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A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

A new type of nerve cell involved in itch perception was discovered.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

UC.145 may be a new biomarker for predicting gastric cancer.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Hair follicle-derived IL-7 and IL-15 are crucial for maintaining skin-resident memory T cells and could be targeted for treating skin diseases and lymphoma.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

WIF1 helps keep skin stem cells inactive to prevent excessive cell growth.

Type II spiral ganglion neurites avoid high concentrations of laminin and fibronectin.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

The gp130 receptor helps in tissue regeneration and disease progression, and manipulating it could improve healing and prevent disease.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

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

A specific mutation in PA-PLA1α causes abnormal hair growth.

Overexpression of ΔNLef1 in mouse skin leads to hair loss, cysts, and skin tumors.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

AIMP1 can boost hair growth by increasing stem cell activity.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

Lamins are vital for cell survival, organ development, and preventing premature aging.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

NM2 and RLC phosphorylation are essential for normal inner ear hair cell function.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

ERULUS is crucial for root hair growth by controlling calcium levels.

A genetic variant in the KRT25 gene causes tightly curled hair.

Unconventional lymphocytes are important for quick immune responses and healing of skin and mucosal barriers.

Collagen XXII is a marker for tissue junctions, aiding in structural integrity and found in muscles, heart, skin, and arthritic joints.

A mutation in the KRT25 gene causes woolly hair and hair loss.

LncRNAs play a crucial role in muscle regulation and could help develop treatments for Duchenne muscular dystrophy.