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Latest Paper:
Mangiferin present in Curcuma amada was extracted with the help of microwave assisted extraction (MAE). The extraction solvent used was ethanol, which is eco-friendly and reduced the risk of environmental hazard. The mangiferin content was found to increase until 500 W, but decreased as the microwave power was increased further. A similar threshold was also obtained for microwave irradiation time. Following a mathematical analysis, an optimal mangiferin yield of 41 μg/mL was obtained from an extraction time of 15.32 s for a microwave power of 500 W.
[My paper]
N Baillie,
S Tkachenko,
J Zhang,
P Bosted,
S Bültmann,
M E Christy,
H Fenker,
K A Griffioen,
C E Keppel,
S E Kuhn,
W Melnitchouk,
V Tvaskis,
K P Adhikari,
D Adikaram,
M Aghasyan,
M J Amaryan,
M Anghinolfi,
J Arrington,
H Avakian,
H Baghdasaryan,
M Battaglieri,
A S Biselli,
D Branford,
W J Briscoe,
W K Brooks,
V D Burkert,
D S Carman,
A Celentano,
S Chandavar,
G Charles,
P L Cole,
M Contalbrigo,
V Crede,
A D'Angelo,
A Daniel,
N Dashyan,
R De Vita,
E De Sanctis,
A Deur,
B Dey,
C Djalali,
G Dodge,
J Domingo,
D Doughty,
R Dupre,
D Dutta,
R Ent,
H Egiyan,
A El Alaoui,
L El Fassi,
L Elouadrhiri,
P Eugenio,
G Fedotov,
S Fegan,
A Fradi,
M Y Gabrielyan,
N Gevorgyan,
G P Gilfoyle,
K L Giovanetti,
F X Girod,
W Gohn,
E Golovatch,
R W Gothe,
L Graham,
B Guegan,
M Guidal,
N Guler,
L Guo,
K Hafidi,
D Heddle,
K Hicks,
M Holtrop,
E Hungerford,
C E Hyde,
Y Ilieva,
D G Ireland,
M Ispiryan,
E L Isupov,
S S Jawalkar,
H S Jo,
N Kalantarians,
M Khandaker,
P Khetarpal,
A Kim,
W Kim,
P M King,
A Klein,
F J Klein,
A Klimenko,
V Kubarovsky,
S V Kuleshov,
N D Kvaltine,
K Livingston,
H Y Lu,
I J D Macgregor,
Y Mao,
N Markov,
B McKinnon,
T Mineeva,
B Morrison,
H Moutarde,
E Munevar,
P Nadel-Turonski,
A Ni,
S Niccolai,
I Niculescu,
G Niculescu,
M Osipenko,
A I Ostrovidov,
L Pappalardo,
K Park,
S Park,
E Pasyuk,
S Anefalos Pereira,
S Pisano,
S Pozdniakov,
J W Price,
S Procureur,
Y Prok,
D Protopopescu,
B A Raue,
G Ricco,
D Rimal,
M Ripani,
G Rosner,
P Rossi,
F Sabatié,
M S Saini,
C Salgado,
D Schott,
R A Schumacher,
E Seder,
Y G Sharabian,
D I Sober,
D Sokhan,
S Stepanyan,
S S Stepanyan,
P Stoler,
S Strauch,
M Taiuti,
W Tang,
M Ungaro,
M F Vineyard,
E Voutier,
D P Watts,
L B Weinstein,
D P Weygand,
M H Wood,
L Zana,
B Zhao
Hampton University, Hampton, Virginia 23668 16 University of Houston, Houston, Texas 77204, USA and College of William and Mary, Williamsburg, Virginia 23187, USA.
We report on the first measurement of the F_{2} structure function of the neutron from the semi-inclusive scattering of electrons from deuterium, with low-momentum protons detected in the backward hemisphere. Restricting the momentum of the spectator protons to ≲100 MeV/c and their angles to ≳100° relative to the momentum transfer allows an interpretation of the process in terms of scattering from nearly on-shell neutrons. The F_{2}^{n} data collected cover the nucleon-resonance and deep-inelastic regions over a wide range of Bjorken x for 0.65<Q^{2}<4.52 GeV^{2}, with uncertainties from nuclear corrections estimated to be less than a few percent. These measurements provide the first determination of the neutron to proton structure function ratio F_{2}^{n}/F_{2}^{p} at 0.2≲x≲0.8 with little uncertainty due to nuclear effects.
[My paper]
S Abrahamyan,
Z Ahmed,
H Albataineh,
K Aniol,
D S Armstrong,
W Armstrong,
T Averett,
B Babineau,
A Barbieri,
V Bellini,
R Beminiwattha,
J Benesch,
F Benmokhtar,
T Bielarski,
W Boeglin,
A Camsonne,
M Canan,
P Carter,
G D Cates,
C Chen,
J-P Chen,
O Hen,
F Cusanno,
M M Dalton,
R De Leo,
K de Jager,
W Deconinck,
P Decowski,
X Deng,
A Deur,
D Dutta,
A Etile,
D Flay,
G B Franklin,
M Friend,
S Frullani,
E Fuchey,
F Garibaldi,
E Gasser,
R Gilman,
A Giusa,
A Glamazdin,
J Gomez,
J Grames,
C Gu,
O Hansen,
J Hansknecht,
D W Higinbotham,
R S Holmes,
T Holmstrom,
C J Horowitz,
J Hoskins,
J Huang,
C E Hyde,
F Itard,
C-M Jen,
E Jensen,
G Jin,
S Johnston,
A Kelleher,
K Kliakhandler,
P M King,
S Kowalski,
K S Kumar,
J Leacock,
J Leckey 4th,
J H Lee,
J J Lerose,
R Lindgren,
N Liyanage,
N Lubinsky,
J Mammei,
F Mammoliti,
D J Margaziotis,
P Markowitz,
A McCreary,
D McNulty,
L Mercado,
Z-E Meziani,
R W Michaels,
M Mihovilovic,
N Muangma,
C Muñoz-Camacho,
S Nanda,
V Nelyubin,
N Nuruzzaman,
Y Oh,
A Palmer,
D Parno,
K D Paschke,
S K Phillips,
B Poelker,
R Pomatsalyuk,
M Posik,
A J R Puckett,
B Quinn,
A Rakhman,
P E Reimer,
S Riordan,
P Rogan,
G Ron,
G Russo,
K Saenboonruang,
A Saha,
B Sawatzky,
A Shahinyan,
R Silwal,
S Sirca,
K Slifer,
P Solvignon,
P A Souder,
M L Sperduto,
R Subedi,
R Suleiman,
V Sulkosky,
C M Sutera,
W A Tobias,
W Troth,
G M Urciuoli,
B Waidyawansa,
D Wang,
J Wexler,
R Wilson,
B Wojtsekhowski,
X Yan,
H Yao,
Y Ye,
Z Ye,
V Yim,
L Zana,
X Zhan,
J Zhang,
Y Zhang,
X Zheng,
P Zhu
Yerevan Physics Institute, Yerevan, Armenia.
We report the first measurement of the parity-violating asymmetry A_{PV} in the elastic scattering of polarized electrons from ^{208}Pb. A_{PV} is sensitive to the radius of the neutron distribution (R_{n}). The result A_{PV}=0.656±0.060(stat)±0.014(syst) ppm corresponds to a difference between the radii of the neutron and proton distributions R_{n}-R_{p}=0.33_{-0.18}^{+0.16} fm and provides the first electroweak observation of the neutron skin which is expected in a heavy, neutron-rich nucleus.
[My paper]
S Chatrchyan,
V Khachatryan,
A M Sirunyan,
A Tumasyan,
W Adam,
T Bergauer,
M Dragicevic,
J Erö,
C Fabjan,
M Friedl,
R Frühwirth,
V M Ghete,
J Hammer,
M Hoch,
N Hörmann,
J Hrubec,
M Jeitler,
W Kiesenhofer,
M Krammer,
D Liko,
I Mikulec,
M Pernicka,
B Rahbaran,
C Rohringer,
H Rohringer,
R Schöfbeck,
J Strauss,
A Taurok,
F Teischinger,
P Wagner,
W Waltenberger,
G Walzel,
E Widl,
C-E Wulz,
V Mossolov,
N Shumeiko,
J Suarez Gonzalez,
S Bansal,
L Benucci,
T Cornelis,
E A De Wolf,
X Janssen,
S Luyckx,
T Maes,
L Mucibello,
S Ochesanu,
B Roland,
R Rougny,
M Selvaggi,
H Van Haevermaet,
P Van Mechelen,
N Van Remortel,
A Van Spilbeeck,
F Blekman,
S Blyweert,
J D'Hondt,
R Gonzalez Suarez,
A Kalogeropoulos,
M Maes,
A Olbrechts,
W Van Doninck,
P Van Mulders,
G P Van Onsem,
I Villella,
O Charaf,
B Clerbaux,
G De Lentdecker,
V Dero,
A P R Gay,
G H Hammad,
T Hreus,
A Léonard,
P E Marage,
L Thomas,
C Vander Velde,
P Vanlaer,
J Wickens,
V Adler,
K Beernaert,
A Cimmino,
S Costantini,
G Garcia,
M Grunewald,
B Klein,
J Lellouch,
A Marinov,
J McCartin,
A A Ocampo Rios,
D Ryckbosch,
N Strobbe,
F Thyssen,
M Tytgat,
L Vanelderen,
P Verwilligen,
S Walsh,
E Yazgan,
N Zaganidis,
S Basegmez,
G Bruno,
L Ceard,
J De Favereau De Jeneret,
C Delaere,
T du Pree,
D Favart,
L Forthomme,
A Giammanco,
G Grégoire,
J Hollar,
V Lemaitre,
J Liao,
O Militaru,
C Nuttens,
D Pagano,
A Pin,
K Piotrzkowski,
N Schul,
N Beliy,
T Caebergs,
E Daubie,
G A Alves,
M Correa Martins Junior,
D De Jesus Damiao,
T Martins,
M E Pol,
M H G Souza,
W L Aldá Júnior,
W Carvalho,
A Custódio,
E M Da Costa,
C De Oliveira Martins,
S Fonseca De Souza,
D Matos Figueiredo,
L Mundim,
H Nogima,
V Oguri,
W L Prado Da Silva,
A Santoro,
S M Silva Do Amaral,
L Soares Jorge,
A Sznajder,
T S Anjos,
C A Bernardes,
F A Dias,
T R Fernandez Perez Tomei,
E M Gregores,
C Lagana,
F Marinho,
P G Mercadante,
S F Novaes,
Sandra S Padula,
V Genchev,
P Iaydjiev,
S Piperov,
M Rodozov,
S Stoykova,
G Sultanov,
V Tcholakov,
R Trayanov,
M Vutova,
A Dimitrov,
R Hadjiiska,
A Karadzhinova,
V Kozhuharov,
L Litov,
B Pavlov,
P Petkov,
J G Bian,
G M Chen,
H S Chen,
C H Jiang,
D Liang,
S Liang,
X Meng,
J Tao,
J Wang,
X Wang,
Z Wang,
H Xiao,
M Xu,
J Zang,
Z Zhang,
C Asawatangtrakuldee,
Y Ban,
S Guo,
Y Guo,
W Li,
S Liu,
Y Mao,
S J Qian,
H Teng,
S Wang,
B Zhu,
W Zou,
A Cabrera,
B Gomez Moreno,
A F Osorio Oliveros,
J C Sanabria,
N Godinovic,
D Lelas,
R Plestina,
D Polic,
I Puljak,
Z Antunovic,
M Dzelalija,
M Kovac,
V Brigljevic,
S Duric,
K Kadija,
J Luetic,
S Morovic,
A Attikis,
M Galanti,
J Mousa,
C Nicolaou,
F Ptochos,
P A Razis,
M Finger,
M Finger Jr,
Y Assran,
A Ellithi Kamel,
S Khalil,
M A Mahmoud,
A Radi,
A Hektor,
M Kadastik,
M Müntel,
M Raidal,
L Rebane,
A Tiko,
V Azzolini,
P Eerola,
G Fedi,
M Voutilainen,
S Czellar,
J Härkönen,
A Heikkinen,
V Karimäki,
R Kinnunen,
M J Kortelainen,
T Lampén,
K Lassila-Perini,
S Lehti,
T Lindén,
P Luukka,
T Mäenpää,
T Peltola,
E Tuominen,
J Tuominiemi,
E Tuovinen,
D Ungaro,
L Wendland,
