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The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

TM-β-CD improves finasteride's solubility and delivery, while β-CD offers better long-term release.

TSC2 is crucial for proper hair follicle development and patterning.

Dynlt3 is important for melanosome transport and skin coloration.

FDG PET/CT can improve cancer treatment plans in dogs.

Igf1r helps regulate hair growth cycles.

Vitamin D receptor helps control hair growth and could be used to treat certain skin tumors.

Tofacitinib significantly improved hair loss and lesions in a patient with overlapping autoimmune disorders.

The research found a way to develop hair growth materials by targeting a specific signaling pathway.

Six African American women experienced hair loss after switching to a new HIV medication.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

FLRG and follistatin have different roles in wound healing.

New methods efficiently isolate dermal papilla cells from hair follicles, preserving their characteristics better than traditional methods.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

Recombinant human TSG-6 speeds up wound healing in diabetic mice.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Chlorinated compounds like TCDD can cause skin issues and chloracne by affecting cell behavior.

Trichothiodystrophy causes unusual hair and developmental issues.

FGF18 controls hair growth rest phase.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

A specific gene mutation causes sparse, brittle hair in a family.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Androgen-deprivation therapies increase the risk of certain heart conditions, but testosterone treatment may help.

Regulatory T cells help prevent autoimmunity and have potential for treating autoimmune diseases.