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

Protein kinase C epsilon may promote skin cancer development after UV exposure by affecting nearby cells.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

CCCA can affect both genders and all ages, and it has a genetic component.

The Swedish neonatal screening program effectively detects PKU, galactosaemia, and biotinidase deficiency with low false positives.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

CCCA mainly affects Black women and is linked to high-tension hairstyles, heating tools, chemical relaxants, and genetics.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

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

Specific keratin gene mutations can cause monilethrix.

Men with early balding may have a higher risk of prostate issues, and surgery for prostate cancer has a slight survival benefit over radiation.

Bald areas have lower cell growth, more DNA damage, and increased cell death.

Shorter CAG repeats in a specific gene may increase male hormone activity and symptoms like acne and excess hair in women with PCOS.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

DNA analysis can help tailor alopecia treatment.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

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

Disruptions in mammary stem cell division can lead to cancer, but targeting these processes might help treat breast cancer.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

Both HLA-B and MICA are independently linked to alopecia areata.

5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

The extracellular matrix affects where tumors can start in the body.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Suppressing very long chain fatty acids is linked to skin cancer.

Using finasteride or dutasteride does not increase the risk of male breast cancer.