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The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Dupilumab is being tested for many new skin, respiratory, and gastrointestinal conditions.

Certain microRNAs in the fluid around eggs are linked to Polycystic Ovary Syndrome and may help diagnose it.

The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

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

Hoxc genes control hair growth through Wnt signaling.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

The study developed a tool to predict how gut microbes process foods and drugs, showing that similar compounds often share metabolic pathways and effects.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

Skin organoids are a promising new model for studying human skin development and testing treatments.

ΔNp63α stops TAp73β from working in skin cancer by blocking its access to specific genes, not by directly interacting with it.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Endoglin is crucial for proper hair growth cycles and stem cell activation in mice.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

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

Researchers identified specific genes that are important for mouse skin cell development and healing.

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

miR-140-5p in certain cell vesicles helps hair growth by boosting cell proliferation.

Genes related to pigmentation, body rhythms, and behavior change during hares' seasonal coat color transition, with a common genetic mechanism in two hare species.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.