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A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A new method was created to analyze certain chemicals in the urine of alopecia areata patients, revealing they have higher metanephrine content. This method can also be used for other related diseases.

Using a special laser and skin medication together successfully cleared a skin condition in a pregnant woman.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

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

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

The study concluded that the new wound model can be used to evaluate skin regeneration and nerve growth.

Activin A and follistatin control when ear hair cells form in mice.

Activin A promotes ear hair cell development, while follistatin delays it.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Researchers found a specific immune receptor in patients that causes severe skin reactions to a drug.

Macroalgae compounds offer sustainable, effective benefits for cosmetics.

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

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

The skin is a complex barrier that protects the body, regulates temperature, and helps with immune responses.

Surgeons suggested a standard system for hair transplant methods to improve communication and results.

Cosmetic residues on individual hairs can be identified and differentiated using ATR FT-IR microspectroscopy.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Scientists made a chemical (compound 4e) that can be applied on skin to reduce oil production, which can help with acne, but it might cause skin sensitivity to light.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

Hair's internal fibers are arranged in a pattern that doesn't let much water in, and treatments like oils and heat change how much water hair can absorb.

The study developed a method to detect minoxidil and its sulfate form, found that minoxidil sulfate is temperature-sensitive, and identified a way to potentially increase its stability for hair loss treatment.

The conclusion is that effective cancer treatment often requires a combination of therapies, but must be carefully managed due to serious side effects and the risk of immunosuppression.

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

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.