太傻超级论坛's Archiver

moonol 发表于 2007-6-12 09:06

[Paper Help] 英文全文 Request (Working now)

If you need full-text of a English scientific research paper for Biological, pharmaceutical and Medical Researches, ;`k T&O+T p
you can request it by providing the information as following:
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~T)`IoA.G&t a [b]Title:                                      [/b][b]required[/b]!{4XJd`bh1r!]jQ"j
[b]Author(s):                              [/b][b]required[/b]
3`6va K'u H4i_ [b]Name of Journal:                  [/b][b]required[/b]
y&_#YJdO"X\6gf [b]Year:[/b]
[cYeTa| [b]Volume:[/b]
q!l%y(zHa KVL [b]Issue:[/b]
"AtXQ Sq [b]Page: Start from __ to __[/b]*re;}XH,W4X4~ [Mr
[b]PubMed ID:                            required[/b] R+aPM!t x6_6Q

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Your email box for receiving files:(prefer gmail.com,yahoo.com).z:^BYa'W0c
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[b]Rules:[/b]
1Et,Nz5j/V6t+Z!j   Up to two papers for each request and Up to six papers per ID, per week.6K'gB B;G`I)G
  Paper can not be older than year of 1995. EVa+jdo;b5`
  English publications only. Other lauguages articals are not acceptable.
n#^iEf!~ZJk   Research Articals and Reviews only. News, letters, are not acceptable.
!?9AfC%jS`#}`
^.w(Hi]"~ L;Z   Do not leave your request into my Email boxes and message boxes here.9~ _$At/wta6Dv

P+q|TE   You can post your requests by replying this thread here, I will keep checking this post very two days.
'Z)K#rc.Z [b]  If the paper you want can not be identified by PubMed, It will be less likely that I can get it for you.
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[3D\,P#Q7]TIu/wv Other Aspects:
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[/b]The time to process your request will depends on size of file, journal types, etc. Normally, it will take 2 days and should not longer than one week.;m&IS9gx4B%N
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I will send paper in PDF form mostly that can be open in any PDF reviewer software such as Adobe PDF reader, Devonthink pro, etc.Gb8t j1f-tiYt

vnN M+` Before you submit your request, please use google.com (Enligsh version) to search the paper your want. In this way, you can pretty sure that the paper is not available in a downloadable form.
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|`V8s%a_A7X Thank you and good luck..G1~Cya t4A3b
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[[i] 本帖最后由 moonol 于 2008-7-7 07:24 编辑 [/i]]

flandy 发表于 2007-6-12 22:31

功德一件啊,支持
d#o9UN1gl @ 我们学校的数据库超级好,我要是有空也可以帮忙找
El)@/Zc"GK| G7Uc2b!Iz)jQV9E
[[i] 本帖最后由 flandy 于 2007-6-14 00:29 编辑 [/i]]

卡卡罗特 发表于 2007-6-13 00:20

再次感谢下moonol

kangxz 发表于 2007-6-13 10:32

真乃大侠啊!

lonemen 发表于 2007-6-15 09:03

非常感谢,可是求助要发到哪个版呢?

flandy 发表于 2007-6-15 09:56

直接回复这个帖子,我会不定期来看看,斑竹也会来的kNy~Q!L
不过是生物医学相关的

alfredyu2004 发表于 2007-6-15 13:45

支持一下,大好人啊!

hhades 发表于 2007-6-15 23:37

支持一个sT1m/|5T? X$^.s
大家资源互补互助吧~~

lonemen 发表于 2007-6-16 10:50

[quote]原帖由 [i]flandy[/i] 于 2007-6-15 09:56 发表 [url=http://www.taisha.org/bbs/redirect.php?goto=findpost&pid=8900453&ptid=843050][img]http://www.taisha.org/bbs/images/common/back.gif[/img][/url]+CA2Q F9^V*h
直接回复这个帖子,我会不定期来看看,斑竹也会来的,X}!}%[ B(tN
不过是生物医学相关的 [/quote]
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好的,非常感谢! akXj,Q3X
不知道可以求整本书不?

