DOCSLIB.ORG

Ernst-Günter Afting, Ph.D., M.D. (Name of Person(S) Filing Proxy Statement, If Other Than the Registrant)

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Ernst-Günter Afting, Ph.D., M.D. (Name of Person(S) Filing Proxy Statement, If Other Than the Registrant) SCHEDULE 14A INFORMATION (Rule 14a-101) PROXY STATEMENT PURSUANT TO SECTION 14(a) OF THE SECURITIES EXCHANGE ACT OF 1934 (Amendment No. ) Filed by the Registrant [ ] Filed by a party other than the Registrant [X] Check the appropriate box: [ ] Preliminary Proxy Statement [ ] Confidential, for Use of the Commission Only (as permitted by Rule 14a-6(e)(2)) [ ] Definitive Proxy Statement [ ] Definitive Additional Materials [X] Soliciting Material under §240.14a-12 Sorrento Therapeutics, Inc. (Name of Registrant as Specified in Its Charter) Ernst-Günter Afting, Ph.D., M.D. (Name of Person(s) Filing Proxy Statement, if other Than the Registrant) Payment of Filing Fee (Check the appropriate box): [X] No fee required. [ ] Fee computed on table below per Exchange Act Rules 14a-6(i)(4) and 0-11. (1) Title of each class of securities to which transaction applies: (2) Aggregate number of securities to which transaction applies: (3) Per unit price or other underlying value of transaction computed pursuant to Exchange Act Rule 0-11 (set forth the amount on which the filing fee is calculated and state how it was determined): (4) Proposed maximum aggregate value of transaction: (5) Total fee paid: [ ] Fee paid previously with preliminary materials. [ ] Check box if any part of the fee is offset as provided by Exchange Act Rule 0-11(a)(2) and identify the filing for which the offsetting fee was paid previously. Identify the previous filing by registration statement number, or the Form or Schedule and the date of its filing. (1) Amount Previously Paid: (2) Form, Schedule or Registration Statement No.: (3) Filing Party: (4) Date Filed: On August 8, 2012, Ernst-Günter Afting (“Afting”) delivered a notice (the “Nomination Letter”) to the Corporate Secretary of Sorrento Therapeutics, Inc. (“Sorrento”, or the “Company”) of his intent to nominate a new slate of directors for election to the board of directors of the Company at the Company’s 2012 annual meeting of stockholders (the “2012 Annual Meeting”) to be held on September 6, 2012, or any adjournment or postponement thereof. The Nomination Letter is incorporated herein and attached hereto as Exhibit 1. SECURITY HOLDERS ARE ADVISED TO READ THE PROXY STATEMENT AND OTHER DOCUMENTS RELATED TO THE SOLICITATION OF PROXIES BY AFTING FROM THE STOCKHOLDERS OF SORRENTO FOR USE AT ITS 2012 ANNUAL MEETING WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION, INCLUDING INFORMATION RELATING TO THE PARTICIPANT IN SUCH PROXY SOLICITATION. WHEN COMPLETED, A DEFINITIVE PROXY STATEMENT AND A FORM OF PROXY WILL BE AVAILABLE AT NO CHARGE AT THE SECURITIES AND EXCHANGE COMMISSION’S WEBSITE AT HTTP://WWW.SEC.GOV. IN ADDITION, THE PARTICIPANT IN THIS PROXY SOLICITATION WILL PROVIDE COPIES OF THE DEFINITIVE PROXY STATEMENT (IF AND WHEN AVAILABLE) WITHOUT CHARGE UPON REQUEST. INFORMATION RELATING TO THE PARTICIPANT IN A POTENTIAL PROXY SOLICITATION IS CONTAINED IN EXHIBIT 1 HERETO AND IS INCORPORATED HEREIN. EXHIBIT 1 Ernst-Günter Afting, Ph.D., M.D. Meisenweg 21 D-82152 Krailling Germany BY OVERNIGHT MAIL AND FACSIMILE (858-210-3759) August 8, 2012 Sorrento Therapeutics, Inc. 6042 Cornerstone Ct. West, Suite B San Diego, California 92121 Attention: Corporate Secretary Stockholder Nomination of Directors Dear Sir or Madam: I, Ernst-Günter Afting, am the owner of record of 925,430 shares of common stock, par value $0.0001 per share (“Common Stock”), and the beneficial owner of an additional 40,000 shares of Common Stock, of Sorrento Therapeutics, Inc., a Delaware corporation (the “Company”). In accordance with Section 1(2)(c) of Article I of the Company’s Bylaws (the “Bylaws”), I hereby nominate