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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

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

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

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

Ablative CO2 laser resurfacing tightens skin by destroying and regenerating skin layers.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

A specific RNA increases hair stem cell growth and skin healing by affecting a protein through interaction with a microRNA.

NKCC1 transporters help control neuron excitability and inhibition.

The new SLICC criteria for diagnosing lupus are more sensitive and accurate than the old criteria.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

GLABRA2 represses root hair formation by inhibiting a specific gene.

RCDP NCs are promising anti-aging cosmetic ingredients that improve skin health by reducing oxidative stress and enhancing cell function.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

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

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Club-like receptors detect light touch but not whisking.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

NIR-II imaging effectively tracked stem cells that helped repair facial nerve defects in rats.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.