Search

everythinglearnresearchcommunity

for

Search:↓

Reflectance confocal microscopy is useful for diagnosing and monitoring skin diseases, but it has limitations and requires expertise for correct use.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

Paxillin may help manage androgen-related disorders like PCOS by stabilizing androgen receptor proteins.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

NIR-II imaging effectively tracked stem cells that helped repair facial nerve defects in rats.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

A new gene variant causes glucocorticoid resistance in a mother and son.

CK 19 expression is higher in more severe skin cancers.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.

A certain type of skin cell, marked by EGFR, produces a lot of IGF1 and helps hair follicles grow back faster.

Basal cell carcinoma mostly starts from cells in the upper skin layers, not hair follicle stem cells.

A specific genetic deletion in goats affects cashmere yield and thickness.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Calcium signaling in skin cells is crucial for communication and regeneration.

Specific RNA patterns are linked to alopecia areata.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

Deleting Rac1 in the skin depletes stem cells and damages hair follicles.

CRISPR-Cas9 can successfully edit genes in large mammals like Cashmere goats.

Trichilemmoma, BCC, and SCC tumors have different stem cell marker expressions.

The article's correction clarifies scientific and methodological concerns about miR-200c-3p's role in alopecia areata.

A specific RNA, circNlgn, contributes to heart damage and scarring caused by the cancer drug doxorubicin.

Ber‐EP4 marks cells related to the secondary hair germ in hair follicles.

Keratinocyte gene expression is controlled by multiple modules with specific binding sites.