“Rochelle and I worked together at BRT, where she was a Study Director and I was the QA Manager. She was the key contact for many immunotoxicity studies and had to liaison with Sponsors, QA, and laboratory personnel. Her reports were skillfully written and she was always willing to explain scientific nuances to someone less experienced. She is talented, supportive of colleagues and clients, and has excellent time management skills. She fosters a collaborative environment and working with her was always a pleasure. ”
Rochelle Mills
Managing Partner & Senior Medical Writer at SRM Management Science Company
Richmond, Virginia, United States
731 followers
500+ connections
Richmond, Virginia, United States
731 followers
500+ connections
About
PhD scientist with expertise in the fields of medical writing, regulatory submissions, clinical and nonclinical summaries, oncology, immunotherapy, infectious disease (antibacterial, antifungal, and antiviral), vaccines and adjuvants, pain management, cardiology, and toxicology. Excited to contribute to well-designed studies and communicate critical data and results in written or oral form. Invigorated by team work and collaboration.
Interested in networking and collaboration to advance research and progress personally as a scientific/regulatory writer. Also interested in advancing the careers of women in science through mentoring and education.
Specialties: Regulatory & Scientific Writing, Project Management, GCP, GLP & Nonclinical, Oncology, Immunology/Immunotherapy, Toxicology, Vaccines, Infectious Disease.
Activity
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I am really proud of the GIVAX team that is pushing a new vaccine concept to fight GI viral infections. An oral vaccine for infant protection…
I am really proud of the GIVAX team that is pushing a new vaccine concept to fight GI viral infections. An oral vaccine for infant protection…
Liked by Rochelle Mills
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First LinkedIn post ever! I did a thing that I think is cool. Check it out! https://lnkd.in/gYRb6wVj
First LinkedIn post ever! I did a thing that I think is cool. Check it out! https://lnkd.in/gYRb6wVj
Liked by Rochelle Mills
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Today, I was promoted to Associate Professor of Psychiatry & Behavioral Sciences and Pediatrics (with tenure) at the The George Washington University…
Today, I was promoted to Associate Professor of Psychiatry & Behavioral Sciences and Pediatrics (with tenure) at the The George Washington University…
Liked by Rochelle Mills
Experience
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Managing Partner & Senior Medical Writer
SRM Management Science Company
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Graduate Women in Science, Research Triangle Chapter
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President
Graduate Women in Science, Research Triangle Chapter
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Secretary
Graduate Women in Science, Research Triangle Chapter
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Graduate Research Assistant (NIH Ruth L. Kirschstein National Research Service Award Trainee)
North Carolina State University
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Education
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North Carolina State University
PhD Immunology, minor biotechnology
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Activities and Societies: Lectured on quantitative PCR for graduate students and in an immunology laboratory for DVM students. Manuscript co-reviewer for Blood. Mentored two DVM students in the Merck-Merial Veterinary Scholars Program. Recruited and mentored a high school student during a semester-long research project. NCSU College of Veterinary Medicine Graduate Student Association Secretary. NC DNA Day Mentor. Organized science outreach activities for Dr. Gregg Dean’s laboratory.
Ruth L. Kirschstein National Research Service Award Trainee in the NCSU Molecular Biotechnology Training Program, 2006-2008.
Keystone Symposia HIV Pathogenesis Student Travel Scholarship, 2008. -
University of Alabama
BS Microbiology and Immunology
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Activities and Societies: Howard Hughes Medical Research Intern in 2003 and 2004. Tutored for the University of Alabama Rural Science Scholars Program. Managed an undergraduate summer intern.
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Volunteer Experience
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Secretary
Graduate Student Association, College of Veterinary Medicine (NCSU)
- 1 year
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Chapter Adviser
Graduate Women in Science, Rho Tau Chapter
- 2 years 1 month
Science and Technology
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Chair, Chapter Establishment Committee
Graduate Women in Science, National
- 2 years
Science and Technology
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Member, Programs Committee
Immunotoxicology Specialty Section, Society of Toxicology
- 1 year 3 months
Science and Technology
Publications
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Murine Gammaherpesvirus-68 (MHV-68) is Not Horizontally Transmitted Amongst Laboratory Mice by Cage Contact
Journal of Immunotoxicology
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An Alphavirus Vector-Based Tetravalent Dengue Vaccine Induces a Rapid and Protective Immune Response in Macaques That Differs Qualitatively from Immunity Induced by Live Virus Infection
Journal of Virology
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Regulatory T cell depletion prior to acute feline immunodeficiency virus infection does not alter disease pathogenesis.
