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The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

Recombinant Filaggrin-2 microneedles effectively promote hair growth and repair in hair loss.

LncRNA RP11-818024.3 helps hair growth and recovery in hair loss by boosting cell survival and reducing cell death.

PDF2 senses specific lipids and regulates root growth and gene expression in Arabidopsis.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

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

TCDD disrupts skin stem cells, causing skin issues like chloracne.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

A specific gene mutation causes a severe skin disorder in a family.

lncRNA MRPS28 regulates hair follicle development in cashmere goats, affecting cashmere quality.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Women with pattern hair loss may have more stress in their bodies due to a lack of NRF2, a protein. Eating healthy and losing weight could help reduce this stress and improve hair loss. NRF2 boosters might also help treat this type of hair loss.

Scientists made a carbon-14 labeled version of a drug with a 48% yield and over 99% purity.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Dermal EZH2 controls skin cell development and hair growth in mice.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

A rabbit gene important for hair development was identified and detailed.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

CSC is linked to mineralocorticoid receptor damage, stress, and steroid use, with treatments including drugs and laser therapies to prevent eye damage.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

Killing specific cells in hair follicles can lead to hair growth problems in mice.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.