scholarly article | Q13442814 |
P50 | author | Kim L. McBride | Q37371145 |
P2093 | author name string | Nikki J Seagraves | |
P2860 | cites work | Coordinating tissue interactions: Notch signaling in cardiac development and disease | Q26822995 |
The incidence of congenital heart disease | Q29614195 | ||
The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations | Q30776464 | ||
The polymorphism architecture of mouse genetic resources elucidated using genome-wide resequencing data: implications for QTL discovery and systems genetics | Q31120643 | ||
Genealogies of mouse inbred strains | Q33806120 | ||
jumonji gene is essential for the neurulation and cardiac development of mouse embryos with a C3H/He background | Q33870890 | ||
Mouse models of human phenylketonuria | Q33961407 | ||
Ethanol teratogenesis in five inbred strains of mice | Q34181659 | ||
Heterogeneity of genetic modifiers ensures normal cardiac development | Q34193363 | ||
Epidemiology of noncomplex left ventricular outflow tract obstruction malformations (aortic valve stenosis, coarctation of the aorta, hypoplastic left heart syndrome) in Texas, 1999-2001 | Q34338168 | ||
National Institutes of Health Consensus Development Conference Statement: phenylketonuria: screening and management, October 16-18, 2000. | Q34388027 | ||
The cephalic neural crest exerts a critical effect on forebrain and midbrain development | Q35080427 | ||
Developmental anatomy of the heart: a tale of mice and man. | Q35581652 | ||
Effects of dietary management of phenylketonuria on long-term cognitive outcome | Q36154575 | ||
Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics. | Q36829209 | ||
Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pedia | Q36829213 | ||
Reduced EGFR causes abnormal valvular differentiation leading to calcific aortic stenosis and left ventricular hypertrophy in C57BL/6J but not 129S1/SvImJ mice | Q37264435 | ||
NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling | Q37294787 | ||
An efficient SNP system for mouse genome scanning and elucidating strain relationships. | Q37496419 | ||
Pathogenesis of cognitive dysfunction in phenylketonuria: review of hypotheses. | Q37685646 | ||
The effects of high phenylalanine concentration on chick embryonic development | Q37827351 | ||
Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies | Q40364201 | ||
Effect of maternal blood phenylalanine level on mouse maternal phenylketonuria offspring | Q40671745 | ||
Early human development and the chief sources of information on staged human embryos | Q41212347 | ||
The international study of pregnancy outcome in women with maternal phenylketonuria: report of a 12-year study | Q41722149 | ||
Nasomaxillary hypoplasia and severe orofacial clefting in a child of a mother with phenylketonuria | Q41922943 | ||
Congenital heart disease in maternal phenylketonuria: report from the Maternal PKU Collaborative Study | Q43592447 | ||
Emotional outcome of adolescents and young adults with early and continuously treated phenylketonuria | Q43793544 | ||
Developmental neurotoxicity: do similar phenotypes indicate a common mode of action? A comparison of fetal alcohol syndrome, toluene embryopathy and maternal phenylketonuria | Q44019760 | ||
How practical are recommendations for dietary control in phenylketonuria? | Q44061671 | ||
Congenital cardiovascular malformations: questions on inheritance. Baltimore-Washington Infant Study Group | Q45884803 | ||
Metabolic phenotypes of phenylketonuria. Kinetic and molecular evaluation of the Blaskovics protein loading test. | Q45927134 | ||
Effects of genetic background on cardiovascular anomalies in the Ts16 mouse | Q46419766 | ||
Frontal lobe-dependent functions in treated phenylketonuria: blood phenylalanine concentrations and long-term deficits in adolescents and young adults | Q46497893 | ||
Abnormal expression of genes associated with development and inflammation in the heart of mouse maternal phenylketonuria offspring | Q46705037 | ||
Blood phenylalanine monitoring for dietary compliance among patients with phenylketonuria: comparison of methods | Q46897326 | ||
Cardiac neural crest cells provide new insight into septation of the cardiac outflow tract: aortic sac to ventricular septal closure. | Q52188159 | ||
Cardiovascular Defects among the Progeny of Mouse Phenylketonuria Females | Q52193955 | ||
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project | Q57315750 | ||
Life span of specified-pathogen-free (MRC category 4) mice and rats | Q70729585 | ||
Characterization of mutations at the mouse phenylalanine hydroxylase locus | Q73269192 | ||
Patterning the vertebrate heart | Q74399546 | ||
Conotruncal myocardium arises from a secondary heart field | Q77102388 | ||
Seeking causes: Classifying and evaluating congenital heart defects in etiologic studies | Q80867983 | ||
Generation n + 1: Projected numbers of babies born to women with PKU compared to babies with PKU in the United States in 2009 | Q83865274 | ||
P433 | issue | 4 | |
P921 | main subject | phenylketonuria | Q194041 |
teratogenicity | Q56246640 | ||
maternal phenylketonuria | Q68430440 | ||
P304 | page(s) | 650-658 | |
P577 | publication date | 2012-08-08 | |
P1433 | published in | Molecular Genetics and Metabolism | Q6895949 |
P1476 | title | Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences | |
P478 | volume | 107 |
Q26744450 | Genetic Evaluation and Use of Chromosome Microarray in Patients with Isolated Heart Defects: Benefits and Challenges of a New Model in Cardiovascular Care |
Q41929459 | Methylome repatterning in a mouse model of Maternal PKU Syndrome. |
Q90842272 | RNA-Seq analysis in an avian model of maternal phenylketonuria |
Q90428534 | Uric acid: a potent molecular contributor to pluripotent stem cell cardiac differentiation via mesoderm specification |
Search more.