PLoS ONE
Feline immunodeficiency virus (FIV) infection in cats follows a disease course similar to HIV-1, including a short acute phase characterized by high viremia, and a prolonged asymptomatic phase characterized by low viremia and generalized immune dysfunction. CD4+CD25hiFoxP3+ immunosuppressive regulatory T (Treg) cells have been implicated as a possible cause of immune dysfunction during FIV and HIV-1 infection, as they are capable of modulating virus-specific and inflammatory immune responses…
Feline immunodeficiency virus (FIV) infection in cats follows a disease course similar to HIV-1, including a short acute phase characterized by high viremia, and a prolonged asymptomatic phase characterized by low viremia and generalized immune dysfunction. CD4+CD25hiFoxP3+ immunosuppressive regulatory T (Treg) cells have been implicated as a possible cause of immune dysfunction during FIV and HIV-1 infection, as they are capable of modulating virus-specific and inflammatory immune responses. Additionally, the immunosuppressive capacity of feline Treg cells has been shown to be increased during FIV infection. We have previously shown that transient in vivo Treg cell depletion during asymptomatic FIV infection reveals FIV-specific immune responses suppressed by Treg cells. In this study, we sought to determine the immunological influence of Treg cells during acute FIV infection. We asked whether Treg cell depletion prior to infection with the highly pathogenic molecular clone FIV-C36 in cats could alter FIV pathogenesis. We report here that partial Treg cell depletion prior to FIV infection does not significantly change provirus, viremia, or CD4+ T cell levels in blood and lymphoid tissues during the acute phase of disease. The effects of anti-CD25 mAb treatment are truncated in cats acutely infected with FIV-C36 as compared to chronically infected cats or FIV-naïve cats, as Treg cell levels were heightened in all treatment groups included in the study within two weeks post-FIV infection. Our findings suggest that the influence of Treg cell suppression during FIV pathogenesis is most prominent after Treg cells are activated in the environment of established FIV infection.
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In vivo depletion of CD4+CD25hi regulatory T cells is associated with improved antiviral responses in cats chronically infected with feline immunodeficiency virus.
Virology
Regulatory T (Treg) cells are activated and suppress immune responses during infection, and are characterized as CD4(+)CD25(hi)FOXP3(+). Ex vivo studies demonstrate that Treg cells potentially suppress anti-HIV-1 T cell responses. Lentivirus-induced CD4(+)CD25(hi) Treg cells were first described in feline immunodeficiency virus (FIV)-infected cats. In the present study we demonstrate that anti-feline CD25 monoclonal antibody (mAb) therapy depletes Treg cells in FIV-infected cats for 4 weeks and…
Regulatory T (Treg) cells are activated and suppress immune responses during infection, and are characterized as CD4(+)CD25(hi)FOXP3(+). Ex vivo studies demonstrate that Treg cells potentially suppress anti-HIV-1 T cell responses. Lentivirus-induced CD4(+)CD25(hi) Treg cells were first described in feline immunodeficiency virus (FIV)-infected cats. In the present study we demonstrate that anti-feline CD25 monoclonal antibody (mAb) therapy depletes Treg cells in FIV-infected cats for 4 weeks and does not exacerbate viral replication or proinflammatory cytokine production. Significant FIV-specific immune responses are revealed in Treg cell-depleted cats. These anti-FIV effector cells exist prior to Treg cell depletion and are not expanded while Treg cells are depleted. Importantly, cats receiving the Treg cell-depleting mAb are able to produce a robust humoral response to new antigen. We propose that short-term in vivo Treg cell depletion during chronic HIV-1 infection could provide a window of opportunity for therapeutic vaccination in individuals with controlled viral replication.
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In vivo depletion of CD4+CD25+ regulatory T cells in cats.
