Pages that link to "Q33964982"
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The following pages link to Identification of a methylation imprint mark within the mouse Gnas locus (Q33964982):
Displaying 50 items.
- Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution (Q21092496) (← links)
- Methylation levels at IGF2 and GNAS DMRs in infants born to preeclamptic pregnancies (Q21266667) (← links)
- A novel STX16 deletion in autosomal dominant pseudohypoparathyroidism type Ib redefines the boundaries of a cis-acting imprinting control element of GNAS (Q24531505) (← links)
- Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS-based heterotopic ossification (Q24654579) (← links)
- Global transcriptome analysis of the C57BL/6J mouse testis by SAGE: evidence for nonrandom gene order (Q24793092) (← links)
- The GNAS complex locus and human diseases associated with loss-of-function mutations or epimutations within this imprinted gene (Q26852157) (← links)
- Gene Dosage Effects at the Imprinted Gnas Cluster (Q27316512) (← links)
- GNAS locus and pseudohypoparathyroidism (Q28235038) (← links)
- Imprinting of the G(s)alpha gene GNAS1 in the pathogenesis of acromegaly (Q28360510) (← links)
- Identification of the control region for tissue-specific imprinting of the stimulatory G protein alpha-subunit (Q28508007) (← links)
- Maternal inheritance of the Gnas cluster mutation Ex1A-T affects size, implicating NESP55 in growth (Q28592629) (← links)
- Targeted deletion of the Nesp55 DMR defines another Gnas imprinting control region and provides a mouse model of autosomal dominant PHP-Ib (Q28593878) (← links)
- The evolution of mammalian genomic imprinting was accompanied by the acquisition of novel CpG islands (Q28742697) (← links)
- Selective resistance to parathyroid hormone caused by a novel uncoupling mutation in the carboxyl terminus of G alpha(s). A cause of pseudohypoparathyroidism type Ib. (Q31456359) (← links)
- The importance of imprinting in the human placenta. (Q33628787) (← links)
- A comprehensive transcript map of the mouse Gnas imprinted complex (Q33678495) (← links)
- Imprinted Nesp55 influences behavioral reactivity to novel environments (Q33724476) (← links)
- The function of non-coding RNAs in genomic imprinting (Q33761870) (← links)
- Alternative Gnas gene products have opposite effects on glucose and lipid metabolism. (Q33821507) (← links)
- Uncoupling antisense-mediated silencing and DNA methylation in the imprinted Gnas cluster. (Q33859387) (← links)
- A novel variant of Inpp5f is imprinted in brain, and its expression is correlated with differential methylation of an internal CpG island (Q33862945) (← links)
- Discordance between genetic and epigenetic defects in pseudohypoparathyroidism type 1b revealed by inconsistent loss of maternal imprinting at GNAS1 (Q33905190) (← links)
- Expanded methyl-sensitive cut counting reveals hypomethylation as an epigenetic state that highlights functional sequences of the genome (Q33908086) (← links)
- Retrotransposition and genomic imprinting (Q34022943) (← links)
- Deletion of the noncoding GNAS antisense transcript causes pseudohypoparathyroidism type Ib and biparental defects of GNAS methylation in cis (Q34032076) (← links)
- The role of GNAS and other imprinted genes in the development of obesity. (Q34099397) (← links)
- Imprints of disease at GNAS1. (Q34206380) (← links)
- A GNAS1 imprinting defect in pseudohypoparathyroidism type IB (Q34457845) (← links)
- The role of tissue-specific imprinting as a source of phenotypic heterogeneity in human disease. (Q34467097) (← links)
- Potent constitutive cyclic AMP-generating activity of XLαs implicates this imprinted GNAS product in the pathogenesis of McCune-Albright syndrome and fibrous dysplasia of bone. (Q34493975) (← links)
- Pseudohypoparathyroidism: one gene, several syndromes (Q34547669) (← links)
- Effects of deficiency of the G protein Gsα on energy and glucose homeostasis (Q34883776) (← links)
- Ontogeny of CpG island methylation and specificity of DNMT3 methyltransferases during embryonic development in the mouse (Q34968030) (← links)
- The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals (Q35113579) (← links)
- Epigenetic properties and identification of an imprint mark in the Nesp-Gnasxl domain of the mouse Gnas imprinted locus. (Q35170038) (← links)
- Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies (Q35221453) (← links)
- Genetics of Pituitary Tumors: Focus on G-Protein Mutations (Q35552656) (← links)
- Imprinting status of Galpha(s), NESP55, and XLalphas in cell cultures derived from human embryonic germ cells: GNAS imprinting in human embryonic germ cells (Q35613804) (← links)
- Bio-CAP: a versatile and highly sensitive technique to purify and characterise regions of non-methylated DNA (Q35780054) (← links)
- New mutations at the imprinted Gnas cluster show gene dosage effects of Gsα in postnatal growth and implicate XLαs in bone and fat metabolism but not in suckling (Q35807252) (← links)
- Loss of XLαs (extra-large αs) imprinting results in early postnatal hypoglycemia and lethality in a mouse model of pseudohypoparathyroidism Ib. (Q35921843) (← links)
- Studies of the regulation and function of the Gs alpha gene Gnas using gene targeting technology (Q36076341) (← links)
- The influence of non-coding RNAs on allele-specific gene expression in mammals (Q36088917) (← links)
- Q-RRBS: a quantitative reduced representation bisulfite sequencing method for single-cell methylome analyses. (Q36214540) (← links)
- Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS (Q36259714) (← links)
- Non-Coding RNAs at the Gnas and Snrpn-Ube3a Imprinted Gene Loci and Their Involvement in Hereditary Disorders (Q36433565) (← links)
- How imprinting centres work (Q36436525) (← links)
- Imprinting the Gnas locus. (Q36436567) (← links)
- Resistance to growth hormone releasing hormone and gonadotropins in Albright's hereditary osteodystrophy (Q36514109) (← links)
- Intracytoplasmic sperm injection--an assisted reproduction technique that should make us cautious about imprinting deregulation (Q36524664) (← links)