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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Recent selection on immune response genes was identified across seven ethnicities.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

Somatic BHD mutations are rare in Japanese renal tumors.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The balance between cell renewal and differentiation controls the growth of cancerous cells in mouse skin.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Certain gene variations increase the risk of alopecia areata in Koreans.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Alopecia can be caused by multicentric reticulohistiocytosis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

HPV-150 and HPV-151 are rare skin viruses linked to warts and some skin cancers.

A unique gene mutation was found in a family with monilethrix.

A gene mutation in mice causes permanent hair loss and skin issues.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.