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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

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

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

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

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Low-penetration genes might help personalize colorectal cancer prevention.

Certain gene variations may increase the risk and severity of alopecia areata.

A specific gene variant may increase the risk of developing Alopecia Areata.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new genetic variant in the EEF2K gene may contribute to polycystic ovary syndrome.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Variation in the TCHH gene affects wool curliness in sheep.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

A new gene mutation linked to a skin condition was found in a Spanish family.

A specific mutation in PA-PLA1α causes abnormal hair growth.