天天灌水 发表于 2007-6-16 20:49

回复 #2 flandy 的帖子

你们学校数据库权限很高吗?哪里啊,能不能偷偷告诉我?

moonol 发表于 2007-6-17 11:49

sorry, I can not do that..school ID links to my bank account.:)

天天灌水 发表于 2007-6-17 16:53

哦,国外高校数据库总的来说确实比一般国内权限要高不少

flandy 发表于 2007-6-18 10:56

[quote]原帖由 [i]天天灌水[/i] 于 2007-6-16 20:49 发表 [url=http://bbs.taisha.org/redirect.php?goto=findpost&pid=8910499&ptid=843050][img]http://bbs.taisha.org/images/common/back.gif[/img][/url]2?*SqgWb/B"D8t
你们学校数据库权限很高吗?哪里啊,能不能偷偷告诉我? [/quote]n*b2R"q-}
不行,PID account才能登陆

天天灌水 发表于 2007-6-18 20:52

原来都是国外的啊

风蚀 发表于 2007-6-20 01:24

回复 #1 moonol 的帖子

GREAT!!!!::80 ::p7

cryptlord 发表于 2007-6-20 18:39

楼主好人啊。。。。。。。::z4

cryptlord 发表于 2007-6-22 15:50

title: Fresh and dry. )\8q ~'ReS;E7i
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author: Philip Ball
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%Qp]`d#OGY\ journal: nature.'e$hS~Dm{+f"G.N
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year: July 2000.
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Philip Ball finds out how a kind of sugar might help preserve things as diverse as fruit and frozen human tissue.
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别的信息不清楚了,多谢各位帮忙!我的邮箱:   [email]ursoulismine@gmail.com[/email]

Maxyuan 发表于 2007-6-22 20:49

那个......可以帮我找找关于"LEPTIN" 方面的文章么?最好是能有老美教授的邮箱的那些版本,或者一些REVIEW比较好.想知道有哪些教授在做这个东西^^?.X;PQF)R
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对不起,因为目前自己也不是非常了解具体内容,所以只能给这么点信息,可能有点乱.......对不起如果您有时间的话就简单帮帮忙吧,不管怎样,小弟谢过先.....
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7r*GcH/\x P$u;P 小弟的邮箱....    [email]maxyuan1007@gmail.com[/email]
8US+jTC k%P%d ::p4

moonol 发表于 2007-6-23 01:38

回复 #18 Maxyuan 的帖子

if you do not know what you want, other people will less likely know...
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8J.^#IiT+w] Keep looking for and let me know.

moonol 发表于 2007-6-23 01:40

I think you request a news rather than a research article..And I do not have right to access Nature news for you.T8@PY%v~ rW
May someother people help you out..
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Mh(\Z.C1?JM [quote]原帖由 [i]cryptlord[/i] 于 2007-6-22 01:50 发表 [url=http://bbs.taisha.org/redirect.php?goto=findpost&pid=8959004&ptid=843050][img]http://bbs.taisha.org/images/common/back.gif[/img][/url]
-Rj2r ^;b*VQ\ title: Fresh and dry. 6j3Ov7|fL
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author: Philip Ball
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s+bi9Z!FF4^%v_ journal: nature.
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year: July 2000.
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Philip Ball finds out how a kind of sugar might help preserve things as diverse as fruit and frozen human ... [/quote]

lzen5 发表于 2007-6-23 12:10

is this what it is?
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this is the text version, not sure how legal this is, but anyway.&Om~}C9B0y

Z0[l7H/_ I cant find the one you want, do you have the issue number.
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Biophysics: Science in motion:l0V3F8Bc4v
Philip Ball1ue3xuO
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'If it moves, it's biology', goes the saying, but the moment one asks how it moves, physics intervenes. Between the release of chemical energy and the buzz of a fly's wing there is a host of minor mechanical miracles. At the other end of the scale, cooperative motions of groups of organisms ranging from bacteria to fish and humans can influence the movements of individuals. Can it be a coincidence that both fish and slime mould cells swarm in the same patterns (Fig. 1)? A workshop  in Budapest last month showed how physical and biological sciences can collaborate to explain these miracles of motion.
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e F y]#w'N Figure 1: Swirling vortex motion is a mode of collective swarming behaviour exhibited by both fish (left) and slime mould cells (right).
,KG]XpOA~ L High resolution image and legend (46K)
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Motion in biology is a cascade of mechanical transduction processes, from the molecular scales of time and length upwards. At every level in this hierarchy, biological motion provides perhaps the ideal testing ground for the current migration of physicists towards biological problems. At the molecular level, the two have long been blended in conventional biophysics, which has been revitalized by single-molecule probe techniques. It is hard to imagine how, without these, one could unravel the secrets of muscle proteins such as titin — the spring that gives relaxed muscle its elasticity. For example, the inequivalence of stretching and contracting in individual titin molecules can be attributed to rapid unfolding and slow refolding of repetitive protein domains (M. Kellermayer, Pécs Univ., Hungary).HP6c&Mh
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But whereas the movements of motor proteins like myosin and kinesin and springs like titin are being decoded residue by residue, it appears that something else may be needed to convert protein movements into the motion of whole cells. Migrating cells are central to embryo development and wound healing.@ `:^&N c5P{H
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Myosin typically collects at the trailing edge of the cell to pull it in the direction of motion, whereas a polymerizing network of actin pushes the leading edge forward (G. Borisy, Univ. Wisconsin-Madison). How can actin, a relatively limp filamentary polymer, develop any force to push on the cell membrane? The answer, it seems, is that repeated branching of the polymers, at an angle close to 70°, ensures a constant supply of short filaments at the front edge of the network. These are stiff enough to generate the necessary force. The branching is initiated on the inside of the membrane itself by a membrane-bound protein called Wasp, which activates a second protein, Arp 2/3, to secure itself to actin and provide a junction for a branching filament. MH }T!T