the following persons to stand for election to be directors of the Company at the Company’s next annual meeting of its stockholders (the “2012 Annual Meeting”): Henry Ji, Kim D. Janda, M. Scott Salka, David Webb, Cam Gallagher, Richard Vincent and Ernst-Günter Afting (collectively, the “Nominees”). Based on the Company’s proxy materials filed with the Securities and Exchange Commission (the “SEC”) on July 31, 2012, the 2012 Annual Meeting is scheduled to take place on September 6, 2012. According to the Bylaws, nominations for director candidates may be submitted to the Company’s secretary not later than the close of business on August 10, 2012 for voting/consideration at the 2012 Annual Meeting. Capitalized terms used without definition herein shall have the meanings provided in the Bylaws. Dr. Henry Ji is the beneficial owner of 58,404,032 shares of the Company’s Common Stock. Dr. Kim Janda is the beneficial owner of 197,500 shares of the Company’s Common Stock. Mr. M. Scott Salka has no beneficial ownership of the Company’s Common Stock. Dr. David Webb is the beneficial owner of 12,500 shares of the Company’s Common Stock. Mr. Cam Gallagher has no beneficial ownership of the Company’s Common Stock. Mr. Richard Vincent is the beneficial owner of 225,000 shares of the Company’s Common Stock. Each of the above nominees and I have consented to be nominated (Henry Ji, Kim D. Janda, M. Scott Salka, David Webb, Cam Gallagher, Richard Vincent and I are sometimes collectively referred to herein as the “Group”). Ernst- Günter Afting, as the “nominating person”, is the “Record Stockholder” as defined in the Bylaws and is solely proposing the Nominees. Except as set forth in this letter, there are no “affiliates” or “associates” of the Nominating Person or the Nominees. 1 It is my firmly held belief that the Company is in need of new leadership and a fresh perspective on the Board of Directors of the Company (the “Board”). The election of Henry Ji, Ph.D., Kim D. Janda, Ph.D., M. Scott Salka, David Webb, Ph.D., Cam Gallagher, Richard Vincent and Ernst-Günter Afting, all experienced, individually or collectively, with deep antibody and industry expertise, broad understanding of the operational, pre-clinical and clinical development, financial and strategic issues facing public and private companies both domestically and internationally, should significantly improve the oversight function of the Board. This letter provides the information required by Section 1(4) of Article I of the Bylaws (“Section 1(4)”). While I am complying with Section 1(4) of the Bylaws, I expressly reserve the right to challenge the validity and lawfulness of certain purported requirements set forth therein, and nothing herein shall constitute a waiver of such rights or claims. Please note that due to the extensive disclosure requirements set forth in Section 1(4) of the Bylaws, many of which are duplicative or redundant, the information provided herein and in the attachments to this letter shall be deemed responsive to all relevant provisions of the Bylaws notwithstanding any specific reference to a particular section or sections of the Bylaws. As provided in Section 1(4), subject to reserving my rights to challenge the legality or appropriateness of certain provisions of Section 1(4), I will provide any updates or supplements to this notice in the times and in the forms required by Section 1(4). Solicitation Statement I will deliver a proxy statement and form of proxy to holders of at least the percentage of voting power of all of the shares of capital stock of the Company reasonably believed by me to be sufficient to elect the nominees proposed to be nominated by me. Information Required by Section 1(4)(c) of the Bylaws Stockholder Information: Dr. Henry Ji (“Ji”), age 48, PO Box 3531, 6099 Rancho Diegueno, Rancho Santa Fe, CA 92067 (residential) and 6042 Cornerstone Court, Suite B, San Diego, CA 92121 (business). Shares of Common Stock held of record by Ji: 43,154,032. Shares of Common Stock directly or indirectly beneficially owned by Ji, as defined in Section 1(4)(c) of the Bylaws (which number includes the shares owned of record): 58,404,032, comprised of 75,000 shares of Common Stock issuable pursuant to stock options exercisable within 60 days of August 7, 2012, 6,250,000 deemed to be beneficially owned by Dr. Ji in his capacity as one of three controlling persons in the Hongye SD Group, LLC and 52,154,032 shares of common stock held in family trusts, of which Dr. Ji is a co-trustee with his wife Vivian Q. Zhang. Each of Dr. Ji and Vivian Q. Zhang, while acting as co-trustees, have the power to act alone and have those actions binding on both trustees and the trusts’ assets, including voting and dispositive power over the shares of common stock held by the family trusts. Dr. Kim Janda (“Janda”), age 54, 5787 La Jolla Corona Drive, La Jolla, CA 92037 (residential) and 10550 N. Torrey Pines Road, 8CC-582, La Jolla, CA 92037 (business). Shares of Common Stock held of record by Janda: 0. Shares of Common Stock directly or indirectly beneficially 2 owned by Janda, as defined in Section 1(4)(c) of the Bylaws: 197,500, comprised of Common Stock issuable pursuant to stock options exercisable within 60 days of August 7, 2012. M. Scott Salka (“Salka”), age 50, PO Box 3577, Rancho Santa Fe, CA 92067 (residential and business). Shares of Common Stock held of record by Salka and shares of Common Stock directly or indirectly beneficially owned by Salka, as defined in Section 1(4) (c) of the Bylaws: 0. Dr. David Webb (“Webb”), age 67, 2747 Llama Court, Carlsbad, CA 92009 (residential and business). Shares of Common Stock held of record by Webb: 0. Shares of Common Stock directly or indirectly beneficially owned by Webb, as defined in Section 1(4) (c) of the Bylaws: 12,500, comprised of Common Stock issuable pursuant to stock options exercisable within 60 days of August 7, 2012.
Load more

Recommended publications
  • SCRIPPS DISCOVERS FALL 2010 Selective Inhibition of BMK1 Suppresses Tumor Growth
    SC RIPPS DISC OVERS Accelerating Discoveries, Saving Lives A Newsletter for Philanthropists Published Quarterly by The Scripps Research Institute WINTER 2010 | VOL 7 | NO 1 California-Florida RESEARCH UPDATE Scripps Research Scientists Develop Molecular Test Providing a New Pathway for Identifying Obesity and Diabetes Drugs cientists at The Scripps Research Institute The Worm Institute for Research and Medicine have designed a new molecular test that at Scripps Research. Swill allow researchers to look for potential Janda and Amanda Garner, Ph.D., a research drugs targeting a human metabolic enzyme believed associate in his laboratory, described the new to stimulate the appetite and play a role in diabetes. approach—which may also prove useful for The new test, which the scientists call a simple investigating other enzymes involved in a assay, will allow researchers to look through variety of diseases—in an advance, online Early hundreds of thousands of compounds for those that Edition of the journal Angewandte Chemie on have potential to block the action of an enzyme September 15, 2010. known as ghrelin O-acyltransferase (GOAT). If Even though GOAT was only discovered drugs can be found that safely suppress the action recently, in 2008, scientists had speculated for of GOAT, they may help people who have clinical years that it had to exist. After all, its target (ghrelin, problems with appetite, obesity, and diabetes. or the “G” in the acronym GOAT) had been Professor Kim Janda “There hasn’t been a simple screen until now,” known for more than a decade. says Kim D. Janda, Ph.D., a professor in the Ghrelin, a small peptide hormone that is Departments of Chemistry and Immunology mainly produced in the stomach, signals hunger, and Microbial Science, member of The Skaggs typically before meals.
    [Show full text]
  • Dr. Craig W. Lindsley, FRSC
    Dr. Craig W. Lindsley, FRSC Home Address: Laboratory Address I: Laboratory Address II: 9281 Wardley Park Lane Department of Pharmacology VCNDD – Cool Springs Brentwood, TN 37027 MRBIV (Langford), 12478B Innovation Park (615)-891-1470 Vanderbilt Medical Center 393 Nichol Mills Road Nashville, TN 37232-6600 Franklin, TN 37027 E-mail: [email protected]; phone (office): 615-322-8700 Web sites: www.lindsleylab.com; www.vcndd.org; www.appellopharma.com Citizenship: US Date of Birth: February 7, 1970 Marital status: Married (Stacey), six children: Cameron (13), Jayma (11), Paige (10), Madison (6), Logan (4), Luke (2) Education: 1997 – 1999 Postdoctoral Fellow, Harvard University, Cambridge, MA 1992 - 1996 Ph.D., University of California, Santa Barbara, Santa Barbara, CA 1988 - 1992 B.S., Chemistry, California State University, Chico, Chico, CA Academic Appointments, Industrial Positions, Leadership Roles and Research Experience: 01/2018-present University Professor of Chemistry, University Professor of Pharmacology, University Professor of Biochemistry William K. Warren, Jr. Chair in Medicine, Co-Director and Director of Medicinal Chemistry and DMPK, Vanderbilt Center for Neuroscience Drug Discovery; Site Head, VCNDD Cool Springs Innovation Park; Editor-in-Chief, ACS Chemical Neuroscience Member, Vanderbilt Institute of Chemical Biology, VU-Ingram Cancer Center, Vanderbilt Center for Addiction Research Vanderbilt University School of Medicine, Vanderbilt University (Medicinal Chemistry, Drug Discovery, Total Synthesis, Chemical Biology)
    [Show full text]
  • ACNP 57Th Annual Meeting: Panels, Mini-Panels and Study Groups
    www.nature.com/npp ABSTRACTS COLLECTION ACNP 57th Annual Meeting: Panels, Mini-Panels and Study Groups Sponsorship Statement: Publication of this supplement is sponsored by the ACNP. Individual contributor disclosures may be found within the abstracts. Asterisks in the author lists indicate presenter of the abstract at the annual meeting. https://doi.org/10.1038/s41386-018-0265-8 Panel experiments were performed in 8-10-week-old male or female mice on a C57 background. 1. Dissecting the Contributions of Dopamine D1 and D2 Results: We observed dendritic atrophy in NAc D1-MSNs but Receptor-Expressing Neurons in Behaviors Dysregulated in not D2-MSNs in CSDS susceptible mice (P < 0.001). mRNAs of RhoA Neuropsychiatric Illness pathway molecules were significantly altered in D1-MSNs of CSDS susceptible mice (P < 0.05). Genetic overexpression of WT-RhoA in D1-MSNs induced dendritic atrophy and a susceptible outcome to 1.1 Dichotomous Structural Adaptations in Nucleus SSDS (P < 0.01), while DN-RhoA in D1-MSNs restored dendritic Accumbens Neuron Subtypes Underlie Stress Susceptibility complexity and caused a resilient outcome to CSDS (P < 0.05) compared to eYFP controls. RhoA (WT) in D1-MSNs caused reduced time grooming in splash test of female mice, reduced Mary Kay Lobo sucrose preference in male mice, and enhanced time immobile in forced swim test of both sexes (P < 0.05). Increased Egr3, the RhoA University of Maryland School of Medicine, Baltimore, Maryland, transcriptional regulator, in D2-MSNs promotes stress resiliency (P United States < 0.05) by preventing D2-MSN enhanced density of mushroom spines that occurs in stress susceptible mice (P < 0.01), without Background: Ventral striatum (nucleus accumbens-NAc) medium altering dendritic arbor.
    [Show full text]
  • SRI C20-5 Endeavor
    VOLUME EIGHT NUMBER ONE EndeavorSpring 2005 Controlling Addiction Endeavor VOLUME EIGHT NUMBER ONE Spring 2005 Addiction takes an enormous toll on individuals, families, and society as a whole. The direct and indirect public health costs of addiction are estimated to be in the hundreds of billions of dollars yearly. What are the biological bases of addiction? How can we Sandbagging Cancer in the more effectively treat and prevent this terrible disease? This issue Bloodstream of Endeavor features some investigators at The Scripps Research Institute who are helping to answer these questions. A team of scientists led by Scripps Research Institute Professor David A. Cheresh and Research Associate Sara Weis has identified a potential treatment strategy against metastatic cancer cells that has never been tried before. featured page Metastasis is a major problem with cancer because it allows tumor cells to spread to other parts of the body. While solid tumors can be removed surgically or treated An Antidote for Addiction 02 with chemotherapy or radiation, metastatic cells that Kim Janda Uses the Immune System to Fight Drug Abuse have already entered the circulation are capable of opening a passageway through blood vessels in order to spread to various organs throughout the body. The treatment strategy, which showed promise in the Working to Understand the lab, targets a final step of the metastatic cascade—the Brain’s Role in Alcohol Dependence 06 exit of the metastatic cells from the bloodstream— George Koob and Barbara Mason Search for increasing the protective barrier strength of the host Treatments That Work Over the Long-Term blood vessels and preventing tumor cells from exiting the bloodstream to establish a new cancer site.
