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Using special RNA to target a mutant gene fixed hair problems in mice.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

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

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

CDP is crucial for lung and hair follicle cell development.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

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

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The 3D-SeboSkin model effectively simulates Hidradenitis suppurativa and is useful for future research.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

Dermal Papilla Cells grown in 3D and with stem cells better mimic natural hair growth conditions than cells grown in 2D.

Tamoxifen caused hair loss in a 52-year-old woman.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Cysteine-rich keratins evolved independently in mammals, reptiles, and birds for hard skin structures like hair, claws, and feathers.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

CEC levels may be a useful marker for predicting prostate cancer progression.

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

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Gene variation affects prostate issues and hair loss.