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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

Aromatase gene variation may increase female hair loss risk.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Hair loss in balding individuals is linked to changes in specific hair growth-related genes.

Mutation in hairless gene may increase hair loss risk.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Mutation in hairless gene may increase hair loss risk.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

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

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

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

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

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Ficus carica leaf extract may help treat skin disorders by reducing inflammation and androgen effects in skin cells.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Finasteride exposure affects gene expression and anogenital distance in male rat fetuses.

Chicken feather gene mutation helps understand human hair disorders.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.