Cincinnati Children's Hospital Medical Center Jul 2012 - Jun 2014
Associate Professor
Baylor College of Medicine Jul 2012 - Jun 2014
Associate Professor
Cincinnati Children's Hospital Medical Center Jun 2006 - Jun 2012
Assistant Professor
Baylor College of Medicine 2005 - 2006
Assistant Professor, Pediatrics-Gastroenterology
Baylor College of Medicine 2001 - 2005
Postdoctoral Fellow, Genetics
Education:
Baylor College of Medicine 1995 - 2001
Doctorates, Doctor of Philosophy, Molecular Biology
Louisiana State University 1992 - 1995
Bachelors, Bachelor of Science, Biochemistry, Microbiology
Benjamin Franklin High School
Skills:
Genetics Cell Culture Molecular Biology Immunohistochemistry Cell Biology Cancer Western Blotting Science Animal Models Cancer Research Cell Molecular Cloning Pcr Grant Writing Grantsmanship Grant Reviewing University Teaching Biology Mentoring
Us Patents
Nucleic Acid And Amino Acid Sequences For Atp-Binding Cassette Transporter And Methods Of Screening For Agents That Modify Atp-Binding Cassette Transporter
Rando Allikmets - Frederick MD, US Kent L. Anderson - Houston TX, US Michael Dean - Frederick MD, US Mark Leppert - Salt Lake City UT, US Richard A. Lewis - Houston TX, US Yixin Li - Houston TX, US James R. Lupski - Houston TX, US Jeremy Nathans - Baltimore MD, US Amir Rattner - Baltimore MD, US Noah F. Shroyer - Houston TX, US Nanda Singh - Salt Lake City UT, US Philip Smallwood - Woodbine MD, US Hui Sun - Baltimore MD, US
Assignee:
University of Utah Research Foundation - Salt Lake City UT Baylor College of Medicine - Houston TX John Hopkins University - Baltiomore MD The United States of America as represented by the Department of Health and Human Services - Washington DC
The present invention provides nucleic acid and amino acid sequences of an ATP binding cassette transporter and mutated sequences thereof associated with macular degeneration. Methods of detecting agents that modify ATP-binding cassette transporter comprising combining purified ATP binding cassette transporter and at least one agent suspected of modifying the ATP binding cassette transporter an observing a change in at least one characteristic associated with ATP binding cassette transporter. Methods of detecting macular degeneration is also embodied by the present invention.
Methods Of Screening And Diagnostics Using Atp-Binding Cassette Transporter
Rando Allikmets - Frederick MD, US Kent L. Anderson - Houston TX, US Michael Dean - Frederick MD, US Mark Leppert - Salt Lake City UT, US Richard A. Lewis - Houston TX, US Yixin Li - Houston TX, US James R. Lupski - Houston TX, US Jeremy Nathans - Baltimore MD, US Amir Rattner - Baltimore MD, US Noah F. Shroyer - Houston TX, US Nanda Singh - Salt Lake City UT, US Philip Smallwood - Woodbine MD, US Hui Sun - Baltimore MD, US
Assignee:
Baylor College of Medicine - Houston TX The United States of America as represented by the Department of Health and Human Services - Washington DC University of Utah Research Foundation - Salt Lake City UT John Hopkins University - Baltimore MD
The present invention provides nucleic acid and amino acid sequences of an ATP binding cassette transporter and mutated sequences thereof associated with macular degeneration. Methods of detecting agents that modify ATP-binding cassette transporter comprising combining purified ATP binding cassette transporter and at least one agent suspected of modifying the ATP binding cassette transporter an observing a change in at least one characteristic associated with ATP binding cassette transporter. Methods of detecting macular degeneration is also embodied by the present invention.
Methods Of Gene Therapy Using Nucleic Acid Sequences For Atp-Binding Cassette Transporter
Rando Allikmets - Frederick MD, US Kent L. Anderson - Houston TX, US Michael Dean - Frederick MD, US Mark Leppert - Salt Lake City UT, US Richard A. Lewis - Houston TX, US Yixin Li - Houston TX, US James R. Lupski - Houston TX, US Jeremy Nathans - Baltimore MD, US Amir Rattner - Baltimore MD, US Noah F. Shroyer - Houston TX, US Nanda Singh - Salt Lake City UT, US Philip Smallwood - Woodbine MD, US Hui Sun - Baltimore MD, US
Assignee:
Baylor College of Medicine - Houston TX Johns Hopkins University - Baltimore MD University of Utah Research Foundation - Salt Lake City UT United States of America, Represented by the Secretary, Department of Health and Human Services, c/o National Institute of Health - Washington DC
The present invention provides nucleic acid and amino acid sequences of an ATP binding cassette transporter and mutated sequences thereof associated with macular degeneration. Methods of detecting agents that modify ATP-binding cassette transporter comprising combining purified ATP binding cassette transporter and at least one agent suspected of modifying the ATP binding cassette transporter an observing a change in at least one characteristic associated with ATP binding cassette transporter. Methods of detecting macular degeneration is also embodied by the present invention.
