Search

everythinglearnresearchcommunity

for

Search:↓

A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

New SRD5A2 variants may disrupt protein function, aiding diagnosis and treatment of related disorders.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A multidisciplinary approach is crucial for managing Silver-Russell syndrome effectively.

The AMHR2-482A>G gene change is linked to higher PCOS risk.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

The HSD3B1 variant increases hair loss risk in overweight women with PCOS.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

SQSTM1 gene issues may increase the risk of alopecia areata.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A specific gene mutation causes long hair in Angora rabbits.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Genetic factors in PCOS are complex, with potential influences from the MC4R gene.

SFRP2 and PTGDS may be key factors in female hair loss.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

CT60 polymorphism might increase the risk of Alopecia Areata.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

The study found genetic variations in sheep linked to traits like milk production, growth, and health.

Vitamin D receptor gene variations are not linked to alopecia areata.

A specific genetic deletion in goats affects cashmere yield and thickness.