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AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

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.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

TRP channels in the skin are important for sensation and health, and targeting them could help treat skin disorders.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

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

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Early and personalized treatment for hair loss in young people is crucial to prevent permanent damage and should include psychological support.

Hair proteins have weak spots in their α-helical segments.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Parkinson's disease is linked to skin disorders and skin cells help in studying the disease.

Metformin helps regulate menstrual cycles, induce ovulation, and improve pregnancy outcomes in women with PCOS.

New treatments for skin conditions related to the sebaceous gland are being developed based on current research.

The document concludes that hormonal biomarkers are key for diagnosing hyperandrogenemia in women and hypogonadism in men.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Finasteride can cause lasting sexual dysfunction, depression, and other side effects, needing more research for treatment.

Blocking prolactin increases the activity of secondary hair follicles in cashmere goats.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Follicle Stimulating Hormone is important for fertility.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

Vitamin D is important for bones, hair, blood pressure, and breast development.