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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

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

The C-terminal tail of AHF/trichohyalin is essential for organizing keratin filaments in keratinocytes.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

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.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

DHT affects bone growth by altering gene activity in osteoblasts, potentially complicating steroid use.

Artemis protein may help control hair growth and health by influencing cell processes.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Blocking JAK/STAT pathways can help treat hair loss from alopecia areata.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Mutations in the KRT85 gene cause hair and nail problems.

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

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

GLI2 increases follistatin production in human skin cells.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

Human hair follicles can be used to create stem cells that might help clone hair for treating hair loss or helping burn patients.

Minoxidil can reduce functions related to androgen receptors.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

PF-05314882 selectively activates androgen receptors without much effect on prostate and may help in prostate cancer treatment and hair loss prevention.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

The HR protein's role as a repressor is essential for controlling hair growth.

Brain-Derived Neurotrophic Factor (BDNF) slows down hair growth and promotes hair follicle regression.