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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Chemotherapy damages hair follicles, causing hair loss and other cellular changes.

Intermittent fasting slows hair growth by damaging hair follicle cells.

Different types of persistent hair loss after chemotherapy respond differently to treatments.

External factors like certain shampoos, bacterial infections, and parasites might cause hair defects similar to genetic conditions.

EGFR helps control how hair grows and forms without needing p53 protein.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Hair shaft disorders cause fragile, brittle, and abnormal-looking hair.

The hair defect is due to abnormal inner root sheath keratinization.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Hair changes could indicate neurological diseases and help monitor treatment.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

Topical 6% salicylic acid effectively reduced skin plaques in a patient with wooly hair and palmoplantar keratoderma.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Autophagy changes the protein makeup of hair.

Edar signaling is crucial for proper hair follicle development and function.

The 14-3-3σ gene is essential for preventing hair loss.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Hair from people with seborrheic dermatitis is thicker scaled, more damaged, and thinner than healthy hair, and atomic force microscopy can help monitor the condition.

A specific type of skin cell creates an opening for hair to grow out, and problems with this process can lead to skin conditions.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Scientists found cells in hair that are key for growth and color.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

6-Gingerol, found in ginger, may slow down hair growth and could be used for hair removal.