Genetic Engineering to Program Cells

Genetic engineering is a process that alters the genetic structure of an organism by removing or introducing DNA. This technique is being tested to program cells. Discover the latest research on genetic engineering to program cells here.

September 15, 2020
Open Access

Genetic buffering and potentiation in metabolism

PLoS Computational Biology
Juan F Poyatos
September 18, 2020

Reprogramming roadmap reveals route to human induced trophoblast stem cells

Nature
Xiaodong LiuJose M Polo
September 15, 2020
Preprint

Generation of human induced trophoblast stem cells

BioRxiv : the Preprint Server for Biology
G. CASTELLaurent DAVID
September 17, 2020
Open Access

Histone deacetylase HDA-1 modulates mitochondrial stress response and longevity

Nature Communications
Li-Wa ShaoYing Liu
September 16, 2020
Open Access

IL-4Rα signalling in CD4+CD25+FoxP3+ T regulatory cells restrain airway inflammation via limiting local tissue IL-33

JCI Insight
Jermaine KhumaloFrank Brombacher
September 17, 2020
Open Access

Phenotype stability under dynamic brain-tumor environment stimuli maps glioblastoma progression in patients

Science Advances
Vinodh N RajapakseOrit Lavi
September 17, 2020
Review
Open Access

Ionizing Radiation and Translation Control: A Link to Radiation Hormesis?

International Journal of Molecular Sciences
Usha KabilanDmitry Klokov
September 16, 2020

Distinct cell-types in the prostate share an aging signature suggestive of metabolic reprogramming

American Journal of Clinical and Experimental Urology
Preston D CrowellAndrew S Goldstein
September 15, 2020
Review
Open Access

FPAA-based implementation of fractional-order chaotic oscillators using first-order active filter blocks

Journal of Advanced Research
Alejandro Silva-JuárezRui Li
September 17, 2020
Open Access

Extensive SUMO Modification of Repressive Chromatin Factors Distinguishes Pluripotent from Somatic Cells

Cell Reports
Ilan TheurillatAnne Dejean
September 17, 2020
Review
Open Access

Organotypic Culture of Acinar Cells for the Study of Pancreatic Cancer Initiation

Cancers
Carlotta Paoli, Alessandro Carrer
September 18, 2020
Open Access

AGL15 Controls the Embryogenic Reprogramming of Somatic Cells in Arabidopsis through the Histone Acetylation-Mediated Repression of the miRNA Biogenesis Genes

International Journal of Molecular Sciences
Katarzyna NowakMałgorzata D Gaj
September 17, 2020
Open Access

Generation of self-organized sensory ganglion organoids and retinal ganglion cells from fibroblasts

Science Advances
Dongchang XiaoMengqing Xiang
September 17, 2020
Review
Open Access

IL15 synergizes with radiotherapy to reprogram the tumor immune contexture through a dendritic cell connection

Oncoimmunology
Karsten A PilonesSandra Demaria
September 17, 2020
Open Access

A Possible Role of FZD10 Delivering Exosomes Derived from Colon Cancers Cell Lines in Inducing Activation of Epithelial-Mesenchymal Transition in Normal Colon Epithelial Cell Line

International Journal of Molecular Sciences
Maria Principia ScavoGianluigi Giannelli
September 17, 2020
Open Access

Adipocyte Reprogramming by the Transcriptional Coregulator GPS2 Impacts Beta Cell Insulin Secretion

Cell Reports
Karima DrareniNicolas Venteclef
September 16, 2020

Role of cholesterol metabolism in the anticancer pharmacology of selective estrogen receptor modulators

Seminars in Cancer Biology
Diego Gómez-CoronadoMaría E Fernández-Suárez

Sign up to follow this feed and discover related papers.

Related Feeds

AAV-based Gene Therapy

Adeno-associated virus (AAV)-based gene therapy is a biological vector that is being researched to be used as a potential therapeutic option. This gene therapy is designed to insert fragments of DNA into targeted cells to help treat diseases, such as hemophilia a. Discover the latest research on AAV-based gene therapy here.

ALS: Genetics

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized by muscle weakness. ALS is a genetically heterogeneous disorder with several causative genes. Here are the latest discoveries pertaining to the genetics of this disease.

Acute Myeloid Leukaemia & RNA

Acute myeloid leukaemia (AML) is a common hematological type of cancer. As the population ages, there has been a rise in the frequency of AML. RNA expression has been used to see if there are different genetic profiles that exist within AML and whether these may underpin the variations in survival rates. Here is the latest research on AML and RNA.

Adult Kidney Organoids at Single Cell Resolution

Single-cell RNA sequencing of the adult human kidney transcriptome can provide molecular information about cell-specific responses to environmental variables and disease states. This information can provide a dataset to benchmark human kidney organoids. Discover the latest research on adult kidney organoids at single cell resolution here.

Adult Stem Cells

Adult stem cells reside in unique niches that provide vital cues for their survival, self-renewal, and differentiation. They hold great promise for use in tissue repair and regeneration as a novel therapeutic strategies. Here is the latest research.

Allogenic & Autologous Therapies

Allogenic therapies are generated in large batches from unrelated donor tissues such as bone marrow. In contrast, autologous therapies are manufactures as a single lot from the patient being treated. Here is the latest research on allogenic and autologous therapies.

Alzheimer's Disease: Genetics

Alzheimer's disease is a chronic neurodegenerative disease. Discover genetic and epigenetic aspects of Alzheimer’s disease, including genetic markers and genomic structural variations here.

Antisense Oligonucleotide - Therapies For ALS

This feed focuses on antisense oligonucleotide therapies such as Inotersen, Nusinursen, and Patisiran, in neurodegenerative diseases including amyotrophic lateral sclerosis.

Antisense Oligonucleotides: ND

This feed focuses on antisense oligonucleotide therapies such as Inotersen, Nusinursen, and Patisiran, in neurodegenerative diseases including amyotrophic lateral sclerosis.

Artificial Cell Models

This feed focuses on biomimetrics, synthetic biology and bio- and tissue-engineering approaches used for modeling human diseases.

© 2020 Meta ULC. All rights reserved
/feed-previews/genetic-engineering-to-program/f884d981-f108-49ca-8605-a4a2843df4d6