E(D!UBI'Sn But how do new actin monomers add to the advancing tip if it is pushing against the membrane? Here help is on hand from physics, specifically from George Oster's idea of a brownian ratchet. Thermal fluctuations of the flexible actin filaments expose the tip long enough for a new monomer to attach. Once the tip springs back, it ratchets the membrane forward by the length of one monomer. Brownian ratchets have found a life of their own in the physics literature; it is good to know this amounts to more than idle curiosity.
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4}1s|6C^y5v`*\ Granted that cells move, how do they know where to go? Under some circumstances — for example, during chick embryogenesis — tracking specific cells labelled with multicoloured fluorescent proteins seems to indicate a more or less random walk (R. Lansford, California Inst. Technol.). But in vitro studies of nerve cells known as astrocytes seem to show directional streaming motions into unpopulated areas (A. Czirók, Eötvös Univ., Budapest). M. Abercrombie suggested 50 years ago that mutual adhesion was enough to guarantee directional motion at the leading edge of a tissue. But there is directionality behind this edge too, which demands a more complex model.a1_*k1xs;f3_
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Commonly, cell migration is guided by trails of attractant and repellent chemicals: the process of chemotaxis. Single-celled organisms apply this trick too, finding safety in numbers in times of stress. The best studied of these systems is the slime mould Dictyostelium discoideum, which aggregates into a multicellular 'slug' — a kind of 'super-organism' — when food is short. The slug cells differentiate into two types: one forms a long stalk, the other a 'fruiting body' containing spores, which will survive almost indefinitely until revived by favourable conditions. Virtually all stages of this process can now be modelled by making some simple assumptions about cell-to-cell interactions (H. Levine, Univ. California, San Diego).
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K~;b*g6E$K Following migration, the spontaneous sorting of young cells into regions of different cell type can create coherent structures in tissues. This may be nothing more than a variation of the kind of phase separation observed between immiscible fluids (G. Forgács, Clarkson Univ., Potsdam; J. Glazier, Univ. Notre Dame). Differential adhesion between the various cell types, which is mediated by adhesion molecules at the cell surface, may create something analogous to surface tension for a cell cluster, and energy minimization would then take care of the rest. But, as ever in biology, one cannot take it for granted that variables such as surface tension will not change over time in an active cell.
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At the ecosystem level, the 'why' of aggregation behaviour is not so obviously answered as for embryo cells or slime moulds. For animals that form groups, the benefits may depend on a delicate balance between such factors as foraging efficiency, distribution of the spoils and chances of attracting predators (J. Parrish, Univ. Washington). The diversity of spatial patterns arising from the tendency to aggregate offers rich grounds for physical modelling, and is as yet little understood.
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Human behaviour offers another layer of complication: the veneer of social conventions. In social sciences the tradition has been to assume that these dominate — that patterns of motion are dictated primarily by considerations such as courtesy. Hence the challenge posed by simulations in which people are represented by particles moving under little more compunction than that for a particular velocity and for collision avoidance (D. Helbing, Dresden Univ. Technol.). It is unnerving to watch these streams of disk-shaped pedestrians spontaneously arrange themselves into counter-flowing streams in a corridor, or passing in groups through a door before standing back and giving a chance to those coming in the other direction. And most chilling of all is to watch these automata converge on a narrow bottleneck under conditions of mass panic, and collectively block the exit in the crush to escape.'{ MG'y ?M.l

Ket%hLEG There are useful lessons for both parties from this kind of meeting between biology and physics. Even the most conscientious of physicists cannot expect to get all the necessary information from a textbook, nor to be confident without input from biologists that the neglected details are really dispensable or the resemblances between model and experiment more than skin deep. The biologists can learn that approximations are permissible even in the most complex of systems, and that complex behaviour can (even if that does not mean it must) arise from simple principles. As one speaker remarked, to make the interaction work, "we all have to be in the same room."

