Strategies for high-efficiency mutation using the CRISPR/Cas system
S Feng, Z Wang, A Li, X Xie, J Liu, S Li, Y Li… - Frontiers in cell and …, 2022 - frontiersin.org
Clustered regularly interspaced short palindromic repeats (CRISPR)-associated systems
have revolutionized traditional gene-editing tools and are a significant tool for ameliorating …
have revolutionized traditional gene-editing tools and are a significant tool for ameliorating …
Epigenetic and transcriptional regulations prime cell fate before division during human pluripotent stem cell differentiation
Stem cells undergo cellular division during their differentiation to produce daughter cells
with a new cellular identity. However, the epigenetic events and molecular mechanisms …
with a new cellular identity. However, the epigenetic events and molecular mechanisms …
Addressing variability and heterogeneity of induced pluripotent stem cell-derived cardiomyocytes
SM Biendarra-Tiegs, FJ Secreto, TJ Nelson - Cell Biology and …, 2020 - Springer
Induced pluripotent stem cells (iPSCs) offer great promise in the areas of disease modeling,
basic research, drug development, and regenerative medicine. Much of their value comes …
basic research, drug development, and regenerative medicine. Much of their value comes …
A spatially resolved single cell atlas of human gastrulation
RCV Tyser, E Mahammadov, S Nakanoh, L Vallier… - BioRxiv, 2020 - biorxiv.org
Gastrulation is the fundamental process during the embryogenesis of all multicellular
animals through which the basic body plan is first laid down. It is pivotal in generating …
animals through which the basic body plan is first laid down. It is pivotal in generating …
Analysis of endothelial-to-haematopoietic transition at the single cell level identifies cell cycle regulation as a driver of differentiation
G Canu, E Athanasiadis, RA Grandy… - Genome biology, 2020 - Springer
Abstract Background Haematopoietic stem cells (HSCs) first arise during development in the
aorta-gonad-mesonephros (AGM) region of the embryo from a population of haemogenic …
aorta-gonad-mesonephros (AGM) region of the embryo from a population of haemogenic …
[HTML][HTML] Thymine DNA glycosylase regulates cell-cycle-driven p53 transcriptional control in pluripotent cells
Cell cycle progression is linked to transcriptome dynamics and variations in the response of
pluripotent cells to differentiation cues, mostly through unknown determinants. Here, we …
pluripotent cells to differentiation cues, mostly through unknown determinants. Here, we …
Human surface ectoderm and amniotic ectoderm are sequentially specified according to cellular density
Mechanisms specifying amniotic ectoderm and surface ectoderm are unresolved in humans
due to their close similarities in expression patterns and signal requirements. This lack of …
due to their close similarities in expression patterns and signal requirements. This lack of …
Generation of new isogenic models of Huntington's disease using CRISPR-Cas9 technology
M Dabrowska, A Ciolak, E Kozlowska, A Fiszer… - International journal of …, 2020 - mdpi.com
Huntington's disease (HD) is a fatal neurodegenerative disorder caused by the expansion of
CAG repeats in exon 1 of the huntingtin gene (HTT). Despite its monogenic nature, HD …
CAG repeats in exon 1 of the huntingtin gene (HTT). Despite its monogenic nature, HD …
Pol α-primase dependent nuclear localization of the mammalian CST complex
JM Kelich, H Papaioannou, E Skordalakes - Communications Biology, 2021 - nature.com
The human CST complex composed of CTC1, STN1, and TEN1 is critically involved in
telomere maintenance and homeostasis. Specifically, CST terminates telomere extension by …
telomere maintenance and homeostasis. Specifically, CST terminates telomere extension by …
Recapitulating and reversing human brain ribosomopathy defects via the maladaptive integrated stress response
Animal or human models recapitulating brain ribosomopathies are incomplete, hampering
development of urgently needed therapies. Here, we generated genetic mouse and human …
development of urgently needed therapies. Here, we generated genetic mouse and human …