Paper Search Console

Home Search Page About Contact

Journal Title

Title of Journal:

Search In Journal Title:

Abbravation: Journal of Human Genetics

Search In Journal Abbravation:

Publisher

Nature Publishing Group

Search In Publisher:

DOI

10.1002/2015WR018427

Search In DOI:

ISSN

1435-232X

Search In ISSN:
Search In Title Of Papers:

In situ detection of insulinlike growth factor II

Authors: Tetsuro Sohda Kaoru Iwata Hidenobu Soejima Seiichiro Kamimura Hiroshi Shijo Kankatsu Yun
Publish Date: 1998/02
Volume: 43, Issue: 1, Pages: 49-
PDF Link

Abstract

Thank you for visiting naturecom You are using a browser version with limited support for CSS To obtain the best experience we recommend you use a more up to date browser or turn off compatibility mode in Internet Explorer In the meantime to ensure continued support we are displaying the site without styles and JavaScriptTo assess the relationship between insulinlike growth factor II IGF2 and H19 gene expression at the cellular level we have examined the distribution of IGF2 and H19 mRNA by means of in situ hybridization in hepatic malignancies consisting of hepatocellular carcinoma HCC cholangiocellular carcinoma CCC and metastatic liver cancer MLC In HCC 15 of 27 tumors 56 and 11 of 27 tumors 41 demonstrated increased IGF2 and H19 gene expression respectively Of 16 HCCs with increased expression of either IGF2 or H19 10 tumors coexpressed both transcripts at comparable levels Moreover the spatiotemporal distribution and the cellular localization of the two gene transcripts were almost identical suggesting the presence of a reciprocal relation between IGF2 and H19 In addition 5 HCCs showed increased IGF2 expression without concomitant H19 expression whereas 1 HCC showed increased H19 expression without IGF2 transcripts However 11 HCCs showed no IGF2 or H19 expression On the other hand neither IGF2 transcripts nor H19 transcripts were detected in 2 CCCs or 10 MLCs studied The data suggest that IGF2 and/or H19 gene expression may be characteristic of some HCCs


Keywords:

References


.
Search In Abstract Of Papers:
Other Papers In This Journal:

  1. Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome
  2. Mitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications
  3. Distal 15q trisomy with Dandy-Walker malformation in a female infant
  4. Molecular cloning, mapping, and characterization of a novel human gene, MTA1-L1 , showing homology to a metastasis-associated gene, MTA1
  5. G6PD Viangchan (871G>A) is the most common G6PD-deficient variant in the Cambodian population
  6. Mucopolysaccharidosis IVA: A novel splice acceptor site mutation in intron 4 of the N -acetylgalactosamine-6-sulfate sulfatase gene in an afghanistan girl with classical morquio disease
  7. Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence
  8. Isolation of human chromosome 21-specific cosmids and their uses in mapping of cosmid contigs on chromosomal subregions
  9. Novel polymorphism in the 5′-untranslated region of the interleukin-4 gene
  10. A comprehensive method to scan for point mutations of the glucose 6 phosphate dehydrogenase gene
  11. Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non- APOE -ε4 carriers
  12. A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan
  13. The hOGG1 Ser 326 Cys gene polymorphism is associated with decreased insulin sensitivity in subjects with normal glucose tolerance
  14. Concordance and discordance of anencephaly in 109 twin pairs in Japan
  15. Molecular cloning of a novel human gene ( SIRP-B2 ) which encodes a new member of the SIRP/SHPS-1 protein family
  16. Genomic imprinting and its relevance to genetic diseases
  17. No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population
  18. Ret/PTC3 is the most frequent form of gene rearrangement in papillary thyroid carcinomas in Japan
  19. Subsequent pregnancy outcomes in recurrent miscarriage patients with a paternal or maternal carrier of a structural chromosome rearrangement
  20. Cancer-predisposing genes and chromosome mutation
  21. A disease with immune deficiency, skin abscesses, pancytopenia, abnormal bone marrow karyotype, and increased sister chromatid exchanges: An autosomal recessive chromosome instability syndrome?
  22. Allele frequencies of single nucleotide polymorphisms (SNPs) in 40 candidate genes for gene-environment studies on cancer: data from population-based Japanese random samples
  23. Analysis of the HLA-DRw9 antigen using two-dimensional gel electrophoresis and alloantisera
  24. High heritability of bone size at the hip and spine in Chinese
  25. Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes
  26. Amelioration of prolidase deficiency in fibroblasts using adenovirus mediated gene transfer
  27. A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia
  28. Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain α-keto acid dehydrogenase complex
  29. Common coding variant in the TCF7L2 gene and study of the association with type 2 diabetes in Japanese subjects
  30. Saliva acid phosphatases and amylase in Senoi and Aboriginal Malays and superoxide dismutase in various racial groups of peninsular Malaysia
  31. High prevalence of Southeast Asian ovalocytosis in Malays with distal renal tubular acidosis
  32. Linkage study of dominantly inherited olivo-ponto-cerebellar atrophy (OPCA) and Holmes' ataxia
  33. A common functional exon polymorphism in the microsomal triglyceride transfer protein gene is associated with type 2 diabetes, impaired glucose metabolism and insulin levels
  34. Study of AZFc partial deletion gr/gr in fertile and infertile Japanese males
  35. Genetic polymorphism of the a subunit of human coagulation factor XIII in Japanese
  36. Mutational analysis of ATP7B gene in Egyptian children with Wilson disease: 12 novel mutations

Search Result: