journal888's Mykytyn:K [5 articles] Export Sort

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	Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin [My Copy] Proc Natl Acad Sci U S A, Vol. 101, No. 47. (2004), pp. 16588-93. by D. Y. Nishimura, M. Fath, R. F. Mullins, et al.C. Searby, M. Andrews, R. Davis, J. L. Andorf, K. Mykytyn, R. E. Swiderski, B. Yang, R. Carmi, E. M. Stone, V. C. Sheffield posted to bbs cilia mouse 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

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journal888's Mykytyn:K [5 articles] Export Sort

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