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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Platelet-rich plasma may improve embryo genetics in IVF.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

New genetic mutations causing hair loss were found in a Chinese family.

Activated platelet-rich plasma helps hair growth by boosting growth factors and cell growth pathways in hair cells.

Researchers created an efficient method to extract DNA from marmoset hair, reducing blood chimerism.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Removing the p75 gene in mouse skin cells didn't affect their skin or hair growth.

Neuregulin3 affects cell development in the skin and mammary glands.

Blocking mTORC1 reduces skin tumor growth in mice.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

Platelet-rich plasma (PRP) may help promote hair growth and improve graft survival after hair transplantation, but more research is needed to confirm its effectiveness and determine the best dosage.

A gene mutation causes curly hair and hair loss in rats.

RNase L hinders hair follicle regeneration by altering immune signals.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, which could be a new target for treating hair loss and other skin conditions driven by testosterone.

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

The new lab-grown skin model is good for testing sunscreen's protection against DNA damage from UV light.

miR-200a reduces goose fibroblast growth by targeting PITX2 in the Wnt pathway.

A single medium, PRIME AIRLIFT, supports better human hair follicle formation in grafts.

Retinoic acid changes skin cells to mucosal cells with goblet cells, needing TG2/Gh, Gbx1, and TGF-beta.