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Finasteride can cause lasting sexual dysfunction, depression, and other side effects, needing more research for treatment.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Certain gene variations might be linked to severe acne in women but not in men.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Two siblings both had a rare case of alopecia areata at the same time.

COVID-19 may worsen with androgens; anti-androgen drugs could help.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

Redheaded people may have evolved to efficiently make vitamin D in areas with less sunlight.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

New treatments targeting T-cell pathways are needed for better alopecia areata management.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

Hair loss treatment caused more hair loss in a man.

Men with less sun-sensitive skin have lower PSA levels, while men with more sun-sensitive skin have higher PSA levels.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

ESR2 gene linked to female-pattern hair loss.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

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

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

The document concludes that early diagnosis and treatment are key for pediatric hair loss disorders, and addressing the emotional effects on children is important.

The 60-second timed hair count is a reliable and simple way to measure hair shedding at home, showing older women tend to shed more hair than younger women.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Understanding the immune-related causes of Alopecia Areata has led to potential treatments like JAK inhibitors.

Understanding skin structure and development helps diagnose and treat skin disorders.