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

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Sox2-positive cells determine specific hair follicle types in mammals.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

Yak hair follicles adapt to cold through specific gene regulation, enhancing cell growth.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

The research cloned keratin 7 genes from humans, mice, and marsupials, found similarities between human and mouse genes, and discovered new areas of K7 expression in mice.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

KAP6 genes are conserved across species and active in hair follicles.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Blocking certain pathways with kinase inhibitors may help treat cutaneous lupus erythematosus.

The KAP8-1 gene affects skin, hair follicle development, and wool quality in different sheep varieties.

SQSTM1 is linked to increased risk of alopecia areata.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

A gene mutation causes a rare hereditary hair loss, offering potential for new treatments.

DNMT1 may help treat hypospadias by improving cell function and preventing unwanted cell changes.