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

A 72-year-old man was diagnosed with a rare skin form of Rosai-Dorfman disease after years of misdiagnosis.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

The activity of a specific rat enzyme in the prostate and epididymis is highly dependent on the acidity level.

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

Palmaris longus muscle absence is uncommon and not linked to gender, hand side, or finger ratio.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Meis2 is essential for touch sensation and proper nerve connection to touch receptors in certain skin areas of mice.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Bortezomib chemotherapy can cause temporary skin rashes.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

Far-infrared radiation improves stem cell growth and movement, helping heart therapy.

MK-0773 safely increased muscle mass but did not improve muscle strength or function in elderly women with sarcopenia.

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RC48 shows promise for treating certain advanced cancers, but more research is needed.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

RORs may influence cashmere growth cycles.

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Methylation of the 5-AR2 gene may cause resistance to Finasteride in BPH patients.

Accurate protein modeling can help develop new treatments for prostate cancer and other diseases.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Bullous pemphigoid can look like erythema multiforme, so awareness is needed for proper treatment.