Journal of Immunological Methods
To establish a characterized model of regulatory T cell (Treg) depletion in the cat we assessed the kinetics of depletion and rebound in peripheral and central lymphoid compartments after treatment with anti-CD25 antibody as determined by cell surface markers and FOXP3 mRNA expression. An 82% decrease in circulating CD4+CD25+ Tregs was observed by day 11 after treatment. CD4+CD25+ cells were also reduced in the thymus (69%), secondary lymphoid tissues (66%), and gut (67%). Although CD4+CD25+…
To establish a characterized model of regulatory T cell (Treg) depletion in the cat we assessed the kinetics of depletion and rebound in peripheral and central lymphoid compartments after treatment with anti-CD25 antibody as determined by cell surface markers and FOXP3 mRNA expression. An 82% decrease in circulating CD4+CD25+ Tregs was observed by day 11 after treatment. CD4+CD25+ cells were also reduced in the thymus (69%), secondary lymphoid tissues (66%), and gut (67%). Although CD4+CD25+ cells rebound by day 35 post-treatment, FOXP3 levels remain depressed suggesting anti-CD25 antibody treatment has a sustainable diminutive effect on the Treg population. To determine whether CD25+ Treg depletion strategies also deplete activated CD25+ effector cells, cats were immunized with feline immunodeficiency virus (FIV) p24-GST recombinant protein, allowing them to develop a measurable memory response, prior to depletion with anti-CD25 antibody. Anti-FIV p24-GST effector cell activity in peripheral blood after depletion was sustained as determined by antigen-specific T cell proliferation and humoral responses against FIV p24-GST with an ELISA for antigen-specific feline IgG. Furthermore, development of an anti-mouse response in Treg-depleted cats was similar to control levels indicating the retained capacity to respond to a novel antigen. We conclude that despite alterations in CD25+ cell levels during depletion, the feline immune system remains functional. We demonstrate here a model for the study of disease pathogenesis in the context of reduced numbers of immunosuppressive CD4+CD25+ Tregs throughout the feline immune system.
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Plasmid-specified FemABX-like immunity factor in Staphylococcus sciuri DD 4747.
FEMS Microbiology Letters
A plasmid from Staphylococcus sciuri DD 4747 had three open reading frames: a replication gene, an N-acetylmuramyl-l-alanine amidase-like gene, and a gene similar to the lysostaphin endopeptidase resistance gene (epr/lif). The epr-like gene was introduced into S. aureus RN4220; the recombinant strain was more resistant to lysostaphin endopeptidase and its cell wall peptidoglycan contained more serines and fewer glycines than the parental strain with the shuttle vector alone. Based on both its…
A plasmid from Staphylococcus sciuri DD 4747 had three open reading frames: a replication gene, an N-acetylmuramyl-l-alanine amidase-like gene, and a gene similar to the lysostaphin endopeptidase resistance gene (epr/lif). The epr-like gene was introduced into S. aureus RN4220; the recombinant strain was more resistant to lysostaphin endopeptidase and its cell wall peptidoglycan contained more serines and fewer glycines than the parental strain with the shuttle vector alone. Based on both its function and its similarity to femAB, this gene is a member of the femABX-like immunity gene family. Furthermore, this is the first example of a femABX-like immunity gene that is not linked to the gene for the bacteriolytic enzyme against which it specifies immunity.
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The streptococcolytic enzyme zoocin A is a penicillin-binding protein
FEMS Microbiology Letters
Zoocin A is a streptococcolytic enzyme produced by Streptococcus equi subsp. zooepidemicus 4881 that has an unknown site of action on the peptidoglycans of susceptible organisms. Analysis of a mutant strain in which the genes for zoocin A and resistance to zoocin A were inactivated revealed that this strain was more susceptible to β-lactam antibiotics than the parental organism. Purified zoocin A had weak β-lactamase activity, bound radioactive penicillin covalently, and its streptococcolytic…
Zoocin A is a streptococcolytic enzyme produced by Streptococcus equi subsp. zooepidemicus 4881 that has an unknown site of action on the peptidoglycans of susceptible organisms. Analysis of a mutant strain in which the genes for zoocin A and resistance to zoocin A were inactivated revealed that this strain was more susceptible to β-lactam antibiotics than the parental organism. Purified zoocin A had weak β-lactamase activity, bound radioactive penicillin covalently, and its streptococcolytic activity was inhibited by penicillin. Thus, zoocin A is a penicillin-binding protein and presumably is a d-alanyl endopeptidase.
