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A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

VEGF and VEGFR-2 genes influence feather maturity, and specific genetic markers can improve chicken breeding.

Infants with severe KID syndrome may be more prone to serious infections and need close monitoring.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

Dengue fever can cause a temporary type of hair loss called telogen effluvium.

DAB labeling effectively identifies collagen type III and PDGFR in horse skin, but may show false positives.

VHL disease can cause early paragangliomas, needing lifelong monitoring.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

The vitamin D receptor can act without its usual activating molecule, affecting hair growth and skin cancer, but its full range of actions is not well understood.

The patient's hair has unique structural differences with alternating bright and dark bands.

A dog with a hereditary skin condition causing blisters and hair loss survived for a year.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

The study concluded that the new wound model can be used to evaluate skin regeneration and nerve growth.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

cGVHD often severely affects the skin, causing rapid aging and other issues.

Dacomitinib can cause nail and skin issues, but these can be managed without stopping the drug.

A new genetic mutation was found causing hair and eye issues in a boy.

FLCN helps control iron levels in cells.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

The ID2 gene can help distinguish between sensitizers and irritants in skin cells.

Genetic factors alone might not cause pemphigus vulgaris; other factors like birth complications and puberty may trigger it.

Vitamin D receptor helps prevent skin tumors.

A child with a rare vitamin D-resistant condition improved with treatment.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

MSF-VMDNet accurately segments skin cancer images better than existing methods.

Viral reactivation is rare at the time of DRESS diagnosis in the U.S.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.