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

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A specific gene mutation causes different hair defects in Indian monilethrix families.

The MTR gene affects wool quality and production in Chinese Merino sheep.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

A specific gene mutation causes a severe skin disorder in a family.

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

New genes and markers can help breed better cashmere goats.

Portable point-of-care testing can improve quick and accurate genetic disorder detection.

CAG repeat numbers in the AR gene likely don't affect hair loss in Korean men.

Researchers found two new genetic variants linked to Alzheimer's disease.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

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

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Longer TA repeats in the SRD5A2 gene may increase acne risk in Chinese people.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

The AR gene is linked to male-pattern baldness, TNFSF4 to heart disease, SLC19A3 to BBGD, MCT8 to a syndrome, and segmental duplications to genetic variation.

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

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

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

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A genetic variant linked to hair thinning in Japanese women was found.

Trichotillomania may have a genetic link to psychiatric disorders.

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