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Studying rare genetic disorders can help us understand and treat common diseases better.

Red blood cell folate levels are reliable indicators of long-term folate status in alopecia areata patients.

Genetically repaired stem cells may treat certain genetic diseases, Th17 cells are key in fighting systemic fungal infections, hair loss in AGA is due to progenitor cell loss, and α-synuclein transfer might contribute to Parkinson's disease progression.

Understanding where cancer cells come from helps create better prevention and treatment methods.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Cathepsin L is essential for normal hair growth and development.

The document concludes that both internal stem cell factors and external influences like the environment and hormones affect hair loss and aging, with potential treatments focusing on these areas.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

More melanoblasts in hair follicles mean better survival and proper hair pigmentation.

Hibiscus rosa-sinensis may help treat various health issues and promote hair growth, but more research is needed for safety.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

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

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

New treatments for male hair loss show promise but need more research for safety and effectiveness.

Indian Gooseberry has potential for cancer prevention and treatment and promotes hair growth.

Bimatoprost increases hair growth in mice without breaking down into other substances.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Following hair transplant surgery, proper self-care is crucial for successful recovery and hair growth.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A new gene variant causes glucocorticoid resistance in a mother and son.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

The document concludes that various signaling pathways and genetic factors are crucial for chicken feather development, affecting poultry quality.

Personalized treatments for hair loss are becoming more effective by using genetic information.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.