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Mice lacking fibromodulin have disrupted healing patterns, leading to abnormal skin repair and scarring.

The study created a mouse model to better understand hair follicle stem cells' role in hair growth and repair.

Krt15+ cells in the mouse intestine resist radiation and can start tumors.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

TLR2 is important for hair growth and can be targeted to treat hair loss.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

miR-182 may help treat hallux valgus by targeting FGF9.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.

Carpronium chloride increases blood flow by widening small blood vessels.

Facial feminization surgery is effective in helping transgender women appear more feminine and has high patient satisfaction.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Nerve growth factor helps cashmere goat hair cells grow by activating a specific protein.

Nelfb is essential for dermal fat development and survival.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

MIM is crucial for hair follicle formation and regeneration by controlling cilia formation and hedgehog signaling through its interaction with Cortactin and Src.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Fluoxetine's effectiveness as an antidepressant in mice depends on a specific protein activity and a 5-minute pretest.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

GhDET2 is crucial for cotton fiber growth.

A rabbit gene important for hair development was identified and detailed.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Plerixafor may help treat pigmentation disorders by promoting skin repigmentation.