journal888's human [12 articles] Export

Recent papers added to journal888's library classified by the tag human. You can also see everyone's human.

	Cilium-generated signaling and cilia-related disorders [My Copy] Laboratory Investigation, Vol. aop, No. current. (21 February 2005) by Junmin Pan, Qian Wang, William J. Snell posted to cilia disease human ift review by journal888 on 2005-05-13 15:21:51 as
	Novel association of RP1 gene mutations with autosomal recessive retinitis pigmentosa. [My Copy] J Med Genet, Vol. 42, No. 5. (May 2005), pp. 436-438. by S. Khaliq, A. Abid, M. Ismail, et al.A. Hameed, A. Mohyuddin, P. Lall, A. Aziz, K. Anwar, S. Q. Mehdi posted to human retinitis-pigmentosa by journal888 on 2005-05-07 01:32:36 as
	Cilia and flagella revealed: from flagellar assembly in Chlamydomonas to human obesity disorders [My Copy] Cell, Vol. 117, No. 6. (2004), pp. 693-7. by W. J. Snell, J. Pan, Q. Wang posted to axoneme bibtex-import chlamy cilia disease human review by journal888 on 2005-04-23 06:42:38 as
	Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2) [My Copy] Hum Mol Genet, Vol. 10, No. 8. (2001), pp. 865-74. by D. Y. Nishimura, C. C. Searby, R. Carmi, et al.K. Elbedour, L. V. Van Maldergem, A. B. Fulton, B. L. Lam, B. R. Powell, R. E. Swiderski, K. E. Bugge, N. B. Haider, A. E. Kwitek Black, L. Ying, D. M. Duhl, S. W. Gorman, E. Heon, A. Iannaccone, D. Bonneau, L. G. Biesecker, S. G. Jacobson, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:28 as
	Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly. [My Copy] Proc Natl Acad Sci U S A, Vol. 101, No. 23. (Jun 2004), pp. 8664-9. by Kirk Mykytyn, Robert F. Mullins, Michael Andrews, et al.Annie P. Chiang, Ruth E. Swiderski, Baoli Yang, Terry Braun, Thomas Casavant, Edwin M. Stone, Val C. Sheffield posted to bbs cilia flagella human by journal888 on 2005-04-23 06:42:27 as
	Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome [My Copy] Nat Genet, Vol. 31, No. 4. (2002), pp. 435-8. by K. Mykytyn, D. Y. Nishimura, C. C. Searby, et al.M. Shastri, H. J. Yen, J. S. Beck, T. Braun, L. M. Streb, A. S. Cornier, G. F. Cox, A. B. Fulton, R. Carmi, G. Luleci, S. C. Chandrasekharappa, F. S. Collins, S. G. Jacobson, J. R. Heckenlively, R. G. Weleber, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:27 as
	Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1) [My Copy] Am J Hum Genet, Vol. 72, No. 2. (2003), pp. 429-37. by K. Mykytyn, D. Y. Nishimura, C. C. Searby, et al.G. Beck, K. Bugge, H. L. Haines, A. S. Cornier, G. F. Cox, A. B. Fulton, R. Carmi, A. Iannaccone, S. G. Jacobson, R. G. Weleber, A. F. Wright, R. Riise, R. C. Hennekam, G. Luleci, S. Berker Karauzum, L. G. Biesecker, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:27 as
	Identification of the gene that, when mutated, causes the human obesity syndrome BBS4 [My Copy] Nat Genet, Vol. 28, No. 2. (2001), pp. 188-91. by K. Mykytyn, T. Braun, R. Carmi, et al.N. B. Haider, C. C. Searby, M. Shastri, G. Beck, A. F. Wright, A. Iannaccone, K. Elbedour, R. Riise, A. Baldi, A. Raas Rothschild, S. W. Gorman, D. M. Duhl, S. G. Jacobson, T. Casavant, E. M. Stone, V. C. Sheffield posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:27 as
	Distribution of Indian hedgehog and its receptors patched and smoothened in human chronic pancreatitis [My Copy] J Endocrinol, Vol. 178, No. 3. (2003), pp. 467-78. by H. Kayed, J. Kleeff, S. Keleg, M. W. Buchler, H. Friess posted to hedgehog human bibtex-import by journal888 on 2005-04-23 06:42:22 as
	Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome [My Copy] Nat Genet, Vol. 26, No. 1. (2000), pp. 67-70. by N. Katsanis, P. L. Beales, M. O. Woods, et al.R. A. Lewis, J. S. Green, P. S. Parfrey, S. J. Ansley, W. S. Davidson, J. R. Lupski posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:22 as
	Molecular genetics of autosomal recessive polycystic kidney disease [My Copy] Mol Genet Metab, Vol. 81, No. 2. (2004), pp. 75-85. by P. C. Harris, S. Rossetti posted to human pkd bibtex-import by journal888 on 2005-04-23 06:42:22 as
	Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport [My Copy] Genes Dev, Vol. 18, No. 13. (2004), pp. 1630-42. by O. E. Blacque, M. J. Reardon, C. Li, et al.J. Mccarthy, M. R. Mahjoub, S. J. Ansley, J. L. Badano, A. K. Mah, P. L. Beales, W. S. Davidson, R. C. Johnsen, M. Audeh, R. H. Plasterk, D. L. Baillie, N. Katsanis, L. M. Quarmby, S. R. Wicks, M. R. Leroux posted to bbs cilia human bibtex-import by journal888 on 2005-04-23 06:42:16 as

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bibtex-import	310
pancreas	87
hedgehog	37
cilia	31
diabetes	23
review	22
smo	15
stem-cell	14
human	12
mouse	11
beta-cell	10
ift	10
bbs	9
endoderm	8
shh	7
zebrafish	7
drosophila	5
insulin	5
wnt	5
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ptc	4
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enu	3
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knockout	2
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node	2
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polaris	2
tg737	2
ablation	1
alpha-cell	1
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cloning	1
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pericentrin	1
phosphorylation	1
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pkd2	1
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ra	1
retinitis-pigmentosa	1
revire	1
rfx4	1
skin	1
small-molecule	1
sox17	1
sprouty	1
ventricle	1
xenopus	1

journal888's human [12 articles] Export

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