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Keratin proteins are essential for keeping the cells in the human colon healthy and stable.

The p53 protein has complex, sometimes contradictory functions, including tumor suppression and promoting cell survival.

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

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Cholesterol balance is important for hair health, and problems with it can lead to hair loss conditions.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Seborrheic dermatitis is influenced by diet, genetics, and psychological factors.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

Nitric Oxide has potential in medicine, especially for infections and heart treatments, but its short life and delivery challenges limit its use.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

Identified genes linked to male-pattern baldness may help develop new treatments.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

Actinic keratosis is a sun-induced skin condition that can potentially turn into skin cancer and requires various treatments to prevent this.

Actinic keratosis is a sun-induced skin condition that can potentially turn into skin cancer and requires treatment to prevent malignancy.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

MSC-protein helps regenerate gum tissue and bone.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Two mouse mutations cause similar hair loss despite different skin changes.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

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.

Taking Propecia might lead to the development of cataracts.