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Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Sun exposure and genetics increase skin cancer risk from precancerous lesions.

K15 is a reliable marker for studying stem cells in dog hair follicle tumors.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

Early onset female hair loss is linked to lower hair density, scalp issues, and certain genetic factors.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Keratins 8 and 14 can help identify and diagnose benign skin tumors.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

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

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

17b-Estradiol in skin affects hair growth and tumor promotion.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The PML protein helps prevent skin cancer in mice.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Keratin 17 is crucial for early hair strength and cell survival.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Most genetic mutations causing hypohidrotic ectodermal dysplasia in Russian patients are found in the EDA gene.

A rare gene variant causes hair and nail issues in a family.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.