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The study developed a successful mouse model to study skin infections, highlighting the importance of choosing the right fungal strains.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

A new mouse mutation causes skin and hair defects due to a gene change.

Id2 gene helps keep hair follicle stem cells inactive.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

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

Syndecan-1 is essential for maintaining skin fat and preventing cold stress.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.

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.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Dicer is crucial for hair growth in mice.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

NFIC helps rat dental cells grow and turn into bone-like cells.

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

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.