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Zongliang Jiang

Researcher at Louisiana State University

Publications -  45
Citations -  939

Zongliang Jiang is an academic researcher from Louisiana State University. The author has contributed to research in topics: DNA methylation & Embryo. The author has an hindex of 15, co-authored 37 publications receiving 572 citations. Previous affiliations of Zongliang Jiang include University of Connecticut & Yale University.

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Transcriptional profiles of bovine in vivo pre-implantation development.

TL;DR: This study provides a comprehensive examination of gene activities in bovine embryos and identified little-known potential master regulators of pre-implantation development, demonstrating that bovines are better models for human embryonic development.
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Jak/Stat3 signaling promotes somatic cell reprogramming by epigenetic regulation.

TL;DR: It is concluded that Jak/Stat3 activity plays a fundamental role to promote pluripotency establishment at the epigenetic level, by facilitating DNA demethylation/de novo methylation, and open‐chromatin formation during late‐stage reprogramming.
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Mitochondrial dysfunction and ovarian aging.

TL;DR: Mitochondria are double‐membrane‐bound organelles that are responsible for the generation of most of the cell's energy and have been implicated in cellular senescence in general and ovarian aging in particular.
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Mitochondrial unfolded protein response gene Clpp is required to maintain ovarian follicular reserve during aging, for oocyte competence, and development of pre-implantation embryos.

TL;DR: It is demonstrated that CLPP is required for oocyte and embryo development and oocyte mitochondrial function and dynamics, and absence of CLPP results in mTOR pathway activation, and accelerated depletion of ovarian follicular reserve.
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Mitofusin 1 is required for female fertility and to maintain ovarian follicular reserve

TL;DR: Targeted deletion of mitochondrial fusion protein mitofusin1 (MFN1) in oocytes resulted in female infertility associated with failure to achieve oocyte maturation and a phenotype consistent with accelerated female reproductive aging.