K Banzuzi,
A Korpela,
T Tuuva,
D Sillou,
M Besancon,
S Choudhury,
M Dejardin,
D Denegri,
B Fabbro,
J L Faure,
F Ferri,
S Ganjour,
A Givernaud,
P Gras,
G Hamel de Monchenault,
P Jarry,
E Locci,
J Malcles,
L Millischer,
J Rander,
A Rosowsky,
I Shreyber,
M Titov,
S Baffioni,
F Beaudette,
L Benhabib,
L Bianchini,
M Bluj,
C Broutin,
P Busson,
C Charlot,
N Daci,
T Dahms,
L Dobrzynski,
S Elgammal,
R Granier de Cassagnac,
M Haguenauer,
P Miné,
C Mironov,
C Ochando,
P Paganini,
D Sabes,
R Salerno,
Y Sirois,
C Thiebaux,
C Veelken,
A Zabi,
J-L Agram,
J Andrea,
D Bloch,
D Bodin,
J-M Brom,
M Cardaci,
E C Chabert,
C Collard,
E Conte,
F Drouhin,
C Ferro,
J-C Fontaine,
D Gelé,
U Goerlach,
P Juillot,
M Karim,
A-C Le Bihan,
P Van Hove,
F Fassi,
D Mercier,
C Baty,
S Beauceron,
N Beaupere,
M Bedjidian,
O Bondu,
G Boudoul,
D Boumediene,
H Brun,
J Chasserat,
R Chierici,
D Contardo,
P Depasse,
H El Mamouni,
A Falkiewicz,
J Fay,
S Gascon,
M Gouzevitch,
B Ille,
T Kurca,
T Le Grand,
M Lethuillier,
L Mirabito,
S Perries,
V Sordini,
S Tosi,
Y Tschudi,
P Verdier,
S Viret,
D Lomidze,
G Anagnostou,
S Beranek,
M Edelhoff,
L Feld,
N Heracleous,
O Hindrichs,
R Jussen,
K Klein,
J Merz,
A Ostapchuk,
A Perieanu,
F Raupach,
J Sammet,
S Schael,
D Sprenger,
H Weber,
B Wittmer,
V Zhukov,
M Ata,
J Caudron,
E Dietz-Laursonn,
M Erdmann,
A Güth,
T Hebbeker,
C Heidemann,
K Hoepfner,
T Klimkovich,
D Klingebiel,
P Kreuzer,
D Lanske,
J Lingemann,
C Magass,
M Merschmeyer,
A Meyer,
M Olschewski,
P Papacz,
H Pieta,
H Reithler,
S A Schmitz,
L Sonnenschein,
J Steggemann,
D Teyssier,
M Weber,
M Bontenackels,
V Cherepanov,
M Davids,
G Flügge,
H Geenen,
M Geisler,
W Haj Ahmad,
F Hoehle,
B Kargoll,
T Kress,
Y Kuessel,
A Linn,
A Nowack,
L Perchalla,
O Pooth,
J Rennefeld,
P Sauerland,
A Stahl,
M H Zoeller,
M Aldaya Martin,
W Behrenhoff,
U Behrens,
M Bergholz,
A Bethani,
K Borras,
A Burgmeier,
A Cakir,
L Calligaris,
A Campbell,
E Castro,
D Dammann,
G Eckerlin,
D Eckstein,
A Flossdorf,
G Flucke,
A Geiser,
J Hauk,
H Jung,
M Kasemann,
P Katsas,
C Kleinwort,
H Kluge,
A Knutsson,
M Krämer,
D Krücker,
E Kuznetsova,
W Lange,
W Lohmann,
B Lutz,
R Mankel,
I Marfin,
M Marienfeld,
I-A Melzer-Pellmann,
A B Meyer,
J Mnich,
A Mussgiller,
S Naumann-Emme,
J Olzem,
A Petrukhin,
D Pitzl,
A Raspereza,
P M Ribeiro Cipriano,
M Rosin,
J Salfeld-Nebgen,
R Schmidt,
T Schoerner-Sadenius,
N Sen,
A Spiridonov,
M Stein,
J Tomaszewska,
R Walsh,
C Wissing,
C Autermann,
V Blobel,
S Bobrovskyi,
J Draeger,
H Enderle,
J Erfle,
U Gebbert,
M Görner,
T Hermanns,
R S Höing,
K Kaschube,
G Kaussen,
H Kirschenmann,
R Klanner,
J Lange,
B Mura,
F Nowak,
N Pietsch,
C Sander,
H Schettler,
P Schleper,
E Schlieckau,
A Schmidt,
M Schröder,
T Schum,
H Stadie,
G Steinbrück,
J Thomsen,
C Barth,
J Berger,
T Chwalek,
W De Boer,
A Dierlamm,
G Dirkes,
M Feindt,
J Gruschke,
M Guthoff,
C Hackstein,
F Hartmann,
M Heinrich,
H Held,
K H Hoffmann,
S Honc,
I Katkov,
J R Komaragiri,
T Kuhr,
D Martschei,
S Mueller,
Th Müller,
M Niegel,
A Nürnberg,
O Oberst,
