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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

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

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The protein Gnαs is found more in black mice than white mice and may influence their coat color.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

DNA variants can predict male pattern baldness, with higher risk scores increasing baldness likelihood.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Researchers found two new genetic variants linked to Alzheimer's disease.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

No link found between new male baldness genes and female hair loss.

Hairless gene not strongly linked to baldness.

The study suggests that hypothyroidism may cause alopecia areata.

Scientists found a gene in mice that causes early hearing loss.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.