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A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

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

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

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

The visfatin GT genotype may increase the risk of Alopecia Areata.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Two new gene mutations cause a rare hair disorder.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

VPS13C variants are linked to more severe REM sleep disorder and faster progression to Parkinson's disease.

A unique gene mutation was found in a family with monilethrix.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Two genetic variations in Moa buffalo help them adapt to heat.

Gene variation affects prostate issues and hair loss.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

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

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

DNA virus-induced tumors have consistent isozyme profiles, unlike other tumor types.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.