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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

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

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

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

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

CuATSM speeds up wound healing and reduces scarring.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

CCC1 is essential for pH balance and normal cell function in plants.

TS-13 speeds up hair regrowth after chemotherapy without affecting treatment effectiveness.

TGFβ-2 may cause hair loss in androgenetic alopecia.

Alpha-ketoglutarate protects rabbit skin cells from oxidative damage by activating a specific cell pathway.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Enobosarm significantly increased muscle mass and improved physical function in elderly men and postmenopausal women without serious side effects.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

The enzyme from human skin can cross-link proteins and needs calcium to work.

Taurine may help reduce hair loss by improving hair growth cycles.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

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