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A genetic marker linked to a type of hair loss was found in most patients studied.

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

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Microarray analysis helps find hidden chromosomal changes in patients with intellectual disabilities and birth defects.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

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

Different mutations in the 5 alpha-reductase-2 gene were found in affected individuals in the Dominican Republic, suggesting no common ancestry.

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

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

The TT genotype of a specific SNP in sheep is linked to better wool quality.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

ESR2 gene linked to female-pattern hair loss.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

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

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

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

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Certain MC4R gene variants are linked to higher BMI in obese women with PCOS but do not cause PCOS.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.