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The document concludes that understanding sulfation biology is crucial for creating treatments due to its importance in biological functions and disease.

Four-amino acid part makes enzyme sensitive to finasteride.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

An imbalanced gut and lack of biotin can cause hair loss in mice.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

EGF and KGF signalling prevent hair follicle formation and promote skin cell development in mice.

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

Skin has specialized touch receptors that can tell different sensations apart.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Hair shedding is an active process that could be targeted to treat hair loss.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Follistatin helps hair growth and cycling, while activin prevents it.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

Fat cells are important for healthy skin, hair growth, and healing, and changes in these cells can affect skin conditions and aging.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

A20 protein is crucial for normal skin and hair development.

Certain mice without specific receptors or mast cells don't lose hair from stress.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Both vitiligo and alopecia areata involve an immune response triggered by stress and specific genes, with treatments targeting this pathway showing potential.

The conclusion is that hair growth can be improved by activating hair cycles, changing the surrounding environment, healing wounds to create new hair follicles, and using stem cell technology.

The HR protein's role as a repressor is essential for controlling hair growth.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Prolactin affects when mice shed and grow hair.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.