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Environmental factors can cause mutations in skin proteins, leading to skin disorders.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

Pannexin 3 is important for bone formation and the development of bone cells.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

RU 58841 may treat acne, hair loss, and excessive hair growth.

Sex steroids affect the MafB gene differently in male and female hamsters.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Women with PCOS have similar levels of certain proteins compared to women without PCOS, and these proteins don't independently cause PCOS.

Hair proteins have weak spots in their α-helical segments.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

FA2H is essential for normal fur and sebum production in mice.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

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.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

Changes in testosterone and estrogen receptor genes can affect how men age, influencing body fat, hair patterns, and possibly leading to skin disorders.

Lipopolysaccharides boost wheat seedling growth, but procyanidin B2 weakens this effect.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Metabolic Syndrome is linked to several skin conditions, and stem cell therapy might help treat them.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.