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Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Arctiin helps protect hair cells from damage and death caused by oxidative stress.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

DHT affects hair follicle cells by changing microRNA levels, leading to less cell growth and more cell death.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

The study found new details about human hair growth and suggests that preventing a specific biological pathway could potentially treat hair graying.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

Some skin diseases and their treatments can negatively affect male fertility.

Troxerutin helps protect skin cells from oxidative stress and may be good for treating hair loss.

Biotin and acetazolamide improved hair and nail growth, mental function, and reduced headaches in a child with autism.

Hair changes can indicate systemic diseases or medication effects.

M30 is a promising treatment for preventing hair loss during chemotherapy.

Using rodents for research shows that health problems in the womb can cause diseases later in life.

Key genes can rewire networks, changing skin appendage types.

Light therapy reduces scalp inflammation, boosts hair regrowth with Minoxidil 2%.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

ceRNA networks offer potential treatments for skin aging and wound healing.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

FLCN helps control iron levels in cells.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Heavy metals like arsenic, cadmium, and lead can increase cancer risk and worsen outcomes.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

Blocking both main energy pathways can stop hair follicle stem cell-induced skin cancer growth.