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Leopold Groesser

Showing results (11-20 of 16) with videos related to

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Blood|January 25, 2014
The cytokine midkine supports neutrophil trafficking during acute inflammation by promoting adhesion via β2 integrins (CD11/CD18)Ludwig T Weckbach, Anita Gola, Michael Winkelmann, et al.
Nature Genetics|June 12, 2012
Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndromeLeopold Groesser, Eva Herschberger, Arno Ruetten, et al.
The Journal of Investigative Dermatology|January 23, 2013
Phacomatosis pigmentokeratotica is caused by a postzygotic HRAS mutation in a multipotent progenitor cellLeopold Groesser, Eva Herschberger, Ana Sagrera, et al.
The Journal of Investigative Dermatology|April 23, 2016
Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal NeviAgustí Toll, Luis C Fernández, Tirso Pons, et al.
The Journal of Investigative Dermatology|January 19, 2016
Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal MelanocytosisAnna C Thomas, Zhiqiang Zeng, Jean-Baptiste Rivière, et al.
American Journal of Human Genetics|May 31, 2016
A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones SyndromeStephen R F Twigg, Robert B Hufnagel, Kerry A Miller, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Blood|January 25, 2014
The cytokine midkine supports neutrophil trafficking during acute inflammation by promoting adhesion via β2 integrins (CD11/CD18)Ludwig T Weckbach, Anita Gola, Michael Winkelmann, et al.
Nature Genetics|June 12, 2012
Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndromeLeopold Groesser, Eva Herschberger, Arno Ruetten, et al.
The Journal of Investigative Dermatology|January 23, 2013
Phacomatosis pigmentokeratotica is caused by a postzygotic HRAS mutation in a multipotent progenitor cellLeopold Groesser, Eva Herschberger, Ana Sagrera, et al.
The Journal of Investigative Dermatology|April 23, 2016
Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal NeviAgustí Toll, Luis C Fernández, Tirso Pons, et al.
The Journal of Investigative Dermatology|January 19, 2016
Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal MelanocytosisAnna C Thomas, Zhiqiang Zeng, Jean-Baptiste Rivière, et al.
American Journal of Human Genetics|May 31, 2016
A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones SyndromeStephen R F Twigg, Robert B Hufnagel, Kerry A Miller, et al.
Pageof 2