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Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A20 protein is crucial for normal skin and hair development.

Certain drugs that block specific enzymes can help treat prostate diseases.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

MicroRNAs are crucial in controlling cell signaling, affecting cancer and tissue regeneration.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

The document concludes that accurate diagnosis and treatment are crucial in dermatology, and it presents various findings on skin conditions and treatments.

Keratins are important for skin cell health and their problems can cause diseases.

Minoxidil decreases LH expression, while hydralazine has mixed effects on prolyl and lysyl hydroxylase activities.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

CDP is crucial for lung and hair follicle cell development.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

White blood cells and their traps can slow down the process of new hair growth after a wound.

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

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

S100A3 protein is crucial for hair shaft formation in mice.

The RORα gene is active in different parts of cashmere goat hair follicles and may be influenced by melatonin, especially in December when hair growth changes.

Wnt5a may slow down hair growth in mice.

The molecule Wise is involved in the development of various structures in chick embryos.