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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.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

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A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

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

Low-level light therapy safely improves hair growth and thickness for androgenetic alopecia.

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Drug approvals slowed in 2Q22, but notable drugs like Amvuttra, Camzyos, and Olumiant were approved.

The study found that minor protein differences between curved and straight Japanese hair are unlikely to significantly affect hair structure.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

The research developed methods to test drugs that could protect and restore hair follicle protection in a hair loss condition.

AUC and APL are distinct conditions needing careful clinical assessment.

Ritlecitinib significantly improves scalp hair regrowth in alopecia areata patients over time.

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

A new group called the Asian Association of Hair Restoration Surgeons (AAHRS) has been created.

The LTF gene may help predict and manage nonspecific orbital inflammation.

N‐AOHPA is a promising alternative to traditional surfactants for better hair conditioning.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.