Search

everythinglearnresearchcommunity

for

Search:↓

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

The study found genetic diversity in coat color dilution among Czech pointers in Slovakia.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A certain gene variation can affect protein production and is linked to male pattern baldness.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Different forms of finasteride dissolve and remain stable differently, affecting capsule quality.

The DNMT3B -579G>T polymorphism may increase the risk of colorectal cancer.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Gene variation affects prostate issues and hair loss.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

A unique gene mutation was found in a family with monilethrix.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

A new gene mutation is linked to monilethrix in the studied family.

Certain genetic variations in IGF2BP2 and IGFBP3 are linked to a higher risk of PCOS.