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Mushrooms offer benefits for food, energy, and water security, and have potential uses in health and environmental applications.

Collagen makes skin stiff, and preservation methods greatly increase tissue stiffness.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Drospirenone is a unique progestin with anti-water retention and potential blood pressure benefits, used in birth control and hormone therapy.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

New compounds were found to help increase hair growth and decrease hair loss.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Fat-derived stem cells show promise for skin repair and reducing aging signs but need more research for consistent results.

The telogen phase of hair growth is active and important for preparing hair follicles for regeneration, not just a resting stage.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Three new types of a skin blistering disease were found, caused by specific gene mutations.

A male with aromatase deficiency improved bone health with estradiol treatment.

Loss of keratin K2 causes skin problems and inflammation.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

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

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.