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Mechanisms of Development
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January 29, 2013
Endothelial deletion of ADAM17 in mice results in defective remodeling of the semilunar valves and cardiac dysfunction in adults
Carole L Wilson, Peter J Gough, Cindy A Chang, et al.
Protein Science : a Publication of the Protein Society
|
October 20, 2023
Exploring novel HIV-1 reverse transcriptase inhibitors with drug-resistant mutants: A double mutant surprise
Klarissa Hollander, Albert H Chan, Kathleen M Frey, et al.
Parkinsonism & Related Disorders
|
June 3, 2019
Involuntary movements, vocalizations and cognitive decline
Olafur Sveinsson, Bjarne Udd, Per Svenningsson, et al.
Brain Communications
|
May 7, 2024
Dopaminergic mesolimbic structural reserve is positively linked to better outcome after severe stroke
Liv Asmussen, Benedikt M Frey, Lukas K Frontzkowski, et al.
Respiration; International Review of Thoracic Diseases
|
February 15, 2013
Diagnosis and management of chronic obstructive pulmonary disease: the Swiss guidelines. Official guidelines of the Swiss Respiratory Society
E W Russi, W Karrer, M Brutsche, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 2, 2024
Plasma and platelet lipidome changes in Fabry disease
Bo Burla, Jeongah Oh, Albina Nowak, et al.
Parkinsonism & Related Disorders
|
October 12, 2018
WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred
Olafur Sveinsson, Bjarne Udd, Per Svenningsson, et al.
Transfusion
|
July 12, 2016
Impact of donor ABH-secretor status in ABO-mismatched living donor kidney transplantation
Beatrice Drexler, Andreas Holbro, Joerg Sigle, et al.
Infection
|
March 26, 2026
Clinical and microbial insights into polymicrobial vascular graft infections: a prospective observational study
Catrina I Pedrett, Jana Epprecht, Bruno Ledergerber, et al.
Vox Sanguinis
|
January 16, 2024
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A<sub>3</sub> phenotype
Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, et al.
Page
of 101
Search research articles
Search
Showing results (911-920 of 1,005) with videos related to
Sort By:
Page
of 101
Mechanisms of Development
|
January 29, 2013
Endothelial deletion of ADAM17 in mice results in defective remodeling of the semilunar valves and cardiac dysfunction in adults
Carole L Wilson, Peter J Gough, Cindy A Chang, et al.
Protein Science : a Publication of the Protein Society
|
October 20, 2023
Exploring novel HIV-1 reverse transcriptase inhibitors with drug-resistant mutants: A double mutant surprise
Klarissa Hollander, Albert H Chan, Kathleen M Frey, et al.
Parkinsonism & Related Disorders
|
June 3, 2019
Involuntary movements, vocalizations and cognitive decline
Olafur Sveinsson, Bjarne Udd, Per Svenningsson, et al.
Brain Communications
|
May 7, 2024
Dopaminergic mesolimbic structural reserve is positively linked to better outcome after severe stroke
Liv Asmussen, Benedikt M Frey, Lukas K Frontzkowski, et al.
Respiration; International Review of Thoracic Diseases
|
February 15, 2013
Diagnosis and management of chronic obstructive pulmonary disease: the Swiss guidelines. Official guidelines of the Swiss Respiratory Society
E W Russi, W Karrer, M Brutsche, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 2, 2024
Plasma and platelet lipidome changes in Fabry disease
Bo Burla, Jeongah Oh, Albina Nowak, et al.
Parkinsonism & Related Disorders
|
October 12, 2018
WITHDRAWN: Novel Xp21.1 deletion associated with unusual features in a large McLeod syndrome kindred
Olafur Sveinsson, Bjarne Udd, Per Svenningsson, et al.
Transfusion
|
July 12, 2016
Impact of donor ABH-secretor status in ABO-mismatched living donor kidney transplantation
Beatrice Drexler, Andreas Holbro, Joerg Sigle, et al.
Infection
|
March 26, 2026
Clinical and microbial insights into polymicrobial vascular graft infections: a prospective observational study
Catrina I Pedrett, Jana Epprecht, Bruno Ledergerber, et al.
Vox Sanguinis
|
January 16, 2024
Novel regulatory variant in ABO intronic RUNX1 binding site inducing A<sub>3</sub> phenotype
Gian Andri Thun, Morgan Gueuning, Sonja Sigurdardottir, et al.
Page
of 101