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Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

Ritlecitinib helps regrow hair in people with alopecia totalis and universalis and is safe to use.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

MicroRNAs are crucial for hair growth and skin balance.

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

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

miR-214-3p helps nerve repair and recovery.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

wAMD patients have higher oxidative stress, suggesting antioxidant treatment may help.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Ritlecitinib reduces alopecia areata symptoms by blocking JAK3/TEC signaling and T-cell activity.

Lipid-antigen stimulation may play a role in folliculotropic mycosis fungoides.

Mutations in the P2RY5 gene cause hereditary woolly hair.

The new protocol using Cellutome™ and RCM safely assesses wound healing in detail.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

Sgk3 kinase is essential for normal hair growth in mice.

Ritlecitinib may help treat alopecia areata by protecting hair follicles.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

CD271 is crucial for maintaining healthy skin and preventing inflammation.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.