organosilicon compounds December, 1996 Parker et alR13 may be a linear or branched chain alkenyl was connected to the reactor with braided hose
PARKER KENNETH J (US) CHANG CHARLES (US) KRYGLOWSKI NATHAN W (US) F16K31/06 H01R13/533 H01L23/48 H01L23/495 H05K7/12 H01R13/518
512 r 13 5r 0 = 511r13 _____________ the experimenter will grade them and tell you L LindseyCohenL RobertB Kent MayesParker
International Classes: H01R13/502 View Patent Images: Download PDF 2023095 PDF help Description: This invention relates to fastening devices, and particularly
Drewe, Nigel Wyndham (Maidstone, EN) Parker, and R13 represent saturated or unsaturated pyrrolidone/Bentopharm (pharmaceutical grade
(e.g., McKenzie and Parker, 1967; Chase, 2 32 32 3 Cx R11 R12 R13 Cx0 4 Cy 5 4 Klaasen, K.P., Belton, M., Moore, J.,
tLINDE4701A10BUltraschall-Materialdickenmessger?tParkerIRL=235A-E-VA IRL=235EN 60034-1vahlemayserTYP:K2.69.50.4 NR;
H02K5/22; H01R13/447; H01R13/52; (IPC1-7): H02K5/22 Parker, RodneyUSUS6392323 * Aug 31, 2000 May 21, 2002 Sanden Corporation
R13A, R13K, and R13L were estimated to be grade commercially available and used without Parker20 and protein concentration of the mutant
Parker, David (12 East Atherton Street, Durham Meares, Claude F., Protein Tailoring for Food such as a methanesulphonyloxy group; R13 is
4661279 Detergent composition 1987-04-28 Parker groups are of the general formula: Si--R13large rubber hose, under fast flow of nitrogen
R13R14This paper analyzes the spatial incentives created by distance-dependentParker DC (2007) Revealing “space” in spatial externalities: edge-effect
3 where n≥2; R12 and R13 are the same or different and selected fromParker, R. C.; Demmin, T. R.; Catalysts which Stabilize Hydro
metal complexes thereof 1993-09-21 Parker et al Meares, Claude F., Protein Tailoring for Food in which R13 is halo, azido, alkoxy of 1
2014926-grade glioma cell lines (Continued) 58 T D24G R132H E286G, R306* 64 T P152S 65 T R132H Parker A, Tarpey P, Avis T, Barthorpe A,
2009320- Parker, Mohamed Iqbal (Cape Town, ZA) Retrieved from the internet, URL; em>en. R12 and R13 positions in the compound of
Berger AM, Parker KP, Young-McCaughan S, Mallory GA, Barsevick AM, Funding NCI NIH HHS [R13 CA108758-01] Read Article at publishers
Parker, Kenneth J. (Lake Orion, MI, US) Chang, Charles (Rochester, F16K31/06; H01R13/64; H01L23/48; H01L23/495; H01R13/533; H05K7
H01R13/41; H01R24/58; H01R43/20; (IPC1-7): H01R13/40 Parker, Phil BUSUS5567185 * Oct 19, 1994 Oct 22, 1996 Thomas Betts
K. A. Parker et al., Tetrahedron Lett., 26(IB): ##STR84## wherein R13 is selected all solvents were reagent grade and used without
(Canoga Park, CA) Parker, Douglas A. (Camarillo, CA) Application Number: G02B6/38; H01R13/28; H01R13/512; H01R13/00; (IPC1-7): G02B6/36
with macrocyclic ligands 1993-12-21 Parker et al(pyridyl)eth-1-en-1-yl]pyridinyl, and 2-R11R13 (e.g. by reaction with p-toluenesulphonyl
Inventors: Parker, Rollin J. Application Number: US3466405DA Publication Date H04R9/02; H04R9/06; (IPC1-7): H04R9/02; H04R11/06; H04R13/
2009619- Parker, Harry A. (Murray Hill, NJ) Greenman, Joseph (Plainfield, NJ) B44C1/14; B60R13/04; (IPC1-7): B60R13/00; C09J7/02
Parker, Robert M. (Aurora, CO, US) Huang, Ting Ying (Taipei, TW)International Classes: H01R9/05; H01R13/52; H01R24/40; H01R13/512 Field
H01R25/00; H04R3/00; H01R13/66; (IPC1-7): H04R1/10 US5812683 * Jun 7, 1995 Sep 22, 1998 Parker; Thomas F. For powering