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Steve Seltzsam

Showing results (1-10 of 19) with videos related to

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Translational Oncology|December 17, 2018
In HPV-Positive HNSCC Cells, Functional Restoration of the p53/p21 Pathway by Proteasome Inhibitor Bortezomib Does Not Affect Radio- or ChemosensitivitySteve Seltzsam, Frank Ziemann, Kristin Dreffke, et al.
Oncotarget|December 30, 2017
Roscovitine strongly enhances the effect of olaparib on radiosensitivity for HPV neg. but not for HPV pos. HNSCC cell linesFrank Ziemann, Steve Seltzsam, Kristin Dreffke, et al.
American Journal of Medical Genetics. Part A|September 4, 2024
Genetic Contributions to Lower Urinary Tract DysfunctionLilian R Hiltebeitel, Steve Seltzsam, Chunyan Wang, et al.
Nephron|July 27, 2023
Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal KidneyLuca M Schierbaum, Sophia Schneider, Florian Buerger, et al.
American Journal of Medical Genetics. Part A|September 15, 2021
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tractBixia Zheng, Chunyan Wang, Steve Seltzsam, et al.
American Journal of Medical Genetics. Part A|January 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tractCaroline M Kolvenbach, Bixia Zheng, Lea M Merz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 2, 2021
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tractBixia Zheng, Steve Seltzsam, Chunyan Wang, et al.
American Journal of Medical Genetics. Part A|May 22, 2023
Recessive CHRM5 variant as a potential cause of neurogenic bladderSophia Schneider, Luca Schierbaum, Wessel A C Burger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, et al.
Genes & Diseases|June 13, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding <i>NPHP1</i> deletionsKonstantin Deutsch, Verena Klämbt, Thomas M Kitzler, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Translational Oncology|December 17, 2018
In HPV-Positive HNSCC Cells, Functional Restoration of the p53/p21 Pathway by Proteasome Inhibitor Bortezomib Does Not Affect Radio- or ChemosensitivitySteve Seltzsam, Frank Ziemann, Kristin Dreffke, et al.
Oncotarget|December 30, 2017
Roscovitine strongly enhances the effect of olaparib on radiosensitivity for HPV neg. but not for HPV pos. HNSCC cell linesFrank Ziemann, Steve Seltzsam, Kristin Dreffke, et al.
American Journal of Medical Genetics. Part A|September 4, 2024
Genetic Contributions to Lower Urinary Tract DysfunctionLilian R Hiltebeitel, Steve Seltzsam, Chunyan Wang, et al.
Nephron|July 27, 2023
Prioritization of Monogenic Congenital Anomalies of the Kidney and Urinary Tract Candidate Genes with Existing Single-Cell Transcriptomics Data of the Human Fetal KidneyLuca M Schierbaum, Sophia Schneider, Florian Buerger, et al.
American Journal of Medical Genetics. Part A|September 15, 2021
A truncating NRIP1 variant in an Arabic family with congenital anomalies of the kidneys and urinary tractBixia Zheng, Chunyan Wang, Steve Seltzsam, et al.
American Journal of Medical Genetics. Part A|January 24, 2023
A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tractCaroline M Kolvenbach, Bixia Zheng, Lea M Merz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 2, 2021
Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes for monogenic congenital anomalies of the kidneys and urinary tractBixia Zheng, Steve Seltzsam, Chunyan Wang, et al.
American Journal of Medical Genetics. Part A|May 22, 2023
Recessive CHRM5 variant as a potential cause of neurogenic bladderSophia Schneider, Luca Schierbaum, Wessel A C Burger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 2, 2020
Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)Chen-Han Wilfred Wu, Nina Mann, Makiko Nakayama, et al.
Genes & Diseases|June 13, 2024
Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding <i>NPHP1</i> deletionsKonstantin Deutsch, Verena Klämbt, Thomas M Kitzler, et al.
Pageof 2