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A higher genetic risk score increases the chance of getting benign prostatic hyperplasia and affects treatment outcomes in Han Chinese men.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Low-cost dermoscopes can effectively diagnose early female pattern hair loss.

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

Human placenta helps hair grow back after chemotherapy by blocking cell death and increasing hair follicle growth.

Trichoscopy effectively diagnoses and assesses hair loss severity in androgenetic alopecia and alopecia areata.

The document provides a method to classify human hair growth stages using a model with human scalp on mice, aiming to standardize hair research.

Different tumor cells in one basal cell carcinoma can cause mixed treatment responses, suggesting personalized treatment is needed.

The document concludes that hirsutism is the main sign for diagnosing hyperandrogenism, which requires a detailed patient history and physical exam.

The guidelines aim to find treatable prostate cancer early while avoiding unnecessary tests and treatments.

New mutations in the hairless gene may cause hair loss and affect bone development.

Hair follicle cells change their DNA packaging during growth cycles and when grown in the lab.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Trichoscopy is crucial for diagnosing and managing androgenetic alopecia, showing increased vellus hairs, empty follicles, and fibrosis with severity.

Genetic factors can predict male pattern baldness risk.

Single hair grafting is effective for treating small, localized patches of vitiligo.

Human stem cells were turned into cells similar to those that help grow hair and showed potential for hair follicle formation.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

Researchers found a new mutation causing total hair loss from birth.

Trichoscopy and pathological examination both have unique benefits and cannot completely replace each other in evaluating hair.

The NAMS 2014 recommendations guide healthcare providers on treating health issues in midlife women, emphasizing individualized care and informed decision-making.

Skin aging is due to impaired stem cell mobilization or fewer responsive stem cells.