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Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

Tacrolimus causes fewer acute rejections than cyclosporin A in kidney transplants but doesn't necessarily improve kidney function after one year; cardiovascular risks and side effects vary between the two drugs.

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

The meeting discussed vitamin D3's role in fighting tuberculosis, potential treatments for skin conditions like psoriasis, and hair follicle regeneration as a possible solution for hair loss.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Rapamycin reduces age-related hearing cell loss in mice, but acarbose does not.

People with alopecia areata often have lower levels of vitamin D, zinc, and folate, but more research is needed to understand if supplements can help treat it.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

Eph/ephrin signaling is important for skin cell behavior and could be targeted to treat skin diseases.

Acne in dark skin is influenced by environmental factors and can lead to hyperpigmentation, with various treatment options available.

Sox2 controls hair color by affecting pigment production in hair follicles.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Blocking the Wnt pathway could lead to new treatments for cancer and tissue repair but requires careful development to avoid side effects.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.

New genes and pathways are important for testosterone production and male sexual development.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The conclusion is that we need more effective hair loss treatments than the current ones, and these could include new drugs, gene and stem cell therapy, hormones, and scalp cooling, but they all need thorough safety testing.

SOX9 is essential for the development of various organs and hair follicles.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.