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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

A genetic variant in goats is linked to cashmere growth.

Two gene variants cause white spots in cattle.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Hairless gene not strongly linked to baldness.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Targeting amphiregulin may improve treatment for fibrotic diseases and cancer.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

Pregnancy increases certain GABA_A receptors in rat brains, influenced by steroid levels.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Different ACE2 gene versions may affect COVID-19 impact based on age and suggest some hair loss drugs could be potential treatments.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

Ultra-high molecular weight poly-γ-glutamic acid may help promote hair growth.

Scientists discovered two versions of a new human hair keratin gene.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

MPA increases cancer spread by boosting Eph A2 activity.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.