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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.

Certain IL-18 gene variations may increase the risk of alopecia areata.

Finasteride helps female-pattern hair loss.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

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

Mutation in hairless gene may increase hair loss risk.

Mutation in hairless gene may increase hair loss risk.

Pregnancy-related hormone changes affect Y1 receptor gene expression in mice.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

The Cashmere goat hair keratin gene is crucial for hair structure.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

A mouse gene mutation increases the risk of skin cancer.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

ASLNC168501 may help restore hair growth in androgenetic alopecia by improving hair follicle stem cell function.

Hair follicles are crucial for maintaining skin barrier function.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

PIEZO1 helps keep hair follicle stem cells inactive, affecting hair growth.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

The 4C32 gene may help in mouse skin development and differentiation.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

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

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.