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A new DSG4 gene mutation causes hair defects in a young girl.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Immortalized rat dermal papilla cells can still induce hair growth.

ALRV5XR effectively increases hair density in men with androgenetic alopecia without adverse effects.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Peptide nanoparticles can effectively deliver CRISPR-Cas9 to target KRAS mutations in cancer.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

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

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

A 4kb fragment of the desmocollin 3 promoter targets gene expression to specific skin and hair follicle areas.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

Cell membrane-coated nanoparticles could improve gene therapy by enhancing delivery and targeting of nucleic acids.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

ALRV5XR significantly improves hair density in women with hair loss and is well-tolerated.