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The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

The document concludes that more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

The androgen receptor's shape-changing ability helps it function but can lead to cancer treatment resistance.

Curcuma aeruginosa Roxb. may help treat hair loss by affecting specific biological pathways.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Lysophospholipids like LPA and S1P are important for hair growth, immune responses, and vascular development, and could be targeted for treating diseases.

Understanding how acne develops in different diseases could lead to new treatments.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

RNA delivery is best for in-body use, while RNP delivery is good for outside-body use. Both methods are expected to greatly impact future treatments.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

The document discussed hair loss causes and treatments but didn't give a final summary.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Chicken feather growth involves specific genes and shares similarities with hair development.

DNA methylation changes in women with PCOS could be used as disease markers and suggest new treatment targets.

Inactive stem cells in hair follicles and muscles can avoid detection by the immune system.

Testosterone may influence COVID-19 severity and outcomes.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Schizophrenia risk genes may affect early brain development, contributing to the disease.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

High MUC-18/MCAM levels in blood indicate a worse outlook for melanoma patients.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

A man's chest hair turned white after a shingles infection, possibly due to virus-damaged pigment cells.