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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Oral contraceptives lower testosterone levels in women, especially those with certain genetic traits, and may be linked to increased breast cancer risk.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The meeting highlighted major advances in skin research, including new findings on skin microbes, genetic links to skin diseases, and improved treatments for various conditions.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Different types of stem cells exist within individual skin layers, and they can adapt to damage, transplantation, or tumor growth. These cells are regulated by their environment and genetic factors. Tumor growth is driven by expanding, genetically altered cells, not long-lived mutant stem cells. There's evidence of cancer stem cells in skin tumors. Other cells, bacteria, and genetic factors help maintain balance and contribute to disease progression. A method for growing mini organs from single cells has been developed.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Scientists developed a method to grow human fetal skin and digits in a lab for 3-4 weeks, which could help study skin features and understand genetic interactions in tissue formation.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Curcumin may help reverse aging by targeting specific genes.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

Thymosin β4 helps increase hair growth in Cashmere goats.

A new gene mutation causes long hair in some Maine Coon cats.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.