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A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

Whiskers can form without sensory nerves or Foxd1, thanks to Meis2 in mesenchymal cells.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

Early diagnosis of skin conditions linked to rickets is crucial to prevent growth and bone issues.

Vitamin D and calcium are essential for normal hair growth.

A new method allows detailed, continuous imaging of crustacean leg regeneration without harming the cells.

Terrestrial vertebrates have balanced keratin gene clusters, unlike teleost fish.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

TIP39 and PTH2R help control calcium levels and skin cell development.

TGF-β and FGF pathways are crucial for skin development and regeneration.

Gene regulatory regions evolve faster than protein coding regions, allowing new gene relationships without changing transcription factors.

RANKL causes lymph nodes to grow by making certain cells multiply.

Gujian oral liquid reduces osteoarthritis symptoms by targeting inflammation.

Noggin promotes skin tumors by activating Wnt and Shh pathways.

Scientists created a functional 3D skin system from stem cells that can be transplanted into wounds.

The OVOL1-OVOL2 axis is important for hair follicle differentiation and can help diagnose certain hair-related tumors.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Cornification is the process where living skin cells die to create a protective barrier, and problems with it can cause skin diseases.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Skin organoids can model tuberculosis infection and help test treatments.

Ichthyoses are genetic skin disorders that affect the skin's barrier function.

Hoxc13 gene is essential for hair, nail, and papilla development.

A new method to study dog skin diseases using lab-grown skin cells was developed.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

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