A Oehler,
J Ott,
T Peiffer,
G Quast,
K Rabbertz,
F Ratnikov,
N Ratnikova,
M Renz,
S Röcker,
C Saout,
A Scheurer,
P Schieferdecker,
F-P Schilling,
M Schmanau,
G Schott,
H J Simonis,
F M Stober,
D Troendle,
J Wagner-Kuhr,
T Weiler,
M Zeise,
E B Ziebarth,
G Daskalakis,
T Geralis,
S Kesisoglou,
A Kyriakis,
D Loukas,
I Manolakos,
A Markou,
C Markou,
C Mavrommatis,
E Ntomari,
L Gouskos,
T J Mertzimekis,
A Panagiotou,
N Saoulidou,
E Stiliaris,
I Evangelou,
C Foudas,
P Kokkas,
N Manthos,
I Papadopoulos,
V Patras,
F A Triantis,
A Aranyi,
G Bencze,
L Boldizsar,
C Hajdu,
P Hidas,
D Horvath,
A Kapusi,
K Krajczar,
F Sikler,
V Veszpremi,
G Vesztergombi,
N Beni,
J Molnar,
J Palinkas,
Z Szillasi,
J Karancsi,
P Raics,
Z L Trocsanyi,
B Ujvari,
S B Beri,
V Bhatnagar,
N Dhingra,
R Gupta,
M Jindal,
M Kaur,
J M Kohli,
M Z Mehta,
N Nishu,
L K Saini,
A Sharma,
A P Singh,
J Singh,
S P Singh,
S Ahuja,
B C Choudhary,
A Kumar,
S Malhotra,
M Naimuddin,
K Ranjan,
V Sharma,
R K Shivpuri,
S Banerjee,
S Bhattacharya,
S Dutta,
B Gomber,
S Jain,
R Khurana,
S Sarkar,
R K Choudhury,
D Dutta,
S Kailas,
V Kumar,
A K Mohanty,
L M Pant,
P Shukla,
T Aziz,
S Ganguly,
M Guchait,
A Gurtu,
M Maity,
G Majumder,
K Mazumdar,
G B Mohanty,
B Parida,
A Saha,
K Sudhakar,
N Wickramage,
S Dugad,
N K Mondal,
H Arfaei,
H Bakhshiansohi,
S M Etesami,
A Fahim,
M Hashemi,
H Hesari,
A Jafari,
M Khakzad,
A Mohammadi,
M Mohammadi Najafabadi,
S Paktinat Mehdiabadi,
B Safarzadeh,
M Zeinali,
M Abbrescia,
L Barbone,
C Calabria,
S S Chhibra,
A Colaleo,
D Creanza,
N De Filippis,
M De Palma,
L Fiore,
G Iaselli,
L Lusito,
G Maggi,
M Maggi,
N Manna,
B Marangelli,
S My,
S Nuzzo,
N Pacifico,
A Pompili,
G Pugliese,
F Romano,
G Selvaggi,
L Silvestris,
G Singh,
S Tupputi,
G Zito,
G Abbiendi,
G Barozzi,
A C Benvenuti,
D Bonacorsi,
S Braibant-Giacomelli,
L Brigliadori,
P Capiluppi,
A Castro,
F R Cavallo,
M Cuffiani,
G M Dallavalle,
F Fabbri,
A Fanfani,
D Fasanella,
P Giacomelli,
C Grandi,
S Marcellini,
G Masetti,
M Meneghelli,
A Montanari,
F L Navarria,
F Odorici,
A Perrotta,
F Primavera,
A M Rossi,
T Rovelli,
G Siroli,
R Travaglini,
S Albergo,
G Cappello,
M Chiorboli,
S Costa,
R Potenza,
A Tricomi,
C Tuve,
G Barbagli,
V Ciulli,
C Civinini,
R D'Alessandro,
E Focardi,
S Frosali,
E Gallo,
S Gonzi,
M Meschini,
S Paoletti,
G Sguazzoni,
A Tropiano,
L Benussi,
S Bianco,
S Colafranceschi,
D Piccolo,
P Fabbricatore,
R Musenich,
A Benaglia,
F De Guio,
L Di Matteo,
S Fiorendi,
S Gennai,
A Ghezzi,
S Malvezzi,
R A Manzoni,
A Martelli,
A Massironi,
D Menasce,
L Moroni,
M Paganoni,
D Pedrini,
S Ragazzi,
N Redaelli,
S Sala,
T Tabarelli de Fatis,
S Buontempo,
C A Carrillo Montoya,
N Cavallo,
A De Cosa,
O Dogangun,
F Fabozzi,
A O M Iorio,
L Lista,
M Merola,
P Paolucci,
P Azzi,
N Bacchetta,
P Bellan,
D Bisello,
A Branca,
R Carlin,
P Checchia,
T Dorigo,
U Dosselli,
F Fanzago,
F Gasparini,
U Gasparini,
A Gozzelino,
K Kanishchev,
S Lacaprara,
I Lazzizzera,
M Loreti,
M Margoni,
M Mazzucato,
A T Meneguzzo,
M Nespolo,
L Perrozzi,
