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Stanford Chem-H Presentation (PDF)
KiNativ® In situ kinase profiling Stanford University ChEM-H confidential @KiNativPlatform Principle of the KiNativ platform • ATP (or ADP) acyl phosphate binds to, and covalently modifies Lysine residues in the active site • Thus, ATP acyl phosphate with a desthiobiotin tag can be used capture and quantitate kinases in a complex lysate Acyl phosphate Desthiobiotin tag ATP 2 ATP acyl phosphate probe covalently modifies kinase in the active site Lysine 2 Lysine 1 3 ATP acyl phosphate probe covalently modifies kinase in the active site Lysine 2 Lysine 1 4 Samples trypsinized, probe-labeled peptides captured with streptavidin, and analyzed by targeted LC-MS2 Identification Quantitation Explicit determination of peptide Integration of signal from MS2 sequence and probe modification site fragment ions from MS2 spectrum 5 Comprehensive Coverage of Protein and Lipid Kinases Protein kinases Atypical kinases Green: Kinases detected on KiNativ Red: Kinases not detected on KiNativ ~80% of known protein and atypical kinases identified on the platform http://www.kinativ.com/coverage/protein-lipid.html 6 Profiling compound(s) on the KiNativ platform Control sample – add probe Sample: Lysate derived from any cell line or tissue from ANY species Treated sample – add inhibitor followed by probe Inhibited kinase Green: Kinases Blue: Probe Gray: Non-kinases Red: Inhibitor 7 Profiling compound(s) on the KiNativ platform Control sample – add probe MS signalMS Sample: Lysate derived from any cell line or tissue from ANY species Treated sample – add inhibitor -
Town of South Hadley, Ma 2019 Street Listing V No
TOWN OF SOUTH HADLEY, MA 2019 STREET LISTING V NO. APT. NAME BORN OCCUPATION PCT V NO. APT. NAME BORN OCCUPATION PCT ABBEY LN ABBEY ST Con't U 125 CLEGG COLIN H 12/22/1992 CONCRETE FINISH E D 1 ROSARIO NORMA 04/08/1971 HOME MAKER E D 125 CLEGG SHEILA 08/13/1954 UNDERWRITER E D 1 SANTIAGO JUAN R 11/27/1995 STUDENT E U 130 CRAWFORD WALTER H 11/17/1950 HUMAN SERV E 1 SANTIAGO THALIAN 03/17/1998 STUDENT E U 130 ROBINSON PATRICIA E 09/20/1946 HUMAN RES DIR E U 3 KALVINEK JENNIFER P 07/26/1971 SEAMSTRESS E U 132 NAPIORKOWSKI LISA A 05/15/1967 COA ASST DIR E 3 SPINNEY PAYTON 12/09/1994 UNKNOWN E U 132 NAPIORKOWSKI THOMAS A 01/28/1965 SHIPPING/RECEIV E D 5 GARCIA SARAH P 11/26/1980 AT HOME E U 134 STJACQUES BARBARA J 08/11/1957 ADMIN ASST E D 5 GONZALEZ ONIX O 09/14/1980 UNKNOWN E U 134 STJACQUES PAUL L 05/12/1954 MECHANIC E U 7 RIVERA LIZ J 04/24/1988 UNKNOWN E U 137 TAYLOR MAUREEN A 12/02/1955 HOMEMAKER E U 9 ALVES ROBERT A 04/08/1953 UNKNOWN E U 137 TAYLOR THOMAS B 10/08/1953 SHEET METAL E 9 BOISVERT WILLIAM 07/01/1955 UNKNOWN E U 139 KUROWSKI LINDA R 04/01/1947 LIBRARIAN E 9 LEWIS ROBERT 11/27/1954 UNKNOWN E U 140 VANKRUININGEN SHARON A 04/23/1960 CUSTOMER SERVIC E 9 PETE ROBERT 05/12/1937 UNKNOWN E R 143 BRUSO LINDSAY M 06/02/1986 OPTICAL TECH E 9 SCANLON SHAUN 09/18/1957 UNKNOWN E R 143 BRUSO JEREMY H 04/27/1984 SALES E 11 ALEXANDER KAREN 07/27/1953 DISABLED E R 147 LAMONTAGNE SEAN L 05/02/1968 MECHANICAL ENG E 11 GEMME LILLIAN 08/24/1928 DISABLED E R 147 LAMONTAGNE ROXANNE M 01/28/1966 DISABLED E R 11 LAROCHE DEBRA L 12/30/1956 DISABLED -
Hamilton County (Ohio) Naturalization Records – Surname M
