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Oliver Gross

Showing results (71-80 of 148) with videos related to

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International Journal of Molecular Sciences|January 30, 2019
Kidney Injury by Variants in the <i>COL4A5</i> Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental GlomerulosclerosisJenny Frese, Matthias Kettwig, Hildegard Zappel, et al.
Human Pathology|December 17, 2009
Interstitial inflammation in Alport syndromeJan Jedlicka, Afschin Soleiman, Dan Draganovici, et al.
Molecular Medicine (Cambridge, Mass.)|September 27, 2021
Addressing the 'hypoxia paradox' in severe COVID-19: literature review and report of four cases treated with erythropoietin analoguesMartin Begemann, Oliver Gross, Dominik Wincewicz, et al.
Pediatric Nephrology (Berlin, Germany)|June 25, 2013
Diagnosis of Alport syndrome--search for proteomic biomarkers in body fluidsMichael Pohl, Karin Danz, Oliver Gross, et al.
The Journal of Urology|February 24, 2018
Diagnostic Accuracy of Multiparametric Magnetic Resonance Imaging and Fusion Guided Targeted Biopsy Evaluated by Transperineal Template Saturation Prostate Biopsy for the Detection and Characterization of Prostate CancerAshkan Mortezavi, Olivia Märzendorfer, Olivio F Donati, et al.
Kidney International|March 20, 2018
Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working GroupClifford E Kashtan, Jie Ding, Guido Garosi, et al.
Scientific Reports|October 12, 2022
Effect of composition and thermal history on deformation behavior and cluster connections in model bulk metallic glassesNico Neuber, Maryam Sadeghilaridjani, Nandita Ghodki, et al.
Kidney International|January 13, 2012
Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutationsJohanna Temme, Frederick Peters, Katharina Lange, et al.
Frontiers in Pediatrics|December 19, 2019
The Hypomorphic Variant p.(Gly624Asp) in <i>COL4A5</i> as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport SyndromeEva Pauline Macheroux, Matthias C Braunisch, Stephanie Pucci Pegler, et al.
Proteome Science|December 20, 2014
Effects of mycophenolate mofetil on kidney function and phosphorylation status of renal proteins in Alport COL4A3-deficient miceDarinka Todorova Petrova, Frank Christian Schultze, Gunnar Brandhorst, et al.
Pageof 15

Showing results (71-80 of 148) with videos related to

Sort By:
Pageof 15
International Journal of Molecular Sciences|January 30, 2019
Kidney Injury by Variants in the <i>COL4A5</i> Gene Aggravated by Polymorphisms in Slit Diaphragm Genes Causes Focal Segmental GlomerulosclerosisJenny Frese, Matthias Kettwig, Hildegard Zappel, et al.
Human Pathology|December 17, 2009
Interstitial inflammation in Alport syndromeJan Jedlicka, Afschin Soleiman, Dan Draganovici, et al.
Molecular Medicine (Cambridge, Mass.)|September 27, 2021
Addressing the 'hypoxia paradox' in severe COVID-19: literature review and report of four cases treated with erythropoietin analoguesMartin Begemann, Oliver Gross, Dominik Wincewicz, et al.
Pediatric Nephrology (Berlin, Germany)|June 25, 2013
Diagnosis of Alport syndrome--search for proteomic biomarkers in body fluidsMichael Pohl, Karin Danz, Oliver Gross, et al.
The Journal of Urology|February 24, 2018
Diagnostic Accuracy of Multiparametric Magnetic Resonance Imaging and Fusion Guided Targeted Biopsy Evaluated by Transperineal Template Saturation Prostate Biopsy for the Detection and Characterization of Prostate CancerAshkan Mortezavi, Olivia Märzendorfer, Olivio F Donati, et al.
Kidney International|March 20, 2018
Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working GroupClifford E Kashtan, Jie Ding, Guido Garosi, et al.
Scientific Reports|October 12, 2022
Effect of composition and thermal history on deformation behavior and cluster connections in model bulk metallic glassesNico Neuber, Maryam Sadeghilaridjani, Nandita Ghodki, et al.
Kidney International|January 13, 2012
Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutationsJohanna Temme, Frederick Peters, Katharina Lange, et al.
Frontiers in Pediatrics|December 19, 2019
The Hypomorphic Variant p.(Gly624Asp) in <i>COL4A5</i> as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport SyndromeEva Pauline Macheroux, Matthias C Braunisch, Stephanie Pucci Pegler, et al.
Proteome Science|December 20, 2014
Effects of mycophenolate mofetil on kidney function and phosphorylation status of renal proteins in Alport COL4A3-deficient miceDarinka Todorova Petrova, Frank Christian Schultze, Gunnar Brandhorst, et al.
Pageof 15