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Proteins like aPKC and PDGF-AA, substances like adenosine and ATP, and adipose-derived stem cells all play important roles in hair growth and health, and could potentially be used to treat hair loss and skin conditions.

ERG increases SOX9, promoting prostate cancer growth and invasion.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

Melatonin directly affects mouse hair follicles and may influence hair growth.

The KRTAP36-2 gene in sheep affects wool yield.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

FGF5 gene mutations cause long hair in domestic cats.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Combination pharmacotherapy is generally more effective for treating keloids and hypertrophic scars.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

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

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

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