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The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

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

Sfrp2 increases during hair follicle catagen phase and slows keratinocyte growth.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Rice husk and bran extracts from the Bue Bang 3 CMU variety can potentially treat hair loss due to their antioxidant, anti-inflammatory, and anti-androgenic properties.

PAD type III enzyme is specific to rat skin and hair follicles.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

Mutations in the KRT85 gene cause hair and nail problems.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A boy with severe Vitamin D-resistant rickets did not respond to treatment and lacked a common symptom, suggesting a need for alternative treatments.

Two types of 5α-reductase are in dog skin, which might make dutasteride better than finasteride for treating dog hair loss.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Mutations in the SNRPE gene cause hereditary hair loss.

Methylated gene parts may cause finasteride-resistance in some enlarged prostate patients.

5α-reductase is essential for male sexual development and its inhibitors have potential in treating various conditions related to hormone action.

CD98hc's role in skin health decreases with age.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A new gene variant causes curly coats in some dog breeds.

The androgen receptor's shape-changing ability helps it function but can lead to cancer treatment resistance.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The equine epididymis mainly uses type 1 5α-reductase, and both finasteride and dutasteride can inhibit its activity.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.