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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Pregnancy-related hormone changes affect Y1 receptor gene expression in mice.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A KRT32 gene variant causes loose anagen hair syndrome.

Certain IL-18 gene variations may increase the risk of alopecia areata.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

The 4C32 gene may help in mouse skin development and differentiation.

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Activated protein C helps protect mice from long-term radiation damage.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

A49T gene variant linked to higher prostate cancer risk, lower hormone levels, and slightly reduced balding risk.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

Mutations in specific llama genes may affect fiber quality for textiles.

NDRG1 protein helps infantile hemangioma, a common infant tumor, to grow, and its mismanagement by FOXO1 protein plays a big role in causing the tumor.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

ASLNC168501 can help treat hair loss by restoring hair follicle stem cell function.

Lef1 helps stem cells become hair cells by interacting with specific signaling pathways.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.