Search

everythinglearnresearchcommunity

for

Search:↓

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

CCC1 is essential for pH balance and normal cell function in plants.

A rare genetic deletion in the KRT1 gene causes unique skin symptoms in a family.

Fatty acid transport protein 4 is essential for skin and hair development.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

HSPC016 gene is important for hair growth.

Blocking the Wnt/β‐catenin pathway can speed up wound healing, reduce scarring, and improve cartilage repair.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

PTHrP regulates various normal body functions, including bone development, skin, and muscle function.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

QLT0267 stops hair follicle cell growth and movement.

Certain herbal compounds, especially from bitter melon, can inhibit cancer growth and promote hair growth by blocking PAK1.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

Four specific genes are linked to keloid formation and could be potential treatment targets.

Mice can regenerate ear tissue without the p53 protein.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

Blocking mTORC1 reduces skin tumor growth in mice.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.