Search

everythinglearnresearchcommunity

for

Search:↓

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Cadd4 effectively reduces cholesterol levels without side effects.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

A specific gene change in APCDD1 increases the risk of hair loss.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Genetic variants in specific genes cause a type of hair loss.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

A genetic marker linked to a type of hair loss was found in most patients studied.

Genetic variations may affect how well finasteride works for BPH patients.

Targeting CXXC5 and GSK-3β may help treat male pattern baldness.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

Ceramide synthase 4 is essential for maintaining skin barrier health.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.