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Epimorphin, a protein, plays a key role in the development of hair follicles in human fetuses, but it doesn't help in maintaining the stem cell population of the follicular skin layer.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Modulating Cytochrome P450 activity could help develop new skin disease treatments.

Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

A specific gene mutation causes congenital hair loss.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

The AVET system effectively delivers genes to human keratinocytes and may help treat skin diseases.

Fluorescence can effectively measure acne treatment progress.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Feather patterns are influenced by enhancers and chromatin looping, and the structure of protein complexes important for hair growth has been detailed.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High levels of male hormones, insulin resistance, and obesity are closely linked and worsen polycystic ovary syndrome, but more research is needed to improve treatments.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.