Daniel Hogan Email & Phone Number
@tocagen.com
3 phones found area 650 and 858
LinkedIn matched
Who is Daniel Hogan? Overview
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Daniel Hogan is listed as Director of Food Science and Product Development at Alpine Bio, a with 69 employees, based in San Mateo, California, United States. AeroLeads shows a work email signal at tocagen.com, phone signal with area code 650, 858, and a matched LinkedIn profile for Daniel Hogan.
Daniel Hogan previously worked as Director Food Science and Product Development at Nobell Foods and Research Fellow at Impossible Foods. Daniel Hogan holds Phd, Molecular Biology, Biochemistry, Genomics from Stanford University School Of Medicine.
Email format at Alpine Bio
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AeroLeads found 1 current-domain work email signal for Daniel Hogan. Compare company email patterns before reaching out.
About Daniel Hogan
Daniel Hogan is a Director of Food Science and Product Development at Alpine Bio. He possess expertise in biochemistry, cell culture, molecular biology, cell biology, assay development and 15 more skills.
Listed skills include Biochemistry, Cell Culture, Molecular Biology, Cell Biology, and 16 others.
Daniel Hogan's current company
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Daniel Hogan work experience
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Director Food Science And Product Development
Current
Research Fellow
Bioinformatics Scientist
• Identification of predictive biomarkers for retroviral gene therapy (Toca511) targeting glioblastoma multiforme.• Development of minimally invasive diagnostics for glioblastoma multiforme.
Scientist, Group Leader Basic Mechanisms Project Team
• Developed new design principles for oligonucleotide therapeutics targeting microRNAs (anti-miRs) that were incorporated into Regulus’ first developmental candidate RG101.• Identified mRNAs whose increased expression correlated with undesirable effects associated with some anti-miRs in model organisms using molecular profiling data, providing an integral component of the drug discovery cascade.• Defined the mechanism of action of anti-miRs in vivo. • Designed cell culture assays to eliminate pro-inflammatory and cytotoxic anti-miRs.• Characterized intra-tissue and intracellular trafficking of anti-miRs in mouse liver using biochemical separation techniques.• Established workflow to quantify anti-miR levels in specific cell types and subcellular compartments in mouse livers.• Presented research findings to Board of Directors and Scientific Advisory Board on several occasions.
Postdoctoral Research Associate, Advisors: Pat Brown And Dan Hershlag
• Analyzed DNA microarray data from hundreds of human adipocyte samples in order to characterize site-specific developmental and physiological programs.• Developed a ribosome footprinting/RNA sequencing method to systematically map the location of ribosome-associated chaperone interactions with nascent polypeptides.
Phd Student, Dept Of Biochemistry, Advisors: Pat Brown And Dan Herschlag
• Systematically identified the RNA targets of 40 RNA-binding proteins in yeast by affinity immunopurification and DNA microarray hybridization.• Discovered an extensive combinatorial system for post-transcriptional regulation involving dozens or even hundreds of RNA-binding proteins.• Developed a method to systematically identify the mRNAs recruited to Argonuate proteins by specific microRNAs.• Applied a novel systematic translation profiling method to dissect the mechanism of action of microRNA-mediated regulation of gene expression.• Co-developed a method to systematically identify the nascent polypeptides associated with specific molecular chaperones.
Fulbright Scholar, Advisor: Hans Lipps
• Used subtractive cDNA screen to Identify mRNAs differentially expressed during macronuclear development in Stylonchia lemnae.• Identified PIWI protein as being differentially expressed during macronuclear development and proposed PIWI-associated small RNAs from parental macronucleus guide DNA recombination events.• Developed RNAi method for stichotrichous ciliates by feeding them E. coli engineered to produce dsRNA of the gene of interest.
Undergraduate Researcher, Advisor: David Prescott
• Developed a method to eliminate contaminating macronuclear DNA from micronuclear DNA preparations in stichotrichous ciliates.• Demonstrated the order of IES insertion and gene scrambling of the actin I gene in stichotrichous ciliates, which we published in PNAS.
Daniel Hogan education
Phd, Molecular Biology, Biochemistry, Genomics
Bachelor Of Science (Bs), Mcd Biology, Biochemistry With A Minor In Math
Frequently asked questions about Daniel Hogan
Quick answers generated from the profile data available on this page.
What company does Daniel Hogan work for?
Daniel Hogan works for Alpine Bio.
What is Daniel Hogan's role at Alpine Bio?
Daniel Hogan is listed as Director of Food Science and Product Development at Alpine Bio.
What is Daniel Hogan's email address?
AeroLeads has found 1 work email signal at @tocagen.com for Daniel Hogan at Alpine Bio.
What is Daniel Hogan's phone number?
AeroLeads has found 3 phone signal(s) with area code 650, 858 for Daniel Hogan at Alpine Bio.
Where is Daniel Hogan based?
Daniel Hogan is based in San Mateo, California, United States while working with Alpine Bio.
What companies has Daniel Hogan worked for?
Daniel Hogan has worked for Alpine Bio, Nobell Foods, Impossible Foods, Tocagen Inc., and Regulus Therapeutics.
How can I contact Daniel Hogan?
You can use AeroLeads to view verified contact signals for Daniel Hogan at Alpine Bio, including work email, phone, and LinkedIn data when available.
What schools did Daniel Hogan attend?
Daniel Hogan holds Phd, Molecular Biology, Biochemistry, Genomics from Stanford University School Of Medicine.
What skills is Daniel Hogan known for?
Daniel Hogan is listed with skills including Biochemistry, Cell Culture, Molecular Biology, Cell Biology, Assay Development, In Vivo, Genetics, and Pcr.
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