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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.

The assay effectively identifies compounds that affect immune cell activation.

Advancements in measuring chromatin accessibility at single-cell level improve understanding of gene regulation.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Farudodstat can prevent hair follicle immune damage linked to alopecia areata.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Forensic DNA phenotyping can predict physical traits from DNA but faces challenges in knowledge and ethics.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

DRDE-07 shows promise for treating skin diseases due to its favorable properties.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

Mitochondrial DNA from nails and hair can be effectively analyzed for forensic use.

Peptide-based PROTACs show promise in targeting hard-to-treat proteins, especially for cancer therapy.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

JAK inhibition may help manage autoimmune conditions in Down syndrome.

The chitosan/PDRN polyplex improved wound healing in diabetic rats.

JAK inhibitors helped treat hair loss in two people with Down syndrome.

Different autoantibody groups in pediatric SLE are linked to specific symptoms and disease outcomes.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Raltitrexed conjugates are less potent than the free drug but more effective at high concentrations.

The new method is 1000 times more sensitive for measuring hair growth.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Some synthetic carbohydrate receptors, especially compounds 3 and 15, show strong potential for treating Zika virus.

PDI helps restore over-bleached hair's strength and structure by attaching special peptides.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Human liver enzyme DHEA ST helps process minoxidil.

New treatments for Hepatitis C show promise but need more research to confirm their safety and effectiveness for clinical use.

Targeting SIRT1 with antisense oligonucleotides could be a promising treatment for hair loss.

Patients with Systemic Sclerosis have much higher levels of GDF-15, which could help predict organ involvement and guide treatment.