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| 1 | Identification of genes involved in bamboo fiber development显示文摘 | Rai V Ghosh J S Pal A | | 0，，1： | 1 |
| 2 | Dermatomyositis associated with acute myelocytic leukemia 显示文摘 | Shrivastav A Kumar V Pal J | 2010 | Rheumatol Int2010，30，5： | 1 |
| 3 | Adefovir dipivoxil in the treatment of chn,nic hepatitis B virus infection 显示文摘 | Hadziyannis S J Pal atheodoridis G V | 2004 | Expert Rev Anti Infect Ther2004，2，4： | 1 |
| 4 | Epigenetieally silenced GNG4 inhibits SDFlalpha/CXCR4 signaling in mes- enchymal glioblastoma显示文摘 | Pal J Patil V Mondal B | 2016 | Genes Cancer2016，7，34： | 1 |
| 5 | Hepatitis C virus RNA replication requires a conserved structural motif within the transmembrane domain of the NS5B RNA-dependent RNA polymerase显示文摘 | Brass V Gouttenoire J Wahl A Pal Z Blum H E Penin F Moradpour D | | 0，，21： | 1 |
| 6 | Identification of genes involved in bamboo fiber development显示文摘 | Rai V Ghosh J S Pal A | 2011 | Gene2011，，478： | 1 |
| 7 | Sequence and analysis ofchromosome 3 of the plant Arabidopsis thaliana显示文摘 | Salanoubat M Lemcke K Rieger M Ansorge W Unseld M Fartmann B Vaile G Blocker H Pcrez-Alonso M Obennaier B Delseny M Boutry M Grivell L A Mache R Puigdomenech P De Simone V Choisne N Artiguenave F Robert C Brottier P Wincker P Cattolico L Weissenbach J Saurin W Quetier F Schafer M Mu||er-Auer S Gabel C Fuchs M Benes V Wurmbach E Drzonek H Erfle H Jordan N Bangert S Wiedelmann R Kranz H Voss H Holland R Brandt P Nyakatura G Vezzi A D' Angelo M Pallavicini A Toppo S Simionati B Conrad A Homischer K Kauer G Lohnert T H Nordsiek G Reichelt J Scharfe M Schon O Bargues M Terol J Climent J Navarro P CoUado C Perez-Perez A Ottenwalder B Duchemin D Cooke R Laudie M Berger-Llauro C Pumelle B Masuy D de Haan M Maarse A C Alcaraz J P Cottet A Casacuberta E Monfort A Argiriou A Flores M Liguori R Vitale D Mannhaupt G Haase D Schoof H Rudd S Zaccaria P Mewes H W Mayer K F Kaul S Town C D Koo H L Tailon L J Jenkins J Rooney T Rizzo M Waits A Utterback T Fujii C Y Shea T P Creasy T H Haas B Maiti R Wu D Peterson J Van Aken S Pal G Militscher J Sellers P Gill J E Feldblyum T V Preuss D Lin X Nierman W C Salzberg S L White O Venter J C Fraser C M Kaneko T Nakamura Y Sato S Kato T Asamizu E Sasamoto S Kimura T Idesawa K Kawashiraa K Kishida Y Kiyokawa C Kohara M Matsumoto kl Matsuno A Muraki A Nakayama S Nakazaki N Shinpo S Takeuchi C Wada T Watanabe A Yamada M Yasuda M Tabata S | 2000 | Nature2000，408，6814： | 1 |
| 8 | Evidence of genet- ic drift and reassortment in infectious bursal disease virus and emergence of outbreaks in poultry farms in India显示文摘 | PATEL A K PANDEY V C PAL J K | 2016 | Virus Disease2016，27，2： | 1 |
| 9 | Impactof left ventricular assist device bridging on post-transplantoutcomes 显示文摘 | PAL J D PIACENTINO V CUEVAS A D | 2009 | The Annals of Thoracic Surgery2009，88，5： | 1 |
| 10 | Predicting heats of formation of energetic materials using quantum mechanical calculations显示文摘 | Rice B M Pal S V Hare J | 1999 | Combustion and Flame1999，118，： | 1 |
| 11 | The tomato genome sequence provides insights into fleshy fruit evolution 显示文摘 | Sato S Tabata S Hirakawa H Asamizu E Shlrasawa K Isobe S Kaneko T Nakamura Y Shibata D Aoki K Egholm M Knight J Bogden R Li C Shuang Y Xu X Pan S Cheng S Liu X Ren Y Wang J Albiero A Dal Pero F Todesco S Van Eck J Buels R M Bombarely A Gosselin J R Huang M Leto J A Menda N Strickler S Mao L Gao S Tecle I Y York T Zheng Y Vrebalov JT Lee J Zhong S Mueller L A Stiekema W J Ribeca P Alioto T Yang W Huang S Du Y Zhang Z Gao J Guo Y Wang X Li Y He J Li C Cheng Z Zuo J Ren J Zhao J Yan L Jiang H Wang B Li H Li Z Fu F Chen B Feng Q Fan D Wang Y Ling H Xue Y Ware D McCombie W R Lippman Z B Chia J M Jiang K Pasternak S Gelley L Kramer M Anderson L K Chang S B Royer S M Shearer L A Stack S M Rose J K Xu Y Eannetta N Matas A J McQuinn R Tanksley S D Camara F Guiga R Rombauts S Fawcett J Van de Peer Y Zamir D Liang C Spannagl M Gundlach H Bruggmann R Mayer K Jia Z Zhang J Ye Z Bishop G J Butcher S Lopez-Cobollo R Buchan D Filippis I Abbott J Dixit R Singh M Singh A Pal J K Pandit A Singh P K Mahato A K Gaikwad V D Sharma R R Mohapatra T Singh N K Causse M Rothan C Schiex T Noirot C Bellec A Klopp C Delalande C Berges H Mariette J Frasse P Vautrin S Zouine M Latch6 A Rousseau C Regad F Pech J C Philippot M Bouzayen M Pericard P Osorio S Fernandez del Carmen A Monforte A Granell A Fernandez-Mufioz R Conte M Lichtenstein G Carrari F De Bellis G Fuligni F