Title: A systematic search for new mammalian noncoding RNAs indicates little conserved intergenic transcription.
Journal: BMC Genomics. 2005; 6: 104
Authors: Babak T, Blencowe BJ, Hughes TR.
More
Title: Microarray analysis of fiber cell maturation in the lens.
Journal: FEBS Lett. Author manuscript; available in PMC 2006 March 15.
PMCID: 1401504
Authors: Ivanov D, Dvoriantchikova G, Pestova A, Nathanson L, Shestopalov VI.
More
Title: 12-oxo-phytodienoic acid triggers expression of a distinct set of genes and plays a role in wound-induced gene expression in Arabidopsis.
Journal: Plant Physiol, Vol 139, Issue 3: 1268-83
Authors: Nozomi Taki, Yuko Sasaki-Sekimoto, Takeshi Obayashi, Akihiro Kikuta, Koichi Kobayashi, Takayuki Ainai, Kaori Yagi, Nozomu Sakurai, Hideyuki Suzuki, Tatsuru Masuda, Ken-ichiro Takamiya, Daisuke Shibata, Yuichi Kobayashi and Hiroyuki Ohta
More
Title: 13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients.
Journal: Journal of Medical Genetics 2007;44:e60
Authors: Lucia Ballarati, Elena Rossi, Maria Teresa Bonati, Stefania Gimelli, Paola Maraschio, Palma Finelli, Sabrina Giglio, Elisabetta Lapi, Maria Francesca Bedeschi, Silvana Guerneri, Giulia Arrigo, Maria Grazia Patricelli, Teresa Mattina, Oriana Guzzardi, Vanna Pecile, Adalgisa Police, Gioacchino Scarano, Lidia Larizza, Orsetta Zuffardi, Daniela Giardino
More
Title: 2-methoxyestradiol inhibits the anaphase-promoting complex and protein translation in human breast cancer cells.
Journal: Cancer Res. 2007 Jan 15;67(2):702-8.
Authors: Bhati R, Gokmen-Polar Y, Sledge GW Jr, Fan C, Nakshatri H, Ketelsen D, Borchers CH, Dial MJ, Patterson C, Klauber-DeMore N.
More
Title: 22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
Journal: Am J Hum Genet. 2008 Jan;82(1):214-21
Authors: Ben-Shachar S, Ou Z, Shaw CA, Belmont JW, Patel MS, Hummel M, Amato S, Tartaglia N, Berg J, Sutton VR, Lalani SR, Chinault AC, Cheung SW, Lupski JR, Patel A
More
Title: A 1 Mb minimal amplicon at 8p11–12 in breast cancer identifies new candidate oncogenes.
Journal: Oncogene (2005) 24, 5235–5245
Authors: Maria J Garcia, Jessica C M Pole, Suet-Feung Chin, Andrew Teschendorff, Ali Naderi, Hilal Ozdag, Maria Vias, Tanja Kranjac, Tatiana Subkhankulova, Claire Paish, Ian Ellis, James D Brenton, Paul A W Edwards and Carlos Caldas
More
Title: A 17p11.2 germline deletion in a patient with Smith-Magenis syndrome and neuroblastoma.
Journal: J Med Genet. 2005 Jan;42(1):e3.
Authors: Hienonen T, Sammalkorpi H, Isohanni P, Versteeg R, Karikoski R, Aaltonen LA.
More
Title: A 2.6 Mb deletion of 6q24.3–25.1 in a patient with growth failure, cardiac septal defect, thin upperlip and asymmetric dysmorphic ears.
Journal: Eur J Med Genet. 2007 Jul-Aug;50(4):315-21
Authors: R. Caselli, M.A. Mencarelli, F.T. Papa, V. Uliana, S. Schiavone, M. Strambi, C. Pescucci, F. Ariani, V. Rossi, I. Longo, I. Meloni, A. Renieri and F. Mari
More
Title: A 580kb microdeletion in 17q21.32 associated with mental retardation, microcephaly, cleft palate, and cardiac malformation.
Journal: Eur J Med Genet. 2008 Jan-Feb;51(1):74-80. Epub 2007 Oct 2
Authors: Rooryck C, Burgelin I, Stef M, Taine L, Thambo JB, Lacombe D, Arveiler B
More
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
>