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A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

Very-long-chain acyl-CoA synthetases and fatty acid transport proteins play key roles in fatty acid metabolism and lipid processing in different tissues.

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

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

ATP helps prevent skin damage from vandetanib by reducing stress.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

Vitamin A helps rabbit skin cells grow and survive heat stress.

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

Cyclic nucleotide-gated channels are crucial for proper root hair growth and calcium balance in plants.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Transglutaminases work through a ping-pong mechanism, and human plasma and platelet transglutaminases have similar catalytic subunits.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Phospholipase Cδ1 is crucial for normal skin and hair development.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

Iron influences root hair growth during phosphate starvation by affecting auxin distribution and vesicle trafficking.

Protein Kinase C shows promise for cancer treatment, but more research is needed to develop effective inhibitors.

Freeze-dried platelet-rich plasma boosts bone growth in gum treatment.

Hairless protein can block vitamin D activation in skin cells.

Cepharanthine may help treat Equid herpesvirus type 8 by reducing oxidative stress.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

Removing part of the vitamin D receptor stops vitamin D from working properly.

The method identified and measured ten compounds from Eclipta prostrata, showing significant enzyme inhibitory effects.

A new compound, HTPI, promotes hair growth by protecting cells from damage and regulating energy use.