Jianhua Xiong

headshot of Jianhua Xiong
jianhua.xiong@emory.edu

Dr. Jianhua Xiong is an Assistant Professor of Urology at Emory University School of Medicine. The laboratory investigates the metabolic regulation of cell fate and function, with a focus on urological disorders and cancer. Research explores how fatty acids influence cell behavior in T cells, endothelial cells, and cancer cells. A multidisciplinary approach integrates cell and molecular biology, biochemistry, super-resolution imaging, transcriptomics, proteomics, metabolomics, histology, tissue studies, and mouse models to understand cellular mechanisms and identify potential therapeutic strategies.

Assistant Professor
Additional Research

Biochemicals

Bioinformatics

Biotechnology

Cancer Immunotherapy

Health & Life Sciences

University, College, and School/Department
Google Scholar
https://scholar.google.com/citations?user=sAVc7gIAAAAJ&hl=en

Daniel Hass

Assistant Professor Daniel Hass
dthass@emory.edu
Profile Page

Vision is energy-intensive. Mutations that impair a person's ability to generate energy disproportionately affect vision. Common diseases that cause blindness may also be related to a failure of the eye to generate sufficient energy to serve its needs. Our goal is to understand the metabolic function of individual cells in visual tissues, primarily the retina and retinal pigment epithelium. We want to know which cells in the eye carry out particular metabolic processes (glycogen synthesis, nucleotide synthesis, etc.), what causes a cell to be metabolically 'wired' as it is, the extent to which retina generates metabolic intermediates de novo vs. from circulating, and the extent to which neurodegenerative diseases such as age-related macular degeneration and glaucoma are linked to metabolic impairments.

Assistant Professor
Office
Emory Clinic B, Room 5602
University, College, and School/Department

Kyle Allison

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kyle.r.allison@emory.edu
Website

Kyle Allison is a bioengineer and chemical engineer whose research has focused on understanding the behavior of bacteria in order to improve antibiotics. The Allison Lab tracks individual bacteria using microscopy approaches they developed.  Kyle and his lab have made foundational discoveries in the metabolite potentiation of antibiotics, the resuscitation of persistent bacteria, and the multicellularity of E. coli (the best-studied unicellular organism).  Kyle was named to the first “30 under 30” list in Science by Forbes Magazine and received the NIH Director’s Early Independence Award to bypass traditional postdoctoral training. His research has been published in Nature, PNAS, Molecular Systems Biology, Nature Methods, Nature Chemical Biology, and other journals.  Kyle also holds a master’s degree in literature and wrote his thesis on James Joyce’s Finnegans Wake.

Assistant Professor, Department of Medicine/Infectious Disease, Emory University
Phone
404-727-6974
Office
Emory HSRB E146
Additional Research

Antibiotics, Systems Biology, Multicellularity

Research Focus Areas
Google Scholar
https://scholar.google.com/citations?user=Gn-HTRUAAAAJ&hl=en
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Jacob Berchuck

Jacob Berchuck's profile picture
jberchuck@emory.edu
https://www.theberchucklab.org/

Dr. Jacob Berchuck is a Medical Oncologist at the Winship Cancer Institute and Assistant Professor in the Department of Hematology and Medical Oncology at Emory University School of Medicine. Prior to joining Emory, Dr. Berchuck was an Assistant Professor of Medicine at Harvard Medical School and a Medical Oncologist at the Dana-Farber Cancer Institute. In addition to caring for patients, Dr. Berchuck leads a translational research lab focused on utilizing "liquid biopsy" tools that enable multi-omic profiling of tumor-derived cell-free DNA circulating in the bloodstream to pioneer advances that transform how we manage and treat individuals living with cancer. The core research objectives of the Berchuck Lab include include developing biomarkers to guide treatment decisions, working towards a future where a simple blood draw can enable real-time insights to choose the right treatment for the right patient at the right time, and studying mechanisms of therapeutic resistance. Dr. Berchuck’s research has been published in several high-impact journals, including Nature Medicine, Cancer Cell, Annals of Oncology, JAMA Oncology, Clinical Cancer Research, and others.