moonol 发表于 2007-6-23 14:32

thanx Lzen5

moonol 发表于 2007-7-15 00:45

奇怪,大家都想陶瓷.但是都不想读文章.
0FD_j](r_ 那怎么行,呵呵

d.rain 发表于 2007-7-15 09:24

陶瓷是申请以后的事了。。。以后的事。。根据你申请的教授的研究方向,多读他的文章,去陶瓷

liuruya212 发表于 2007-11-4 03:04

Publication Type: Journal Article; Research Support, Non-U.S. Gov't 9r*y&{9}2D_ k+]"N)s
Title: Generation of a constitutively active mutant of human GPR48/LGR4, a G-protein-coupled receptor. 6B7l Br^l;D#E:GAu
Author(s): Gao, Yun; Kitagawa, Kyoko; Shimada, Mai; Uchida, Chiharu; Hattori, Takayuki; Oda, Toshiaki; Kitagawa, Masatoshi 9x*W9h(gR2E^
Source:  Hokkaido Igaku Zasshi 81 (2) : 101-5, 107, 109 2006 Mar ][mO Q'm
ISSN: 0367-6102
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V4j xe2}8Seix Title: Expression pattern of the orphan receptor LGR4/GPR48 gene in the mouse 9Kil;r o
Author(s): Van Schoore G, Mendive F, Pochet R, Vassart G
4YY$?MU Source: HISTOCHEMISTRY AND CELL BIOLOGY 124 (1): 35-50 JUL 2005 .{*hz'W4aiX+H
IDS Number: 961GI DjP3t'X)j9e}
ISSN: 0948-6143 @i%~COI

1K`@0ZrtY;d Cytogenet Cell Genet. 2000;89(1-2):2-5.
&d'MA"Xssu Chromosomal localization of GPR48, a novel glycoprotein hormone receptor like GPCR, in human and mouse with radiation hybrid and interspecific backcross mapping.
6b8xB,o(R,q[-[3s;n6_:A Loh ED, Broussard SR, Liu Q, Copeland NG, Gilbert DJ, Jenkins NA, Kolakowski LF Jr.
0E;~"|)bSAv3`L PMID: 10894923 [PubMed - indexed for MEDLINE]^ ?EI8l(f!Gd
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我想要三篇文章。谢谢楼主啦!!!真是大好人呀!!!!

liuruya212 发表于 2007-11-4 03:05

对不起,忘了留email::p4
6?J0rn%rg s [email]liuruya212@gmail.com[/email]

moonol 发表于 2007-11-4 14:34

the second one is sent to your mailbox..the first and third one are in process of delivery. may take 2 ~3days

moonol 发表于 2007-11-7 04:15

回复 25# liuruya212 的贴子

all you three paper are sent to your gmail box..-BC_[K Q ['I
please let me know if you do not get them..i just can keep the copyright of these papers for one week.
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[[i] 本帖最后由 moonol 于 2007-11-6 14:17 编辑 [/i]]

沧海逍遥 发表于 2007-11-7 22:06

Thanks a million!!sf&BMf9d
You did a great job!#aj$g5H9s:e ~"t
Title: Improved Production of Mycelial Biomass and Ganoderic Acid by Submerged Culture    of Ganoderma lucidum SB97 Using Complex Media
hJKYQ%[[o&l Author: Peng Xu, Zhong-Yang Ding, Zhu Qian, Chang-Xin Zhao and Ke-Chang Zhang@2L8Z6n~4^
Journal: Enzyme and Microbial TechnologywI9S!~9p
Year: 2007, article in press0S%t8tN/H,p;iQ
My e-mail: [email]xupeng1122@hotmail.com[/email]

moonol 发表于 2007-11-11 00:34

回复 29# 沧海逍遥 的贴子

paper is sent to your mail box

lockeryin 发表于 2007-11-25 22:39

IDrugs. 2005 Jun;8(6):491-6.9]iv[y
Receptorome screening for CNS drug discovery.
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Vortherms TA, Roth BL. _6H;X3B*i~4O0B

