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All HPV vaccine studies should be registered and published to reduce reporting bias.

Twist1 is crucial for UVB-induced skin cancer development.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

HGF activator helps convert HGF to its active form, promoting hair growth.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The yeast found in a sea lion's skin lesion was almost identical to that on healthy skin, suggesting environmental factors may affect fungal growth and the cause of the lesion is unclear.

The child has a scaly rash and fever, but tests show no infection.

Serotype 4 of Ureaplasma showed the highest pathogenicity in female mice.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

MRI can effectively image skin structures noninvasively.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Deleting Twist1 in skin cells reduces UVB-induced skin cancer risk.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

A possible link exists between hair follicle abnormalities, hair loss, and muscle weakness.

Progeria, a disease that causes early aging, is linked to a gene mutation and helps us understand normal aging.

A mutation in the human hairless gene causes alopecia universalis.

Hair loss in Rhesus macaques may be caused by a skin allergy-related condition.

Hair follicle stem cells can become heart muscle cells.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

A 13-year-old boy with a rare genetic condition survived a heart attack and improved with treatment.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Human placenta hydrolysate may help treat COVID-19 by reducing virus replication and boosting immune response.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

Capsaicin, found in chili peppers, can slow down hair growth by affecting skin cells and hair follicles.

Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.