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Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

The document concludes that anti-dsDNA antibodies are not unique to SLE and their use as indicators is doubtful, highlighting the need for better understanding and classification of the disease.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Regenerative therapies show promise for treating vitiligo and alopecia areata.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

New drugs for heart disease may be developed from molecules secreted by stem cells.

R-spondins and their receptors help increase bone growth and may be used to treat bone loss diseases.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

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

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Stress can worsen skin conditions and affect mental health, so doctors should include stress management in skin treatment.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Certain inhibitors can potentially treat prostate cancer and other hormone-dependent conditions by controlling sex hormone levels in cells.

Non-immune factors play a significant role in alopecia areata.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Researchers found a new mutation causing total hair loss from birth.

Mice with autoimmune hair loss showed signs of heart problems.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

Hair follicles are essential for skin health, aiding in hair growth, wound healing, and immune function.

Exosomes are important for skin health and could help diagnose and treat skin diseases.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.