Pages that link to "Q24294226"
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The following pages link to Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid (Q24294226):
Displaying 50 items.
- cytochrome P450 family 26 subfamily B member 1 (Q21110764) (← links)
- Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2 (Q21202852) (← links)
- Danio rerio: the Janus of the bone from embryo to scale (Q26775731) (← links)
- A Genetic-Pathophysiological Framework for Craniosynostosis (Q26784240) (← links)
- Current perspectives on the use of alternative species in human health and ecological hazard assessments (Q26825743) (← links)
- Nuclear receptors in bone physiology and diseases (Q26853017) (← links)
- p53 and TAp63 promote keratinocyte proliferation and differentiation in breeding tubercles of the zebrafish (Q27318144) (← links)
- Application of synthetic photostable retinoids induces novel limb and facial phenotypes during chick embryogenesis in vivo (Q28655707) (← links)
- 500,000 fish phenotypes: The new informatics landscape for evolutionary and developmental biology of the vertebrate skeleton (Q28728345) (← links)
- Excessive dietary intake of vitamin A reduces skull bone thickness in mice (Q33585182) (← links)
- The ontology of craniofacial development and malformation for translational craniofacial research (Q33699401) (← links)
- Osterix/Sp7 limits cranial bone initiation sites and is required for formation of sutures (Q33792803) (← links)
- Impact of retinoic acid exposure on midfacial shape variation and manifestation of holoprosencephaly in Twsg1 mutant mice (Q35041346) (← links)
- Vitamin a is a negative regulator of osteoblast mineralization (Q35067782) (← links)
- Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses. (Q35809894) (← links)
- Cutaneous retinoic acid levels determine hair follicle development and downgrowth (Q36407832) (← links)
- Human cytochromes P450 in health and disease (Q36512912) (← links)
- Zebrafish Craniofacial Development: A Window into Early Patterning (Q36593756) (← links)
- Retinoic acid-induced premature osteoblast-to-preosteocyte transitioning has multiple effects on calvarial development (Q36855971) (← links)
- The FaceBase Consortium: a comprehensive resource for craniofacial researchers (Q37120516) (← links)
- Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation (Q37186044) (← links)
- Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency. (Q37514812) (← links)
- Retinoic Acid Excess Impairs Amelogenesis Inducing Enamel Defects. (Q37565800) (← links)
- Cytochrome P450 oxidoreductase deficiency caused by R457H mutation in POR gene in Chinese: case report and literature review (Q37698004) (← links)
- Using transgenic reporters to visualize bone and cartilage signaling during development in vivo. (Q38028948) (← links)
- The role of vertebrate models in understanding craniosynostosis (Q38032780) (← links)
- A bone to pick with zebrafish (Q38178279) (← links)
- Roles of retinoic acid signaling in normal and abnormal development of the palate and tongue (Q38199181) (← links)
- Electron Transfer Pathways in Cholesterol Synthesis (Q38582147) (← links)
- Gain-of-Function Mutations in RARB Cause Intellectual Disability with Progressive Motor Impairment (Q38818972) (← links)
- Building and maintaining joints by exquisite local control of cell fate (Q38942837) (← links)
- Accelerated Skeletal Maturation in Disorders of Retinoic Acid Metabolism: A Case Report and Focused Review of the Literature (Q38944874) (← links)
- Transcription factor TLX1 controls retinoic acid signaling to ensure spleen development (Q40663410) (← links)
- Electron transfer by human wild-type and A287P mutant P450 oxidoreductase assessed by transient kinetics: functional basis of P450 oxidoreductase deficiency (Q42266862) (← links)
- Defective CYP26B1 causes RHFCA (Q45316472) (← links)
- Citalopram and sertraline exposure compromises embryonic bone development (Q46280055) (← links)
- Generating retinoic acid gradients by local degradation during craniofacial development: One cell's cue is another cell's poison. (Q48249810) (← links)
- Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31. (Q48317391) (← links)
- Defective CYP26B1 does not 4-hydroxylate atRA (Q50289151) (← links)
- CYP26A1,B1,C1 4-hydroxylate atRA (Q50299011) (← links)
- Excessive retinoic acid impaired proliferation and differentiation of human fetal palatal chondrocytes (hFPCs). (Q50427082) (← links)
- Functional bone histology of zebrafish reveals two types of endochondral ossification, different types of osteoblast clusters and a new bone type (Q50506130) (← links)
- Retinol-binding protein 4 downregulation during osteogenesis and its localization to non-endocytic vesicles in human cranial suture mesenchymal cells suggest a novel tissue function (Q50791162) (← links)
- Mucopolysaccharidosis IIIB and mild skeletal anomalies: coexistence of NAGLU and CYP26B1 missense variations in the same patient in a Chinese family. (Q52615495) (← links)
- Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability. (Q52653945) (← links)
- Direct activation of chordoblasts by retinoic acid is required for segmented centra mineralization during zebrafish spine development. (Q52719724) (← links)
- Genetic advances in craniosynostosis. (Q52795305) (← links)
- All-Trans Retinoic Acid-Induced Craniofacial Malformation Model: A Prenatal and Postnatal Morphological Analysis. (Q53057253) (← links)
- Congenital adrenal hyperplasia. (Q53249380) (← links)
- Retinoic Acid Maintains Function of Neural Crest-Derived Ocular and Craniofacial Structures in Adult Zebrafish. (Q55318589) (← links)