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Immune cells are essential for early hair and skin development and healing.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

The authors maintain that shorter androgen receptor alleles may lead to milder COVID-19 by positively affecting the immune response, not due to changes in testosterone levels or activity.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Skin's epithelial stem cells are crucial for repair and maintenance, and understanding them could improve treatments for skin problems.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Effective treatments for spinal and bulbar muscular atrophy are not yet available; more research is needed.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Researchers identified genes and proteins that may influence wool thickness in sheep.

No clear link between specific gene and hair loss in Mexican brothers.

Male pattern baldness involves genetics, hormones, and needs better treatments.

Female Pattern Hair Loss affects women's self-esteem and needs more research for better treatment.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Hair gets thinner, grayer, and changes texture with age due to genetics, environment, and cellular changes, affecting the growth cycle.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.