Hamilton County Naturalization Records – Surname M Applicant Age Country of Origin Departure Date Departure Port Arrive Date Entry Port Declaration Dec Date Vol Page Folder Naturalization Naturalization Date Maag, Frederick 46 Oldenburg Bremen New Orleans T 11/01/1852 5 132 F F Maag, Frederick 46 Oldenburg Bremen New Orleans T 11/01/1854 6 258 F F Maag, Sebastian 31 Baden Liverpool New York T 01/02/1858 16 296 F F Maahan, James 32 Ireland Toronto Buffalo T 01/20/1852 24 37 F F Maas, Anton 30 Prussia Bremen New York T 01/17/1853 7 34 F F Maas, Carl 18 Mannheim, Germany ? ? T 05/04/1885 T F Maas, Garrett William 25 Holland Rotterdam New York T 11/15/1852 5 287 F F Maas, Garrett William 25 Holland Rotterdam New York T 11/15/1852 6 411 F F Maas, Jacob 55 Germany Rotterdam New York F ? T T Maas, John 55 Germany Havre New York F ? T T Maas, John William 28 Holland Rotterdam New Orleans T 09/27/1848 22 56 F F Maas, Julius J. 48 Germany Bremen New York F ? T T Maas, Leonardus Aloysius 37 Holland Rotterdam New Orleans T 03/01/1852 24 6 F F Maass, F.W. 45 Hanover Bremen Baltimmore T 11/02/1860 18 3 F F Macalusa, Michael 23 Italy Palermo New York T 3/18/1903 T F MacAvoy, Henry 48 England Liverpool New York T 10/26/1891 T F MacDermott, Joseph England ? ? T 2/26/1900 T F Machenheimer, Christoph 29 Hesse Darmstadt Havre New York T 02/19/1850 2 100 F F Machnovitz, Moses 50 Russia Bremen Baltimore T 4/27/1900 T F Maciejensky, Martin 28 Prussia Hamburg New York T 04/28/1854 8 280 F F Maciejensky, Martin 28 Prussia Hamburg New York T 04/28/1854 9 151 F -
2008 Annual Report Committee: Keith A
TOWN OF NORTH ATTLEBOROUGH 2008 ANNUAL REPORT TOWN OF NORTH ATTLEBOROUGH 2008 ANNUAL REPORT Cover Photography – Patty Hitchcock: “The Gasholder” Winning Photograph in the Massachusetts Municipal Association’s 2009 State Calendar Contest 2008 Annual Report Committee: Keith A. Mueller and Judith Chafetz-Sulfaro Printing: Sir Speedy Printing, North Attleborough, MA Editor and Coordinator: Judith Chafetz-Sulfaro Photographs courtesy of Patty Hitchcock The 2008 Annual Report of the Town of North Attleborough has been dedicated to the memory of the employees, retirees, and committee members who passed away in 2008. Your contributions to our town have been immeasurable. You remain in our thoughts and will live on in our hearts forever. Rest in Peace, Dear Friends. Town of North Attleborough Employees, Retirees, and Committee Members Who Passed Away in 2008 DEPARTMENT, BOARD NAME DATE OR COMMITTEE Edward G. Lambert, Jr. January 10, 2008 Chairman, Retirement Board George E. Landry January 28, 2008 Highway Department; RTM Carol Paquette February 15, 2008 Town Clerk/Tax Collector Renaldo J. Chelotti February 23, 2008 School Department Harriet Wilmarth February 29, 2008 School Department John Flynn March 2, 2008 Bus Driver, Council on Aging Arthur Gelichauf, Jr. March 6, 2008 Town Accountant William J. McKeon March 29, 2008 Fire Department Gerald F. Dugan May 12, 2008 NAED Susan Nelson May 21, 2008 Board of Selectmen, 1st female Gilberte M. Hebert September 7, 2008 Secretary, Retirement Board John L. Thorp September 7, 2008 Fire Commissioner; RTM Town Moderator, Advisory Board to Veterans’ Council Katherine E. Dupelle October 24, 2008 School Department Lester E. Caldwell November 24, 2008 Chief, North Attleborough Fire Department; Board of Selectmen Eugene R. -
Pharmacologic Considerations in the Disposition of Antibodies and Antibody-Drug Conjugates in Preclinical Models and in Patients
