| scholarly article | Q13442814 |
| P2093 | author name string | Gilbert DJ | |
| Jenkins NA | |||
| Copeland NG | |||
| Hernandez L | |||
| Piras G | |||
| Stewart CL | |||
| Kozlov S | |||
| Escalante-Alcalde D | |||
| El Kharroubi A | |||
| P2860 | cites work | Regulation of apoptosis and cell cycle arrest by Zac1, a novel zinc finger protein expressed in the pituitary gland and the brain | Q24309817 |
| Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene | Q24312044 | ||
| epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D | Q24314855 | ||
| hZAC encodes a zinc finger protein with antiproliferative properties and maps to a chromosomal region frequently lost in cancer | Q24317330 | ||
| Multiple mouse chromosomal loci for dynein-based motility | Q24329086 | ||
| The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform | Q24678511 | ||
| Identification of a zinc-finger gene at 6q25: a chromosomal region implicated in development of many solid tumors | Q28238130 | ||
| A mouse model for Prader-Willi syndrome imprinting-centre mutations | Q28271033 | ||
| Evidence against a major role of PEG1/MEST in Silver-Russell syndrome | Q28286061 | ||
| Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries | Q29618999 | ||
| Development and applications of a molecular genetic linkage map of the mouse genome | Q33650255 | ||
| Expression of retroviral vectors in transgenic mice obtained by embryo infection | Q33928812 | ||
| Expression of foreign genes from retroviral vectors in mouse teratocarcinoma chimaeras. | Q33932178 | ||
| A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross | Q33956856 | ||
| Differential activity of maternally and paternally derived chromosome regions in mice | Q34198480 | ||
| Role of paternal and maternal genomes in mouse development | Q34261845 | ||
| Completion of mouse embryogenesis requires both the maternal and paternal genomes | Q34267351 | ||
| Muscular dystrophies and the dystrophin-glycoprotein complex | Q34425741 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6q. | Q35431945 | ||
| Variable and tissue-specific hormone resistance in heterotrimeric Gs protein alpha-subunit (Gsalpha) knockout mice is due to tissue-specific imprinting of the gsalpha gene | Q36214949 | ||
| Screening for imprinted genes by allelic message display: identification of a paternally expressed gene impact on mouse chromosome 18 | Q36561256 | ||
| Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality | Q36731073 | ||
| Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus | Q36921900 | ||
| Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome | Q37964406 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| Expression and methylation of imprinted genes during in vitro differentiation of mouse parthenogenetic and androgenetic embryonic stem cell lines | Q41464133 | ||
| Androgenetic mouse embryonic stem cells are pluripotent and cause skeletal defects in chimeras: implications for genetic imprinting | Q41727650 | ||
| Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting | Q46630830 | ||
| Localisation of the imprinted gene neuronatin, Nnat, confirms and refines the location of a second imprinting region on mouse chromosome 2. | Q47738227 | ||
| Comparisons of genomic structures and chromosomal locations of the mouse aldose reductase and aldose reductase-like genes | Q47977298 | ||
| Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest | Q48016474 | ||
| Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M. | Q48060772 | ||
| Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization | Q48071136 | ||
| Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting | Q48084682 | ||
| A functional analysis of imprinting in parthenogenetic embryonic stem cells. | Q52216378 | ||
| Production of chimeras between embryonic stem cells and embryos. | Q52228433 | ||
| High resolution mapping of chromosome 6 deletions in cervical cancer. | Q53422516 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Craniofacial abnormalities, agenesis of the corpus callosum, polysyndactyly and abnormal skin and gut development--the Curry Jones syndrome | Q56384722 | ||
| Loss of expression of the candidate tumor suppressor gene ZAC in breast cancer cell lines and primary tumors | Q57287558 | ||
| Loss of heterozygosity on the long arm of chromosome 6 in breast cancer: possibly four regions of deletion | Q57287621 | ||
| epsilon-sarcoglycan replaces alpha-sarcoglycan in smooth muscle to form a unique dystrophin-glycoprotein complex | Q64381267 | ||
| Detection of frequent allelic loss of 6q23-q25.2 in microdissected human breast cancer tissues | Q73363385 | ||
| Genetics of silver-russell syndrome | Q77146774 | ||
| Paternal uniparental disomy of chromosome 6 and transient neonatal diabetes mellitus | Q77813273 | ||
| Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl | Q78247577 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3308-3315 | |
| P577 | publication date | 2000-05-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines | |
| P478 | volume | 20 |
| Q53413310 | A gain-of-glycosylation mutation associated with myoclonus-dystonia syndrome affects trafficking and processing of mouse ε-sarcoglycan in the late secretory pathway. |
| Q28208083 | A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids |
| Q35221526 | A survey for novel imprinted genes in the mouse placenta by mRNA-seq |
| Q38028387 | A survey of tissue-specific genomic imprinting in mammals |
| Q34063055 | Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models |
| Q35688598 | Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models |
| Q34206423 | Alteration of striatal dopaminergic neurotransmission in a mouse model of DYT11 myoclonus-dystonia |
| Q28296892 | Altered expression and loss of heterozygosity of the LOT1 gene in ovarian cancer |
| Q50683487 | Analysis of imprinted messenger RNA expression during bovine preimplantation development. |
| Q31147226 | Antisense transcripts with FANTOM2 clone set and their implications for gene regulation |
| Q33405733 | At least ten genes define the imprinted Dlk1-Dio3 cluster on mouse chromosome 12qF1 |
| Q63446335 | Biochemistry and Biology of ARHI (DIRAS3), an Imprinted Tumor Suppressor Gene Whose Expression Is Lost in Ovarian and Breast Cancers |
| Q48318024 | Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6 |
| Q24647126 | Characterization of conserved and nonconserved imprinted genes in swine |
| Q34882530 | Chromosome-wide identification of novel imprinted genes using microarrays and uniparental disomies. |
| Q28185777 | Classification and genetics of dystonia |
| Q36804837 | Comparative analysis of human chromosome 7q21 and mouse proximal chromosome 6 reveals a placental-specific imprinted gene, TFPI2/Tfpi2, which requires EHMT2 and EED for allelic-silencing |
| Q36793471 | Cooperativity of imprinted genes inactivated by acquired chromosome 20q deletions |
| Q24677959 | DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency |
| Q31742998 | DNA demethylation reactivates a subset of imprinted genes in uniparental mouse embryonic fibroblasts |
| Q52006521 | Disruption of parental-specific expression of imprinted genes in uniparental fetuses. |
| Q40485526 | Does the cytotoxic effect of transient amyloid oligomers from common equine lysozyme in vitro imply innate amyloid toxicity? |
| Q30497374 | Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce. |
| Q28279818 | Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight |
| Q37239952 | Engineering animal models of dystonia |
| Q38166841 | Epigenetic deregulation of genomic imprinting in humans: causal mechanisms and clinical implications |
| Q37801493 | Epigenetics and the placenta |
| Q36930029 | Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes |
| Q34507201 | Establishment of the primary imprint of the HYMAI/PLAGL1 imprint control region during oogenesis |
| Q24616239 | Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia |
| Q30999843 | Exclusive paternal expression and novel alternatively spliced variants of epsilon-sarcoglycan mRNA in mouse brain. |
| Q48770799 | Expression pattern of Zac1 mouse gene, a new zinc-finger protein that regulates apoptosis and cellular cycle arrest, in both adult brain and along development |
| Q82457009 | Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes |
| Q55010158 | FACS-Seq analysis of Pax3-derived cells identifies non-myogenic lineages in the embryonic forelimb. |
| Q97549607 | Gene expression profiling identifies the role of Zac1 in cervical cancer metastasis |
| Q46581076 | Genetic evidence for a maternal effect locus controlling genomic imprinting and growth |
| Q34407791 | Genome patterns of selection and introgression of haplotypes in natural populations of the house mouse (Mus musculus). |
| Q37642342 | Genome wide screening of candidate genes for improving piglet birth weight using high and low estimated breeding value populations |
| Q21145256 | Genomic imprinting in mammals: emerging themes and established theories |
| Q36436530 | Genomic imprinting in the placenta |
| Q35561940 | Germline and somatic imprinting in the nonhuman primate highlights species differences in oocyte methylation. |
| Q47099407 | Identification of Plagl1/Zac1 binding sites and target genes establishes its role in the regulation of extracellular matrix genes and the imprinted gene network |
| Q33680910 | Identification of a large novel imprinted gene cluster on mouse proximal chromosome 6. |
| Q34994392 | Identification of novel imprinted genes in a genome-wide screen for maternal methylation. |
| Q21092496 | Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution |
| Q34939534 | Identification of the mouse paternally expressed imprinted gene Zdbf2 on chromosome 1 and its imprinted human homolog ZDBF2 on chromosome 2. |
| Q26829945 | Imprinted Zac1 in neural stem cells |
| Q33622341 | Imprinted genes: identification by chromosome rearrangements and post-genomic strategies |
| Q49123992 | Imprinting and expression analysis of a non-coding RNA gene in the mouse Dlk1-Dio3 domain |
| Q37543706 | Imprinting and extraembryonic tissues-mom takes control |
| Q34086461 | Involvement of PLAGL2 in activation of iron deficient- and hypoxia-induced gene expression in mouse cell lines |
| Q28217017 | LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer |
| Q40571620 | Loss of expression of ZAC/LOT1 in squamous cell carcinomas of head and neck |
| Q28592236 | Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome |
| Q41900340 | Lot1 is a key element of the pituitary adenylate cyclase-activating polypeptide (PACAP)/cyclic AMP pathway that negatively regulates neuronal precursor proliferation |
| Q28603472 | Mammalian-specific genomic functions: Newly acquired traits generated by genomic imprinting and LTR retrotransposon-derived genes in mammals |
| Q74312289 | Mechanisms of genomic imprinting |
| Q48760908 | Members of the Plag gene family are expressed in complementary and overlapping regions in the developing murine nervous system. |
| Q36659593 | Metabolic changes in DYT11 myoclonus-dystonia |
| Q37882600 | Milestones in dystonia |
| Q28214758 | Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome |
| Q41878236 | Myoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain. |
| Q28204029 | Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype |
| Q36872209 | Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease |
| Q38867221 | PLAGL1: an important player in diverse pathological processes. |
| Q37089178 | Paternal and maternal genomes confer opposite effects on proliferation, cell-cycle length, senescence, and tumor formation |
| Q33380215 | Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation |
| Q38314252 | Prostate cancer cells use genetic and epigenetic mechanisms for progression to androgen independence. |
| Q46416808 | Reduced striatal D2 receptor binding in myoclonus-dystonia |
| Q28762910 | Retrotransposon silencing by DNA methylation can drive mammalian genomic imprinting |
| Q39172425 | Role of DNA methylation in imprinting disorders: an updated review |
| Q35458473 | Roles of imprinted genes in neural stem cells |
| Q28198998 | Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation |
| Q34465575 | Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions |
| Q37437882 | Spatial link between nucleoli and expression of the Zac1 gene |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q36417552 | The PcG gene Sfmbt2 is paternally expressed in extraembryonic tissues |
| Q28182925 | The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted |
| Q34992967 | The genetics of the Silver-Russell syndrome |
| Q34559930 | The human HYMAI/PLAGL1 differentially methylated region acts as an imprint control region in mice |
| Q42680409 | The mouse Zac1 locus: basis for imprinting and comparison with human ZAC. |
| Q37088920 | The pathophysiological basis of dystonias. |
| Q35207966 | The potential role of gene duplications in the evolution of imprinting mechanisms |
| Q34190554 | The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome |
| Q51992629 | Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promoters. |
| Q24540824 | Transcriptional activities of the zinc finger protein Zac are differentially controlled by DNA binding |
| Q33389173 | Transcriptome-wide identification of novel imprinted genes in neonatal mouse brain |
| Q34097249 | Undetectable and Decreased Expression of KIAA1949 (Phostensin) Encoded on Chromosome 6p21.33 in Human Breast Cancers Revealed by Transcriptome Analysis |
| Q42515181 | White matter abnormalities in gene-positive myoclonus-dystonia |
| Q24301866 | ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome |
| Q37338991 | ZAC1 is up-regulated by hypertonicity and decreases sorbitol dehydrogenase expression, allowing accumulation of sorbitol in kidney cells |
| Q42483072 | Zac1 Regulates the Differentiation and Migration of Neocortical Neurons via Pac1. |
| Q34412930 | Zac1 is expressed in progenitor/stem cells of the neuroectoderm and mesoderm during embryogenesis: differential phenotype of the Zac1-expressing cells during development |
| Q42754267 | Zac1 plays a key role in the development of specific neuronal subsets in the mouse cerebellum. |
| Q53590915 | Zac1 promotes a Müller glial cell fate and interferes with retinal ganglion cell differentiation in Xenopus retina. |
| Q42456228 | Zinc finger protein Zac1 is expressed in chondrogenic sites of the mouse |
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