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The QR 678 hair growth treatment was safe and effective for hair regrowth in men and women.

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

CCL5 is important for the hair growth potential of human dermal papilla cells.

A preauricular crease is common in people with coronary artery disease.

Cyproterone acetate temporarily reduces hair growth in women with idiopathic hirsutism but doesn't change hormone levels.

A simple, precise method was created for estimating Tamsulosin and Finasteride in medicine using common lab solvents, showing good precision and stability.

PCOS is the main cause of hirsutism, often linked to insulin resistance.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

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.

New cryomicroneedles can improve hair growth and regeneration.

Caribine from traditional Chinese medicine may help treat hair loss.

The therapies improved ejaculation disorders and sexual function in middle-aged men.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

Scientists created a new 3D skin model from cells of plucked hairs that works like real skin and is easier to get.

Home-use light devices can significantly reduce hair but are less effective on very dark skin and slower than professional devices.

The method is quick and effective for testing steroid 5 alpha-reductase inhibitors.

Fullerene C60 shows promise as a new treatment for various skin conditions.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Women of reproductive age with polycystic ovary syndrome often experience hair loss.

Increasing calcium sensing receptor speeds up skin and hair development in mice.

Cetuximab can cause unusual hair growth and hair loss.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

Lack of functional CYLD in mice leads to early aging and cancer.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Optimal conditions for extracting beneficial compounds from Carthamus caeruleus L. rhizomes were identified, improving efficiency.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.