scholarly article | Q13442814 |
P356 | DOI | 10.1042/BSR20090009 |
P698 | PubMed publication ID | 19435464 |
P2093 | author name string | Erin N McMurray | |
Jennifer V Schmidt | |||
Eric D Rogers | |||
P2860 | cites work | Alterations in glucose homeostasis in SSTR1 gene-ablated mice. | Q46889446 |
Fine genetic mapping defines the genetic order of Pax9, Tcf3a, and Acrodysplasia (Adp). | Q52212555 | ||
Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
Identification and characterization of two novel brain-derived immunoglobulin superfamily members with a unique structural organization | Q24316343 | ||
Cloning and functional characterization of a family of human and mouse somatostatin receptors expressed in brain, gastrointestinal tract, and kidney | Q24337883 | ||
The FK506-binding protein 25 functionally associates with histone deacetylases and with transcription factor YY1. | Q24535726 | ||
The small subunits of human and mouse DNA polymerase epsilon are homologous to the second largest subunit of the yeast Saccharomyces cerevisiae DNA polymerase epsilon | Q24546252 | ||
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M | Q24654206 | ||
Computational and experimental identification of novel human imprinted genes | Q24684684 | ||
Dapper, a Dishevelled-associated antagonist of beta-catenin and JNK signaling, is required for notochord formation | Q27638891 | ||
Wnt/Frizzled activation of Rho regulates vertebrate gastrulation and requires a novel Formin homology protein Daam1 | Q28214701 | ||
Polar overdominance at the ovine callipyge locus | Q28281525 | ||
Abnormal lung development and cleft palate in mice lacking TGF-beta 3 indicates defects of epithelial-mesenchymal interaction | Q28284617 | ||
Comparative analysis of structure, expression and PSD95-binding capacity of Lrfn, a novel family of neuronal transmembrane proteins | Q28504528 | ||
A crucial role of WW45 in developing epithelial tissues in the mouse | Q28508988 | ||
Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain | Q28511651 | ||
Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1 | Q28589840 | ||
Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice | Q28591920 | ||
Loss of imprinting at the Dlk1-Gtl2 locus caused by insertional mutagenesis in the Gtl2 5' region | Q33259112 | ||
Identification of a new imprinted gene, Rian, on mouse chromosome 12 by fluorescent differential display screening | Q34085531 | ||
Specific expression and regulation of the new melanoma inhibitory activity-related gene MIA2 in hepatocytes | Q34177232 | ||
A census of mammalian imprinting. | Q34430259 | ||
Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding | Q34487703 | ||
Estrogen receptor isoform-specific regulation of the retinoblastoma-binding protein 1 (RBBP1) gene: roles of AF1 and enhancer elements. | Q34551804 | ||
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. | Q35211749 | ||
Tissue-specific expression of Cre recombinase from the Tgfb3 locus | Q36726025 | ||
Mouse CD-RAP/MIA gene: structure, chromosomal localization, and expression in cartilage and chondrosarcoma | Q36853053 | ||
Three Dact gene family members are expressed during embryonic development and in the adult brains of mice | Q38311014 | ||
Cloning of a retinoic acid-sensitive mRNA expressed in cartilage and during chondrogenesis | Q41228936 | ||
TRIM9 is specifically expressed in the embryonic and adult nervous system | Q42520295 | ||
Identification and comparative expression analyses of Daam genes in mouse and Xenopus | Q45144347 | ||
P433 | issue | 2 | |
P304 | page(s) | 119-124 | |
P577 | publication date | 2009-11-23 | |
P1433 | published in | Bioscience Reports | Q2790714 |
P1476 | title | Imprinting analysis in the Acrodysplasia region of mouse chromosome 12. | |
P478 | volume | 30 |
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