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Courses
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American College of Toxicology: Toxicology for Pharmaceutical and Regulatory Scientists (April 2016)
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Projects
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Presentation: Managing Your Online Professional Network
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See projectPresented hour-long seminars about maximizing the utility of LinkedIn and networking to six groups from 2012-2015.
• RTI International, RTP, NC, June 2012
• The Church of Jesus Christ of Latter-day Saints, Durham, NC, September 2012
• University of Alabama at Birmingham Graduate Career Awareness and Trends (UAB GCAT), Birmingham, AL, September 2012
• University of North Carolina-Chapel Hill Career Symposium for Graduate Students and Post-doctoral Scholars, February 2013 (with…Presented hour-long seminars about maximizing the utility of LinkedIn and networking to six groups from 2012-2015.
• RTI International, RTP, NC, June 2012
• The Church of Jesus Christ of Latter-day Saints, Durham, NC, September 2012
• University of Alabama at Birmingham Graduate Career Awareness and Trends (UAB GCAT), Birmingham, AL, September 2012
• University of North Carolina-Chapel Hill Career Symposium for Graduate Students and Post-doctoral Scholars, February 2013 (with Katherine Nobles)
• The Church of Jesus Christ of Latter-day Saints, Raleigh, NC, February 2014
• Duke University Women in Science & Engineering, Durham, NC, January 2015
Honors & Awards
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American Society for Virology Postdoctoral Fellow Travel Award
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Keystone Symposia HIV Pathogenesis Student Travel Scholarship
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Ruth L. Kirschstein National Research Service Award Trainee
NIH/NCSU Molecular Biotechnology Training Program
Participated 2006-2008.
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Howard Hughes Medical Research Intern
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Howard Hughes Medical Research Intern
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Organizations
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American Medical Writers Association
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Society of Toxicology
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Graduate Women in Science
President, Secretary, Chapter Adviser, Chapter Establishment Committee Chair
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Women in Bio
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American Society for Virology
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American Association of Immunologists
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American Society for Microbiology
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Recommendations received
7 people have recommended Rochelle
Join now to viewMore activity by Rochelle
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It's not about the people, it's about the RIGHT people! #TheinSeptionDifference #PeoplePurposePerformance
It's not about the people, it's about the RIGHT people! #TheinSeptionDifference #PeoplePurposePerformance
Liked by Rochelle Mills
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AnaBios Corporation
We're still accepting abstracts for our Translational Research Grant, with the winning academic scientist awarded $15,000 in tissue samples to advance their #translationalresearch project. Learn more about the grant and submission guidelines on our website. Submission deadline is June 30. #DrugDiscovery #HeartResearch #PainResearch #Toxicology #EarlyHumanInsights
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Biochemical Society
Have you read the latest issue of Essays in Biochemistry? Computational Biology provides an in-depth introduction into the subject, including reviews covering computational methods and models. Read the issue: https://ow.ly/Kbmm50SSMUx Portland Press
1 Comment -
Ruby Hu
Mastery of pipetting techniques is fundamental for lab success, and it sets a strong foundation for every project. When selecting Co-op students, I spend three hours to a hands-on "pipette interview" with each candidate. This process gives them a deep look at the role, helping them decide if it’s the right fit, while also allowing us to evaluate key skills. During the session, candidates learn to follow protocols, work with precision, and show their organizational habits — all essential traits for lab work. Even if they might not ultimately join us, I’m confident those hours spent training are valuable for their journey, adding a practical skill to their toolkit.
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Mia Edgerton-Fulton
The ASCB virtual biotech courses have been so enlightening so far! There are 2 days left, and I can’t wait to gain more knowledge on how to prepare for my next career stage! 🧬👩🏽🔬 This course will allow me to spread my knowledge to those in the Scholarly Scouts™️ community who are interested in learning more about how biotech companies work!😃 #biotech #biopharma #careerdevelopment
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Davood Bashash
I would highly recommend taking a look at our publication. https://lnkd.in/dBQwFqbU TITLE CAR NK cell therapy in hematologic malignancies and solid tumors; obstacles and strategies to overcome the challenges ABSTRACT Adoptive cell treatment (ACT) utilizing chimeric antigen receptors (CAR) diverts the specificity of safe cells against a target-specific antigen and portrays exceptional potential for cancer treatment. While CAR T cell treatment has risen as a breakthrough with unprecedented results within the therapeutic procedures of human malignancies, different deficiencies including challenging and costly generation processes, strict patient qualification criteria, and undesirable toxicity have ruined its application. Unlike T cells, the application of natural killer (NK) cells has attracted consideration as a reasonable alternative owing to the major histocompatibility complex (MHC)-independency, shorter life expectancy, the potential to create an off-the-shelf immune product, and potent antitumor properties. In this article, we provide an updated review of the differences between CAR T and CAR NK cells, current enhancements in CAR NK design, the available sources for collecting NK cells, and strategies for the transduction step of the CARs to NK cells. Furthermore, we focus on the published and ongoing preclinical and clinical studies of CAR NK treatment strategies both in hematologic malignancies and solid tumors. We also discuss limitations and plausible solutions to improve the perseverance, function, safety, and efficacy of CAR NK cells with a special focus on solid tumors.
