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Patients with hidradenitis suppurativa have higher levels of cell-free DNA in their blood.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

Shorter CAG repeats may cause hair and skin issues, while longer ones may link to acne.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

The IRF2BP2 gene affects sheep fleece quality by influencing fiber traits.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Researchers found 15 new genetic links to skin traits in Japanese women.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

STK11 gene polymorphism does not predict metformin response in PCOS.

5% topical minoxidil improves hair density and quality in monilethrix patients.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

A mouse gene mutation increases the risk of skin cancer.

New genes linked to male pattern baldness were found on chromosome 20p11.

Metformin increases FSH levels in PCOS, and KISS1 gene variations may influence PCOS development.

Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

Early detection of specific VDR mutations is crucial for effective treatment and better dental outcomes in children with hereditary vitamin D–resistant rickets.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Finasteride works better for baldness in people with shorter gene repeats.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

TCF7L2 gene polymorphism is linked to alopecia areata, but it doesn't affect the success of PRP or conventional treatments.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.