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

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Forensic hair analysis for drugs is now more reliable and accurate.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Significant progress was made in understanding PXE, but effective treatments are still needed.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Genetic marker rs12558842 strongly linked to male hair loss.

Sunscreens with higher SPF and UVA filters offer the best protection against skin aging from UVA rays.

Minoxidil can reduce functions related to androgen receptors.

Birt–Hogg–Dubé syndrome is a rare genetic condition causing skin lesions, lung cysts, and a higher chance of kidney cancer.

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

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Stem cells from whiskers can be transplanted to stimulate hair growth.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Targeting specific genes in certain pathways may help treat male pattern baldness.

Sex hormones affect brain cells differently in males and females.

A new ethical skin model using stem cells offers a reliable alternative for dermatological research.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Androgens cause oil-producing skin cells with androgen receptors to mature and produce more oil.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Mouse models help understand alopecia areata and find treatments.