Pages that link to "Q22009166"

The following pages link to A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region (Q22009166):

Displaying 50 items.

• Makorin ring finger protein 3 (Q21109300) (← links)
• Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome (Q21261463) (← links)
• Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15 (Q22253999) (← links)
• Phylogenetic conservation of the makorin-2 gene, encoding a multiple zinc-finger protein, antisense to the RAF1 proto-oncogene (Q24291785) (← links)
• Identification of Four Highly Conserved Genes between Breakpoint Hotspots BP1 and BP2 of the Prader-Willi/Angelman Syndromes Deletion Region That Have Undergone Evolutionary Transposition Mediated by Flanking Duplicons (Q24532789) (← links)
• Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the Prader-Willi deletion region, which Is highly expressed in brain (Q24534447) (← links)
• Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control (Q24539092) (← links)
• The non-coding RNAs as riboregulators (Q24607004) (← links)
• Regulatory long non-coding RNAs and neuronal disorders (Q24632237) (← links)
• Epigenetic principles and mechanisms underlying nervous system functions in health and disease (Q24657549) (← links)
• The putatively functional Mkrn1-p1 pseudogene is neither expressed nor imprinted, nor does it regulate its source gene in trans (Q24670569) (← links)
• An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus (Q24678820) (← links)
• Computational discovery of sense-antisense transcription in the human and mouse genomes (Q24803676) (← links)
• An update on the genetic causes of central precocious puberty (Q26741326) (← links)
• A new pathway in the control of the initiation of puberty: the MKRN3 gene (Q26861068) (← links)
• Natural antisense transcripts (Q27020939) (← links)
• Genetic & epigenetic approach to human obesity (Q28084624) (← links)
• Parent-specific complementary patterns of histone H3 lysine 9 and H3 lysine 4 methylation at the Prader-Willi syndrome imprinting center (Q28361223) (← links)
• Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4 (Q28941781) (← links)
• Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: efficient identification of known microduplications and identification of a novel microduplication in ASMT. (Q30484771) (← links)
• Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14. (Q30495343) (← links)
• Antisense transcripts with FANTOM2 clone set and their implications for gene regulation (Q31147226) (← links)
• Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region (Q33316874) (← links)
• Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3. (Q33682471) (← links)
• The vertebrate makorin ubiquitin ligase gene family has been shaped by large-scale duplication and retroposition from an ancestral gonad-specific, maternal-effect gene (Q33776161) (← links)
• The uniqueness of the imprinting mechanism (Q33885040) (← links)
• Disruption of the bipartite imprinting center in a family with Angelman syndrome (Q34020745) (← links)
• RNA-directed DNA methylation. (Q34041209) (← links)
• Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759. (Q34118711) (← links)
• The role of genomic imprinting in human developmental disorders: lessons from Prader-Willi syndrome (Q34190554) (← links)
• Central precocious puberty caused by mutations in the imprinted gene MKRN3. (Q34348835) (← links)
• DNA methylation in genomic imprinting, development, and disease (Q34378421) (← links)
• Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints (Q34389945) (← links)
• A novel MKRN3 missense mutation causing familial precocious puberty (Q34443581) (← links)
• The human obesity gene map: the 2001 update (Q34557274) (← links)
• The human obesity gene map: the 2005 update (Q34567973) (← links)
• Regulatory elements associated with paternally-expressed genes in the imprinted murine Angelman/Prader-Willi syndrome domain (Q34579857) (← links)
• Non-coding ribonucleic acids--a class of their own? (Q34801141) (← links)
• The human obesity gene map: the 2002 update (Q35084465) (← links)
• The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals (Q35113579) (← links)
• The role of imprinted genes in fetal growth abnormalities (Q35295496) (← links)
• Distinct phenotypes distinguish the molecular classes of Angelman syndrome (Q35436435) (← links)
• The neurobiology of mouse models syntenic to human chromosome 15q. (Q35680716) (← links)
• The human obesity gene map: the 2003 update (Q35715184) (← links)
• Temporal and developmental requirements for the Prader-Willi imprinting center (Q35807517) (← links)
• Changing images of the gene (Q36492692) (← links)
• The human hypothalamus in metabolic and episodic disorders. (Q36550599) (← links)
• RNAs of the human chromosome 15q11-q13 imprinted region (Q36625658) (← links)
• Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans (Q36744063) (← links)
• Conserved characteristics of heterochromatin-forming DNA at the 15q11-q13 imprinting center (Q36745813) (← links)