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New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Some alternative treatments for hair loss might work, but more research is needed.

Lipase H is important for hair follicle function and shaping hair fibers.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

Androgens like testosterone affect skin health and can lead to conditions such as acne and hair loss, with various treatments available.

Long scalp hair evolved for cooling and social signaling.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Oestrogens are key for bone growth during puberty in both boys and girls.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

New partnerships, clinical trials, and drug approvals marked progress in therapeutic delivery in July 2018.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Skin problems are common in Lupus patients and can indicate the disease's severity, requiring specific treatments and lifestyle changes.

The document concludes that recognizing and treating cutaneous lupus erythematosus early is crucial for managing the skin and potential systemic symptoms.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Alopecia Areata causes hair loss and needs treatments that address both physical and emotional health.

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Corticosteroids are the most effective treatment for Satoyoshi syndrome.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.