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LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

Atoh1 expression can create new Merkel cells in the skin.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

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

Targeting ornithine decarboxylase can help prevent skin cancer.

Citrullinated proteins from Porphyromonas gingivalis may contribute to rheumatoid arthritis.

Enzymes called PADIs play a key role in hair growth and loss.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Activating autophagy in dogs with certain diseases improves their skin and hair.

A new amino acid derivative, ATS, improves hair texture and moisture, making it easier to straighten curly hair.

INTASYL is a promising, adaptable RNAi technology for treating skin cancers.

Hypaphorine from a fungus changes the internal structure of Eucalyptus root hairs, stopping their growth.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

Id2 gene helps keep hair follicle stem cells inactive.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Increased LC3 gene expression may be linked to premature graying of hair.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Nano-PROTACs could improve drug targeting and delivery by using nanotechnology.

Catalytic antibodies are early indicators and active participants in the development of systemic lupus erythematosus.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Phospholipids help plant proteins move by regulating receptor interactions.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

MEGA PROTAC improves prediction and ranking of protein complexes better than existing methods.

The gene for Marie Unna hereditary hypotrichosis is located on chromosome 8p21, near the hairless gene.

LHTric-1 is a specific antibody useful for studying hair and nail formation.