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New mutations in hair keratin genes cause the rare hair disorder monilethrix.

CGRP MAbs treatment for migraines may also improve rosacea symptoms, but more research is needed to confirm its effectiveness and safety.

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

SHPro® improved urinary symptoms and erectile function in men and is safe.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Haplogroup X found in Altaian population supports Amerindian origin.

Scientists created iodinated arylhydantoins and arylthiohydantoins that could potentially be used for imaging prostate cancer. Some versions with specific side-chains showed high potential for this use.

MC1R gene variations affect skin, hair color, UV sensitivity, and melanoma risk.

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

Long non-coding RNA Xist plays a key role in sex bias in lupus and rheumatoid arthritis, especially in females.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

A man's skin cancer improved and some of his hair grew back after treatment with a special light therapy and a medication.

Smaller substituents at C-17 enhance the inhibitory activity of progesterone derivatives on 5alpha-reductase.

The system helps monitor hair properties using RGB video microscopy.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Rosacea severely affects the quality of life for many patients in China, especially young adults and those with appearance-related jobs.

Using cans with beans improves Rex rabbits' growth, meat quality, and hair follicle density.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.