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LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Memory T cells in the skin balance staying put and moving into the blood, clustering around hair follicles, and increasing in number after infection.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

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

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Basonuclin helps identify and track hair follicle development and cycling in mice.

A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Treat limited stage small cell lung cancer with chemotherapy and radiation, and consider preventive brain radiation for better survival chances.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Genetic marker rs12558842 strongly linked to male hair loss.

Sweet syndrome can be the only sign of hairy cell leukemia relapse.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

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

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

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

CCCA can affect both genders and all ages, and it has a genetic component.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Cigarette smoke condensates increase tumor-promoting markers in mouse skin, especially around hair follicles.

ILC1-like cells can cause alopecia areata by themselves.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

The human K5 promoter controls specific gene expression in skin cells, with key regulatory elements near the TATA box.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.