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Higher MIF levels in alopecia areata patients suggest it could be a treatment target and disease predictor.

BMP signaling affects hair color by interacting with the MC-1R pathway.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Azelaic acid helps protect hair cells from UV damage and encourages hair growth by increasing certain gene expressions and proteins.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Monilethrix, a genetic hair disorder causing fragile hair, affects three generations in a family.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

Maslinic acid from olive extracts promotes hair growth like minoxidil.

The study maps how genes are regulated during mouse hair growth.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

Dermal EZH2 controls skin cell development and hair growth in mice.

Selenium imbalance can cause hair loss and skin issues.

miR-3606-3p reduces skin fibrosis by blocking key signaling pathways.

Two specific genes are more active during hair growth in mice.

Certain genes control the color of human hair by affecting pigment production.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

Researchers identified specific genes that are important for mouse skin cell development and healing.

Nicastrin deficiency may cause skin cell damage and pigmentation disorders in humans, similar to effects seen in fish.

Treatment with moisturizers improved the skin condition of a girl with a rare genetic skin disorder.

Id2 gene helps keep hair follicle stem cells inactive.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Spiny mice regenerate skin better than laboratory mice due to larger hair bulges, more stem cells, and different collagen ratios.

Fibroblasts can be turned into melanocytes for potential skin treatments.

Certain miRNAs might be involved in a hair loss condition called frontal fibrosing alopecia and could possibly help in its diagnosis.