Search

everythinglearnresearchcommunity

for

Search:↓

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Blocking YAP/TAZ could be a new way to treat skin cancer.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Patched1 helps prevent tumors by controlling cell growth.

The 14-3-3σ gene is essential for preventing hair loss.

AP-1 controls tumor cell type by affecting key signaling pathways.

Rhino mice show significant meibomian gland changes, making them a potential model for studying gland disorders.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

Antizyme slows skin tumor growth by reducing cell growth in mice.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

New LSS gene variants help understand congenital hypotrichosis 14 better.

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.

Vitamin D receptor knockout mice have significant motor impairments but no cognitive deficits.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

Loss of Dnmt3a and Dnmt3b leads to more aggressive skin tumors, but blocking PPAR-γ can reduce this effect.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Cetaceans lost hair genes to adapt to water.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

β-catenin, Shh, and Bmp signaling control hair follicle development.

Hair shaft miniaturization leads to hair follicle stem cell loss, suggesting Piezo1 as a potential treatment target.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.