Methods Of Gene Therapy Using Nucleic Acid Sequences For Atp-Binding Cassette Transporter
Rando Allikmets - Frederick MD, US Kent L. Anderson - Houston TX, US Michael Dean - Frederick MD, US Mark Leppert - Salt Lake City UT, US Richard A. Lewis - Houston TX, US Yixin Li - Houston TX, US James R. Lupski - Houston TX, US Jeremy Nathans - Baltimore MD, US Amir Rattner - Baltimore MD, US Noah F. Shroyer - Houston TX, US Nanda Singh - Salt Lake City UT, US Philip Smallwood - Woodbine MD, US Hui Sun - Baltimore MD, US
Assignee:
Baylor College of Medicine - Houston TX John Hopkins University - Baltimore MD The United States of America as represented by the Secretary, Department of Health and Human Services - Washington DC University of Utah Research Foundation - Salt Lake City UT
International Classification:
A61K 48/00 A61K 38/43 C07H 21/02
US Classification:
514 44R, 536 231, 424 941
Abstract:
The present invention provides nucleic acid and amino acid sequences of an ATP binding cassette transporter and mutated sequences thereof associated with macular degeneration. Methods of detecting agents that modify ATP-binding cassette transporter comprising combining purified ATP binding cassette transporter and at least one agent suspected of modifying the ATP binding cassette transporter an observing a change in at least one characteristic associated with ATP binding cassette transporter. Methods of detecting macular degeneration is also embodied by the present invention.
Methods Of Gene Therapy Using Nucleic Acid Sequences For Atp-Binding Cassette Transporter
Rando Allikmets - Frederick MD, US Kent L. Anderson - Houston TX, US Michael Dean - Frederick MD, US Mark Leppert - Salt Lake City UT, US Richard A. Lewis - Houston TX, US Yixin Li - Houston TX, US James R. Lupski - Houston TX, US Jeremy Nathans - Baltimore MD, US Amir Rattner - Baltimore MD, US Noah F. Shroyer - Houston TX, US Nanda Singh - Salt Lake City UT, US Philip Smallwood - Woodbine MD, US Hui Sun - Baltimore MD, US
The present invention provides nucleic acid and amino acid sequences of an ATP binding cassette transporter and mutated sequences thereof associated with macular degeneration. Methods of detecting agents that modify ATP-binding cassette transporter comprising combining purified ATP binding cassette transporter and at least one agent suspected of modifying the ATP binding cassette transporter an observing a change in at least one characteristic associated with ATP binding cassette transporter. Methods of detecting macular degeneration is also embodied by the present invention.
Methods And Systems For Converting Precursor Cells Into Intestinal Tissues Through Directed Differentiation
James M. Wells - Cincinnati OH, US Jason R. Spence - Cincinnati OH, US Aaron M. Zorn - Cincinnati OH, US Noah F. Shroyer - Cincinnati OH, US
Assignee:
CHILDREN'S HOSPITAL MEDICAL CENTER - Cincinnati OH
International Classification:
C12N 5/071
US Classification:
435 29, 435377
Abstract:
The generation of complex organ tissues from human embryonic and pluripotent stem cells (PSCs) remains a major challenge for translational studies. It is shown that PSCs can be directed to differentiate into intestinal tissue in vitro by modulating the combinatorial activities of several signaling pathways in a step-wise fashion, effectively recapitulating in vivo fetal intestinal al development. The resulting intestinal “organoids” were three-dimensional structures consisting of a polarized, columnar epithelium surrounded by mesenchyme that included a smooth muscle-like layer. The epithelium was patterned into crypt-like SOX9-positive proliferative zones and villus-like structures with all of the major functional cell types of the intestine. The culture system is used to demonstrate that expression of NEUROG3, a pro-endocrine transcription factor mutated in enteric anendocrinosis is sufficient to promote differentiation towards the enteroendocrine cell lineage. In conclusion, PSC-derived human intestinal tissue should allow for unprecedented studies of human intestinal development, homeostasis and disease.
Nucleic Acid And Amino Acid Sequences For Atp-Binding Cassette Transporter And Methods Of Screening For Agents That Modify Atp-Binding Cassette Transporter
Rando Allikmets - Frederick MD Kent L. Anderson - Houston TX Michael Dean - Frederick MD Mark Leppert - Salt Lake City UT Richard A. Lewis - Houston TX Yixin Li - Houston TX James R. Lupski - Houston TX Jeremy Nathans - Baltimore MD Amir Rattner - Baltimore MD Noah F. Shroyer - Houston TX Nanda Singh - Salt Lake City UT Philip Smallwood - Woodbine MD Hui Sun - Baltimore MD
Assignee:
University of Utah Research Foundation - Salt Lake City UT Baylor College of Medicine - Houston TX Johns Hopkins University - Baltimore MD The United States of America as represented by the Department of Health and Human Services - Washington DC
The present invention provides nucleic acid and amino acid sequences of an ATP binding cassette transporter and mutated sequences thereof associated with macular degeneration. Methods of detecting agents that modify ATP-binding cassette transporter comprising combining purified ATP binding cassette transporter and at least one agent suspected of modifying the ATP binding cassette transporter an observing a change in at least one characteristic associated with ATP binding cassette transporter. Methods of detecting macular degeneration is also embodied by the present invention.
Engineering Novel Enteroid Models For Understanding Human Enteric Disease
- Houston TX, US Reid Laurence Wilson - Houston TX, US Christopher Stewart - Houston TX, US Joseph Petrosino - Houston TX, US Robert Allen Britton - Houston TX, US Jane Grande-Allen - Houston TX, US Noah F. Shroyer - Houston TX, US Mary K. Estes - Houston TX, US
An anaerobic chamber system to evaluate human enteric disease is described herein that can be used to test therapeutic components. In specific embodiments, the anaerobic chamber is used to determine the effect of one or more bacterial communities on ex vivo enteroid cultures. In one application, the anaerobic chamber system is used to determine the efficacy of therapeutic components in ameliorating human enteric disease using personalized medicine.
The current study in Nature represents the latest step in years of stem cell and organoid research at Cincinnati Childrens, much of which has been led by James Wells, PhD, and Noah Shroyer, PhD. Wells is a scientist in the divisions of Developmental Biology and Endocrinology at Cincinnati Children
Date: Oct 19, 2014
Category: Health
Source: Google
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