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Publications by Aaron N. Cranston
The RetC620R Mutation Affects Renal and Enteric Development in a Mouse Model of Hirschsprung's Disease
American Journal of Pathology
Forensic Medicine
Pathology
Related publications
A Novel Corrective Pullthrough Surgery in a Mouse Model of Hirschsprung's Disease
Journal of Pediatric Surgery
Medicine
Child Health
Surgery
Pediatrics
Perinatology
Hepatocyte Growth Factor Prevents Renal Fibrosis and Dysfunction in a Mouse Model of Chronic Renal Disease.
Journal of Clinical Investigation
Medicine
Hirschsprung's Disease in Infancy.
BMJ
Hirschsprung's Disease in the Neonatal Period
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Erythrocyte Acetylcholinesterase in Hirschsprung's Disease.
Journal of Clinical Pathology
Medicine
Forensic Medicine
Pathology
Mutation of the Sry-Related Sox10 Gene in Dominant Megacolon, a Mouse Model for Human Hirschsprung Disease
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Loss of Enteric Dopaminergic Neurons and Associated Changes in Colon Motility in an MPTP Mouse Model of Parkinson's Disease
Experimental Neurology
Developmental Neuroscience
Neurology
The MOUSE BPK MUTATION, a MODEL OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) and Jcpk, a PHENOTYPICALLY DISTINCT PKD MUTATION, ARE ALLELIC. • 2151
Pediatric Research
Child Health
Pediatrics
Perinatology
Genetic Model System Studies of the Development of the Enteric Nervous System, Gut Motility and Hirschsprung’s Disease
Neurogastroenterology and Motility
Endocrine
Physiology
Gastroenterology
Autonomic Systems
