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Zinc Fingers
NR2F1 mutations cause optic atrophy with intellectual disability., Bosch, Daniëlle G. M., Boonstra Nienke F., Gonzaga-Jauregui Claudia, Xu Mafei, de Ligt Joep, Jhangiani Shalini, Wiszniewski Wojciech, Muzny Donna M., Yntema Helger G., Pfundt Rolph, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.303-9, (2014) Abstract
Zebrafish
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Gerhard, Daniela S., Wagner Lukas, Feingold Elise A., Shenmen Carolyn M., Grouse Lynette H., Schuler Greg, Klein Steven L., Old Susan, Rasooly Rebekah, Good Peter, et al. , Genome research, 2004 Oct, Volume 14, Issue 10B, p.2121-7, (2004) Abstract
A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies., Khanna, Hemant, Davis Erica E., Murga-Zamalloa Carlos A., Estrada-Cuzcano Alejandro, Lopez Irma, den Hollander Anneke I., Zonneveld Marijke N., Othman Mohammad I., Waseem Naushin, Chakarova Christina F., et al. , Nature genetics, 2009 Jun, Volume 41, Issue 6, p.739-45, (2009) Abstract
Gene therapy rescues cilia defects and restores olfactory function in a mammalian ciliopathy model., McIntyre, Jeremy C., Davis Erica E., Joiner Ariell, Williams Corey L., Tsai I-Chun, Jenkins Paul M., McEwen Dyke P., Zhang Lian, Escobado John, Thomas Sophie, et al. , Nature medicine, 2012 Sep, Volume 18, Issue 9, p.1423-8, (2012) Abstract
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum., Davis, Erica E., Zhang Qi, Liu Qin, Diplas Bill H., Davey Lisa M., Hartley Jane, Stoetzel Corinne, Szymanska Katarzyna, Ramaswami Gokul, Logan Clare V., et al. , Nature genetics, 2011 Mar, Volume 43, Issue 3, p.189-96, (2011) Abstract
Young Adult
NR2F1 mutations cause optic atrophy with intellectual disability., Bosch, Daniëlle G. M., Boonstra Nienke F., Gonzaga-Jauregui Claudia, Xu Mafei, de Ligt Joep, Jhangiani Shalini, Wiszniewski Wojciech, Muzny Donna M., Yntema Helger G., Pfundt Rolph, et al. , American journal of human genetics, 2014 Feb 6, Volume 94, Issue 2, p.303-9, (2014) Abstract
Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype., Perrault, Isabelle, Estrada-Cuzcano Alejandro, Lopez Irma, Kohl Susanne, Li Shiqiang, Testa Francesco, Zekveld-Vroon Renate, Wang Xia, Pomares Esther, Andorf Jean, et al. , PloS one, 2013, Volume 8, Issue 1, p.e51622, (2013) Abstract
The genetic basis of DOORS syndrome: an exome-sequencing study., Campeau, Philippe M., Kasperaviciute Dalia, Lu James T., Burrage Lindsay C., Kim Choel, Hori Mutsuki, Powell Berkley R., Stewart Fiona, Félix Têmis Maria, van den Ende Jenneke, et al. , Lancet neurology, 2014 Jan, Volume 13, Issue 1, p.44-58, (2014) Abstract
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease., Guo, Dong-Chuan, Papke Christina L., Tran-Fadulu Van, Regalado Ellen S., Avidan Nili, Johnson Ralph Jay, Kim Dong H., Pannu Hariyadarshi, Willing Marcia C., Sparks Elizabeth, et al. , American journal of human genetics, 2009 May, Volume 84, Issue 5, p.617-27, (2009) Abstract
Next-generation sequencing-based molecular diagnosis of a Chinese patient cohort with autosomal recessive retinitis pigmentosa., Fu, Qing, Wang Feng, Wang Hui, Xu Fei, Zaneveld Jacques E., Ren Huanan, Keser Vafa, Lopez Irma, Tuan Han-Fang, Salvo Jason S., et al. , Investigative ophthalmology & visual science, 2013 Jun, Volume 54, Issue 6, p.4158-66, (2013) Abstract
Xylella
Comparative analysis of ESTs involved in grape responses to Xylella fastidiosa infection., Lin, Hong, Doddapaneni Harshavardhan, Takahashi Yuri, and Walker Andrew M. , BMC plant biology, 2007, Volume 7, p.8, (2007) Abstract
Xenopus laevis
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)., Gerhard, Daniela S., Wagner Lukas, Feingold Elise A., Shenmen Carolyn M., Grouse Lynette H., Schuler Greg, Klein Steven L., Old Susan, Rasooly Rebekah, Good Peter, et al. , Genome research, 2004 Oct, Volume 14, Issue 10B, p.2121-7, (2004) Abstract
X Chromosome
130 kb of DNA sequence reveals two new genes and a regional duplication distal to the human iduronate-2-sulfate sulfatase locus., Timms, K. M., Lu F., Shen Y., Pierson C. A., Muzny D. M., Gu Y., Nelson D. L., and Gibbs R. A. , Genome research, 1995 Aug, Volume 5, Issue 1, p.71-8, (1995) Abstract
