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PPAR-γ helps control skin oil glands and inflammation, and its disruption can cause hair loss diseases.

Zebrafish helped find new ways to prevent drug-induced hair cell death and potential treatments for hearing loss.

TGM3 is important for skin and hair structure and may help diagnose cancer.

MILL molecules are unique immune proteins in mice that don't need TAP to appear on cell surfaces.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

Different types of persistent hair loss after chemotherapy respond differently to treatments.

A new mouse model for vitiligo helps study immune responses and potential treatments.

Cepharanthine has many medicinal uses but needs improvement for better effectiveness.

Cobalt is important for health but too much or too little can cause health problems, and its environmental buildup is a concern.

Special proteins are important for skin balance, healing, and aging, and affect skin stem cells.

Mesenchymal stem cells could help treat aging-related diseases better than current methods.

Understanding how Regulatory T Cells work could help create treatments for certain skin diseases and cancers.

Non-biologic immunosuppressive drugs are crucial for treating autoimmune and chronic inflammatory skin diseases.

Scientists can use engineered microbes to make L-aspartate and related chemicals, but there's still room to improve their efficiency.

Sex hormones affect hair growth and loss, and treatments for related hair diseases include various medications, hair transplantation, and light therapy.

No single ideal JAK inhibitor for alopecia areata has been determined; JAK3 inhibitors may be promising with fewer side effects.

A genetic mutation linked to longer life and less disease was found in the Amish, and a drug is being developed to replicate these benefits.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

The document concludes that the girl's hairlessness is likely inherited from her parents.

The document concludes that proper diagnosis and treatment of hair shaft disorders require understanding their unique causes and avoiding hair-damaging practices.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

New treatments for skin and hair repair show promise, but further improvements are needed.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.