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

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Vitamin D 1α-hydroxylase is crucial for bone health and vitamin D metabolism.

Thymosin beta 4 protects cells from damage by blocking a harmful microRNA and boosting a protective gene.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Stem cell niche exit in C. elegans is influenced by Sh1 cell membrane protrusions.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Lhx2 helps retinal cells respond to signals for eye development.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Finasteride helps female-pattern hair loss.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

RXRα is crucial for hair growth and skin cell function.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

The dfRootChip revealed how Arabidopsis roots adapt and grow in uneven conditions.

New compounds may help treat heart disease by activating specific potassium channels.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

FOXN1 mutations can cause varying immune and physical issues, with severity influenced by gene activity and possibly other factors.

ACOD1 deficiency worsens hair loss by causing cell aging and mitochondrial problems, but 4-OI may help.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.