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No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Certain gut bacteria may increase or decrease the risk of male pattern baldness.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

CD201+ fascia progenitors are essential for wound healing and could be targeted for treating skin conditions.

High TSPEAR levels in colorectal cancer predict worse outcomes.

High TSPEAR levels in colorectal cancer predict worse outcomes.

New treatments targeting specific genes show promise for treating keratin disorders.

Altered retinoid metabolism in cicatricial alopecia suggests a balanced vitamin A diet may prevent the condition.

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

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Dutasteride injections can help hair growth in androgenic alopecia but need more research for long-term use.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

Hair growth and health are influenced by factors like age, environment, and nutrition, and are controlled by various molecular pathways. Red light can promote hair growth, and understanding these processes can help treat hair-related diseases.

Altering maternal cortisol during pregnancy can improve wool growth in Merino sheep.

New research shows that skin diversity is influenced by different types of dermal fibroblasts and their development, especially involving the Wnt/β-catenin pathway.

Aging reduces skin stem cell function, leading to changes like hair loss and slower wound healing.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Lgr5 is a marker for active, self-renewing stem cells in the intestine and skin, important for tissue maintenance.

High doses of cyproterone acetate increase the risk of brain tumors in women, but the risk decreases after stopping the medication.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Stem cells compete for space using cell adhesion, and mutations can affect their competitive success, with implications for tissue health and disease.

Lower zinc levels may predict less effective hair loss treatment.