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The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.

Quercitrin may help treat hair loss by promoting hair growth and improving cell health.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Certain immune cells are more common on the top of the head and might help predict or treat common hair loss.

SFRP2 and PTGDS may be key factors in female hair loss.

No clear link between androgen receptor variation and hair loss, but more research needed.

Caffeine can protect scalp hair follicles from damage caused by UV radiation.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

Hidradenitis suppurativa is caused by genetic factors, inflammation, bacteria, hormones, and lifestyle factors like obesity and smoking.

Dermal Papilla cells are a promising tool for evaluating hair growth treatments.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Longer CAG and GGN repeats increase alopecia risk, but no significant link to post-finasteride syndrome found.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.