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People with hidradenitis suppurativa often have lower vitamin D levels, weaker hip bones, and altered bone metabolism markers.

Two mouse mutations cause similar hair loss despite different skin changes.

Chitosan slows root hair growth and causes a buildup of callose at low concentrations, but at high concentrations, it only inhibits growth without callose buildup.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

The document concludes that specific dermoscopic features can help diagnose different facial red skin conditions.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

The exact cause of growth hormone-responsive alopecia in dogs is unclear.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

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

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Hair loss in men is common, treatable, but not curable.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Removing p16INK4a from skin cells can lead to faster and more clumped growth, which might help with hair growth.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Keratin's mechanical properties are influenced by hydrogen bonds and secondary structure, and can be improved with the SPD-2 peptide.

Signaling pathways are crucial for hair growth in goats.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

The EDAR gene greatly affects hair thickness in Asian populations.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

Nanoparticles with more oleic acid improved the delivery and stability of the drug spironolactone.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

Transplant success has improved with better immunosuppressive drugs and donor matching.