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A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Higher cell number PRP improves hair density and diameter more than lower cell number PRP.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Transplant success has improved with better immunosuppressive drugs and donor matching.

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

Loss of keratin K2 causes skin problems and inflammation.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

Non-surgical procedures can help reduce wrinkles and stimulate skin repair by understanding skin aging at the molecular level.

New therapies are being developed that target integrin pathways to treat various diseases.

Understanding how acne develops in different diseases could lead to new treatments.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Products should be called 'sperm-safe' only after thorough, well-designed tests.

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

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Tiny RNA molecules help control the growth of plant hairs.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

FGF13 gene changes cause excessive hair growth in a rare condition.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.