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A rare case of a transplant patient developing a skin condition linked to HPV-49.

CD8A and FOXD2-AS1 may be key for diagnosing and treating alopecia areata.

A mutation in the KRTHB5 gene causes hair and nail issues.

We need more research to better understand human hair follicle stem cells for improved treatments for hair loss and skin cancer.

miR-200c-3p could help diagnose and treat alopecia areata.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Grasp protein helps maintain skin health after UVB exposure.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

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

EZH2 is essential for hair growth and skin cell development.

The hedgehog signalling pathway is key in skin development and basal cell carcinoma, offering insights for prevention and treatment.

Keratin 15 cells from hair follicles help develop and maintain skin tumors in mice.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A mutation in the human hairless gene causes alopecia universalis.

Keratin-associated proteins help link filaments and affect keratin's strength.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A trial showed that a new treatment is safe and effective for male pattern baldness, with most participants growing new hair.

Higher levels of IL-1R1 and hsa-miR-19b-3p may help diagnose and predict alopecia areata severity.

Keratin-associated proteins are crucial for hair strength and structure.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Hex gene plays a crucial role in starting feather development in chick embryos.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.