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Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Male and female hair loss have different genetic causes.

Abnormal Wnt signaling in hair follicle stem cells can lead to acne-like cysts.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

Hypothyroidism may cause certain types of hair loss.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

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 research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

The symposium highlighted the importance of genetics in understanding and treating complex skin diseases.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Melanogenesis-related proteins may trigger immune responses in alopecia areata patients.

Reduced Stx17 expression may contribute to Alopecia Areata.

Male pattern baldness is partly caused by specific genes, but most genetic factors are still unknown.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

JAK inhibitors can effectively reverse hair loss in people with alopecia areata.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

CD8+ T cells are involved in alopecia areata and may cause disease relapse.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Atopic dermatitis increases the risk of some autoimmune diseases.

Finasteride reduces opioid use and withdrawal symptoms in animals.

The CORIN gene variant causes the golden color in Siberian cats.

Mast cells and CD8 T cells interact closely in skin diseases, affecting each other's behavior and contributing to conditions like psoriasis and eczema.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.