antibodies Review Pharmacologic Considerations in the Disposition of Antibodies and Antibody-Drug Conjugates in Preclinical Models and in Patients Andrew T. Lucas 1,2,3,*, Ryan Robinson 3, Allison N. Schorzman 2, Joseph A. Piscitelli 1, Juan F. Razo 1 and William C. Zamboni 1,2,3 1 University of North Carolina (UNC), Eshelman School of Pharmacy, Chapel Hill, NC 27599, USA; [email protected] (J.A.P.); [email protected] (J.F.R.); [email protected] (W.C.Z.) 2 Division of Pharmacotherapy and Experimental Therapeutics, UNC Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; [email protected] 3 Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-919-966-5242; Fax: +1-919-966-5863 Received: 30 November 2018; Accepted: 22 December 2018; Published: 1 January 2019 Abstract: The rapid advancement in the development of therapeutic proteins, including monoclonal antibodies (mAbs) and antibody-drug conjugates (ADCs), has created a novel mechanism to selectively deliver highly potent cytotoxic agents in the treatment of cancer. These agents provide numerous benefits compared to traditional small molecule drugs, though their clinical use still requires optimization. The pharmacology of mAbs/ADCs is complex and because ADCs are comprised of multiple components, individual agent characteristics and patient variables can affect their disposition. To further improve the clinical use and rational development of these agents, it is imperative to comprehend the complex mechanisms employed by antibody-based agents in traversing numerous biological barriers and how agent/patient factors affect tumor delivery, toxicities, efficacy, and ultimately, biodistribution. -
Récidive À Long Terme Du Syndrome De Vasoconstriction Cérébral Réversible : Suivi Prospectif De 173 Patients Rosalie Boitet
Récidive à long terme du syndrome de vasoconstriction cérébral réversible : suivi prospectif de 173 patients Rosalie Boitet To cite this version: Rosalie Boitet. Récidive à long terme du syndrome de vasoconstriction cérébral réversible : suivi prospectif de 173 patients. Médecine humaine et pathologie. 2018. dumas-02955583 HAL Id: dumas-02955583 https://dumas.ccsd.cnrs.fr/dumas-02955583 Submitted on 2 Oct 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution - NonCommercial - ShareAlike| 4.0 International License UNIVERSITÉ DE MONTPELLIER FACULTÉ DE MÉDECINE MONTPELLIER-NIMES THÈSE Pour obtenir le titre de DOCTEUR EN MÉDECINE Présentée et soutenue publiquement Par Rosalie BOITET Le 22 juin 2018 RÉCIDIVE A LONG TERME DU SYNDROME DE VASOCONSTRICTION CÉRÉBRAL RÉVERSIBLE : SUIVI PROSPECTIF DE 173 PATIENTS Directeur de thèse : Professeur Anne DUCROS JURY Président : Professeur Pierre LABAUGE Assesseurs : Professeur Anne DUCROS Professeur Éric THOUVENOT Docteur Caroline ARQUIZAN UNIVERSITÉ DE MONTPELLIER -
Kyntheum, INN-Brodalumab
ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS 1 This medicinal product is subject to additional monitoring. This will allow quick identification of new safety information. Healthcare professionals are asked to report any suspected adverse reactions. See section 4.8 for how to report adverse reactions. 1. NAME OF THE MEDICINAL PRODUCT Kyntheum 210 mg solution for injection in pre-filled syringe 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each pre-filled syringe contains 210 mg brodalumab in 1.5 ml solution. 