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A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

Two enzymes regulate androgen receptor activity, affecting treatments for androgen insufficiency and benign prostatic hyperplasia.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Non-coding RNAs help control hair growth in cashmere goats.

Lack of KSR1 stops certain skin tumors in mice.

Gsdma3 affects hair growth by controlling Wnt5a, which influences hair cell development.

Ocu-miR-205 affects hair density in Rex rabbits by influencing cell processes and signaling pathways.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

A specific mutation in PA-PLA1α causes abnormal hair growth.

The gene HDC is important for the development of hair follicles in newborn mice.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

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

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

The conclusion is that a treatment called cp-asiAR can reduce hair loss and promote hair growth, making it a potential new therapy for androgenetic alopecia.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

New mutations in the hairless gene may cause hair loss and affect bone development.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

GLI2 increases follistatin production in human skin cells.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.