    [Show full text]
  • Director's Report
    ``` DIRECTOR’S REPORT to the National Advisory Council on Drug Abuse September 2020 Nora D. Volkow, M.D. Director National Institute on Drug Abuse TABLE OF CONTENTS RESEARCH HIGHLIGHTS ............................................................................................................ 1 GRANTEE HONORS AND AWARDS ......................................................................................... 23 STAFF HONORS AND AWARDS ................................................................................................ 25 STAFF CHANGES .......................................................................................................................... 26 IN MEMORIAM .............................................................................................................................. 33 RESEARCH HIGHLIGHTS BASIC AND BEHAVIORAL RESEARCH Structure Of The Neurotensin Receptor 1 In Complex With β-arrestin 1 Huang W, Masureel M, Qianhui Q, Janetzko J, Asuka I, Kato HE, Robertson MJ, Nguyen KC, Glenn JS, Skiniotis G, Kobilka BK. Nature. March 2020. 579:303-308. Arrestin proteins bind to active, phosphorylated G-protein-coupled receptors (GPCRs), thereby preventing G-protein coupling, triggering receptor internalization and affecting various downstream signalling pathways. Although there is a wealth of structural information detailing the interactions between GPCRs and G proteins, less is known about how arrestins engage GPCRs. Here we report a cryo-electron microscopy structure of full-length human neurotensin receptor
    [Show full text]
  • Feasibility, Rationale and Prospects for Therapeutic Cocaine Vaccines
    James Shearer & Richard P. Mattick Feasibility, rationale and prospects for therapeutic cocaine vaccines NDARC Technical Report No. 168 FEASIBILITY, RATIONALE AND PROSPECTS FOR THERAPEUTIC COCAINE VACCINES James Shearer & Richard P. Mattick Technical Report Number 168 ISBN: 1 877027 56 1 THIS REPORT WAS FUNDED BY THE AUSTRALIAN GOVERNMENT DEPARTMENT OF HEALTH AND AGEING ©NATIONAL DRUG AND ALCOHOL RESEARCH CENTRE, UNIVERSITY OF NEW SOUTH WALES, SYDNEY, 2003. 2 TABLE OF CONTENTS EXECUTIVE SUMMARY...................................................................................................4 ACKNOWLEDGEMENTS..................................................................................................5 1. BACKGROUND TO COCAINE USE.......................................................................6 1.1 Prevalence of cocaine use ................................................................................6 1.2 Nature of cocaine harms..................................................................................6 1.3 Treatment for cocaine use disorders...............................................................7 2. INTRODUCTION TO COCAINE VACCINES ..........................................................8 2.1 General principles of immunotherapy ............................................................8 2.2 Rationale ...........................................................................................................8 2.3 Mechanism........................................................................................................9
    [Show full text]
  • The Scripps Research Institute
    FALL 2006 VOLUME NINE / NUMBER TWO NON-PROFIT U.S. POSTAGE PAID PERMIT 751 SAN DIEGO, CA THE SCRIPPS RESEARCH INSTITUTE A PUBLICATION OF THE SCRIPPS RESEARCH INSTITUTE Office of Communications—TPC30 ENDEAVOR 10550 North Torrey Pines Road La Jolla, California 92037 www.scripps.edu PUBLISHER: Keith McKeown EDITOR: Mika Ono Benedyk DESIGN: Miriello Grafico PRODUCTION: Miriello Grafico Kevin Fung COVER ILLUSTRATION: Carey Sookocheff PORTRAIT PHOTOGRAPHY: Dana Neibert Bruce Hibbs PRINTING: Precision Litho © 2006 All material copyrighted by The Scripps Research Institute. “What’s important is the work these people are doing. They should have the glory.” HELEN DORRIS Donor Profile: Helen Dorris THE SCRIPPS RESEARCH INSTITUTE Helen Dorris is part of the Scripps Research family. Busy researchers greet her in the hallway and stop to discuss current projects. More than a sup- ENDEAVOR porter, she is their friend. Helen takes a keen interest in the neurosciences and has helped bring several researchers to Scripps Research to explore the mysteries of Alzheim- er’s, schizophrenia, and other brain disorders. VOLUME NINE / NUMBER TWO FALL 2006 She is proud of the research she supports but shies away from taking any credit. “What’s important is the work these people are doing,” she says. “They should have the glory.” 17 Helen Dorris has made several gifts of real estate to Scripps Research to establish a fellowship to study schizophrenia and to create both the Helen L. FEATURES: ALSO: Dorris Child and Adolescent Neuro-Psychiatric Disorder Institute and the Harold L. Dorris Neurological Research Institute. BEHIND THE SCENES The institutes, now the home of some of the world’s top brain research- ers, uncover the pathological basis of neurological and psychiatric disorders and expedite the discovery of promising new therapeutic approaches.
