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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Researchers created a new mouse model for studying scleroderma.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

FOXC1 boosts SFRP1 in hair loss, suggesting new treatments.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Sp6 promotes tooth development by reducing follistatin levels.

A protein called COMP is part of the connective tissue in normal human hair follicles and may be important for hair health.

N6-methyladenosine affects hair follicle development differently in Rex and Hycole rabbits.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

SQSTM1 gene issues may increase the risk of alopecia areata.

A specific gene mutation causes woolly hair and hair loss.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

FoxN1 overexpression in young mice harms immune cell and skin development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A new method using stem cell membranes to deliver Minoxidil improved hair growth in mice better than Minoxidil alone.

MED1 affects skin wound healing differently in young and old mice.

Wnt1a from stem cells boosts hair growth and regeneration in mice.

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

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

ZIP10 is crucial for skin development and maintaining healthy skin.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Matriptase is crucial for skin, hair, and immune cell health, and its imbalance can lead to cancer.