Search

everythinglearnresearchcommunity

for

Search:↓

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

A new gene mutation causes insulin resistance in a girl and her mother.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

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

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

Gene linked to common hair loss found, may lead to new treatments.

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

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Hairless gene not strongly linked to baldness.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

A gene mutation causes curly hair and hair loss in rats.

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

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Haplogroup X found in Altaian population supports Amerindian origin.

The treatment effectively promotes hair regrowth in androgenetic alopecia without causing skin irritation.

New genes linked to male pattern baldness were found on chromosome 20p11.

Certain gene variations increase the risk of alopecia areata in Koreans.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

A new gene causes hairlessness and skin cysts in rats.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

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

These gene variations are not linked to alopecia areata in Egyptians.

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

The TIP1 gene is crucial for normal plant cell growth in Arabidopsis.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.