    [Show full text]
  • Scientists Design Nicotine Vaccine That Provokes Robust Immune Response 12 January 2015
    Scientists design nicotine vaccine that provokes robust immune response 12 January 2015 When a promising nicotine vaccine failed in clinical that it did not single out the most common form of trials a few years ago, scientists from The Scripps nicotine for attack. Nicotine has two forms that look Research Institute (TSRI) were determined to keep like mirror images of each other—one is a "right- trying to help smokers overcome their addiction. handed" version and one is a "left-handed" version. Even though 99 percent of the nicotine found in Now the team has designed a more effective tobacco is the left-handed version, the previous nicotine vaccine and proven that the structures of vaccine elicited antibodies against both. molecules used in vaccines is critical. The study was published recently in the Journal of Medicinal Janda believes that was a waste of immune Chemistry. response. "This is a case where something very simple was overlooked," he said. "This study provides new hope that one could make a nicotine vaccine that succeeds in clinical Improving the Response trials," said Kim Janda, the Ely R. Callaway Jr. Professor of Chemistry and member of the Skaggs In the new study, the researchers elicited a more Institute for Chemical Biology at TSRI. robust antibody response by creating a vaccine from only left-handed nicotine haptens. To do this, Targeting Nicotine they prepared haptens as a 50-50 mixture and as pure right-handed or pure left-handed versions of According to the National Cancer Institute, nicotine, so they could use the two versions smoking is the leading cause of eight types of together or separately.
    [Show full text]
  • 21 September 2012 | $10 CREDIT: MIKE KEMP/GETTY IMAGES SPECIALSECTION
    21 September 2012 | $10 CREDIT: MIKE KEMP/GETTY IMAGES SPECIALSECTION Disease INTRODUCTION Prevention CONTENTS It Takes More Than News 1468 Task Force’s Prevention Advice an Apple a Day Proves Hard to Swallow Public Health Measures in Disease Prevention AS MODELS FOR PREVENTION RESEARCH, INFECTIOUS DISEASES HAVE SET A HIGH standard. Thanks to the development and widespread distribution of vaccines and 1471 Will an Aspirin a Day Keep Cancer anti microbial drugs, we now live in a world free of smallpox, nearly free of polio, Away? Wondering How the Wonder Drug Works and with declining rates of malaria and AIDS. These victories (some still partial) have resulted in people living longer and acute infectious diseases being super- 1473 Tackling America’s Eating Habits, seded in many countries as a public health priority by long-term noncommuni- One Store at a Time cable diseases. Heart disease, metabolic disease, cancer, and respiratory disease 1476 Uncertain Verdict as Vitamin D together account for 60% of all deaths worldwide and 80% of deaths in low- and Goes On Trial middle-income countries. Global projections for dementia are particularly alarm- 1479 Chronic Disease Vaccines Need ing: By the year 2050, the disorder may affect more than 100 million people. Shot in the Arm Logic dictates that preventing these diseases is a better approach than treat- Review ing people after they have become ill. In many cases, the knowledge and tools needed for prevention appear to be in place. A number of these killer diseases 1482 Can Noncommunicable Diseases share risk factors that can be modifi ed by lifestyle changes—for example, by Be Prevented? Lessons from Studies of Populations and Individuals eliminating tobacco use, eating less processed food, and increasing physical M.
