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Showing results (271-280 of 318) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|January 30, 2013
Matrix metalloproteinase-9 of tubular and macrophage origin contributes to the pathogenesis of renal fibrosis via macrophage recruitment through osteopontin cleavageThian Kui Tan, Guoping Zheng, Tzu-Ting Hsu, et al.
Molecular Therapy. Nucleic Acids|March 23, 2017
Limiting Thymic Precursor Supply Increases the Risk of Lymphoid Malignancy in Murine X-Linked Severe Combined ImmunodeficiencySamantha L Ginn, Claus V Hallwirth, Sophia H Y Liao, et al.
Journal of the American Society of Nephrology : JASN|January 4, 2018
Potentiating Tissue-Resident Type 2 Innate Lymphoid Cells by IL-33 to Prevent Renal Ischemia-Reperfusion InjuryQi Cao, Yiping Wang, Zhiguo Niu, et al.
JHEP Reports : Innovation in Hepatology|September 11, 2023
Type 2 innate lymphoid cells are protective against hepatic ischaemia/reperfusion injuryQi Cao, Ruifeng Wang, Zhiguo Niu, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 28, 2019
Promotion of β-catenin/Foxo1 signaling ameliorates renal interstitial fibrosisPadmashree Rao, Min Pang, Xi Qiao, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 10, 2024
Patient, Parental, and Health Professional Perspectives on Growth in Children With CKDJustin G Wu, Chandana Guha, Anastasia Hughes, et al.
The Medical Journal of Australia|May 4, 2005
Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in AustraliaSamantha L Ginn, Julie A Curtin, Belinda Kramer, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 27, 2022
Perspectives of Clinicians on Shared Decision Making in Pediatric CKD: A Qualitative StudyJasmijn Kerklaan, Camilla S Hanson, Simon Carter, et al.
JCI Insight|August 10, 2018
Direct recognition of hepatocyte-expressed MHC class I alloantigens is required for tolerance inductionMoumita Paul-Heng, Mario Leong, Eithne Cunningham, et al.
Human Molecular Genetics|January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaMinal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Pageof 32

Showing results (271-280 of 318) with videos related to

Sort By:
Pageof 32
Laboratory Investigation; a Journal of Technical Methods and Pathology|January 30, 2013
Matrix metalloproteinase-9 of tubular and macrophage origin contributes to the pathogenesis of renal fibrosis via macrophage recruitment through osteopontin cleavageThian Kui Tan, Guoping Zheng, Tzu-Ting Hsu, et al.
Molecular Therapy. Nucleic Acids|March 23, 2017
Limiting Thymic Precursor Supply Increases the Risk of Lymphoid Malignancy in Murine X-Linked Severe Combined ImmunodeficiencySamantha L Ginn, Claus V Hallwirth, Sophia H Y Liao, et al.
Journal of the American Society of Nephrology : JASN|January 4, 2018
Potentiating Tissue-Resident Type 2 Innate Lymphoid Cells by IL-33 to Prevent Renal Ischemia-Reperfusion InjuryQi Cao, Yiping Wang, Zhiguo Niu, et al.
JHEP Reports : Innovation in Hepatology|September 11, 2023
Type 2 innate lymphoid cells are protective against hepatic ischaemia/reperfusion injuryQi Cao, Ruifeng Wang, Zhiguo Niu, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 28, 2019
Promotion of β-catenin/Foxo1 signaling ameliorates renal interstitial fibrosisPadmashree Rao, Min Pang, Xi Qiao, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 10, 2024
Patient, Parental, and Health Professional Perspectives on Growth in Children With CKDJustin G Wu, Chandana Guha, Anastasia Hughes, et al.
The Medical Journal of Australia|May 4, 2005
Treatment of an infant with X-linked severe combined immunodeficiency (SCID-X1) by gene therapy in AustraliaSamantha L Ginn, Julie A Curtin, Belinda Kramer, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 27, 2022
Perspectives of Clinicians on Shared Decision Making in Pediatric CKD: A Qualitative StudyJasmijn Kerklaan, Camilla S Hanson, Simon Carter, et al.
JCI Insight|August 10, 2018
Direct recognition of hepatocyte-expressed MHC class I alloantigens is required for tolerance inductionMoumita Paul-Heng, Mario Leong, Eithne Cunningham, et al.
Human Molecular Genetics|January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemiaMinal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Pageof 32