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A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

DNAJB9 cfRNA could help diagnose and treat female hair loss.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

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

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

PRMT5 inhibitors effectively fight adenoid cystic carcinoma in salivary glands.

A new treatment using nanoliposomes can improve hair regrowth in androgenetic alopecia.

A gene-based model predicts lung adenocarcinoma outcomes and helps guide treatment decisions.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

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

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

LGD1069 effectively prevents breast tumors in mice without toxicity.

Key circRNAs play a role in wool follicle development, aiding in breeding better quality wool sheep.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

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

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

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

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