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The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Cross-section trichometry is an accurate method to measure hair loss and growth.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

Low iron levels may be linked to some types of hair loss in women.

People with atopic dermatitis are more likely to develop other skin conditions due to shared genetics and immune pathways.

Hair disorders are caused by a complex mix of biology, genetics, hormones, and environmental factors, affecting hair growth and leading to conditions like alopecia.

Alopecia Areata is an autoimmune disease affecting hair follicles, influenced by genetic and environmental factors, with rodent models being essential for research.

People with Inflammatory Bowel Disease often lose hair due to stress, medication side effects, or lack of nutrients, and treatment depends on the specific cause.

Targeting immune tolerance issues in Alopecia Areata could restore hair growth and maintain remission.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Certain gut bacteria may protect against alopecia areata, while others may increase the risk.

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

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

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Darker hair colors may increase the risk of alopecia areata, while lighter hair colors may decrease it.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

No link found between new male baldness genes and female hair loss.

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Regulatory T cells are essential for normal and improved wound healing in mice.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Certain genetic variants increase the risk of resistance to hormone therapy in prostate cancer patients.

Patients using social media have mixed feelings about alopecia treatments, noting hair growth but also frustration with treatment recurrence.