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Mice can regenerate ear tissue without the p53 protein.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

The study concluded that hair loss in Indian women is not significantly linked to anemia or thyroid problems, but checking thyroid function could help those with ongoing hair loss.

The document concludes that unruly hair can be congenital or acquired, often lacks specific treatments, and can be managed with oils and short hairstyles.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

miR-140-5p in certain cell vesicles helps hair growth by boosting cell proliferation.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

Keratinocytes help keep hair follicle cells and skin cells separate in 3D cultures, which is important for hair growth research.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Substances from dental stem cells might help treat hair loss.

Lanyu pigs show that partial-thickness wounds can partially regenerate important skin structures, which may help improve human skin healing.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Researchers found a gene mutation responsible for a rare hair loss condition.

Children with short anagen syndrome usually see their hair condition improve as they get older.

Genomic approach finds new possible treatments for hair loss.

Loose Anagen Syndrome is more common in females and may be inherited, often confused with other hair disorders, and lacks evidence for biotin treatment effectiveness.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

EDA and EDAR are important for hair follicle development in cashmere goats and affect other related genes.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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

Different combinations of human hair keratins affect how hair fibers form.

A 72-year-old man had severe fatigue, weight loss, and frequent loose stools.

Loose Anagen Hair syndrome occurs in dark-skinned children and often improves on its own.