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M Steinert

Showing results (321-330 of 359) with videos related to

Pageof 36
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Cell|May 11, 2015
Quantifying Memory CD8 T Cells Reveals Regionalization of ImmunosurveillanceElizabeth M Steinert, Jason M Schenkel, Kathryn A Fraser, et al.
Nature Genetics|January 1, 1996
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneV De Laurenzi, G R Rogers, D J Hamrock, et al.
Optics Express|February 25, 2016
Image formation properties and inverse imaging problem in aperture based scanning near field optical microscopyS Schmidt, A E Klein, T Paul, et al.
The Journal of Investigative Dermatology|September 1, 1996
A novel H1 mutation in the keratin 1 chain in epidermolytic hyperkeratosisJ M Yang, K Nam, K B Park, et al.
Cancer|September 26, 2006
Correlation of immunophenotype with progression-free survival in patients with gastrointestinal stromal tumors treated with imatinib mesylateLucian R Chirieac, Jonathan C Trent, Dejka M Steinert, et al.
The Journal of Investigative Dermatology|October 31, 2002
Two novel mutations in the keratin 1 gene in epidermolytic hyperkeratosisDong-Youn Lee, Kwang-Sung Ahn, Cha-Hui Lee, et al.
Cell|June 15, 1990
Identification of a major keratinocyte cell envelope protein, loricrinT Mehrel, D Hohl, J A Rothnagel, et al.
Optics Letters|November 15, 2016
High speed and high resolution table-top nanoscale imagingG K Tadesse, R Klas, S Demmler, et al.
Acta Dermato-Venereologica|December 2, 1998
Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratodermaJ M Yang, S Lee, H J Kang, et al.
Journal of Molecular Biology|May 10, 2000
The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assemblyH Herrmann, S V Strelkov, B Feja, et al.
Pageof 36

Showing results (321-330 of 359) with videos related to

Sort By:
Pageof 36
Cell|May 11, 2015
Quantifying Memory CD8 T Cells Reveals Regionalization of ImmunosurveillanceElizabeth M Steinert, Jason M Schenkel, Kathryn A Fraser, et al.
Nature Genetics|January 1, 1996
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneV De Laurenzi, G R Rogers, D J Hamrock, et al.
Optics Express|February 25, 2016
Image formation properties and inverse imaging problem in aperture based scanning near field optical microscopyS Schmidt, A E Klein, T Paul, et al.
The Journal of Investigative Dermatology|September 1, 1996
A novel H1 mutation in the keratin 1 chain in epidermolytic hyperkeratosisJ M Yang, K Nam, K B Park, et al.
Cancer|September 26, 2006
Correlation of immunophenotype with progression-free survival in patients with gastrointestinal stromal tumors treated with imatinib mesylateLucian R Chirieac, Jonathan C Trent, Dejka M Steinert, et al.
The Journal of Investigative Dermatology|October 31, 2002
Two novel mutations in the keratin 1 gene in epidermolytic hyperkeratosisDong-Youn Lee, Kwang-Sung Ahn, Cha-Hui Lee, et al.
Cell|June 15, 1990
Identification of a major keratinocyte cell envelope protein, loricrinT Mehrel, D Hohl, J A Rothnagel, et al.
Optics Letters|November 15, 2016
High speed and high resolution table-top nanoscale imagingG K Tadesse, R Klas, S Demmler, et al.
Acta Dermato-Venereologica|December 2, 1998
Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratodermaJ M Yang, S Lee, H J Kang, et al.
Journal of Molecular Biology|May 10, 2000
The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assemblyH Herrmann, S V Strelkov, B Feja, et al.
Pageof 36