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

VILLIN4 helps root hair growth by organizing actin with calcium.

Acinetobacter strain A1-4-2 can safely clean water pollutants.

The ACE1 gene variant doesn't affect long-COVID symptoms.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

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.

MCHR2 gene duplications may be linked to alopecia areata.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Arabidopsis PCaP2 helps plants survive drought by linking ABA and SA signals.

Activin A helps heal skin wounds and protects the brain after injury.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

Overexpression of ALK2 in hair follicles disrupts skin development and slows wound healing.

Precise objectives can improve student achievement in health education.

Blocking adenosine A2B receptor may prevent or treat hearing loss.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

REV7 is crucial for genome stability and cancer treatment, making it a potential target for therapy.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

The vitamin D receptor has many roles in the body beyond managing calcium, affecting the immune system, hair growth, muscles, fat, bone marrow, and cancer cells.

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

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Avacopan may cause unexpected side effects, so early monitoring is important.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.