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Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

People with premature hair graying have an imbalance between harmful and protective molecules in their body, hinting that antioxidants might help.

Double-stranded RNA helps regenerate hair follicles by increasing retinoic acid production and signaling.

Researchers successfully isolated and identified key markers of stem cell-enriched human hair follicle bulge cells.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

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

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

No link found between specific genes and female pattern hair loss.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Human hair follicle stem cells can be isolated using specific markers for potential therapeutic use.

Alopecia areata can be triggered by specific immune cells without genetic or environmental factors.

Androgen conjugates might be better indicators of skin sensitivity to hormones in women with excessive hair growth.

New treatments are needed for PCOS that target its genetic, hormonal, and metabolic causes.

Women with low SHBG levels and a high 3a-diol G to SHBG ratio are likely to experience female pattern baldness, possibly due to a slight excess of androgens affecting sensitive hair bulbs.

Hair loss is caused by genetics and hormones, diagnosed through examination and biopsy, and treated with medications or surgery.

Calcium reduces involucrin in rat hair bulbs but doesn't affect filaggrin and Kdap.

Men using steroids or finasteride to look more attractive may harm their fertility and sexual function, creating a paradox where they seem fit but may be less able to reproduce.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Targeting colon cancer stem cells might lead to better treatment results.

Melasma is now considered a skin aging disorder caused by sun exposure in people with a genetic tendency, which impacts treatment and prevention approaches.

Scientists found a gene in mice that causes early hearing loss.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Human scalp fat stem cells showed improved cartilage-like development on a special scaffold with freeze-thaw treatment.