Assistant Professor of Hematology and Medical Oncology
Additional Research

Cancer Biology, Diagnostics

University, College, and School/Department
https://www.linkedin.com/in/jberchuck/

Anupam Patgiri

Anupam Patgiri's profile picture
anupam.patgiri@emory.edu
https://patgirilab.org/

Anupam received his bachelor’s degree from Gauhati University (India) and a master’s degree in chemistry from the Indian Institute of Technology Guwahati (India). He then moved to New York City to pursue a Ph.D. in chemical biology in Prof. Bobby Arora’s lab at NYU. In the Arora lab, Anupam developed chemical inhibitors of therapeutically relevant protein-protein interactions. His thesis project resulted in the discovery of the first direct inhibitor of oncoprotein Ras. Anupam then spent a short stint as a postdoctoral fellow in Prof. Tarun Kapoor’s lab at the Rockefeller University before moving to Prof. Vamsi Mootha’s lab at Harvard Medical School. In the Mootha lab, Anupam engineered an enzyme called “LOXCAT” as a potential therapy for mitochondrial disease. In his independent lab at Emory University, Anupam is developing strategies to restore mitochondrial and metabolic homeostasis in disease as potential therapies. 

Education

Postdoctoral Fellow Harvard Medical School 

Postdoctoral Fellow Rockefeller University 

Ph.D. New York University 

MSc Indian Institute of Technology Guwahati, India

BSc Gauhati University, India  

Awards and Honors

Keystone Symposia Future of Science Fund Scholarship (2020)

Tosteson & Fund Medical Discovery Fellowship (2017)

Helen Hay Whitney Postdoctoral Fellowship (2013-16)

Margaret and Herman Sokol Scholarship at NYU (2010-2011)

GATE fellowship, Govt. of India (2006)

Junior Research Fellowship, Govt. of India (2005)

Summer Research Fellowship, Indian Academy of Sciences (2004)

Assistant Professor
University, College, and School/Department

Anthony Law

Anthony Law's profile picture
anthony.law@emory.edu
Lab Website

Anthony B. Law, MD, PhD, is an assistant professor in the Department of Otolaryngology at Emory University School of Medicine. A board certified head and neck surgeon, Dr. Law's clinical interest include the diagnosis and treatment of diseases and pathology of the upper aerodigestive tract, particularly laryngeal cancer. He treats disorders involving voice, airway, and swallowing using a wide array of techniques ranging from open surgery, endoscopic minimally invasive surgery, and laser surgery.

Dr. Law earned his MD and also his PhD in biophysics and biochemistry from the University of North Carolina in Chapel Hill, NC. He completed his residency in otolaryngology/head & neck surgery and his fellowship in laryngology at University of Washington in Seattle, WA.

Dr. Law's primary research interests lay in modeling of complex biology and clinical systems. He has broad experience in mathematical modeling and computational models. Historically, he has used machine learning to predict rates and locations of metastasis in head and neck squamous cell carcinoma. His current focus is in applying machine learning to characterize and categorize pathology of the larynx.

Assistant Professor, Department of Otolaryngology, Head and Neck Surgery
Phone
(404) 778-0278
University, College, and School/Department

Zachary Danziger

Zachary Danziger's profile picture
zachary.danziger@emory.edu
https://scholarblogs.emory.edu/danziger/

The effortlessness of moving your body belies the lurking complexity driving it. We are trying to understand how the nervous system makes something so complicated as controlling a human body feel so natural. We use human subjects studies, animal experiments, mathematical biology, and artificial intelligence to understand neural control of movement. New theories and insight promise advances in physical therapy, human-machine collaboration, brain-computer interfaces, neural modulation of peripheral reflexes, and more.

Associate Professor Division of Physical Therapy, Department of Rehabilitation Medicine
Associate Professor, W.H. Coulter Department of Biomedical Engineering
Phone
404-712-4801
University, College, and School/Department

Shoichiro Ono, Ph.D.

