Embryonic Development News and Research

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Embryonic development or embryogenesis is the process by which the embryo is formed and develops. It starts with the fertilization of the ovum, egg, which, after fertilization, is then called a zygote. The zygote undergoes rapid mitotic divisions, the formation of two exact genetic replicates of the original cell, with no significant growth (a process known as cleavage) and cellular differentiation, leading to development of an embryo.

Novel method makes genetic analyses possible for all regions of the intestine

With its length and multitude of folds and protrusions, the intestine represents the largest contact surface between our body and the food taken up from the outside.

23 Jan 2023

Research reveals the cellular origin of cancer-associated fibroblasts

A type of cell that plays a key role in pancreatic cancer can trace its origin back to a structure that forms during embryonic development, new research at MUSC Hollings Cancer Center shows.

20 Jan 2023

Study reveals how new cells join existing tissues by reading mechanical information

Integration is not only a problem of social significance among humans, but also an issue for the cells that form us as humans.

12 Jan 2023

Researchers identify novel gene mechanism in most aggressive kidney cancers

In a new study from the Johns Hopkins Kimmel Cancer Center, researchers described a novel mechanism of tumor formation in kidney cancers driven by overexpression of the mechanistic target of rapamycin complex 1 (mTORC1) signaling pathway with loss of the tuberous sclerosis complex (TSC) tumor suppressor gene.

3 Jan 2023

'Epigenetic fingerprints' of prenatal alcohol exposure could be biomarkers to detect developmental disorders

Alcohol exposure in early pregnancy can change gene function during the tightly regulated embryonic development, and consequently cause developmental disorders - especially neurodevelopmental disorders.

3 Jan 2023

Study provides insights into the coordinated dance of nerve and vascular cells

Nerve cells need a lot of energy and oxygen. They receive both through the blood. This is why nerve tissue is usually crisscrossed by a large number of blood vessels.

21 Dec 2022

New mutations near known genes could contribute to the increase in cleft lip and palate risk

Cleft lip and palate are among the most common congenital malformations, which are mainly due to genetic causes.

16 Dec 2022

Scientists uncover how FoxH1 factor binds to specific points in the genome

Transcription factors are proteins that interact with DNA to regulate the function of some genes. Generally, a single transcription factor binds to several regions in the genome as it orchestrates complex cellular responses, which require the activation or inhibition of several genes.

15 Dec 2022

Animal study pinpoints a gene that is vital for development of earliest social behaviors

Little is known about how social behavior develops in the earliest stages of life. But most animals––including humans––are born with an innate ability to interact socially or form bonds with others. And that contributes to success throughout life.

24 Nov 2022

Scientists provide metrics for organ development

Organs in the human body have complex networks of fluid-filled tubes and loops. They come in different shapes and their three-dimensional structures are differently connected to each other, depending on the organ.

21 Nov 2022

Gene may play a broader role in embryonic organ development

An international study led by the medical Faculty of the University of Bonn has identified a gene that plays an important role in the development of the human embryo. If it is altered, malformations of various organ systems can result.

15 Nov 2022

Researchers illuminate the role of extracellular vesicles in cancer progression

The advent of cell phones, the internet, and various messaging platforms has allowed for faster and broader communication worldwide.

10 Nov 2022

Study finds possible treatment strategy for Feingold syndrome type 1

A decrease in protein synthesis in cells of the developing gut contributes to a rare genetic disorder, and an inexpensive nutritional supplement may help reverse that decrease, according to a new study publishing November 1st in the open access journal PLOS Biology by Yun-Fei Li of Zhejiang University School of Medicine in Hangzhou, China, and colleagues. The finding is an advance in understanding the pathogenesis of the disease, and may lead to new treatments.

2 Nov 2022

Embryonic Development News and Research

Further Reading

Novel method makes genetic analyses possible for all regions of the intestine

Research reveals the cellular origin of cancer-associated fibroblasts

Study reveals how new cells join existing tissues by reading mechanical information

Researchers identify novel gene mechanism in most aggressive kidney cancers

'Epigenetic fingerprints' of prenatal alcohol exposure could be biomarkers to detect developmental disorders

Study provides insights into the coordinated dance of nerve and vascular cells

New mutations near known genes could contribute to the increase in cleft lip and palate risk

Scientists uncover how FoxH1 factor binds to specific points in the genome

Animal study pinpoints a gene that is vital for development of earliest social behaviors

Scientists provide metrics for organ development

Gene may play a broader role in embryonic organ development

Researchers illuminate the role of extracellular vesicles in cancer progression

Study finds possible treatment strategy for Feingold syndrome type 1

New breakthrough in understanding how deletion of certain genes can lead to cancer growth

Ancient viral DNA in human genomes protects cells against present-day viruses

Researchers propose guidelines and methods for consistently generating high-quality brain organoids

Live imaging and cellular barcoding reveal how new stem cells are vetted for quality

Researchers identify key gene network responsible for severe tooth enamel defects

Medulloblastomas originate much earlier in pregnancy than previously thought and may be preventable

New genetic discovery improves understanding of congenital heart disease

Achieving and maintaining ISO 27001 and BS 10012 certifications

Expanding research and clinical options for children with cancer

Examining how pain could play a direct protective role in the gut

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