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Intravenous calcium therapy is a safe and effective treatment for a rare type of rickets.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

K6hf is a unique protein found only in a specific layer of hair follicles.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Recombinant keratins can form useful structures for medical applications, overcoming natural keratin limitations.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

Scientists found out how a specific protein in human hair cuticles behaves and is structured.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

Removing p16INK4a from skin cells can lead to faster and more clumped growth, which might help with hair growth.

10.5% of sheep in Ismailia, Egypt, had Sarcoptes scabiei, causing skin issues.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

Disabling the FGF5 gene in sheep leads to longer wool.

A gene mutation in Lama3 is linked to a common type of hair loss.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

Ro stress hindered ginseng root growth and ginsenoside production, but increased certain hormones and affected gene regulation related to plant growth and stress responses.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.