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About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

Th22 cells are essential for Tβ15-induced hair growth in mice.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

The K15 promoter effectively targets stem cells in the hair follicle bulge.

IL-15 promotes hair growth and protects hair follicles.

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The DiLiCre mouse model is an effective tool for precise genome editing using light.

A 17-year-old female with adrenogenital syndrome produces very high levels of androgens, which prevent complete feminization despite high estrogen doses.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

Gamma-ray exposure improves genome editing efficiency in mice using the i-GONAD method.

Keratin 15 is not a reliable sole marker for identifying epidermal stem cells because it's found in various cell types.

The N-K GM Series offers highly selective, eco-friendly medicines targeting harmful microbes, free for personal use.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

MEGA PROTAC improves prediction and ranking of protein complexes better than existing methods.