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Mithun Rudrapal
Our upcoming book Computational Methods for Rational Drug Design featuring cutting-edge computational methods and tools that are being employed in the development of cost-effective and therapeutically efficacious next-generation drug candidates to combat grievous lifestyle diseases and malicious infectious illness. https://lnkd.in/g4ZYjD92 #computationaltools #RDD #drugdesign #drugdiscovery #cost-effective drugs #safe and #effective drug #next-generation drug candidates
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John Trant
k! That moment a very small percentage of you have been waiting for! After an almost 18 month hiring freeze...we are hiring postdocs! Our first position is for an analytical instrumental chemist! See the PDF below, and visit the group page! #Chempostdoc https://trantteam.ca/ (The ad is attached about mid-way down the page...Adding a direct link doesn't seem to work) The pay is Canadian. Sorry. Tell our funding agencies to give us more money. But it is a comfortable life in Windsor, which is...aggressively a fine place to live. Safe, culturally enriched, but not a sexy party town like Montreal or Syracuse. I promise good science, good colleagues, good chance for soft skill enrichment, the most interdisciplinary academic chem research team anywhere (I'm open to challengers!), and a reasonable boss (once he's had his coffee). Feel free to share with anyone who is looking. We hire the person, not the CV. Good people are welcome. Bigots can go jump off a short pier. NOTE: I am getting a ton of approaches and messages over LinkedIn for this. I understand why, but don't do that. There are clear instructions in the ad. If you can't follow clear instructions, then I think we might not have a good working relationship. The application process is designed to be equitable--if you want to apply, use it. There is a lot of detail as to what we are looking for, if you don't meet the minimum skillset criteria, others do. I will be VERY surprised if we find anyone who has ALL the preferred experience (so don't select out on that). Your cover letter is your chance to discuss WHY you meet the criteria, both minimal and preferred, and what else you can do too. That's what a cover letter is for. I read them first. Consequently, I will not be considering applications that do not follow the process. Questions are fine, but I think most of what I can talk about at this point is in the ad, and I haven't received any questions in all the contacts on this position yet.
9 Comments -
Stephanie M King
At ASMS in Anaheim today? Then stop by Adam King's poster TP466 (Metabolomics: Untargeted Metabolite Profiling II) - High throughput plasma profiling of human liver disease samples using rapid chromatography and a multi-reflecting time-of-flight mass spectrometer. Yuriy Pyatkivskyy will be there to talk you through the poster outlining research investigating human liver disease in collaboration with Elizabeth Want and Ana Sánchez Lorenzo from Imperial College London Highlighting the RApid Microbore Metabolic Profiling (RAMMP) methodology and the novel vacuum jacketed column technology (VJC), on the SELECT SERIES MRT mass spectrometer. High-throughput profiling (<4 mins/sample), excellent mass accuracy (<1 ppm) and high mass resolution (200K FWHM @m/z 811) all at the rapid acquisition rate of 30 Hz. #waterscorporation #ASMS24 #selectseries #MRT #VJC #metabolomics #collaboration #highthroughput #Massspec #lifeatwaters
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ACS Publications
Check out the latest Special Issue from Inorganic Chemistry! This Special Issue highlights contemporary research into different strategies for synthesizing and understanding molecular Zintl anions, clusters, and solid-state phases. Read now: https://go.acs.org/bBM
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Otis Rothenberger
Sorry for the delay in posting CheMagic Model Kit Examples. The NIH/NCI/CACTVS admins transferred the Chemical Identifier Resolver to a new server, and the adjustments took some time. Actually, they are still going on. A model kit has many chemistry education and business uses, and in the era of the Internet, I felt that users should be able to share a model kit - classroom, Zoom, FaceBook, LinkedIn, etc. In normal operation, the model in the model kit window should be editable by all members of a sharing group discussion anywhere in the world with the same ShareID button setting (9 digit number). I do reserve one number for myself (192837465) that only allows me to use the PutShare button to change the model in the window for all discussion participants. During a normal discussion, use of the GetShare button would reveal the latest group edit of the shared model. 