    [Show full text]
  • Director's Report 2/96
    Director's Report 2/96 Director's Report to the National Advisory Council on Drug Abuse February, 1996 Index Research Findings Basic Research Behavioral Research Clinical & Services Research AIDS Research Epidemiology, Etiology and Prevention Research Intramural Research Program Activities Congressional Affairs International Activities Meetings/Conferences Media and Education Activities Planned Meetings Publications Staff Highlights Grantee Honors [Office of Director] [First Report Section] Archive Home | Accessibility | Privacy | FOIA (NIH) | Current NIDA Home Page The National Institute on Drug Abuse (NIDA) is part of the National Institutes of Health (NIH) , a component of the U.S. Department of Health and Human Services. Questions? _ See our Contact Information. https://archives.drugabuse.gov/DirReports/DirRep296/DirectorRepIndex.html[11/16/16, 8:31:17 PM] Director's Report 2/96 - Basic Research Director's Report to the National Advisory Council on Drug Abuse February, 1996 Research Findings Basic Research Cocaine Immunization Kim Janda, Ph.D., Rocio Carrera, M.A., George Koob, Ph.D. and colleagues at the Scripps Research Institute have demonstrated, for the first time, the ability to immunize rats against some of the stimulant effects of cocaine. The animals were treated for 35 days with a conjugated analog of cocaine that is more resistant to metabolism by esterases and that is recognized by the body as a foreign substance. Antibodies were produced in the rats which prevented the subsequent administration of cocaine from producing its CNS stimulatory effects. Cocaine levels in the brains of these animals were reduced from 50 to 75% from those of rats not subjected to the 35-day pretreatment regimen.
    [Show full text]
  • Cv Roberto.Pdf
    CURRICULUM VITAE Personal Details Name: Marisa Roberto Home Address: 3950 Mahaila Avenue, Apt U23, San Diego, California 92122 Work Address: Department of Neuroscience, SP30-1150, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. Contact Details: Tel: (858) 784-7262; Fax: (858) 784-7405 E-mail: [email protected] Education: B.A. equivalent 1991-1996: University of Pisa (Italy); Degree: Biological Sciences; 110/110 cum laude Title of experimental thesis: "Mechanisms of modulation of the Na+/K+-ATPasic pump in the T neurons of the leech Hirudo medicinalis by a sea-weed biotoxin.” PhD 1997-2001: University of Pisa (Italy) and The Scripps Research Institute (USA). May 4 2001: Title of experimental PhD thesis: “The neuropeptide PACAP-38 and ethanol alter the synaptic transmission in rat CA1 hippocampal slices.” Laboratory experience: 1994-1996: Electrophysiology laboratory (research group of Prof. M. Brunelli), Department of Physiology and Biochemistry, University of Pisa, Pisa, Italy. August-December 1996: Leonardo da Vinci UETP (University Enterprises Training Partnership) Fellowship Trainee, Neuronal Development and Biochemistry, The Brabraham Institute of Cambridge, UK, (advisor: Prof. Simon Luckman). 1996-1997: Lab training (advisors: Profs. M. Brunelli and A. Felicioli). February 1997-May 2001: PhD in “Basic Neuroscience,” Department of Physiology and Biochemistry, University of Pisa, Italy (advisor: Prof. M. Brunelli). February-December 1999: PhD Fellowship Training, Department of Neuropharmacology, The Scripps Research Institute, La Jolla, CA (advisors: Profs: G.R. Siggins and D.L. Gruol). May 2001-2003: Postdoctoral Fellowship, Department of Neuropharmacology, The Scripps Research Institute, La Jolla, CA (advisor: Prof. G.R. Siggins).
    [Show full text]
  • ON the BORDER Info & Insights from the Interface Between Energy Healing & Science
    ON THE BORDER Info & insights from the interface between energy healing & science April 2016 Welcome to the April 2016 edition of 'On the Border'.. For those of you new to ‘On the Border’, this is Jayne's monthly Ezine newsletter about the latest information and insights into energy fields, healing and science. Each month I share with you some of the latest research and how it applies to healing, energy work & (daily) life. There is also a 'Freebie' section where you get something for nothing, gratis. Are you wanting to learn the basics of healing and energy work? There is a beginners ‘Heal! En jezelf ook’ in May- July (DEADLINE for registration is SATURDAY 30th APRIL). And the last Self- Healing Circle before the summer is upon us takes place on 25th April. Please consult Jayne’s Calendar below for details and links to the workshops and trainings I have planned for the coming few months. Immune to Addiction? WShen neuroscientist George Koob proposed creating a vaccine for addiction 25 years ago, his colleagues thought he was wasting his time. The immune system evolved to prevent infections, not highs from illegal drugs. Prevailing wisdom holds that treating addiction requires months or years of psychotherapy to help addicts change their thought patterns, a difficult process that does not consistently work. But Koob, then at the Scripps Research Institute, wanted addicts to be able to see their doctor for a shot that could keep them from getting high when their motivation to stay clean waned. His premise was simple. Vaccines against infectious diseases work by priming the body to produce antibodies that stick to the invading pathoge, preventing it from causing illness.
    [Show full text]