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Khun Zaw Latt

Showing results (1-10 of 17) with videos related to

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Frontiers in Medicine|November 12, 2021
Lessons From APOL1 Animal ModelsTeruhiko Yoshida, Khun Zaw Latt, Jurgen Heymann, et al.
Frontiers in Medicine|November 15, 2021
Glomerular Kidney Diseases in the Single-Cell EraKhun Zaw Latt, Jurgen Heymann, Teruhiko Yoshida, et al.
F1000Research|September 3, 2020
Jupyter notebook-based tools for building structured datasets from the Sequence Read ArchiveMatthew N Bernstein, Ariella Gladstein, Khun Zaw Latt, et al.
Kidney International Reports|January 16, 2023
Transcriptomic Analysis of Human Podocytes <i>In Vitro</i>: Effects of Differentiation and <i>APOL1</i> GenotypeTeruhiko Yoshida, Khun Zaw Latt, Avi Z Rosenberg, et al.
Human Genome Variation|April 16, 2016
Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individualsXiaoxi Liu, Minae Kawashima, Taku Miyagawa, et al.
Human Genome Variation|April 16, 2016
Erratum: Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individualsXiaoxi Liu, Minae Kawashima, Taku Miyagawa, et al.
Biorxiv : the Preprint Server for Biology|January 13, 2025
Preeclampsia in mice carrying fetuses with APOL1 risk variantsTeruhiko Yoshida, Khun Zaw Latt, Shashi Shrivastav, et al.
Scientific Reports|October 24, 2018
Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous NephropathyKhun Zaw Latt, Kenjiro Honda, Myo Thiri, et al.
Biorxiv : the Preprint Server for Biology|April 24, 2023
APOL1 kidney risk variants in glomerular diseases modeled in transgenic miceTeruhiko Yoshida, Khun Zaw Latt, Briana A Santo, et al.
Journal of the American Society of Nephrology : JASN|May 6, 2024
Single-Cell Transcriptional Signatures of Glomerular Disease in Transgenic Mice with APOL1 VariantsTeruhiko Yoshida, Khun Zaw Latt, Briana A Santo, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Frontiers in Medicine|November 12, 2021
Lessons From APOL1 Animal ModelsTeruhiko Yoshida, Khun Zaw Latt, Jurgen Heymann, et al.
Frontiers in Medicine|November 15, 2021
Glomerular Kidney Diseases in the Single-Cell EraKhun Zaw Latt, Jurgen Heymann, Teruhiko Yoshida, et al.
F1000Research|September 3, 2020
Jupyter notebook-based tools for building structured datasets from the Sequence Read ArchiveMatthew N Bernstein, Ariella Gladstein, Khun Zaw Latt, et al.
Kidney International Reports|January 16, 2023
Transcriptomic Analysis of Human Podocytes <i>In Vitro</i>: Effects of Differentiation and <i>APOL1</i> GenotypeTeruhiko Yoshida, Khun Zaw Latt, Avi Z Rosenberg, et al.
Human Genome Variation|April 16, 2016
Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individualsXiaoxi Liu, Minae Kawashima, Taku Miyagawa, et al.
Human Genome Variation|April 16, 2016
Erratum: Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individualsXiaoxi Liu, Minae Kawashima, Taku Miyagawa, et al.
Biorxiv : the Preprint Server for Biology|January 13, 2025
Preeclampsia in mice carrying fetuses with APOL1 risk variantsTeruhiko Yoshida, Khun Zaw Latt, Shashi Shrivastav, et al.
Scientific Reports|October 24, 2018
Identification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous NephropathyKhun Zaw Latt, Kenjiro Honda, Myo Thiri, et al.
Biorxiv : the Preprint Server for Biology|April 24, 2023
APOL1 kidney risk variants in glomerular diseases modeled in transgenic miceTeruhiko Yoshida, Khun Zaw Latt, Briana A Santo, et al.
Journal of the American Society of Nephrology : JASN|May 6, 2024
Single-Cell Transcriptional Signatures of Glomerular Disease in Transgenic Mice with APOL1 VariantsTeruhiko Yoshida, Khun Zaw Latt, Briana A Santo, et al.
Pageof 2