Peter G. Kim

ORCID: 0000-0002-8716-8759
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About
Contact & Profiles
Research Areas
  • Zebrafish Biomedical Research Applications
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Pluripotent Stem Cells Research
  • Pregnancy and preeclampsia studies
  • CRISPR and Genetic Engineering
  • Epigenetics and DNA Methylation
  • Gout, Hyperuricemia, Uric Acid
  • Hedgehog Signaling Pathway Studies
  • Liver Disease Diagnosis and Treatment
  • Neonatal Respiratory Health Research
  • Mesenchymal stem cell research
  • Hematopoietic Stem Cell Transplantation
  • Acute Myeloid Leukemia Research
  • Eosinophilic Disorders and Syndromes
  • Genetic Associations and Epidemiology
  • Immune Cell Function and Interaction
  • Biomedical Ethics and Regulation
  • Infectious Diseases and Mycology
  • Erythrocyte Function and Pathophysiology
  • Developmental Biology and Gene Regulation
  • Renal and related cancers
  • Immune cells in cancer
  • Hematological disorders and diagnostics
  • Nerve injury and regeneration
  • Nuclear Receptors and Signaling

Dana-Farber Cancer Institute
2012-2023

Harvard University
2012-2023

Broad Institute
2021-2023

Massachusetts Institute of Technology
2023

Harvard Stem Cell Institute
2012-2016

Howard Hughes Medical Institute
2011-2016

Boston Children's Hospital
2012-2016

Dana-Farber/Boston Children's Cancer and Blood Disorders Center
2015

Brigham and Women's Hospital
2009-2012

Lexington City Schools
2006

Osteoporosis is caused by an imbalance of osteoclasts and osteoblasts, occurring in close proximity to hematopoietic cells the bone marrow. Recurrent somatic mutations that lead expanded population mutant blood termed clonal hematopoiesis indeterminate potential (CHIP). Analyzing exome sequencing data from UK Biobank, we found CHIP be associated with increased incident osteoporosis diagnoses decreased mineral density. In murine models, hematopoietic-specific Dnmt3a, most commonly mutated...

10.1084/jem.20211872 article EN cc-by-nc-sa The Journal of Experimental Medicine 2021-10-26

Gout is a common inflammatory arthritis caused by precipitation of monosodium urate (MSU) crystals in individuals with hyperuricemia. Acute flares are accompanied secretion proinflammatory cytokines, including interleukin-1β (IL-1β). Clonal hematopoiesis indeterminate potential (CHIP) an age-related condition predisposing to hematologic cancers and cardiovascular disease. CHIP associated elevated IL-1β, thus we investigated as risk factor for gout. To test the clinical association between...

10.1182/blood.2022015384 article EN cc-by-nc-nd Blood 2022-06-17
Waihay J. Wong Connor A. Emdin Alexander G. Bick Seyedeh M. Zekavat Abhishek Niroula and 95 more James P. Pirruccello Laura E. Dichtel Gabriel K. Griffin Md Mesbah Uddin Christopher J. Gibson Veronica Kovalcik Amy Lin Marie McConkey Amélie Vromman Rob S. Sellar Peter G. Kim Mridul Agrawal Joshua S. Weinstock Michelle T. Long Bing Yu Rajarshi Banerjee Rowan C. Nicholls Andrea Dennis Matt Kelly Po−Ru Loh Steve McCarroll Eric Boerwinkle Ramachandran S. Vasan Siddhartha Jaiswal Andrew D. Johnson Raymond T. Chung Kathleen E. Corey Daniel Levy Christie M. Ballantyne Namiko Abe Gonçalo R. Abecasis François Aguet Christine M. Albert Laura Almasy Álvaro Alonso Seth A. Ament Peter Anderson Pramod Anugu Deborah Applebaum‐Bowden Kristin Ardlie Dan E. Arking Donna K. Arnett Allison E. Ashley‐Koch Stella Aslibekyan Tim Assimes Paul L. Auer Dimitrios Avramopoulos Najib Ayas Adithya Balasubramanian John Barnard Kathleen C. Barnes R. Graham Barr Emily Barron‐Casella Lucas Barwick Terri H. Beaty Gerald J. Beck Diane M. Becker Lewis C. Becker Rebecca Beer Amber L. Beitelshees Emelia J. Benjamin Takis Benos Marcos Bezerra Larry Bielak Joshua C. Bis Thomas W. Blackwell John Blangero Nathan R. Blue Donald W. Bowden Russell P. Bowler Jennifer A. Brody Ulrich Broeckel Jai Broome Deborah Brown Karen Bunting Esteban G. Burchard Carlos D. Bustamante Erin Buth Brian E. Cade Jonathan Cardwell Vincent J. Carey Julie Carrier April P. Carson Cara L. Carty Richard Casaburi Juan P. Romero James F. Casella Peter J. Castaldi Mark Chaffin Christy Chang Yi–Cheng Chang Daniel I. Chasman Sameer Chavan Bo-Juen Chen Wei‐Min Chen

10.1038/s41586-023-05857-4 article EN Nature 2023-04-12

Hematopoietic stem cells (HSCs) emerge from aortic endothelium via the endothelial-to-hematopoietic transition (EHT). The molecular mechanisms that initiate and regulate EHT remain poorly understood. Here, we show adenosine signaling regulates hematopoietic progenitor cell (HSPC) development in zebrafish embryos. receptor A2b is expressed vascular before HSPC emergence. Elevated levels increased runx1+/cmyb+ HSPCs dorsal aorta, whereas blocking pathway decreased HSPCs. Knockdown of disrupted...

10.1084/jem.20141528 article EN The Journal of Experimental Medicine 2015-04-13

During development, the hematopoietic lineage transits through hemogenic endothelium, but signaling pathways effecting this transition are incompletely characterized. Although Hedgehog (Hh) pathway is hypothesized to play a role in patterning blood formation, early embryonic lethality of mice lacking Hh precludes such analysis. To determine for we assessed effect altered differentiating mouse ES cells, cultured embryos, and developing zebrafish embryos. In cells yolk sac cultures, addition...

10.1073/pnas.1214361110 article EN Proceedings of the National Academy of Sciences 2012-12-12

Fluid shear stress promotes the emergence of hematopoietic stem cells (HSCs) in aorta–gonad–mesonephros (AGM) developing mouse embryo. We determined that AGM is enriched for expression targets protein kinase A (PKA)–cAMP response element-binding (CREB), a pathway activated by fluid stress. By analyzing CREB genomic occupancy from chromatin-immunoprecipitation sequencing (ChIP-seq) data, we identified bone morphogenetic (BMP) as potential regulator CREB. chemical modulation PKA–CREB and BMP...

10.1084/jem.20141514 article EN The Journal of Experimental Medicine 2015-04-13

Abstract Chronic liver disease is a major public health burden worldwide. Despite various injury mechanisms, progression of chronic follows common pathway inflammation, and fibrosis. We examined the association between clonal hematopoiesis indeterminate potential (CHIP) in 58,358 individuals from four prospective cohorts with whole exome sequencing data (Framingham Heart Study, Atherosclerosis Risk Communities UK Biobank Mass General Brigham Biobank). CHIP was associated an increased risk...

10.1101/2022.01.17.22269409 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2022-01-24
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