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Immunofluorescence tomography is a cost-effective method for creating detailed 3-D images of tissues.

Men with less sun-sensitive skin have lower PSA levels, while men with more sun-sensitive skin have higher PSA levels.

The MtAnn3 gene affects root hair growth and is influenced by cytokinin.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

A new gene mutation causes insulin resistance in a girl and her mother.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Ciclosporin can cause excessive hair growth even with testosterone blockers.

Polarized microscopy helps identify hair irregularities in genetic disorders.

The clinic-based hair fall count method is accurate and reliable.

Home photobiomodulation therapy can improve life quality and mobility for disabled individuals.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Graphene oxide and indole-3-acetic acid together inhibit root growth in Brassica napus L. by affecting multiple plant hormone pathways.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Hox genes control hair growth patterns in mammals by regulating stem cell activity in the skin.

Genetic factors, skin barrier, immune function, and obesity influence risk of fungal skin infections.

Humans lost body hair relatively recently in evolution.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

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

Disruptions in epidermal polarity genes can lead to skin diseases.

The composition with carnitine, thioctic acid, and saw palmetto extract may effectively reduce inflammation in hair follicle cells.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Gene regulation could revolutionize hair color by altering pigmentation from within.

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

Certain gene variations increase the risk of alopecia areata in Koreans.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Home-use lasers and IPL devices are unlikely to directly cause paradoxical hair growth; it may be linked to inflammation or hormonal issues.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.