1 ml solution contains 140 mg brodalumab. Brodalumab is a recombinant human monoclonal antibody produced in Chinese Hamster Ovary (CHO) cells. For the full list of excipients, see section 6.1. 3. PHARMACEUTICAL FORM Solution for injection (injection) The solution is clear to slightly opalescent, colourless to slightly yellow and free from particles. 4. CLINICAL PARTICULARS 4.1 Therapeutic indications Kyntheum is indicated for the treatment of moderate to severe plaque psoriasis in adult patients who are candidates for systemic therapy. 4.2 Posology and method of administration Kyntheum is intended for use under the guidance and supervision of a physician experienced in the diagnosis and treatment of psoriasis. Posology The recommended dose is 210 mg administered by subcutaneous injection at weeks 0, 1, and 2 followed by 210 mg every 2 weeks. Consideration should be given to discontinuing treatment in patients who have shown no response after 12-16 weeks of treatment. Some patients with initial partial response may subsequently improve with continued treatment beyond 16 weeks. Special populations Elderly (aged 65 years and over) No dose adjustment is recommended in elderly patients (see section 5.2). -
Revised 6/29/2020 GEORGIA MEDICAID FEE-FOR-SERVICE
GEORGIA MEDICAID FEE-FOR-SERVICE BIOLOGIC IMMUNOMODULATORS PA SUMMARY Preferred Non-Preferred Arcalyst (rilonacept) Actemra subcutaneous (tocilizumab) Benlysta subcutaneous (belimumab) Cimzia (certolizumab) Enbrel (etanercept) Cosentyx (secukinumab) Humira (adalimumab) Dupixent (dupilumab) Ilaris (canakinumab) Fasenra Pen (benralizumab autoinjector)Kevzara Xeljanz (tofacitinib) (sarilumab) Xeljanz XR (tofacitinib extended-release) Kineret (anakinra) Nucala Pen (mepolizumab autoinjector) Olumiant (baricitinib) Orencia subcutaneous (abatacept) Otezla (apremilast) Rinvoq (upadacitinib) Siliq (brodalumab) Simponi (golimumab) Stelara (ustekinumab) Skyrizi (risankizumab) Taltz (ixekizumab) Tremfya (guselkumab) The drug names above include all available oral or subcutaneous formulations under the same primary name. LENGTH OF AUTHORIZATION: Varies NOTES: ▪ All preferred and non-preferred products require prior authorization. Intravenous (IV) formulations of the biologic immunomodulators are not covered under Pharmacy Services. ▪ The criteria details below are for the outpatient pharmacy program. If a medication is being administered in a physician’s office or clinic, then the medication must be billed through the DCH physician services program and not the outpatient pharmacy program. Information regarding the physician services program is located at www.mmis.georgia.gov. PA CRITERIA: Actemra Subcutaneous ❖ Approvable for members 2 years of age or older with a diagnosis of moderately to severely active polyarticular juvenile idiopathic arthritis -
Meeting Minutes Page 1 of 22
DEPARTMENT OF HEALTH BOARD OF RESPIRATORY CARE GENERAL BUSINESS MEETING GENERAL RULES REVIEW July 13, 2012 Minutes Grand Hyatt Tampa Bay 2900 Bayport Drive Tampa, FL 33607 (813) 874-1234 Call the Meeting to Order and Roll Call: Bayyinah Sherrod, RRT, Chair, called the general business meeting to order at 8:30 a.m. Those present for the meeting, included the following: Members Present Staff Present Bayyinah Sherrod, RRT, Chair Allen Hall, Executive Director Bradley Killion, RRT Jessica Sapp, Program Operations Administrator Dick Fields, RRT Kevin Barrett, CRT Board Counsel Rachel Clark, Board