N Pozzobon,
P Ronchese,
F Simonetto,
E Torassa,
M Tosi,
S Vanini,
P Zotto,
G Zumerle,
U Berzano,
M Gabusi,
S P Ratti,
C Riccardi,
P Torre,
P Vitulo,
M Biasini,
G M Bilei,
B Caponeri,
L Fanò,
P Lariccia,
A Lucaroni,
G Mantovani,
M Menichelli,
A Nappi,
F Romeo,
A Santocchia,
S Taroni,
M Valdata,
P Azzurri,
G Bagliesi,
T Boccali,
G Broccolo,
R Castaldi,
R T D'Agnolo,
R Dell'orso,
F Fiori,
L Foà,
A Giassi,
A Kraan,
F Ligabue,
T Lomtadze,
L Martini,
A Messineo,
F Palla,
F Palmonari,
A Rizzi,
A T Serban,
P Spagnolo,
R Tenchini,
G Tonelli,
A Venturi,
P G Verdini,
L Barone,
F Cavallari,
D Del Re,
M Diemoz,
C Fanelli,
M Grassi,
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L Borrello,
D Carlsmith,
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J Efron,
E Friis,
L Gray,
K S Grogg,
M Grothe,
R Hall-Wilton,
M Herndon,
A Hervé,
P Klabbers,
J Klukas,
A Lanaro,
C Lazaridis,
J Leonard,
R Loveless,
A Mohapatra,
I Ojalvo,
G A Pierro,
I Ross,
A Savin,
W H Smith,
J Swanson
Yerevan Physics Institute, Yerevan, Armenia.
A search for a Higgs boson in the four-lepton decay channel H→ZZ, with each Z boson decaying to an electron or muon pair, is reported. The search covers Higgs boson mass hypotheses in the range of 110<m_{H}<600 GeV. The analysis uses data corresponding to an integrated luminosity of 4.7 fb^{-1} recorded by the CMS detector in pp collisions at sqrt[s]=7 TeV from the LHC. Seventy-two events are observed with four-lepton invariant mass m_{4ℓ}>100 GeV (with 13 below 160 GeV), while 67.1±6.0 (9.5±1.3) events are expected from background. The four-lepton mass distribution is consistent with the expectation of standard model background production of ZZ pairs. Upper limits at 95% confidence level exclude the standard model Higgs boson in the ranges of 134-158 GeV, 180-305 GeV, and 340-465 GeV. Small excesses of events are observed around masses of 119, 126, and 320 GeV, making the observed limits weaker than expected in the absence of a signal.
[My paper]
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D Toback,
N Akchurin,
C Bardak,
J Damgov,
P R Dudero,
C Jeong,
K Kovitanggoon,
S W Lee,
T Libeiro,
P Mane,
Y Roh,
A Sill,
I Volobouev,
R Wigmans,
E Yazgan,
E Appelt,
E Brownson,
D Engh,
C Florez,
W Gabella,
A Gurrola,
M Issah,
W Johns,
C Johnston,
P Kurt,
C Maguire,
A Melo,
P Sheldon,
B Snook,
S Tuo,
J Velkovska,
M W Arenton,
M Balazs,
S Boutle,
S Conetti,
B Cox,
B Francis,
S Goadhouse,
J Goodell,
R Hirosky,
A Ledovskoy,
C Lin,
C Neu,
J Wood,
R Yohay,
S Gollapinni,
R Harr,
P E Karchin,
C Kottachchi Kankanamge Don,
P Lamichhane,
M Mattson,
C Milstène,
A Sakharov,
M Anderson,
M Bachtis,
D Belknap,
J N Bellinger,
J Bernardini,
D Carlsmith,
M Cepeda,
S Dasu,
J Efron,
E Friis,
L Gray,
K S Grogg,
M Grothe,
R Hall-Wilton,
M Herndon,
A Hervé,
P Klabbers,
J Klukas,
A Lanaro,
C Lazaridis,
J Leonard,
R Loveless,
A Mohapatra,
I Ojalvo,
G A Pierro,
I Ross,
A Savin,
W H Smith,
J Swanson,
M Weinberg
Yerevan Physics Institute, Yerevan, Armenia.
