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Alloxan diabetes, methylthiouracil, cortisone, and adrenaline affect how white mice hair follicles use glucose and cystine and their cell division.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The fuzzy gene is crucial for controlling hair growth cycles.

Loss of Pten in certain hair follicle stem cells increases skin cancer risk.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

MAA beads improved wound healing in male mice by activating the Shh pathway, but not in females.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

Gingerol may help treat chronic graft-versus-host disease by improving immune cell balance.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

TICE salvage chemotherapy is effective for treating germ-cell tumors with poor prognosis.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Glycyrrhizin may help regrow hair by activating a specific pathway.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

CRISPR/Cas9 gene editing in cashmere goats increases hair follicles and fiber length, boosting cashmere yield.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Cells from concentrated growth factor can become different cell types.

The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

Recombinant gonadotropins improve future fertility in CHH patients.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

PCR genotyping in cre-loxP mice can be inaccurate due to unintended gene deletions in non-target tissues.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Patched1 helps prevent tumors by controlling cell growth.