Genetic contribution of retinoid-related genes to neural tube defects
Journal Article
Overview
publication date
- April 1, 2018
has subject area
- Aldehyde Oxidoreductases - Retinal Dehydrogenase
- Child
- Child, Preschool
- China
- Congenital Abnormalities - Neural Tube Defects
- Cyclohexenes - Tretinoin
- Environment and Public Health - Case-Control Studies
- Environment and Public Health - Cohort Studies
- Enzymes and Coenzymes - Retinoic Acid 4-Hydroxylase
- Flavoproteins - Retinal Dehydrogenase
- Health Care Evaluation Mechanisms - Case-Control Studies
- Health Care Evaluation Mechanisms - Cohort Studies
- Hemeproteins - Retinoic Acid 4-Hydroxylase
- Humans
- Infant
- Infant, Newborn
- Investigative Techniques - Case-Control Studies
- Investigative Techniques - Cohort Studies
- Metalloproteins - Retinal Dehydrogenase
- Mixed Function Oxygenases - Retinoic Acid 4-Hydroxylase
- Morphogenesis - Embryonic Development
- Mutation
- Nervous System Diseases - Neural Tube Defects
- Pigments, Biological - Tretinoin
- Polyenes - Tretinoin
- Receptors, Cytoplasmic and Nuclear - Receptors, Retinoic Acid
- Reproduction - Embryonic Development
- Terpenes - Tretinoin
- Transcription Factors - Receptors, Retinoic Acid
Date in CU Experts
- February 2, 2018 1:14 AM
Full Author List
- Li H; Zhang J; Chen S; Wang F; Zhang T; Niswander L
author count
- 6
citation count
- 11
published in
- Human Mutation Journal
Other Profiles
International Standard Serial Number (ISSN)
- 1059-7794
Electronic International Standard Serial Number (EISSN)
- 1098-1004
Digital Object Identifier (DOI)
Additional Document Info
start page
- 550
end page
- 562
volume
- 39
issue
- 4