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Hair follicle stem cell transplants can reverse liver cirrhosis by blocking harmful cell activation.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Human hair follicle stem cells help repair tendon injuries.

M1 homeopathic complex may help slow melanoma cell growth.

TSC2 is crucial for proper hair follicle development and patterning.

A specific group of skin stem cells was found to help maintain hair follicle cells.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

A new mouse mutation causes skin and hair defects due to a gene change.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

THBS4 helps hair grow by activating hair follicle stem cells.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Human induced pluripotent stem cells can be used to create cells that help grow hair.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Genetically modified stem cells from human hair follicles can lower blood sugar and increase survival in diabetic mice.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

People with hidradenitis suppurativa have a higher risk of heart attacks and strokes.

Activating TRPMLs helps human cells important for hair growth and increases hair growth in mice.

The 5050 MHA42MCS45 hydrogel blend is suitable for repairing load-bearing soft tissues.

EH-MSCs may help treat hair loss by boosting regeneration and reducing inflammation.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.

BMI1 is essential for preventing hair greying and maintaining hair color.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.