Shoichiro Ono, Ph.D. 's profile picture
sono@emory.edu
Website

The Shoichiro's lab primary research interest is the mechanisms that regulate dynamic rearrangement of the actin cytoskeleton during various cellular events including development, cell movement, cytokinesis, and human diseases. We have been studying this problem using the nematode Caenorhabditis elegans as a model system. C. elegans has been used to study many aspects of development, because of its relative simplicity in the body patterning, and application of genetics, molecular biology, biochemistry, and cell biology. We are especially interested in the functions of the actin depolymerizing factor (ADF)/cofilin family of actin-binding proteins, which are required for enhancement of actin filament dynamics. We found that two ADF/cofilin proteins that are generated from the unc-60 gene have different actin-regulating activities. Mutation and expression analyses demonstrated that one of the two ADF/cofilin isoforms (UNC-60B) was specifically required for organized assembly of actin filaments in muscle. ADF/cofilin promotes depolymerization and severing of actin filaments, but tropomyosin inhibits this effect by stabilizing filaments. The other ADF/cofilin isoform (UNC-60A) is highly expressed in early embryos and regulates cytokinesis and embryonic patterning. In addition, we found that actin-interacting protein 1 (AIP1) is a new regulator of muscle actin filaments. AIP1 (UNC-78) specifically interacts with ADF/cofilin-bound actin filaments and enhances filament depolymerization. We also found that the gene product of sup-12 (an RBM24 homolog) regulates alternative splicing of the unc-60 gene and is required for generation of the unc-60B mRNA. We are currently studying functions of these proteins and other regulators of actin dynamics in several developmental aspects in C. elegans.

Associate Professor of Pathology and Laboratory Medicine
Associate Professor of Cell Biology
Phone
404.727.3916
Office
615 Michael Street, Whitehead Biomedical Research Building Room 105N, Atlanta, GA 30322
University, College, and School/Department
Google Scholar
https://scholar.google.com/citations?user=tq7ihbkAAAAJ&hl=en
NCBI

Hyojung Choo

Hyojung Choo 's profile picture
hyojung.choo@emory.edu
Assistant Professor
Phone
404-727-3727
Office
542 Whitehead Research Building, Emory School of Medicine
Additional Research

"Craniofacial muscles are essential muscles for normal daily life. They are involved in facial expressions (facial muscles), blinking and eye movement (eye muscles), as well as speaking and eating (tongue and pharyngeal muscles). Interestingly, craniofacial muscles have differential susceptibility to several muscular dystrophies. For example, craniofacial muscles are the most affected muscles in oculopharyngeal muscular dystrophy but the least affected muscles in Duchenne muscular dystrophy. Among craniofacial muscles, dysfunction of tongue and pharyngeal muscles could cause an eating disability, called dysphagia, afflicts almost 15 million Americans including elderly, neuronal (Parkinson's disease and bulbar-onset amyotrophic lateral sclerosis) and muscular disease (oculopharyngeal muscular dystrophy) patients. However, no cure or therapeutic treatment exists for dysphagia caused by muscular dystrophy. Elucidation of the mechanism(s) behind these differing susceptibilities of craniofacial muscles could lead to development of potential therapeutics targeted to specific skeletal muscles involved in particular types of muscular dystrophy. The mechanisms of skeletal muscles are of interest here because skeletal muscle cells are multinucleated cells. Typically, skeletal muscle cells contain hundreds of nuclei in a single cell since they are generated by fusion of muscle precursor cells during development or by fusion of muscle specific stem cells, called satellite cells, in adult skeletal muscles. However, it is unclear how skeletal muscle cells regulate the quantity and quality of these multi-nuclei. Since craniofacial skeletal muscles, such as extraocular and pharyngeal muscles, have active satellite cell fusion in comparison to limb muscles, they are therefore suitable models to study myonuclear addition and homeostasis."

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