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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2005 | 2 |
2006 | 2 |
2008 | 1 |
2024 | 0 |
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Page 1
Mkks-null mice have a phenotype resembling Bardet-Biedl syndrome.
Hum Mol Genet. 2005 May 1;14(9):1109-18. doi: 10.1093/hmg/ddi123. Epub 2005 Mar 16.
Hum Mol Genet. 2005.
PMID: 15772095
Genetic interaction between Bardet-Biedl syndrome genes and implications for limb patterning.
Tayeh MK, Yen HJ, Beck JS, Searby CC, Westfall TA, Griesbach H, Sheffield VC, Slusarski DC.
Tayeh MK, et al.
Hum Mol Genet. 2008 Jul 1;17(13):1956-67. doi: 10.1093/hmg/ddn093. Epub 2008 Apr 1.
Hum Mol Genet. 2008.
PMID: 18381349
Free PMC article.
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Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function.
Yen HJ, Tayeh MK, Mullins RF, Stone EM, Sheffield VC, Slusarski DC.
Yen HJ, et al. Among authors: tayeh mk.
Hum Mol Genet. 2006 Mar 1;15(5):667-77. doi: 10.1093/hmg/ddi468. Epub 2006 Jan 6.
Hum Mol Genet. 2006.
PMID: 16399798
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Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).
Chiang AP, Beck JS, Yen HJ, Tayeh MK, Scheetz TE, Swiderski RE, Nishimura DY, Braun TA, Kim KY, Huang J, Elbedour K, Carmi R, Slusarski DC, Casavant TL, Stone EM, Sheffield VC.
Chiang AP, et al. Among authors: tayeh mk.
Proc Natl Acad Sci U S A. 2006 Apr 18;103(16):6287-92. doi: 10.1073/pnas.0600158103. Epub 2006 Apr 10.
Proc Natl Acad Sci U S A. 2006.
PMID: 16606853
Free PMC article.
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Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome).
Ferguson PJ, Chen S, Tayeh MK, Ochoa L, Leal SM, Pelet A, Munnich A, Lyonnet S, Majeed HA, El-Shanti H.
Ferguson PJ, et al. Among authors: tayeh mk.
J Med Genet. 2005 Jul;42(7):551-7. doi: 10.1136/jmg.2005.030759.
J Med Genet. 2005.
PMID: 15994876
Free PMC article.
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