Projects per year
Fingerprint Dive into the research topics where New Jersey Medical School (NJMS), Pathology is active. These topic labels come from the works of this organization's members. Together they form a unique fingerprint.
Calcitriol
Medicine & Life Sciences
HL-60 Cells
Medicine & Life Sciences
Neoplasms
Medicine & Life Sciences
DNA
Medicine & Life Sciences
Fetal Blood
Medicine & Life Sciences
Cells
Chemical Compounds
Dendritic Cells
Medicine & Life Sciences
Virus Diseases
Medicine & Life Sciences
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Profiles
Tessa Bergsbaken
- New Jersey Medical School (NJMS), Pathology - ASST PROF-TT
- Cancer Metabolism and Growth Program, CINJ - FULL MEMBER
Person
Projects 1987 2020
Defining The Inflammatory Signals That Regulate Cd8+ T Cell Recruitment And Function In Colorectal Cancer
National Institutes of Health (NIH)
9/1/17 → 8/31/20
Project: Research project
Colorectal Neoplasms
T-Lymphocytes
Neoplasms
Research
Inflammation
Contribution Of Plasmacytoid Dcs To Immune Senescence In Hiv Infection
National Institutes of Health (NIH)
7/15/14 → 6/30/18
Project: Research project
Dendritic Cells
HIV
Infection
HIV Infections
T-Lymphocytes
Imagestream X Mark Ii For Njms Flow Core
National Institutes of Health (NIH)
5/10/14 → 5/9/15
Project: Research project
flow cytometry
laser
apoptosis
image analysis
sorting
Research Output 1962 2019
A Case of Reversible Infantile Respiratory Chain Deficiency Presenting With Hypotonia, Hyperammonemia, and Failure to Thrive
Guerrero, J. C., Pedro, H., Parisotto, S., Heller, D. & Baisre-de Leon, A., Dec 1 2019, In : Pediatric and Developmental Pathology. 22, 6, p. 590-593 4 p.Research output: Contribution to journal › Article
Mitochondrial Myopathies
Hyperammonemia
Failure to Thrive
Muscle Hypotonia
Electron Transport
Adult Diagnosis of Type 1 Fiber Predominance Myopathy Caused by Novel Mutations in the RYR1 Gene
Peddareddygari, L. R., Oberoi, K., Sharer, L. & Grewal, R. P., Jun 1 2019, In : Journal of clinical neuromuscular disease. 20, 4, p. 214-216 3 p.Research output: Contribution to journal › Article
Ryanodine Receptor Calcium Release Channel
Muscular Diseases
Siblings
Mutation
Genes
1
Citation
(Scopus)
Alpha-1 Antitrypsin Deficiency Liver Disease, Mutational Homogeneity Modulated by Epigenetic Heterogeneity With Links to Obesity
Wang, L., Marek, G. W., Hlady, R. A., Wagner, R. T., Zhao, X., Clark, V. C., Fan, A. X., Liu, C., Brantly, M. & Robertson, K. D., Jul 2019, In : Hepatology. 70, 1, p. 51-66 16 p.Research output: Contribution to journal › Article
alpha 1-Antitrypsin Deficiency
Deficiency Diseases
Epigenomics
5-Methylcytosine
Liver Diseases