Finishing a whole-genome shotgun: release 3 of the Drosophila melanogaster euchromatic genome sequence., Celniker, Susan E., Wheeler David A., Kronmiller Brent, Carlson Joseph W., Halpern Aaron, Patel Sandeep, Adams Mark, Champe Mark, Dugan Shannon P., Frise Erwin, et al. , Genome biology, 2002, Volume 3, Issue 12, p.RESEARCH0079, (2002) Abstract
The Drosophila melanogaster Genetic Reference Panel., Mackay, Trudy F. C., Richards Stephen, Stone Eric A., Barbadilla Antonio, Ayroles Julien F., Zhu Dianhui, Casillas Sònia, Han Yi, Magwire Michael M., Cridland Julie M., et al. , Nature, 2012 Feb 9, Volume 482, Issue 7384, p.173-8, (2012) Abstract
Identification of new markers in Xp21 between DXS28 (C7) and DMD., Worley, K. C., Towbin J. A., Zhu X. M., Barker D. F., Ballabio A., Chamberlain J., Biesecker L. G., Blethen S. L., Brosnan P., and Fox J. E. , Genomics, 1992 Aug, Volume 13, Issue 4, p.957-61, (1992) Abstract
Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21., Worley, K. C., Ellison K. A., Zhang Y. H., Wang D. F., Mason J., Roth E. J., Adams V., Fogt D. D., Zhu X. M., and Towbin J. A. , Genomics, 1993 May, Volume 16, Issue 2, p.407-16, (1993) Abstract
Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene., Guo, W., Worley K., Adams V., Mason J., Sylvester-Jackson D., Zhang Y. H., Towbin J. A., Fogt D. D., Madu S., and Wheeler D. A. , Nature genetics, 1993 Aug, Volume 4, Issue 4, p.367-72, (1993) Abstract
Molecular and phenotypic variation in patients with severe Hunter syndrome., Timms, K. M., Bondeson M. L., Ansari-Lari M. A., Lagerstedt K., Muzny D. M., Dugan-Rocha S. P., Nelson D. L., Pettersson U., and Gibbs R. A. , Human molecular genetics, 1997 Mar, Volume 6, Issue 3, p.479-86, (1997) Abstract
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal., Bardoni, B., Zanaria E., Guioli S., Floridia G., Worley K. C., Tonini G., Ferrante E., Chiumello G., McCabe E. R., and Fraccaro M. , Nature genetics, 1994 Aug, Volume 7, Issue 4, p.497-501, (1994) Abstract
Wool
The sheep genome illuminates biology of the rumen and lipid metabolism., Jiang, Yu, Xie Min, Chen Wenbin, Talbot Richard, Maddox Jillian F., Faraut Thomas, Wu Chunhua, Muzny Donna M., Li Yuxiang, Zhang Wenguang, et al. , Science (New York, N.Y.), 2014 Jun 6, Volume 344, Issue 6188, p.1168-73, (2014) Abstract
Wood
Genome, transcriptome, and secretome analysis of wood decay fungus Postia placenta supports unique mechanisms of lignocellulose conversion., Martinez, Diego, Challacombe Jean, Morgenstern Ingo, Hibbett David, Schmoll Monika, Kubicek Christian P., Ferreira Patricia, Ruiz-Duenas Francisco J., Martinez Angel T., Kersten Phil, et al. , Proceedings of the National Academy of Sciences of the United States of America, 2009 Feb 10, Volume 106, Issue 6, p.1954-9, (2009) Abstract
Wolbachia
Widespread lateral gene transfer from intracellular bacteria to multicellular eukaryotes., Dunning Hotopp, Julie C., Clark Michael E., Oliveira Deodoro C. S. G., Foster Jeremy M., Fischer Peter, Muñoz Torres Mónica C., Giebel Jonathan D., Kumar Nikhil, Ishmael Nadeeza, Wang Shiliang, et al. , Science (New York, N.Y.), 2007 Sep 21, Volume 317, Issue 5845, p.1753-6, (2007) Abstract
Functional and evolutionary insights from the genomes of three parasitoid Nasonia species., Werren, John H., Richards Stephen, Desjardins Christopher A., Niehuis Oliver, Gadau Jürgen, Colbourne John K., Werren John H., Richards Stephen, Desjardins Christopher A., Niehuis Oliver, et al. , Science (New York, N.Y.), 2010 Jan 15, Volume 327, Issue 5963, p.343-8, (2010) Abstract
Williams Syndrome
The DNA sequence of human chromosome 7., Hillier, Ladeana W., Fulton Robert S., Fulton Lucinda A., Graves Tina A., Pepin Kymberlie H., Wagner-McPherson Caryn, Layman Dan, Maas Jason, Jaeger Sara, Walker Rebecca, et al. , Nature, 2003 Jul 10, Volume 424, Issue 6945, p.157-64, (2003) Abstract


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