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The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

LC-OCT is a promising tool for diagnosing and monitoring Alopecia areata.

Ca 45 mainly enters rat skin and eye through biosynthesis and may be adsorbed in cartilage and glands.

Visual signs are crucial for accurately diagnosing and treating different types of hair loss in Black patients.

Acorus calamus has potential health benefits but needs more safety research.

A balanced mix of cationic guar gum and anionic surfactants improves hair conditioning and protection.

Liposomal cepharanthine lotion speeds up hair growth in men with early balding.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Aftimoon (Cuscuta reflexa) has various health benefits, including anti-inflammatory and anticonvulsant effects.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A simple enrichment program improves health and reproduction in Calomys callosus.

KAP8.2 gene variations affect cashmere quality in goats.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Avicequinone C, a compound found in the Avicennia marina plant, can reduce hair loss by inhibiting a hormone linked to androgenic alopecia.

Microparticles help caffeic acid stay longer in hair follicles for better treatment of folliculitis.

AUC and APL are distinct conditions needing careful clinical assessment.

Chemotherapy can cause hair changes similar to alopecia areata, which might lead to misdiagnosis.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Both induced and spontaneous AA lymphocytes can cause alopecia areata in mice.

Scarring hair loss found in female pattern; biopsy needed for diagnosis.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

The AAPPO questionnaire is a reliable tool for assessing hair loss impact in alopecia areata patients.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.