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Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Targeting and modifying the stem cell niche can improve regenerative therapies.

Editing the FGF5 gene in sheep increases fine wool growth.

High levels of ST14 and TMEFF1 proteins in ovarian cancer are linked to worse patient outcomes and may be a new treatment target.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

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.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

The document explains how to create detailed biological pathways using genomic data and tools, with examples of hair and breast development.

Laminin-511 may help promote hair growth, while laminin-332 does not affect hair loss.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

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.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Misbehaving hair follicle stem cells can cause hair loss and offer new treatment options.

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

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

The conclusion is that proper signaling is crucial for hair growth and development, and errors can lead to cancer or hair loss.

Anti-acne medications may work by reducing the activity of a protein involved in acne development.

Low selenium levels can extend lifespan but worsen health issues.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

Dengue virus can infect human hair follicle cells and may cause hair loss.

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

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Treg cells help repair and regenerate tissues by interacting with local cells.