A search for signatures of extra spatial dimensions in the diphoton invariant-mass spectrum has been performed with the CMS detector at the LHC. No excess of events above the standard model expectation is observed using a data sample collected in proton-proton collisions at sqrt[s]=7 TeV corresponding to an integrated luminosity of 2.2 fb^{-1}. In the context of the large-extra-dimensions model, lower limits are set on the effective Planck scale in the range of 2.3-3.8 TeV at the 95% confidence level. These limits are the most restrictive bounds on virtual-graviton exchange to date. The most restrictive lower limits to date are also set on the mass of the first graviton excitation in the Randall-Sundrum model in the range of 0.86-1.84 TeV, for values of the associated coupling parameter between 0.01 and 0.10.
[My paper]
Pratik Home,
Biswarup Saha,
Soma Ray,
Debasree Dutta,
Sumedha Gunewardena,
Byunggil Yoo,
Arindam Pal,
Jay L Vivian,
Melissa Larson,
Margaret Petroff,
Patrick G Gallagher,
Vincent P Schulz,
Kenneth L White,
Thaddeus G Golos,
Barry Behr,
Soumen Paul
Department of Pathology and Laboratory Medicine, Smith Intellectual Developmental Disabilities Research Center, Institute of Reproductive Health and Regenerative Medicine, and Departments of Physiology and Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160.
In the preimplantation mouse embryo, TEAD4 is critical to establishing the trophectoderm (TE)-specific transcriptional program and segregating TE from the inner cell mass (ICM). However, TEAD4 is expressed in the TE and the ICM. Thus, differential function of TEAD4 rather than expression itself regulates specification of the first two cell lineages. We used ChIP sequencing to define genomewide TEAD4 target genes and asked how transcription of TEAD4 target genes is specifically maintained in the TE. Our analyses revealed an evolutionarily conserved mechanism, in which lack of nuclear localization of TEAD4 impairs the TE-specific transcriptional program in inner blastomeres, thereby allowing their maturation toward the ICM lineage. Restoration of TEAD4 nuclear localization maintains the TE-specific transcriptional program in the inner blastomeres and prevents segregation of the TE and ICM lineages and blastocyst formation. We propose that altered subcellular localization of TEAD4 in blastomeres dictates first mammalian cell fate specification.
Department of Orthopedics and Traumatology, University Hospital Agostino Gemelli, Catholic University of the Sacred Heart School of Medicine, Largo Agostino Gemelli 1, Rome 00168, Italy.
The prevalence of cardiovascular disease increases with advancing age. Although long-term exposure to cardiovascular risk factors plays a major role in the etiopathogenesis of cardiovascular disease, intrinsic cardiac aging enhances the susceptibility to developing heart pathologies in late life. The progressive decline of cardiomyocyte mitochondrial function is considered a major mechanism underlying heart senescence. Damaged mitochondria not only produce less ATP but also generate increased amounts of reactive oxygen species and display a greater propensity to trigger apoptosis. Given the postmitotic nature of cardiomyocytes, the efficient removal of dysfunctional mitochondria is critical for the maintenance of cell homeostasis, because damaged organelles cannot be diluted by cell proliferation. The only known mechanism whereby mitochondria are turned over is through macroautophagy. The efficiency of this process declines with advancing age, which may play a critical role in heart senescence and age-related cardiovascular disease. The present review illustrates the putative mechanisms whereby alterations in the autophagic removal of damaged mitochondria intervene in the process of cardiac aging and in the pathogenesis of specific heart diseases that are especially prevalent in late life (eg, left ventricular hypertrophy, ischemic heart disease, heart failure, and diabetic cardiomyopathy). Interventions proposed to counteract cardiac aging through improvements in macroautophagy (eg, calorie restriction and calorie restriction mimetics) are also presented.
[My paper]
Mw Stacey,
J Grubb,
A Asmar,
J Pryor,
H Elsayed-Ali,
W Cao,
A Beskok,
D Dutta,
DA Darby,
A Fecteau,
A Werner,
Re Kelly Jr
Frank Reidy Research Center for Bioelectrics, Old Dominion University , Norfolk, VA USA.