Peano C Grandillo S Termolino P Pietrella M Fantini E Falcone G Fiore A Giuliano G Lopez L Facella P Perotta G Daddiego L Bryan G Orozco M Pastor X Torrents D van Schriek M G Feron R M van Oeveren J de Heer P daPonte L Jacobs-Oomen S Cariaso M Prins M van Eijk M J Janssen A van Haaren M J Jungeun Kim S H Kwon S Y Kim S Koo D H Lee S Hur C G Clouser C Rico A Hallab A Gebhardt C Klee K Jocker A Warfsmann J Gobel U Kawamura S Yano K Sherman J D Fukuoka H Negoro S Bhutty S Chowdhury P Chattopadhyay D Datema E Smit S Schijlen E G van de Belt J van Haarst J C Peters S A van Staveren M A Henkens M H Mooyman P J Hesselink T van Ham R C Jiang G Droege M Choi D Kang B C Kim B D Park M Kim S Yeom SI Lee YH Choi Y D Li G Gao J Liu Y Huang S Fernandez-Pedrosa V Collado C Zufiiga S Wang G Cade R Dietrich R A Rogers J Knapp S Fei Z White R A Thannhauser T W Giovannoni J J Botella M A Gilbert L Gonzalez R Goieoechea J L Yu Y Kudrna D Collura K Wissotski M Wing R Meyers BC Gurazada AB Green P J Vyas S M Solanke A U Kumar R Gupta V Sharma A K Khurana P Khurana J P Tyagi A K Dalmay T Mohorianu 1 Waits B Chamala S Barbazuk W B Li J Guo H Lee T H Wang Y Zhang D Paterson A H Wang X Tang H Barone A Chiusano M L Ereolano M R D' Agostino N Di Filippo M Traini A Sanseverino W Frusciante L Seymour G B Elharam M Fu Y Hua A Kenton S Lewis J Lin S Najar F Lai H Qin B Qu C Shi R White D White J Xing Y Yang K Yi J Yao Z Zhou L Roe B A Vezzi A D' Angelo M Zimbello R Sehiavon R Caniato E Rigobello C Campagna D Vitulo N Valle G Nelson D R De Paoli E Szinay D de Jong H H Bai Y Visser R G Klein R Beasley H McLaren K Nicholson C Riddle C Gianese G | 2012 | Nature2012，485，7400： | 1 |
| 12 | Development of magnetic device for cell separation 显示文摘 | Haik Y Pal V Chert C J | 1999 | J Magn Magn Mater1999，194，13： | 1 |
| 13 | Past, present and future of kidney paired donation transplantation in India显示文摘One third of healthy willing living kidney donors are rejected due to ABO blood group incompatibility and donor specific antibody. This increases pre-transplant dialysis duration leading to increased morbidity and mortality on the kidney transplantation waiting list. Over the last decade kidney paired donation is most rapidly increased source of living kidney donors. In a kidney transplantation program dominated by living donor kidney transplantation, kidney paired donation is a legal and valid alternative strategy to increase living donor kidney transplantation. This is more useful in countries with limited resources where ABO incompatible kidney transplantation or desensitization protocol is not feasible because of costs/infectious complications and deceased donor kidney transplantation is in initial stages. The matching allocation, ABO blood type imbalance, reciprocity, simultaneity, geography were the limitation for the expansion of kidney paired donation. Here we describe different successful ways to increase living donor kidney transplantation through kidney paired donation. Compatible pairs, domino chain, combination of kidney paired donation with desensitization or ABO incompatible transplantation, international kidney paired donation, nonsimultaneous, extended, altruistic donor chain and list exchange are different ways to expand the donor pool.In absence of national kidney paired donation program,a dedicated kidney paired donation team will increase access to living donor kidney transplantation in individual centres with team work. Use of social networking sites to expand donor pool, HLA based national kidney paired donation program will increase quality and quantity of kidney paired donation transplantation. Transplant centres should remove the barriers to a broader implementation of multicentre, national kidney paired donation program to further optimize potential of kidney paired donation to increase transplantation of O group and sensitized patients. This review assists in the development of similar programs in other developing countries. | Vivek B Kute Himanshu V Patel Pankaj R Shah Pranjal R Modi Veena R Shah Sayyed J Rizvi Bipin C Pal Manisha P Modi Priya S Shah Umesh T Varyani Pavan S Wakhare Saiprasad G Shinde Vijay A Ghodela Minaxi H Patel Varsha B Trivedi Hargovind L Trivedi | 2017 | World Journal of Transplantation2017，7，2： | 0 |
