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Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Phospholipase A2 enzymes play key roles in skin health and disease.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Exosomes could be a promising way to help repair skin and treat skin disorders.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

New targets for making and using brain-synthesized steroids could lead to better treatments for brain disorders and alcoholism.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The same hormone can affect gene expression differently in various tissues, which could lead to new treatments for conditions like hair loss.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Understanding hair biology is key to developing better treatments for hair and scalp issues.

Advances in genetics may lead to targeted treatments for hair disorders.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

MicroRNAs are important for skin health and could be targets for new skin disorder treatments.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Targeting specific miRNAs may help treat hair follicle issues caused by hydrogen peroxide.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Scientists have made progress in understanding hair follicle stem cells, identifying specific genes and markers, and suggesting their use in treating hair and skin conditions.

Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

HOXC13 is essential for hair and nail development by regulating Foxn1.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

A gene mutation in Lama3 is linked to a common type of hair loss.