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People with severe hair loss (Alopecia Areata) have different scalp bacteria than healthy people, which might help predict the condition's progress.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

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

The EDAR gene greatly affects hair thickness in Asian populations.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

Certain gene variations are not a major cause of male infertility in Nigerian men.

Hair growth is influenced by hormones and goes through different phases; androgens can both promote and inhibit hair growth depending on the body area.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Fat tissue extract may help treat vitiligo by reducing cell stress and promoting skin repair.

Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

Alopecia areata is linked to thyroid autoimmunity but not type 1 diabetes.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Insulin resistance is linked to high male hormone levels in women, often seen in those with PCOS.

Early onset hair loss linked to genetics and androgen levels.

Decorin, a protein, may help start hair growth and could be used to treat hair loss.

Hair loss gene found on chromosome 3q26.

Using both hyaluronic acid compounds together improves skin hydration and reduces wrinkles better than using one alone.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Nanoparticulate systems improve drug delivery by controlling release, protecting drugs, changing absorption and distribution, and concentrating drugs in targeted areas.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.