1. So, let's play. Use the ShareID button to set your model kit ID to 192837465. Note that for this discussion you will not be able to put a model in the window with the PutShare button. 2. If you click the GetShare button, the mess of a molecule that I shared (post image) will load into your model kit. 3. I made the mess of a molecule by loading a small model via the Name button. I then messed it up using the Drag component of the Move button. 4. Normally, you can clean up the model with several clicks of the Optimize button, but in this case it's still a mess. 5. You can REALLY clean up the model by using any of the CIR reload links - L, M, or,S. I'll explain these links more clearly in my next post. Remember, this is a special post where you cannot set a new model with the PutShare button. You can, however, use the GetShare button to load and reload the mess of a molecule that I shared. Aww go ahead and have some fun. You know that you want to. https://lnkd.in/dJ2S7NZW
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Jennifer Harper
BJU's Biology program offers several concentrations. https://lnkd.in/emKxUHZY Biology concentrations enable you to customize your biology program. You can specialize so that you are prepared for a wide variety of graduate programs and careers. Available Concentrations: Biotechnology Cell Biology Zoo and Wildlife Biology Regardless of the route you take, you will have a solid foundation at the molecular, cellular and organismal levels, and have a big-picture context of the interaction of organisms with each other and their environment.
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Hemayet Ullah
This past week, we concluded an intensive hands-on CRISPR workshop as part of the broader impact initiative of our NSF grant. Very amazed to see the student led research results. Students successfully used base editing (B leaf) to revert a mutant phenotype (M leaf) back to the wild-type Ruby red (W) color. Students also used traditional CRISPR to introduce mutation in GFP-expressing gene, providing a fluorescent readout of successful gene editing. After agrobacterium infiltration on day one, students were trained in the - gRNA design and synthesis, Cloning of gRNAs into base editing plasmid, Bacterial expression of CRISPR components, Molecular confirmation of effective CRISPR base editing/mutagenesis via PCR and restriction digestion. Very happy that we could impart so many topics within 5 days and am proud to see students' dedication and quick grasp of these advanced techniques. Their success in completing all planned experiments demonstrates the effectiveness of our hands-on teaching approach. We will organize again in 2025 summer. Program info here: https://lnkd.in/evSmjSXi #CRISPR #GeneEditing #STEMEducation #Biotechnology #UndergraduateResearch #NSFGrant David R. Liu
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Michelle Meyers
https://lnkd.in/giJGpFg9 Inspired by cell biology insights from 50 Trends in Cell Biology (linked above). It is my theory that J Protein functions are being redirected to sustain plant exhalation through the surface cilia. This redirection of protein would diminish leaf output and cytoplast strength in tree branches. This would make branches vulnerable to high winds, thick mulch and doming plants around the trunk of the tree (such as hydrangeas). My art inspired by theses 50 trends is to get your attention, the pattern of homeostasis is interrupted.
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Shiri Yaniv, Ph.D.
Ever wonder what goes into a professional edit of a research proposal or manuscript? It’s more than just polishing the grammar. For grant proposals, I focus on crafting a clear, compelling narrative that aligns with reviewers' priorities, ensuring the aims are concise and impactful. For manuscripts, I help streamline the flow, improve clarity, and highlight the significance of the research for target journals. Whether you're preparing your next funding submission or getting ready to publish, a well-structured, precise document can make all the difference. Let’s connect to discuss how I can help elevate your work!
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Washington University in St. Louis
Effective postdoctoral mentoring goes beyond research supervision—it's about fostering independence and preparing mentees for diverse careers. At WashU, mentorship workshops revealed misalignments between faculty and postdocs in areas like communication, leadership, and career planning. By aligning expectations and offering structured training, faculty can better support postdocs' growth.
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