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The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

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

Researchers found that certain miRNAs, which affect immune system regulation, are differently expressed in mice with a hair loss condition compared to healthy mice.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

A truncated protein linked to breast cancer may change cell adhesion.

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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

New biomarkers and potential treatments for skin diseases were identified.

Found new possible treatments for hair loss.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

RC48 shows promise for treating certain advanced cancers, but more research is needed.

LTBP1 is a key regulator in diseases and a potential target for new treatments.

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

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Exosomal miRNA-218-5p promotes hair growth and development.

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Mutations in the LIPH gene cause woolly hair in a child.

Using special RNA to target a mutant gene fixed hair problems in mice.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

miR-5110 affects alpaca pigmentation by altering specific gene expressions.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A new neural network helps identify key regulators in cell changes, aiding in understanding diseases and finding new treatments.

A new mutation in the HR gene causes hair loss in a specific family.