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Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

SH-MSCs gel can effectively treat alopecia by increasing IL-10 and decreasing TNF-α gene expression.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Women with polycystic ovary syndrome tend to have a longer anogenital distance.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

Diphencyprone is effective for treating patchy hair loss in alopecia areata, but tacrolimus is not.

ATIR101 improves survival in stem cell transplant patients; Australian stem cell treatment decisions are influenced by regulation changes.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Sox13 is a new marker for early hair follicle development and differentiation.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Hoxc genes control hair growth through Wnt signaling.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Human epidermal neural crest stem cells can become bone and skin pigment cells, making them useful for therapies.

FGF5 gene mutations cause long hair in domestic cats.

Mice healed without scars as fetuses but developed scars as adults, suggesting scarless healing might be replicated with further research.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

A mutation in the KRTHB5 gene causes hair and nail issues.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Adding a specific gene to skin cells can help treat skin disorders like psoriasis.

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

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

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