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Cyclophosphamide often causes gastrointestinal issues, hair loss, and low blood cell counts in Chinese patients with autoimmune diseases.

'Eclipta prostrata' plants in Taiwan are infected with 'Candidatus Phytoplasma aurantifolia'.

A new mouse model effectively mimics vitiligo for research and drug testing.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

PTCH gene mutations contribute to basal cell carcinoma development.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Scientists made antibodies to tell cashmere and wool apart, which could improve how we identify animal fibers.

AMH is a reliable marker for diagnosing PCOS.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Diphencyprone can cause unexpected and possibly permanent vitiligo.

CD8+ T cells re-expressing CD45RA may predict treatment resistance in severe alopecia areata.

Specific keratin gene mutations can cause monilethrix.

New genetic variants linked to albinism were found in Pakistani families.

The patient had a severe allergic reaction to gold treatment.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

Fetal skin has unique immune cells different from adult skin.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

Lambs' skin showed similar but more severe responses to a second orf virus infection, involving immune cells and new skin formation.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Bendamustine combined with tucidinostat may effectively treat adult T-cell leukemia.

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.