3h m)@c"t+G9k:Q Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, OH 44106-4935, USA.
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^5Lk#?d"q/tG Z An estimated 50% of currently marketed drugs target G protein-coupled receptors (GPCRs) for a wide variety of indications, including central nervous system (CNS) disorders. Although drug discovery efforts have focused on GPCRs, less than 10% of GPCRs are currently used as drug targets. Thus, GPCRs continue to represent a significant opportunity for future CNS drug development. Identifying the molecular targets of psychoactive compounds may result in the elucidation of novel targets for CNS drug discovery. This commentary will describe discovery-based approaches and provide several recent examples of novel ligand-receptor interactions discovered through systematic screening of the 'receptorome'.
#w]h'X$Z^ d
H+prF#dO z,非常感谢,发到我的MSN邮箱即可,再次感谢。
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tZ`2Kvnn [[i] 本帖最后由 lockeryin 于 2007-11-27 00:51 编辑 [/i]]

moonol 发表于 2007-11-27 00:53

WE are in holiday...
w,x0q0z},^-s5^ You have to wait 2~3 days.. The request is still in process

lockeryin 发表于 2007-11-27 21:17

[quote]原帖由 [i]moonol[/i] 于 2007-11-27 00:53 发表 [url=http://e.taisha.org/redirect.php?goto=findpost&pid=10055001&ptid=843050][img]http://e.taisha.org/images/common/back.gif[/img][/url]6dp H#P9a[fp%oN
WE are in holiday... \ zt.q!Vm
You have to wait 2~3 days.. The request is still in process [/quote]
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Et6aQb:FS OK,打搅,感谢。

moonol 发表于 2007-11-28 05:29

i sent the paper into your hotmail box

lockeryin 发表于 2007-11-28 20:27

[quote]原帖由 [i]moonol[/i] 于 2007-11-28 05:29 发表 [url=http://e.taisha.org/redirect.php?goto=findpost&pid=10061135&ptid=843050][img]http://e.taisha.org/images/common/back.gif[/img][/url]m!BR%dT2G d8S
i sent the paper into your hotmail box [/quote]j(_H}Z
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万分感谢,这篇文章让我的同学都试过了,都说要付费,很佩服楼主的搜文章的本领,哈哈!

jonathanlgd 发表于 2007-12-1 23:20

Title:Mesenchymal stem cells within tumour stroma promote breast cancer metastasis
@7\'CAVn Author(s):Karnoub AE, Dash AB, Vo AP, Sullivan A, Brooks MW, Bell GW, Richardson AL, Polyak K, Tubo R, Weinberg RA:kt(\V-T
Name of Journal: nature
*~dC[Kh} Year:2007
]q?0rY\ Volume:449x*A:mA$K LPs
Issue:7162+k]+[0Ya
Page: Start from 557 to 563
`)@A,iPV7D thanks a lot !!!   great help for me!!     my E-mail:      [email]jonathanlgd@163.com[/email]

moonol 发表于 2007-12-2 01:53

回复 36# jonathanlgd 的贴子

it is a good paper!...
O8cylPC already sent to your email box

jonathanlgd 发表于 2007-12-3 23:33

::16 paper received and it can be read totally. thanks a lot !!! ::31 ::31  Maybe I want some other  papers   in   next  few days becouse our library is short of  enough   resources.  ::p6       thank you again !!!!:loveliness:

jonathanlgd 发表于 2007-12-6 23:06

two papers ,thank you very much!!
UnNrDc:?O-zA p^:Bw Title:  Differential gene expression associated with migration of mesenchymal stem cells to conditioned medium from tumor cells or bone marrow cells.
/fO v8_(r Author(s): Menon LG, Picinich S, Koneru R, Gao H, Lin SY, Koneru M, Mayer-Kuckuk P, Glod J, Banerjee D.(c"y|!@1ypw
Name of Journal: Stem Cells.
$q.O!ag'X;p7v Year:2007@_BY7wnQ I!m
Volume: 25C\:o.W;nn J [
Issue: 2}`? wM h
Page: 520-528
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Pua;j:sZ$R$MF Title:  Mesenchymal stem cells inhibit proliferation and apoptosis of tumor cells: impact on in vivo tumor growth.9@Q OJ$@
Author(s): Ramasamy R, Lam EW, Soeiro I, Tisato V, Bonnet D, Dazzi F9p9{:k&~)et,b
Name of Journal: Leukemia.0R!w~Z3{]_6i w-u%h
Year:2007!}b&?1S${](HR
Volume:21:s'k+w.iC
Issue:21C_ nw3klo!]&\?
Page:304-310^w@:t*hZ*|_*AK1E
thanks a lot !!!   ::31 ::31    my E-mail:      [email]jonathanlgd@163.com[/email]

moonol 发表于 2007-12-7 04:32

回复 39# jonathanlgd 的贴子

paper sent

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