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Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Hyaluronan from Has2 is important for proper wound healing and hair follicle development.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

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

Three siblings with a genetic form of rickets showed different symptoms of the disease.

IL-15 helps maintain hair growth and protects the immune status of hair follicles.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

Specific immune cells cause alopecia areata and blocking certain proteins can prevent it.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21.

Discoid Lupus Erythematosus causes scalp plaques that can lead to hair loss, and antimalarial drugs are effective treatments.

A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Some hair proteins are specific to hair, while others are also found in skin cells.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

Scalp lesions in discoid lupus are more common in women and linked to other autoimmune diseases.

Enhancing Tregs can protect against alopecia areata.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

The dense fine speckled pattern in ANA tests is common in autoimmune diseases, challenging previous beliefs that it was unrelated.

A specific type of immune cell plays a key role in causing alopecia areata and could be a target for treatment.

Two genetic variations in Moa buffalo help them adapt to heat.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

Researchers found a gene mutation responsible for a rare hair loss condition.

Blocking the CCR5 receptor may be a new way to treat hair loss from alopecia areata.

The document suggests a rare skin condition might be caused by a genetic phenomenon.