The spectrum of congenital eye malformations including microphthalmia (small eyes), anophthalmia (absent eyes) and coloboma (ventral eye defects), or MAC, causes blindness in approximately 1 in 10,000 children. We have discovered novel RBP4 coding and SOX3 regulatory mutations in patients with MAC disease. RBP4 encodes plasma retinol binding protein, a lipocalin that transports vitamin A, an essential nutrient for eye development, in the bloodstream. We show RBP4 missense mutations p.A73T and p.A75T alter the ligand-binding pocket, causing autosomal dominant MAC with reduced penetrance and a maternal parent-of-origin effect. Both mutant alleles encode dominant-negative RBPs that bind poorly to vitamin A but strongly to the STRA6 receptor on...
The development of the vertebrate eye is tightly controlled by precise genetic regulations. From a s...
SummaryThe cellular uptake of vitamin A from its RBP4-bound circulating form (holo-RBP4) is a homeos...
Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia (small eye) show...
SummaryGestational vitamin A (retinol) deficiency poses a risk for ocular birth defects and blindnes...
Maternally skewed transmission of traits has been associated with genomic imprinting and oocytederiv...
Background: The retinoic acid (RA) pathway plays a crucial role in both eye morphogenesis and the vi...
Gestational vitamin A (retinol) deficiency poses a risk for ocular birth defects and blindness. We i...
Vitamin A deficiency is the leading cause of preventable blindness in children worldwide and results...
Microphthalmia, anophthalmia, and coloboma (MAC) are distinct abnormalities demonstrating a continuu...
Visual impairment ranges from mild forms that can be corrected with glasses to more severe cases tha...
Chou et al. discover a new mode of maternal inheritance by analyzing human mutations in plasma retin...
The major active retinoid, all-trans retinoic acid, has long been recognized as critical for the dev...
The major active retinoid, all-trans retinoic acid, has long been recognized as critical for the dev...
Microphthalmia, anophthalmia, and coloboma (MAC) are structural congenital eye malformations that ca...
Retinitis Pigmentosa (RP) is a common form of retinal degeneration characterized by photoreceptor de...
The development of the vertebrate eye is tightly controlled by precise genetic regulations. From a s...
SummaryThe cellular uptake of vitamin A from its RBP4-bound circulating form (holo-RBP4) is a homeos...
Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia (small eye) show...
SummaryGestational vitamin A (retinol) deficiency poses a risk for ocular birth defects and blindnes...
Maternally skewed transmission of traits has been associated with genomic imprinting and oocytederiv...
Background: The retinoic acid (RA) pathway plays a crucial role in both eye morphogenesis and the vi...
Gestational vitamin A (retinol) deficiency poses a risk for ocular birth defects and blindness. We i...
Vitamin A deficiency is the leading cause of preventable blindness in children worldwide and results...
Microphthalmia, anophthalmia, and coloboma (MAC) are distinct abnormalities demonstrating a continuu...
Visual impairment ranges from mild forms that can be corrected with glasses to more severe cases tha...
Chou et al. discover a new mode of maternal inheritance by analyzing human mutations in plasma retin...
The major active retinoid, all-trans retinoic acid, has long been recognized as critical for the dev...
The major active retinoid, all-trans retinoic acid, has long been recognized as critical for the dev...
Microphthalmia, anophthalmia, and coloboma (MAC) are structural congenital eye malformations that ca...
Retinitis Pigmentosa (RP) is a common form of retinal degeneration characterized by photoreceptor de...
The development of the vertebrate eye is tightly controlled by precise genetic regulations. From a s...
SummaryThe cellular uptake of vitamin A from its RBP4-bound circulating form (holo-RBP4) is a homeos...
Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia (small eye) show...