's disease]K Beckh, I Sieg, M Stellwaag, et al.
Klinische Wochenschrift|June 1, 1989
Multiple nodular foci in the liver associated with chronic hepatic porphyria after previous treatment of breast cancerW K Lelbach, T R Müller, W Kersjes, et al.
Cardiovascular Surgery (London, England)|March 29, 2003
Do surface modifying additives (SMA) influence blood loss and thrombogenicity in conventional cardiopulmonary bypass for coronary artery bypass grafting?S Martens, G Matheis, G Wimmer-Greinecker, et al.
Health Science Reports|April 20, 2026
Racial Disparities in Time to Treatment of Pancreatic Adenocarcinoma During the COVID-19 Era: A Retrospective Database AnalysisArchana Venkatesan, Raag Patel, Shawn M Doss, et al.
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|November 1, 1971
[Chronic hepatic porphyrias (author's transl)]M Doss, D Look, H Henning, et al.
Transactions of the Association of American Physicians|January 1, 1992
Cloning and expression of the defective genes in delta-aminolevulinate dehydratase porphyria: compound heterozygosity in this hereditary liver diseaseS Sassa, N Ishida, H Fujita, et al.
The New England Journal of Medicine|June 15, 1972
Intermittent acute porphyria--demonstration of a genetic defect in porphobilinogen metabolismU A Meyer, L J Strand, M Doss, et al.
Journal of the American Chemical Society|July 13, 2006
Programmable oligomers for minor groove DNA recognitionRaymond M Doss, Michael A Marques, Shane Foister, et al.
European Journal of Clinical Investigation|April 1, 1991
Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytesS Sassa, H Fujita, M Doss, et al.
Pageof 18