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The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

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.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Aleglitazar and its major metabolite are safe enough to proceed to Phase 3 clinical trials.

Human hair keratins can self-assemble and support cell growth, useful for biomedical applications.

Malassezia yeast linked to hair loss; ketoconazole helps treat it.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

S100A3 protein is crucial for hair shaft formation in mice.

Minoxidil and finasteride are effective for treating hair loss, with dutasteride showing potential but with side effects.

Interferons are effective for some skin conditions and cancers, but can have side effects and need more research for optimal use.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

New cancer treatments are less harmful to hair but can still cause hair loss, color, shape, and growth changes.

Most patients with Tuberous sclerosis had neurological or skin issues, and over half had psychiatric problems.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Procyanidin B-2 is safe to use on skin as a hair growth product.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

Yellow dots look different in various hair loss conditions and can help diagnose them.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

KAP genes are crucial for hair development and show both shared and unique traits in humans, chimpanzees, and baboons.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

Key genes linked to hair growth and cancer were identified in hairless mice.

New genes found linked to balding, may help develop future treatments.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.