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

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Certain genes control the color of human hair by affecting pigment production.

Ceramide synthase 4 is essential for maintaining skin barrier health.

Paeoniflorin protects brain cells by involving a specific protein and neurosteroids.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

p21waf1/cip1 and p27kip1 help in hair follicle differentiation in rats.

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.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

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

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

The ACE1 gene variant doesn't affect long-COVID symptoms.

Human leukocytes and beard hair follicle cells have internal daily clocks, and PER1 and PER3 genes may indicate individual circadian rhythms.

Cyproterone acetate may cause liver cancer at high doses, but is considered safe at recommended doses for approved uses.

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

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Cathepsin L deficiency causes hair and skin issues in mice.

Non-classical 21-hydroxylase deficiency can be missed in newborn screenings and should be considered in cases of early puberty or virilization.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

MTS24 marks a new type of skin cell that helps hair growth and repair.

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

Congenital Adrenal Hyperplasia is mainly caused by enzyme deficiencies, leading to varying symptoms like hormone imbalances and physical changes.