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Cardiovascular Surgery (London, England)
|
August 1, 1997
A critical approach for longitudinal clinical trial of stretch PTFE aortic grafts
D M Shah, R C Darling, P B Kreienberg, et al.
Journal of Medical Genetics
|
August 3, 2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance
K P Burdon, M G Wirth, D A Mackey, et al.
The British Journal of Ophthalmology
|
December 25, 2003
Investigation of crystallin genes in familial cataract, and report of two disease associated mutations
K P Burdon, M G Wirth, D A Mackey, et al.
Medecine Et Maladies Infectieuses
|
July 22, 2018
Management of infective endocarditis and multidisciplinary approach
F Camou, M Dijos, L Barandon, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
February 14, 2025
Super-Resolution Imaging of Nanoscale Inhomogeneities in hBN-Covered and Encapsulated Few-Layer Graphene
Lina Jäckering, Konstantin G Wirth, Lukas Conrads, et al.
Scientific Reports
|
March 2, 2022
Fungal hyphae develop where titanomagnetite inclusions reach the surface of basalt grains
Rebecca A Lybrand, Odeta Qafoku, Mark E Bowden, et al.
The Journal of Cell Biology
|
March 15, 2006
Separase: a universal trigger for sister chromatid disjunction but not chromosome cycle progression
Karin G Wirth, Gordana Wutz, Nobuaki R Kudo, et al.
The British Journal of Ophthalmology
|
June 21, 2005
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes
J D McKay, B Patterson, J E Craig, et al.
Cell
|
July 15, 2006
Resolution of chiasmata in oocytes requires separase-mediated proteolysis
Nobuaki R Kudo, Katja Wassmann, Martin Anger, et al.
Angewandte Chemie (International Ed. in English)
|
February 17, 2025
Elucidating the Role of Electric Fields in Fe Oxidation via an Environmental Atom Probe
Sten V Lambeets, Naseeha Cardwell, Isaac Onyango, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 85) with videos related to
Sort By:
Page
of 9
Cardiovascular Surgery (London, England)
|
August 1, 1997
A critical approach for longitudinal clinical trial of stretch PTFE aortic grafts
D M Shah, R C Darling, P B Kreienberg, et al.
Journal of Medical Genetics
|
August 3, 2004
A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance
K P Burdon, M G Wirth, D A Mackey, et al.
The British Journal of Ophthalmology
|
December 25, 2003
Investigation of crystallin genes in familial cataract, and report of two disease associated mutations
K P Burdon, M G Wirth, D A Mackey, et al.
Medecine Et Maladies Infectieuses
|
July 22, 2018
Management of infective endocarditis and multidisciplinary approach
F Camou, M Dijos, L Barandon, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
February 14, 2025
Super-Resolution Imaging of Nanoscale Inhomogeneities in hBN-Covered and Encapsulated Few-Layer Graphene
Lina Jäckering, Konstantin G Wirth, Lukas Conrads, et al.
Scientific Reports
|
March 2, 2022
Fungal hyphae develop where titanomagnetite inclusions reach the surface of basalt grains
Rebecca A Lybrand, Odeta Qafoku, Mark E Bowden, et al.
The Journal of Cell Biology
|
March 15, 2006
Separase: a universal trigger for sister chromatid disjunction but not chromosome cycle progression
Karin G Wirth, Gordana Wutz, Nobuaki R Kudo, et al.
The British Journal of Ophthalmology
|
June 21, 2005
The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes
J D McKay, B Patterson, J E Craig, et al.
Cell
|
July 15, 2006
Resolution of chiasmata in oocytes requires separase-mediated proteolysis
Nobuaki R Kudo, Katja Wassmann, Martin Anger, et al.
Angewandte Chemie (International Ed. in English)
|
February 17, 2025
Elucidating the Role of Electric Fields in Fe Oxidation via an Environmental Atom Probe
Sten V Lambeets, Naseeha Cardwell, Isaac Onyango, et al.
Page
of 9