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The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Mutations in the KRT16 gene can cause skin and nail disorders.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

The study found that analyzing certain cell signaling pathways is not a reliable method to tell apart two types of skin tumors.

Male pattern baldness is linked to specific genetic variations in the androgen receptor gene.

Afatinib, neratinib, and zanubrutinib could be effective against KRASG12C-mutant tumors.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Certain genetic markers may increase or decrease prostate cancer risk.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Recognizing rare tumor combinations is crucial for accurate diagnosis and treatment.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

MCHR2 gene duplications may be linked to alopecia areata.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Researchers found that hair follicle stem cells can become squamous cell carcinoma due to Ras activation, which could lead to new treatments.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

BAF200 is essential for proper heart and coronary artery formation.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Homozygous K5Cre transgenic mice have wavy hair and faster cancer progression.

miR-22 helps skin cancer grow and spread by activating specific cell signals.

B-Raf and C-Raf are essential for maintaining melanocyte stem cells to prevent hair graying.