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Gwang-Jin Kim

Showing results (11-20 of 19) with videos related to

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Communications Biology|July 1, 2026
Base editing-derived models of human WDR34 and WDR60 disease alleles replicate retrograde intraflagellar transport (IFT) and hedgehog signaling defectsDinu Antony, Elif Yilmaz Güleç, Anna Klawonn, et al.
Innovations in Pharmacy|August 29, 2022
Efficacy and Safety of Innovative Experimental Chimeric Antigen Receptor (CAR) T-cells versus Axicabtagene ciloleucel (Yescarta) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma (LBCL): Matching Adjusted Indirect Comparisons (MAICs) and Systematic ReviewBayarmagnai Weinstein, Bogdan Muresan, Sara Solano, et al.
Developmental Cell|August 26, 2023
Eomes restricts Brachyury functions at the onset of mouse gastrulationKatrin M Schüle, Jelena Weckerle, Simone Probst, et al.
Toxicology and Applied Pharmacology|March 30, 2018
Gene expression profiling of human bronchial epithelial cells exposed to fine particulate matter (PM<sub>2.5</sub>) from biomass combustionDésirée Popadić, Katharina Heßelbach, Sigrid Richter-Brockmann, et al.
Plos Genetics|June 12, 2013
Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humansFranz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, et al.
Nature Genetics|January 17, 2012
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansAnaïs Grall, Eric Guaguère, Sandrine Planchais, et al.
Journal of Medical Genetics|January 22, 2015
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex developmentGwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Communications Biology|July 1, 2026
Base editing-derived models of human WDR34 and WDR60 disease alleles replicate retrograde intraflagellar transport (IFT) and hedgehog signaling defectsDinu Antony, Elif Yilmaz Güleç, Anna Klawonn, et al.
Innovations in Pharmacy|August 29, 2022
Efficacy and Safety of Innovative Experimental Chimeric Antigen Receptor (CAR) T-cells versus Axicabtagene ciloleucel (Yescarta) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma (LBCL): Matching Adjusted Indirect Comparisons (MAICs) and Systematic ReviewBayarmagnai Weinstein, Bogdan Muresan, Sara Solano, et al.
Developmental Cell|August 26, 2023
Eomes restricts Brachyury functions at the onset of mouse gastrulationKatrin M Schüle, Jelena Weckerle, Simone Probst, et al.
Toxicology and Applied Pharmacology|March 30, 2018
Gene expression profiling of human bronchial epithelial cells exposed to fine particulate matter (PM<sub>2.5</sub>) from biomass combustionDésirée Popadić, Katharina Heßelbach, Sigrid Richter-Brockmann, et al.
Plos Genetics|June 12, 2013
Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humansFranz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, et al.
Nature Genetics|January 17, 2012
PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansAnaïs Grall, Eric Guaguère, Sandrine Planchais, et al.
Journal of Medical Genetics|January 22, 2015
Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex developmentGwang-Jin Kim, Elisabeth Sock, Astrid Buchberger, et al.
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Implication of <i>FOXD2</i> dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Kidney International|December 28, 2023
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)Korbinian M Riedhammer, Thanh-Minh T Nguyen, Can Koşukcu, et al.
Pageof 2