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Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.

Topical minoxidil improves hair loss in 80% of women with breast cancer undergoing endocrine therapy.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Selective breeding caused the unique curly hair in Mangalitza pigs.

t-Flavanone helps improve male pattern hair loss by making hair roots stronger.

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

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Key genes linked to hair growth and cancer were identified in hairless mice.

Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

Using special RNA to target a mutant gene fixed hair problems in mice.

Different hair loss types need accurate diagnosis for proper treatment.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Iron deficiency might contribute to hair loss in women.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

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.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

CaV1.2 helps activate hair follicle stem cells without calcium flux.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

A girl with Denys-Drash syndrome was misdiagnosed due to biotin affecting her hormone test results.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Early treatment of acne is crucial to prevent scarring and psychological effects.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.