Investigation of connexin gene expression patterns by in situ hybridization techniques. 2001

M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
Institut de Biologie du Développement de Marseille, Université de la Méditerranée, Marseille, France.

UI MeSH Term Description Entries
D004622 Embryo, Mammalian The entity of a developing mammal (MAMMALS), generally from the cleavage of a ZYGOTE to the end of embryonic differentiation of basic structures. For the human embryo, this represents the first two months of intrauterine development preceding the stages of the FETUS. Embryonic Structures, Mammalian,Mammalian Embryo,Mammalian Embryo Structures,Mammalian Embryonic Structures,Embryo Structure, Mammalian,Embryo Structures, Mammalian,Embryonic Structure, Mammalian,Embryos, Mammalian,Mammalian Embryo Structure,Mammalian Embryonic Structure,Mammalian Embryos,Structure, Mammalian Embryo,Structure, Mammalian Embryonic,Structures, Mammalian Embryo,Structures, Mammalian Embryonic
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D012333 RNA, Messenger RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm. Messenger RNA,Messenger RNA, Polyadenylated,Poly(A) Tail,Poly(A)+ RNA,Poly(A)+ mRNA,RNA, Messenger, Polyadenylated,RNA, Polyadenylated,mRNA,mRNA, Non-Polyadenylated,mRNA, Polyadenylated,Non-Polyadenylated mRNA,Poly(A) RNA,Polyadenylated mRNA,Non Polyadenylated mRNA,Polyadenylated Messenger RNA,Polyadenylated RNA,RNA, Polyadenylated Messenger,mRNA, Non Polyadenylated
D013462 Sulfur Radioisotopes Unstable isotopes of sulfur that decay or disintegrate spontaneously emitting radiation. S 29-31, 35, 37, and 38 are radioactive sulfur isotopes. Radioisotopes, Sulfur
D015336 Molecular Probe Techniques The use of devices which use detector molecules to detect, investigate, or analyze other molecules, macromolecules, molecular aggregates, or organisms. Molecular Probe Technic,Molecular Probe Technics,Molecular Probe Technique,Technic, Molecular Probe,Technics, Molecular Probe,Technique, Molecular Probe,Techniques, Molecular Probe,Probe Technic, Molecular,Probe Technics, Molecular,Probe Technique, Molecular,Probe Techniques, Molecular
D015347 RNA Probes RNA, usually prepared by transcription from cloned DNA, which complements a specific mRNA or DNA and is generally used for studies of virus genes, distribution of specific RNA in tissues and cells, integration of viral DNA into genomes, transcription, etc. Whereas DNA PROBES are preferred for use at a more macroscopic level for detection of the presence of DNA/RNA from specific species or subspecies, RNA probes are preferred for genetic studies. Conventional labels for the RNA probe include radioisotope labels 32P and 125I and the chemical label biotin. RNA probes may be further divided by category into plus-sense RNA probes, minus-sense RNA probes, and antisense RNA probes. Gene Probes, RNA,RNA Probe,Probe, RNA,Probes, RNA,Probes, RNA Gene,RNA Gene Probes
D016612 Paraffin Embedding The infiltrating of tissue specimens with paraffin, as a supporting substance, to prepare for sectioning with a microtome. Embedding, Paraffin
D017403 In Situ Hybridization A technique that localizes specific nucleic acid sequences within intact chromosomes, eukaryotic cells, or bacterial cells through the use of specific nucleic acid-labeled probes. Hybridization in Situ,Hybridization, In Situ,Hybridizations, In Situ,In Situ Hybridizations
D017630 Connexins A group of homologous proteins which form the intermembrane channels of GAP JUNCTIONS. The connexins are the products of an identified gene family which has both highly conserved and highly divergent regions. The variety contributes to the wide range of functional properties of gap junctions. Connexin,Connexin Complex Proteins,Gap Junction Proteins,Gap Junction Channel Proteins,Gap Junction Protein,Junction Protein, Gap,Junction Proteins, Gap

Related Publications

M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2012, Methods in molecular biology (Clifton, N.J.),
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2012, Methods in molecular biology (Clifton, N.J.),
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
October 2007, Parasitology,
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2019, Methods in molecular biology (Clifton, N.J.),
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2024, Methods in molecular biology (Clifton, N.J.),
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
October 1998, Zhonghua bing li xue za zhi = Chinese journal of pathology,
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2009, Nature protocols,
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
April 2012, Journal of visualized experiments : JoVE,
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2012, Methods in molecular biology (Clifton, N.J.),
M Théveniau-Ruissy, and S Alcoléa, and I Marics, and D Gros, and A F Moorman, and W H Lamers
January 2004, Methods in molecular medicine,
Copied contents to your clipboard!