Counsel Consumer Member Office of the Attorney General Shawnta Friday-Stroud, Ph.D., Vice Chair Douglas Dolan, Board Counsel Office of the Attorney General Excused Absent Member Peter Hendriksen, RRT Prosecuting Attorney Cecilie Sykes, DOH, Court Reporter: Assistant General Counsel Dempster & Berryhill Court Reporting Penny Appleton 501 E. Kennedy Blvd Tampa, FL 33602 (813) 229-8225 Dr. Rivenbark was present on behalf of the Professionals Resource Network, Inc. (PRN). To accommodate individuals wishing to address the Board, the Board Chair may adjust the sequence of the agenda items. The minutes reflect the actual sequence of events rather than the original agenda order. DISCIPLINARY PROCEEDINGS Due to participation in the Probable Cause Panel, Ms. Sherrod was recused from Tabs 10 and 11. Dr. Friday-Stroud was directed to chair said Tabs. Mr. Fields was recused from Tabs 1 through 9. MOTION FOR BOARD’S FINAL ORDER AFTER HEARING NOT INVOLVING DISPUTED ISSUES OF MATERIAL FACT TAB 1 Rainey Benton Brown, RRT, DOH Case No: 2011-19366 July 13, 2012 - General Business Meeting Minutes Page 1 of 22 Informal Hearing, (PCP Members – Fields, Nunez) Respondent was present and sworn in by the court reporter. -
JAK Inhibitors for Treatment of Psoriasis: Focus on Selective TYK2 Inhibitors
Drugs https://doi.org/10.1007/s40265-020-01261-8 CURRENT OPINION JAK Inhibitors for Treatment of Psoriasis: Focus on Selective TYK2 Inhibitors Miguel Nogueira1 · Luis Puig2 · Tiago Torres1,3 © Springer Nature Switzerland AG 2020 Abstract Despite advances in the treatment of psoriasis, there is an unmet need for efective and safe oral treatments. The Janus Kinase– Signal Transducer and Activator of Transcription (JAK–STAT) pathway plays a signifcant role in intracellular signalling of cytokines of numerous cellular processes, important in both normal and pathological states of immune-mediated infamma- tory diseases. Particularly in psoriasis, where the interleukin (IL)-23/IL-17 axis is currently considered the crucial pathogenic pathway, blocking the JAK–STAT pathway with small molecules would be expected to be clinically efective. However, relative non-specifcity and low therapeutic index of the available JAK inhibitors have delayed their integration into the therapeutic armamentarium of psoriasis. Current research appears to be focused on Tyrosine kinase 2 (TYK2), the frst described member of the JAK family. Data from the Phase II trial of BMS-986165—a selective TYK2 inhibitor—in psoriasis have been published and clinical results are encouraging, with a large Phase III programme ongoing. Further, the selective TYK2 inhibitor PF-06826647 is being tested in moderate-to-severe psoriasis in a Phase II clinical trial. Brepocitinib, a potent TYK2/JAK1 inhibitor, is also being evaluated, as both oral and topical treatment. Results of studies with TYK2 inhibitors will be important in assessing the clinical efcacy and safety of these drugs and their place in the therapeutic armamentarium of psoriasis. -
Biological Therapies for Atopic Dermatitis: an Update (Review)