Costal cartilage is much understudied compared to the load bearing cartilages. Abnormally grown costal cartilages are associated with the inherited chest wall deformities pectus excavatum and pectus carinatum resulting in sunken or pigeon chest respectively. A lack of understanding of the ultrastructural and molecular biology of costal cartilage is a major confounder in predicting causes and outcomes of these disorders. The present study analyzed the structure of marginal human costal cartilage (ribs 6-10) through scanning electron and atomic force microscopy and identified the presence of straw-like structures running longitudinally. We also demonstrated that chondrocytes tend to occur singly or as doublets and that centrally located cells produce high levels of aggrecan compared to more peripherally located cells measured by immunohistochemistry. Gene expression from mRNA extracted from cartilage showed high levels of decorin expression, likely associated with the large, complex tubular structures running through this cartilage type. COL2A1, ACAN and TIMP1 also showed higher levels of expression compared to ACTB. Analysis of gene expression ratios demonstrate that costal cartilage is under differentiated compared to published ratios for articular cartilage, likely due to the vastly different biomechanical environments of each cartilage type. Further studies need to establish whether findings described here from the costal margins are significantly different to cartilage of the 'true ribs' and how these values change with age.
[My paper]
N Fomin,
J Arrington,
R Asaturyan,
F Benmokhtar,
W Boeglin,
P Bosted,
A Bruell,
M H S Bukhari,
M E Christy,
E Chudakov,
B Clasie,
S H Connell,
M M Dalton,
A Daniel,
D B Day,
D Dutta,
R Ent,
L El Fassi,
H Fenker,
B W Filippone,
K Garrow,
D Gaskell,
C Hill,
R J Holt,
T Horn,
M K Jones,
J Jourdan,
N Kalantarians,
C E Keppel,
D Kiselev,
M Kotulla,
R Lindgren,
A F Lung,
S Malace,
P Markowitz,
P McKee,
D G Meekins,
H Mkrtchyan,
T Navasardyan,
G Niculescu,
A K Opper,
C Perdrisat,
D H Potterveld,
V Punjabi,
X Qian,
P E Reimer,
J Roche,
V M Rodriguez,
O Rondon,
E Schulte,
J Seely,
E Segbefia,
K Slifer,
G R Smith,
P Solvignon,
V Tadevosyan,
S Tajima,
L Tang,
G Testa,
R Trojer,
V Tvaskis,
W F Vulcan,
C Wasko,
F R Wesselmann,
S A Wood,
J Wright,
X Zheng
Los Alamos National Laboratory, Los Alamos, New Mexico 87545, USA and University of Tennessee, Knoxville, Tennessee 37996, USA and University of Virginia, Charlottesville, Virginia 22904, USA.
We present new measurements of electron scattering from high-momentum nucleons in nuclei. These data allow an improved determination of the strength of two-nucleon correlations for several nuclei, including light nuclei where clustering effects can, for the first time, be examined. The data also include the kinematic region where three-nucleon correlations are expected to dominate.
Department of Biotechnology, National Institute of Technology, M. G. Avenue, Durgapur, 713209, West Bengal, India.
Dietzia maris NIT-D, a canthaxanthin producer, was isolated during routine screening of pigment-producing bacteria. Response surface methodology was applied for statistical designing of process parameters for biomass and canthaxanthin production. The effects of four process parameters (considered as independent variables), namely temperature (10-30 °C), pH (4.75-5.75), shaker speed (75-135 rpm) and percentage inoculum (0.5-2.5 %) on the biomass and canthaxanthin yield (considered as dependent variables) were studied. As much as 122 mg L(-1) of canthaxanthin was obtained when Dietzia maris NIT-D was incubated for 120 h at 25 °C and 120 rpm, initial pH and percentage inoculum being 5.5 and 2 % respectively. The pigment yield is the highest reported till date, with Dietzia maris as the test organism. The maximum biomass yield was 7.39 g L(-1) under optimized process parameters. The predicted values were also verified by validation experiments in 5-day fermentation. Different mathematical models were used to describe growth and production, considering the effect of glucose in batch mode. The kinetic constants were calculated by fitting the experimental data to the models. Cell growth was inhibited beyond a glucose concentration of 15 g L(-1). Andrews' model gave the best fit with a R (2) value of 0.9993. During the exponential growth phase, the specific growth rate was found to remain fairly constant with respect to time. There was no inhibitory effect due to intracellular product accumulation for all concentrations of glucose. This observation is the first of its kind, as previous studies have reported that increasing accumulation of intracellular carotenoid exerts greater degree of inhibition on growth.
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