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Dermal papillae cells, important for hair growth, come from multiple cell lines and can be formed by skin cells, regardless of their origin or hair cycle phase. These cells rarely divide, but their ability to shape tissue may contribute to their efficiency in inducing hair growth.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Gene linked to common hair loss found, may lead to new treatments.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

AR gene not major factor in female hair loss; different from male hair loss.

Liposomal anthracyclines are effective and safer for treating multiple myeloma, especially in elderly patients.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

No link found between new male baldness genes and female hair loss.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

5α-Reductase inhibitors can help treat hair loss, acne, and prostate issues by reducing DHT levels.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Mice can regenerate ear tissue without the p53 protein.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

GPR39 is linked to certain cells in the sebaceous gland and helps with skin healing.

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

Researchers found a new mutation causing total hair loss from birth.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.