EXPERIMENTAL AND THERAPEUTIC MEDICINE 17: 1061-1067, 2019 Biological therapies for atopic dermatitis: An update (Review) DIANA DELEANU1-3 and IRENA NEDELEA1,2 1Allergology and Immunology Discipline, ‘Iuliu Hatieganu’ University of Medicine and Pharmacy, 400058 Cluj-Napoca; Departments of 2Allergy and 3Internal Medicine, ‘Professor Doctor Octavian Fodor’ Regional Institute of Gastroenterology and Hepatology, 400162 Cluj-Napoca, Romania Received July 6, 2018; Accepted August 22, 2018 DOI: 10.3892/etm.2018.6989 Abstract. Severe atopic dermatitis, which affects both adults in low-income countries (3). Furthermore, the past decades and children, is a debilitating disorder with a significant decline brought a 2-3-fold increase in prevalence in industrialized of patients' quality of life. Although aetiopathogenic factors countries (3). Generally AD onset is in early childhood, as are currently a topic of study and interpretation, the main one of the first steps of the ‘atopic march’, which describes the features of atopic eczema are skin barrier disturbance and natural history of atopic manifestations, and it is character- immune dysregulation. Severe refractory disease that fails to ized by xerotic skin and acute flare-ups of intensely pruritic improve with conventional therapy may benefit from biologic eczematous lesions (4). Recent studies recognize a predilection therapy. Progress in understanding immunopathology of atopic of AD for persistence in adulthood, with a lifetime prevalence dermatitis have allowed identification of therapeutic molecular accounting for 34.1% (5). Early onset, allergic rhinitis and targets in the field of biological therapy. We reviewed the hand eczema in childhood are high-risk factors for persistent different biological treatments with a focus on novel targeted AD (5). -
Evaluation of Antibody Properties and Clinically Relevant Immunogenicity
Drug Safety https://doi.org/10.1007/s40264-018-00788-w ORIGINAL RESEARCH ARTICLE Evaluation of Antibody Properties and Clinically Relevant Immunogenicity, Anaphylaxis, and Hypersensitivity Reactions in Two Phase III Trials of Tralokinumab in Severe, Uncontrolled Asthma Mats Carlsson1 · Martin Braddock2 · Yuling Li3 · Jihong Wang3 · Weichen Xu3 · Nicholas White4 · Ayman Megally5 · Gillian Hunter6 · Gene Colice5 © The Author(s) 2019 Abstract Introduction Tralokinumab is a monoclonal antibody (mAb) that neutralizes interleukin (IL)-13, a cytokine involved in the pathogenesis of asthma. Objective The objectives of this study were to characterize the potential immunogenic properties of tralokinumab and report data for anti-drug antibodies (ADAs) and hypersensitivity reactions from two phase III clinical trials. Methods The oligosaccharide structure of tralokinumab, Fab-arm exchange, and ADAs were characterized by standard techniques. Hypersensitivity adverse events (AEs) were evaluated in two pivotal clinical trials of tralokinumab in severe, uncontrolled asthma: STRATOS 1 and 2 (NCT02161757 and NCT02194699). Results No galactose-α-1,3-galactose (α-Gal) epitopes were found in the Fab region of tralokinumab and only 4.5% of glycoforms contained α-Gal in the Fc region. Under non-reducing conditions, Fab-arm exchange did not take place with another immunoglobulin (Ig) G 4 mAb (mavrilimumab). However, following glutathione reduction, a hybrid antibody with monovalent bioactivity was detected. ADA incidences (titers) were as follows: STRATOS 1—every 2 weeks (Q2 W) 0.8% (26.0), every 4 weeks (Q4 W) 0.5% (26.0), placebo 0.8% (52.0); STRATOS 2—Q2 W 1.2% (39.0), placebo 0.8% (13.0). Participant-reported hypersensitivity AE rates were as follows: STRATOS 1—Q2 W 25.9%, Q4 W 25.0%, placebo 25.5%; STRATOS 2—Q2 W 13.2%, placebo 9.0%.