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J BRICKMAN, M.D.
M.D.
Specialist
NPI: 1306849831Individual
Specialties, Licenses & Credentials
SpecialistPrimary
Specialist
Code: 174400000X
45042(GA)
Research & Publications (18)
Microsphere-based tracing and molecular delivery in embryonic stem cells.
PMID 19608269·Biomaterials·2009
7-preclinical
Differentiation of embryonic stem cells into anterior definitive endoderm.
PMID 19585461·Curr Protoc Stem Cell Biol·2009
7-preclinical
Microspheres as a vehicle for biomolecule delivery to neural stem cells.
PMID 19524076·N Biotechnol·2009
7-preclinical
Anterior definitive endoderm from ESCs reveals a role for FGF signaling.
PMID 18940732·Cell Stem Cell·2008
7-preclinical
Inhibition of cortical neuron differentiation by Groucho/TLE1 requires interaction with WRPW, but not Eh1, repressor peptides.
PMID 18611861·J Biol Chem·2008
7-preclinical
A novel triple fusion reporter system for use in gene trap mutagenesis.
PMID 17492751·Genesis·2007
7-preclinical
Hex acts with beta-catenin to regulate anteroposterior patterning via a Groucho-related co-repressor and Nodal.
PMID 16936074·Development·2006
7-preclinical
Conserved roles for Oct4 homologues in maintaining multipotency during early vertebrate development.
PMID 16651543·Development·2006
4-observational
Improving patient flow dramatically decreases wait in emergency and inpatient admitting. Roundtable discussion.
PMID 16171236·Mod Healthc·2005
8-other
Characterizing embryonic gene expression patterns in the mouse using nonredundant sequence-based selection.
PMID 14613977·Genome Res·2003
7-preclinical
A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction.
PMID 14561704·J Clin Invest·2003
5-case
Targeted mutagenesis of the Hira gene results in gastrulation defects and patterning abnormalities of mesoendodermal derivatives prior to early embryonic lethality.
PMID 11884616·Mol Cell Biol·2002
7-preclinical
Molecular effects of novel mutations in Hesx1/HESX1 associated with human pituitary disorders.
PMID 11748154·Development·2001
7-preclinical
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia.
PMID 11136712·Hum Mol Genet·2001
5-case
Hex is a transcriptional repressor that contributes to anterior identity and suppresses Spemann organiser function.
PMID 10804173·Development·2000
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 4279 FOREST LAKE DR W
TIFTON, GA 31794 - Phone
- (229) 848-6058
Quick Facts
- NPI
- 1306849831
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 18
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