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Pathologie (Heidelberg, Germany)|April 3, 2024
[Personalized medicine in oncology]Alisa Martina Lörsch, Johannes Jung, Sebastian Lange, et al.Clinical Endocrinology|November 24, 2006
Congenital hypothyroidism caused by new mutations in the thyroid oxidase 2 (THOX2) geneNicole Pfarr, Eckhard Korsch, Stefan Kaspers, et al.Genes, Chromosomes & Cancer|August 8, 2019
Molecular characterization of hepatic epithelioid hemangioendothelioma reveals alterations in various genes involved in DNA repair, epigenetic regulation, signaling pathways, and cell cycle controlCarolin Mogler, Ronald Koschny, Christoph E Heilig, et al.The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Intrafamilial variability of the deafness and goiter phenotype in Pendred syndrome caused by a T416P mutation in the SLC26A4 geneUlrike Napiontek, Guntram Borck, Wiebke Müller-Forell, et al.Pathologie (Heidelberg, Germany)|April 15, 2024
[Molecular pathological analysis through the ages]Maria Walker, Eva-Maria Mayr, Mai-Lan Koppermann, et al.Genes, Chromosomes & Cancer|September 24, 2015
High-throughput diagnostic profiling of clinically actionable gene fusions in lung cancerNicole Pfarr, Albrecht Stenzinger, Roland Penzel, et al.The Journal of Clinical Endocrinology and Metabolism|May 11, 2006
Goitrous congenital hypothyroidism and hearing impairment associated with mutations in the TPO and SLC26A4/PDS genesNicole Pfarr, Guntram Borck, Andrew Turk, et al.International Journal of Molecular Medicine|September 10, 2015
Utility of different massive parallel sequencing platforms for mutation profiling in clinical samples and identification of pitfalls using FFPE tissueJana Fassunke, Florian Haller, Simone Hebele, et al.Journal of Cancer Research and Clinical Oncology|December 10, 2016
Influence of the HER receptor ligand system on sensitivity to cetuximab and trastuzumab in gastric cancer cell linesJulia Kneissl, Anja Hartmann, Nicole Pfarr, et al.The Journal of Clinical Endocrinology and Metabolism|November 22, 2007
Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studiesJohnny Deladoëy, Nicole Pfarr, Jean-Marc Vuissoz, et al.Pageof 12