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Martin Zenker

Showing results (71-80 of 338) with videos related to

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American Journal of Medical Genetics. Part A|June 11, 2021
Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformationsVanessa Franziska Schmidt, Ilse Wieland, Walter A Wohlgemuth, et al.
American Journal of Medical Genetics. Part A|November 1, 2014
Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutationsLuzie Bülow, Christina Lissewski, Rainer Bressel, et al.
European Journal of Medical Genetics|January 24, 2017
Novel FREM1 mutations in a patient with MOTA syndrome: Clinical findings, mutation update and review of FREM1-related disorders literatureOscar F Chacon-Camacho, Martin Zenker, Denny Schanze, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasiaAlireza Baradaran-Heravi, Christian Thiel, Anita Rauch, et al.
Gene Expression Patterns : GEP|October 7, 2021
Galloway-Mowat syndrome: New insights from bioinformatics and expression during Xenopus embryogenesisErnestine Treimer, Kathrin Niedermayer, Sven Schumann, et al.
Anticancer Research|June 4, 2020
Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower LegReinhard E Friedrich, Christian Hagel, Felix K Kohlrusch, et al.
Journal of Inorganic Biochemistry|August 3, 2010
Preparation, 99mTc-labeling and biodistribution studies of a PNA oligomer containing a new ligand derivative of 2,2'-dipicolylamineGilles Gasser, Katrin Jäger, Martin Zenker, et al.
Cell Cycle (Georgetown, Tex.)|August 22, 2006
Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disordersChristian P Kratz, Suzanne Schubbert, Gideon Bollag, et al.
The Journal of Pediatrics|October 16, 2002
Treatment of two patients with Herlitz junctional epidermolysis bullosa with artificial skin bioequivalentsQiu-Jie Jiang, Jan Izakovic, Martin Zenker, et al.
The American Journal of Gastroenterology|August 16, 2008
Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern GermanyFrank Ulrich Weiss, Martin Zenker, Arif Bülent Ekici, et al.
Pageof 34

Showing results (71-80 of 338) with videos related to

Sort By:
Pageof 34
American Journal of Medical Genetics. Part A|June 11, 2021
Mosaic RASopathy due to KRAS variant G12D with segmental overgrowth and associated peripheral vascular malformationsVanessa Franziska Schmidt, Ilse Wieland, Walter A Wohlgemuth, et al.
American Journal of Medical Genetics. Part A|November 1, 2014
Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutationsLuzie Bülow, Christina Lissewski, Rainer Bressel, et al.
European Journal of Medical Genetics|January 24, 2017
Novel FREM1 mutations in a patient with MOTA syndrome: Clinical findings, mutation update and review of FREM1-related disorders literatureOscar F Chacon-Camacho, Martin Zenker, Denny Schanze, et al.
American Journal of Medical Genetics. Part A|July 16, 2008
Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasiaAlireza Baradaran-Heravi, Christian Thiel, Anita Rauch, et al.
Gene Expression Patterns : GEP|October 7, 2021
Galloway-Mowat syndrome: New insights from bioinformatics and expression during Xenopus embryogenesisErnestine Treimer, Kathrin Niedermayer, Sven Schumann, et al.
Anticancer Research|June 4, 2020
Mosaic Neurofibromatosis Type 1 With Multiple Cutaneous Diffuse and Plexiform Neurofibromas of the Lower LegReinhard E Friedrich, Christian Hagel, Felix K Kohlrusch, et al.
Journal of Inorganic Biochemistry|August 3, 2010
Preparation, 99mTc-labeling and biodistribution studies of a PNA oligomer containing a new ligand derivative of 2,2'-dipicolylamineGilles Gasser, Katrin Jäger, Martin Zenker, et al.
Cell Cycle (Georgetown, Tex.)|August 22, 2006
Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disordersChristian P Kratz, Suzanne Schubbert, Gideon Bollag, et al.
The Journal of Pediatrics|October 16, 2002
Treatment of two patients with Herlitz junctional epidermolysis bullosa with artificial skin bioequivalentsQiu-Jie Jiang, Jan Izakovic, Martin Zenker, et al.
The American Journal of Gastroenterology|August 16, 2008
Local clustering of PRSS1 R122H mutations in hereditary pancreatitis patients from Northern GermanyFrank Ulrich Weiss, Martin Zenker, Arif Bülent Ekici, et al.
Pageof 34