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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

A rare EGFR mutation in newborns leads to severe health issues and early death.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Blocking JAK-STAT5 signaling in mice leads to hair growth.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Removing mink's adrenal glands causes their summer fur to grow earlier.

Targeting mTOR in myeloid cells may help reduce psoriasis symptoms.

Certain substances can decrease or increase exploratory behavior in rodents.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A mutation in the Sgkl gene causes defective hair growth in mice.

Androgen receptors in the mouse brain may explain cognitive and mood changes in prostate cancer treatment.

Radiation significantly slows down wound healing in mice.

CD8+ T cells play a key role in graft-versus-host disease in certain mice models.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

ACTH promotes hair growth in mink, but α-MSH does not.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Lack of Evi in skin causes psoriasis-like symptoms in mice.

MPZL3 is crucial for seborrheic dermatitis development.

Mouse genital development depends on male or female hormones for specific features.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Stress can slow hair growth and affect skin color by impacting the body's stress response system.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Androgens can help prevent memory problems caused by apoE4.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.

Meis2 is essential for touch sensation and nerve function in mice.

Young C57BL/6 mice heal better than BALB/c mice, and older mice heal faster but regenerate worse.