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Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Minoxidil decreases LH expression, while hydralazine has mixed effects on prolyl and lysyl hydroxylase activities.

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

CDP is crucial for lung and hair follicle cell development.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Keratin proteins are crucial for healthy skin, but mutations can cause skin disorders with no effective treatments yet.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Keratins are important for skin cell health and their problems can cause diseases.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

A specific protein in chicken embryos links early skin layers to feather development.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

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

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

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

FLRG and follistatin have different roles in wound healing.

Genetics play a role in acne, but how exactly they contribute is not fully understood.