Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

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

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

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

H+-ATPase is crucial for plant growth and can be influenced by microbial compounds, affecting root hair development.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

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

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Aptamers can improve wound healing and promote hair growth.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

PP2Acα is essential for proper hair and skin development.

An Australian with rare hair loss and eye conditions had a gene linked to both, not seen together before.

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