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Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Keratinocytes help heal skin wounds by interacting with immune cells and producing substances that kill pathogens.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Lower SHBG levels may increase the risk of PCOS.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

MicroRNAs play a crucial role in skin and hair health, affecting everything from growth to aging, and could potentially be used in treating skin diseases.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Seasonal changes affect gene activity linked to hair growth in Angora goats, influencing mohair quality.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Robotic hair transplantation with AI offers more reliable, precise, and efficient hair restoration.

Seasonal changes affect gene activity linked to hair growth in Angora goats.

Seasonal changes affect hair growth genes in Angora goats, possibly influencing mohair quality.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

Genetically variant peptides are reliable for forensic identification despite age-related changes in hair proteins.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

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

New DNA analysis and machine learning are advancing forensic science, improving accuracy and expanding into non-human applications.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

Mesenchymal stem cells could help treat aging-related diseases better than current methods.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

The Shen Bai Hair Growing Decoction may help treat hair loss by promoting hair growth and reducing inflammation.

Enzymes play crucial roles in metabolism, health, and disease management.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Calcineurin inhibitors, used in kidney transplants, can cause a wide range of side effects including kidney damage and other health issues.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.