| 14 | International kidney paired donation transplantations to increase kidney transplant of O group and highly sensitized patient: First report from India显示文摘AIM To report the first international living related two way kidney paired donation(KPD) transplantation from India which occurred on 17 th February 2015 after legal per-mission from authorization committee. METHODS Donor recipient pairs were from Portugal and India who were highly sensitized and ABO incompatible with their spouse respectively. The two donor recipient pairs had negative lymphocyte cross-matching, flow cross-matchand donor specific antibody in two way kidney exchange with the intended KPD donor. Local KPD options were fully explored for Indian patient prior to embarking on international KPD. RESULTS Both pairs underwent simultaneous uneventful kidney transplant surgeries and creatinine was 1 mg/d L on tacrolimus based immunosuppression at 11 mo follow up. The uniqueness of these transplantations was that they are first international KPD transplantations in our center.CONCLUSION International KPD will increases quality and quantity of living donor kidney transplantation. This could be an important step to solving the kidney shortage with additional benefit of reduced costs, improved quality and increased access for difficult to match incompatible pairs like O blood group patient with non-O donor and sensitized patient. To the best of our knowledge this is first international KPD transplantation from India. | Vivek B Kute Himanshu V Patel Pankaj R Shah Pranjal R Modi Veena R Shah Sayyed J Rizvi Bipin C Pal Priya S Shah Pavan S Wakhare Saiprasad G Shinde Vijay A Ghodela Umesh T Varyani Minaxi H Patel Varsha B Trivedi Hargovind L Trivedi | 2017 | World Journal of Transplantation2017，7，1： | 0 |
| 15 | Six end-stage renal disease patients benefited from first non-simultaneous single center 6-way kidney exchange transplantation in India显示文摘AIM To avoid desensitization protocols and ABO incompatible kidney transplantation(KT) due to high costs and increased risk of infections from intense immunosuppression.METHODS We present institutional ethical review board- approved study of single center 6-way kidney exchange transplantation. The participants comprised ABO incompatibility(n = 1); positive cross-match and/or presence of donor specific antibody(n = 5). The average time required from registration in kidney paired donation(KPD) registry to find suitable donors was 45 d and time required to perform transplants after legal permission was 2 mo. RESULTS Graft and patient survival were 100%, and 100%, respectively. One patient had biopsy-proven acute borderline T cell rejection(Banff update 2013, type 3). Mean serum creatinine was 0.8 mg/dL at 9 mo followup. The waiting time in KPD was short as compared to deceased donor KT. CONCLUSION We report first non-simultaneous, single center, 6-way kidney exchange transplantation from India. Our experience will encourage other centers in India to undertake this practice. | Vivek B Kute Himanshu V Patel Umesh T Varyani Pankaj R Shah Pranjal R Modi Veena R Shah Sayyed J Rizvi Bipin C Pal Priya S Shah Pavan S Wakhare Vijay A Ghodela Saiprasad G Shinde Varsha B Trivedi Minaxi H Patel Hargovind L Trivedi | 2016 | World Journal of Nephrology2016，5，6： | 0 |
| 16 | Increasing access to kidney transplantation for sensitized recipient through three-way kidney paired donation with desensitization: The first Indian report显示文摘The combination of kidney paired donation(KPD) with desensitization represents a promising method of increasing the rate of living donor kidney transplantation(LDKT) in immunologically challenging patients. Patients who are difficult to match and desensitize due to strong donor specific antibody are may be transplanted by a combination of desensitization and KPD protocol with more immunologically favorable donor. We present our experience of combination of desensitization protocol with three-way KPD which contributed to successful LDKT in highly sensitized end stage renal disease patient. All recipients were discharged with normal and stable allograft function at 24 mo follow up. We believe that this is first report from India where three-way KPD exchange was performed with the combination of KPD and desensitization. The combination of desensitization protocol with KPD improves access and outcomes of LDKT. | Vivek B Kute Himanshu V Patel Pankaj R Shah Pranjal R Modi Veena R Shah Sayyed J Rizvi Bipin C Pal Manisha P Modi Priya S Shah Umesh T Varyani Pavan S Wakhare Saiprasad G Shinde Viajay A Ghodela Minaxi H Patel Varsha B Trivedi Hargovind L Trivedi | 2016 | World Journal of Clinical Cases2016，4，10： | 0 |
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