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Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

HPV8 E6 gene causes growth of certain skin stem cells.

The PP2A-B55α protein is essential for brain and skin development in embryos.

The research found new potential mechanisms in mouse hair growth by studying RNA interactions.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

miRNAs in the Dlk1-Gtl2 region may improve lamb fur quality.

The study found key long non-coding RNAs involved in yak hair growth cycles.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Nitrate helps plants manage phosphate uptake and starvation responses through NIGT1 proteins.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

A specific gene variation in goats is linked to better growth traits.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

AMPK activation may reduce melanoma risk in red-haired individuals.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

RORA boosts autophagy in hair follicle stem cells, potentially aiding hair growth.

Mutations in the LIPH gene cause woolly hair in a child.

Certain gene variations are found in people with polycystic ovary syndrome.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.