agonzale's human [12 articles] Export

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

	A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae. [My Copy] European journal of medical genetics (19 September 2009) by Keiko Shimojima, Takehiko Inoue, Yuji Fujii, Kousaku Ohno, Toshiyuki Yamamoto posted to segmentation human by agonzale on 2009-10-05 01:40:31 as
	Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes [My Copy] Developmental Biology, Vol. 254, No. 1. (01 February 2003), pp. 116-130. by S. Settlejr, R. Rountree, A. Sinha, A. Thacker, K. Higgins, D. Kingsley posted to human segmentation by agonzale on 2009-07-09 02:13:22 as
	Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations [My Copy] Scoliosis, Vol. 2, No. 1. (23 September 2007), 13. by Nader Ghebranious, Cathleen Raggio, Robert Blank, et al.Elizabeth Mcpherson, James Burmester, Lynn Ivacic, Kristen Rasmussen, Jennifer Kislow, Ingrid Glurich, F. Stig Jacobsen, Thomas Faciszewski, Richard Pauli, Oheneba B. Adjei, Philip Giampietro posted to human segmentation by agonzale on 2009-07-09 02:11:50 as
	Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes [My Copy] Hum. Mol. Genet., Vol. 18, No. 6. (15 March 2009), pp. 1110-1121. by Mika Asai-Coakwell, Curtis R. French, Ming Ye, et al.Kamal Garcha, Karin Bigot, Anoja G. Perera, Karen Staehling-Hampton, Silvina C. Mema, Bhaskar Chanda, Arcady Mushegian, Steven Bamforth, Michael R. Doschak, Guang Li, Matthew B. Dobbs, Philip F. Giampietro, Brian P. Brooks, Perumalsamy Vijayalakshmi, Yves Sauve, Marc Abitbol, Periasamy Sundaresan, Veronica van Heyningen, Olivier Pourquie, T. Michael Underhill, Andrew J. Waskiewicz, Ordan J. Lehmann posted to human segmentation by agonzale on 2009-07-09 02:11:08 as
	<I>DLL3</I> as a candidate gene for vertebral malformations [My Copy] American Journal of Medical Genetics Part A, Vol. 140A, No. 22. (2006), pp. 2447-2453. by Philip F. Giampietro, Cathleen L. Raggio, Cory Reynolds, et al.Nader Ghebranious, James K. Burmester, Ingrid Glurich, Kristen Rasmussen, Elizabeth Mcpherson, Richard M. Pauli, Sanjay K. Shukla, Sajid Merchant, F. Stig Jacobsen, Thomas Faciszewski, Robert D. Blank posted to human segmentation by agonzale on 2009-07-09 02:02:06 as
	Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype. [My Copy] American journal of human genetics, Vol. 78, No. 1. (January 2006), pp. 28-37. by D. B. Sparrow, G. Chapman, M. A. Wouters, et al.N. V. Whittock, S. Ellard, D. Fatkin, P. D. Turnpenny, K. Kusumi, D. Sillence, S. L. Dunwoodie posted to human segmentation by agonzale on 2009-05-07 06:31:16 as
	Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis. [My Copy] Human molecular genetics, Vol. 17, No. 23. (1 December 2008), pp. 3761-3766. by D. B. Sparrow, E. Guillén-Navarro, D. Fatkin, S. L. Dunwoodie posted to human segmentation by agonzale on 2009-05-07 06:28:27 as
	Abnormal vertebral segmentation and the notch signaling pathway in man. [My Copy] Developmental dynamics : an official publication of the American Association of Anatomists, Vol. 236, No. 6. (June 2007), pp. 1456-1474. by P. D. Turnpenny, B. Alman, A. S. Cornier, et al.P. F. Giampietro, A. Offiah, O. Tassy, O. Pourquié, K. Kusumi, S. Dunwoodie posted to human segmentation by agonzale on 2009-05-07 06:25:47 as
	A missense T (Brachyury) mutation contributes to vertebral malformations. [My Copy] Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, Vol. 23, No. 10. (October 2008), pp. 1576-1583. by N. Ghebranious, R. D. Blank, C. L. Raggio, et al.J. Staubli, E. McPherson, L. Ivacic, K. Rasmussen, F. S. Jacobsen, T. Faciszewski, J. K. Burmester, R. M. Pauli, O. Boachie-Adjei, I. Glurich, P. F. Giampietro posted to human segmentation by agonzale on 2009-05-06 05:56:22 as
	Mutation of the fucose-specific β1,3 N-acetylglucosaminyltransferase LFNG results in abnormal formation of the spine [My Copy] Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Vol. 1792, No. 2. (February 2009), pp. 100-111. by S. Dunwoodie posted to human segmentation by agonzale on 2009-03-20 08:15:34 as
	Identification of oscillatory genes in somitogenesis from functional genomic analysis of a human mesenchymal stem cell model. [My Copy] Developmental biology, Vol. 305 (May 2007), pp. 172-186. by Dilusha A. William, Biagio Saitta, Joshua D. Gibson, et al.Jeremy Traas, Vladimir Markov, Dorian M. Gonzalez, William Sewell, Douglas M. Anderson, Stephen C. Pratt, Eric F. Rappaport, Kenro Kusumi posted to human segmentation by agonzale on 2009-02-03 07:12:39 as
	Network-based global inference of human disease genes [My Copy] Molecular Systems Biology, Vol. 4 (May 2008) by Xuebing Wu, Rui Jiang, Michael Zhang, Shao Li posted to human by agonzale on 2009-02-03 07:12:35 as

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hedgehog	8
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review	6
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notch	5
equation	5
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mackey-glass	5
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agonzale's human [12 articles] Export

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