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Circular RNA ERCC6 helps activate stem cells important for cashmere goat hair growth by interacting with specific molecules in an m6A modification-dependent way.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Hair loss gene linked to prostate issues.

Epithelial proliferation and hyperkeratosis are linked to gastric ulcers in pigs.

EGF and EGFR are important for goat skin development, increasing from weeks 6 to 21.

ALKBH5 helps wounds heal faster by stabilizing PELI2 mRNA.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Neutrophils quickly respond to skin injury.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

A father and son in Yemen have a genetic condition causing hair loss and nail problems.

Sex steroids affect the MafB gene differently in male and female hamsters.

EGFR is essential for organized skin nerve growth and branching.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Activating PPAR-γ signalling can protect hair follicle stem cells from damage caused by chemotherapy.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.