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Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

A feedback loop between LRH and RSL4 controls root hair growth in Arabidopsis.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

Accurate protein modeling can help develop new treatments for prostate cancer and other diseases.

Get3d protein helps maintain photosynthesis in plants and photosynthetic bacteria.

No significant link was found between the studied genes and female hair loss in the Polish population.

Enzymes called PADIs play a key role in hair growth and loss.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

CD44 variant changes start alopecia areata, but don't maintain it.

Male hormones control a specific gene in hamster skin, with different hormones having varying effects.

DORN1 receptor affects eATP-induced stomatal changes but not eADP in Arabidopsis thaliana.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

The gene HDC is important for the development of hair follicles in newborn mice.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

DGAT1 enzyme helps make diacylglycerols, waxes, and retinyl esters.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Targeting specific genes in certain pathways may help treat male pattern baldness.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

Male hormones and reduced plakoglobin can impair heart electrical function and increase arrhythmia risk in males.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

SQSTM1 gene issues may increase the risk of alopecia areata.

mHa2 and mHa3 keratins have different structures and roles in mouse hair and tongue tissues.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.