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M Jakobs

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The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|May 1, 1998
Prolonged discordant xenograft survival by inhibition of the intrinsic coagulation pathway in complement C6-deficient recipientsF M Jakobs, E A Davis, T White, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|June 17, 1998
Complement contributes to the rejection of complete and class I major histocompatibility complex--incompatible cardiac allograftsZ Qian, F M Jakobs, T Pfaff-Amesse, et al.
Retina (Philadelphia, Pa.)|January 1, 1997
Ophthalmomyiasis interna posterior. Report of a case with optic atrophyE M Jakobs, D A Adelberg, J M Lewis, et al.
Oncotarget|January 18, 2018
Diagnostic performance of <sup>68</sup>Gallium-PSMA-11 PET/CT to detect significant prostate cancer and comparison with <sup>18</sup>FEC PET/CTManuela A Hoffmann, Matthias Miederer, Helmut J Wieler, et al.
Somatic Cell and Molecular Genetics|January 1, 1997
Complementation group assignments in Fanconi anemia fibroblast cell lines from North AmericaP M Jakobs, E Fiddler-Odell, C Reifsteck, et al.
Zeitschrift Fur Rheumatologie|March 10, 2010
[Histopathological degeneration score of fibrous cartilage. Low- and high-grade meniscal degeneration]V Krenn, B Kurz, M G Krukemeyer, et al.
American Journal of Human Genetics|March 31, 2000
Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2P M Jakobs, J F Hess, P G FitzGerald, et al.
Clinical Transplantation|November 15, 1997
The role of CD11b/CD18 mediated neutrophil adhesion in complement deficient xenograft recipientsF M Jakobs, E A Davis, Z Qian, et al.
Der Orthopade|May 19, 2009
[Histopathologic diagnostics in endoprosthetics: periprosthetic neosynovialitis, hypersensitivity reaction, and arthrofibrosis]V Krenn, M Otto, L Morawietz, et al.
Nature Genetics|June 1, 1993
A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi JewsM A Whitney, H Saito, P M Jakobs, et al.
Pageof 6

Showing results (21-30 of 60) with videos related to

Sort By:
Pageof 6
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|May 1, 1998
Prolonged discordant xenograft survival by inhibition of the intrinsic coagulation pathway in complement C6-deficient recipientsF M Jakobs, E A Davis, T White, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|June 17, 1998
Complement contributes to the rejection of complete and class I major histocompatibility complex--incompatible cardiac allograftsZ Qian, F M Jakobs, T Pfaff-Amesse, et al.
Retina (Philadelphia, Pa.)|January 1, 1997
Ophthalmomyiasis interna posterior. Report of a case with optic atrophyE M Jakobs, D A Adelberg, J M Lewis, et al.
Oncotarget|January 18, 2018
Diagnostic performance of <sup>68</sup>Gallium-PSMA-11 PET/CT to detect significant prostate cancer and comparison with <sup>18</sup>FEC PET/CTManuela A Hoffmann, Matthias Miederer, Helmut J Wieler, et al.
Somatic Cell and Molecular Genetics|January 1, 1997
Complementation group assignments in Fanconi anemia fibroblast cell lines from North AmericaP M Jakobs, E Fiddler-Odell, C Reifsteck, et al.
Zeitschrift Fur Rheumatologie|March 10, 2010
[Histopathological degeneration score of fibrous cartilage. Low- and high-grade meniscal degeneration]V Krenn, B Kurz, M G Krukemeyer, et al.
American Journal of Human Genetics|March 31, 2000
Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2P M Jakobs, J F Hess, P G FitzGerald, et al.
Clinical Transplantation|November 15, 1997
The role of CD11b/CD18 mediated neutrophil adhesion in complement deficient xenograft recipientsF M Jakobs, E A Davis, Z Qian, et al.
Der Orthopade|May 19, 2009
[Histopathologic diagnostics in endoprosthetics: periprosthetic neosynovialitis, hypersensitivity reaction, and arthrofibrosis]V Krenn, M Otto, L Morawietz, et al.
Nature Genetics|June 1, 1993
A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi JewsM A Whitney, H Saito, P M Jakobs, et al.
Pageof 6