David H. Stitelman

ORCID: 0000-0001-8067-5830
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About
Contact & Profiles
Research Areas
  • Congenital Diaphragmatic Hernia Studies
  • Neonatal Respiratory Health Research
  • Congenital Anomalies and Fetal Surgery
  • Prenatal Screening and Diagnostics
  • Spinal Dysraphism and Malformations
  • Virus-based gene therapy research
  • Cerebrospinal fluid and hydrocephalus
  • Tissue Engineering and Regenerative Medicine
  • Intestinal Malrotation and Obstruction Disorders
  • Muscle Physiology and Disorders
  • Pediatric Hepatobiliary Diseases and Treatments
  • RNA Interference and Gene Delivery
  • Surgical Simulation and Training
  • Opioid Use Disorder Treatment
  • Gallbladder and Bile Duct Disorders
  • COVID-19 Impact on Reproduction
  • Airway Management and Intubation Techniques
  • Anesthesia and Pain Management
  • Cardiac, Anesthesia and Surgical Outcomes
  • Appendicitis Diagnosis and Management
  • CRISPR and Genetic Engineering
  • Pluripotent Stem Cells Research
  • Gastrointestinal disorders and treatments
  • Esophageal and GI Pathology
  • Preterm Birth and Chorioamnionitis

Yale University
2016-2025

Yale New Haven Hospital
2017-2024

Hartwell Foundation
2022

Case Western Reserve University
2022

Chase Acute Outpatients Hospital
2021

University Medical Center
2020

Yale Cancer Center
2020

University Hospital and Clinics
2020

Children's Center
2010-2014

Children's Hospital of Philadelphia
2004-2014

Genetic diseases can be diagnosed early during pregnancy, but many monogenic disorders continue to cause considerable neonatal and pediatric morbidity mortality. Early intervention through intrauterine gene editing, however, could correct the genetic defect, potentially allowing for normal organ development, functional disease improvement, or cure. Here we demonstrate safe intravenous intra-amniotic administration of polymeric nanoparticles fetal mouse tissues at selected gestational ages...

10.1038/s41467-018-04894-2 article EN cc-by Nature Communications 2018-06-20

Matrix metalloproteinase activity is instrumental in processes of cellular invasion. The interstitial invasion endothelial cells during angiogenesis accompanied by up-regulation several matrix metalloproteinases, including membrane type 1 (MT1-MMP). In this study, we show that stimulated to undergo a three-dimensional extracellular environment increase production the transcription factor Egr-1. Increased binding Egr-1 MT1-MMP promoter correlates with enhanced transcriptional activity,...

10.1074/jbc.274.32.22679 article EN cc-by Journal of Biological Chemistry 1999-08-01

Structural fetal diseases, such as congenital diaphragmatic hernia (CDH) can be diagnosed prenatally. Neonates with CDH are healthy in utero gas exchange is managed by the placenta, but impaired lung function results critical illness from time a baby takes its first breath. MicroRNA (miR) 200b and downstream targets TGF-β pathway critically involved branching morphogenesis. Here, we characterize expression of miR200b at different gestational times using rat model CDH. Fetal rats deficient...

10.1016/j.omtn.2023.04.018 article EN cc-by-nc-nd Molecular Therapy — Nucleic Acids 2023-04-23

In utero gene editing has the potential to modify disease causing genes in multiple developing tissues before birth, possibly allowing for normal organ development, improvement, and conceivably, cure. cystic fibrosis (CF), a that arises from mutations transmembrane conductance regulator (

10.1101/2024.09.04.611031 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2024-09-08

Efficient gene transfer to muscle stem cells (satellite cells) has not been achieved despite broad transduction of skeletal by systemically administered adeno-associated virus serotype 2/9 (AAV-9) in mice. We hypothesized that cellular migration during fetal development would make satellite accessible for following utero intravascular injection. injected AAV-9 encoding green fluorescent protein (GFP) marker into the vascular space mice ranging ages from post-coital day 12 (E12) postnatal 1...

10.1038/mtm.2014.40 article EN cc-by-nc-sa Molecular Therapy — Methods & Clinical Development 2014-01-01

Presently, in vivo methods to efficiently and broadly transduce all major cell types throughout both the central (CNS) peripheral adult nervous system (PNS) are lacking. In this study, we hypothesized that during early fetal development neural populations, including stem cells (NSCs), may be accessible for gene transfer via open groove. To test hypothesis, injected lentiviral vectors encoding a green fluorescent protein (GFP) marker into murine amniotic cavity at embryonic day 8. This method...

10.1038/mt.2010.125 article EN cc-by-nc-nd Molecular Therapy 2010-06-22

Despite a national decrease in emergency department visits the United States during first 10 months of pandemic, preliminary Consumer Product Safety Commission data indicate increased firework-related injuries. We hypothesized an increase injuries 2020 compared to years prior related corresponding consumer firework sales.The National Electronic Injury Surveillance System (NEISS) was queried from 2018 for cases with product codes 1313 (firework injury) and narratives containing "fireworks"....

10.1186/s40621-021-00358-2 article EN cc-by Injury Epidemiology 2021-11-10

Background Advances in Molecular Therapy have made gene editing through systemic or topical administration of reagents a feasible strategy to treat genetic diseases rational manner. Encapsulation therapeutic agents nanoparticles can improve intracellular delivery agents, provided that the are efficiently taken up within target cells. In prior work we had established proof-of-principle carrying mediate site-specific fetal and adult animals vivo results functional disease improvement rodent...

10.1371/journal.pone.0266218 article EN cc-by PLoS ONE 2022-04-06

Infants prenatally suspected of having a choledochal cyst (CDC) typically undergo ultrasound imaging shortly after birth. This study sought to evaluate features on the initial postnatal (IPU) that could identify newborns at risk for early complications.Following IRB approval, patients from four US fetal centers with prenatal suspicion CDC and 2000 2017 were reviewed. Imaging clinical courses assessed.Forty-two had ultrasounds suspicious CDC. Nineteen (45.2%) excluded due diagnostic revision...

10.1080/14767058.2020.1742320 article EN The Journal of Maternal-Fetal & Neonatal Medicine 2020-03-19

To compare institutional practice patterns for gastrostomy tube placement in neonates with duodenal atresia (DA) and trisomy 21.A retrospective review of the Pediatric Health Information System (PHIS) from 2015 to 2018 identified infants <10 days old ICD-10 diagnostic codes DA 21, addition procedure an intestinal bypass or duodenoduodenostomy. This cohort was then queried associated co-morbidities.Two hundred nine were DA, bypass. Fifty-seven (27%) underwent placement. Baseline...

10.1097/mpg.0000000000003227 article EN Journal of Pediatric Gastroenterology and Nutrition 2021-07-07
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