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

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

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

Anti-androgens are effective for female acne but less so for male-pattern hair loss, with side effects similar to birth control pills.

Androgens, like DHT, affect hair growth and treatments like finasteride may help.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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.

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.

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

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.

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

Fluorescence can effectively measure acne treatment progress.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Six new hair loss factors in men not linked to female hair loss.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.