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The research found that PCOS has common genetic factors regardless of how it is diagnosed and is linked to metabolic and reproductive issues.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

The circadian clock affects skin stem cell behavior, impacting aging and cancer risk.

Hair loss and aging are caused by the breakdown of a key protein in hair stem cells.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.

Hormone treatments in transsexual individuals reduce hair growth and oil production in male-to-females and increase them in female-to-males.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

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

Male and female skin differ due to hormones, affecting conditions like hair loss, acne, and skin cancer, and suggesting a need for gender-specific treatments.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

Interferon, especially alfa interferon, is an effective treatment for cutaneous T-cell lymphoma with manageable side effects.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

FGF signaling is a promising target for developing treatments for wounds, metabolic diseases, and cancer.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Cystatin M/E strongly inhibits cathepsin V and cathepsin L, important for skin formation.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

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

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The skin protects the body and is constantly renewed by stem cells; disruptions can lead to cancer.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

Memantine may slightly improve memory in people with Down syndrome, but more research is needed.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

A new gene, JMJD1C, may affect testosterone levels in men.

Zinc deficiency in children can cause skin issues and can be serious if not diagnosed and treated properly.