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*  Chromosome segregation control by Escherichia coli ObgE GTPase - Foti - 2007 - Molecular Microbiology - Wiley Online Library
Hirano, T. (2005) SMC proteins and chromosome mechanics: from bacteria to humans. Philos Trans R Soc Lond B Biol Sci 360: 507- ... Han, J.S., Kang, S., Lee, H., Kim, H.K., and Hwang, D.S. (2003) Sequential binding of SeqA to paired hemi-methylated GATC ... The defects in chromosome partitioning were accompanied by changes in chromosome organization at oriC and ter, visualized by ... Studies of chromosome organization in bacterial cells show that the chromosome is an exquisitely organized and dynamic ...
  http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2958.2007.05811.x/full
*  Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary...
... that in untreated human primary fibroblasts the frequency of anaphase lagging chromosomes for all the 23 chromosome pairs was ... Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary ... Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary ... Merotelic kinetochore orientation versus chromosome mono-orientation in the origin of lagging chromosomes in human primary ...
  http://jcs.biologists.org/content/115/3/507
*  The region 3′ to Xist mediates X chromosome counting and H3 Lys‐4 dimethylation within the Xist gene | The EMBO Journal
The location of the primer pairs is represented on the small map below the graph. A 5 kb region around the DXPas34 locus, which ... Interestingly, comparative sequence analysis has identified a 2 kb region of mouse/human conservation (80610-82632 of Genbank ... A counting process senses the X chromosome/autosome ratio and ensures that X chromosome inactivation (XCI) initiates in the ... Rastan S, Robertson EJ, Rasmussen TP, Mastrangelo MA, Eden A, Pehrson JR, Jaenisch R (1985) X‐chromosome deletions in embryo‐ ...
  http://emboj.embopress.org/content/23/3/594
*  Errors in chromosome segregation during oogenesis and early embryogenesis - WRAP: Warwick Research Archive Portal
Errors in chromosome segregation occurring during human oogenesis and early embryogenesis are very common. Meiotic chromosome ... The crucial events, including meiotic chromosome pairing and recombination, take place from around 11 weeks until birth. ... New insights into human nondisjunction of chromosome 21 in oocytes. PLoS Genet 2008;4(3):e1000033.. 10. Jones KT. Meiosis in ... Munné S, Cohen J. Chromosome abnormalities in human embryos. Hum Reprod Update 1998a;4(6):842-55.. 42. Munné S, Lee A, ...
  http://wrap.warwick.ac.uk/3796/
*  Homologous chromosome - Wikipedia
Humans have a total of 46 chromosomes, but there are only 22 pairs of homologous autosomal chromosomes. The additional 23rd ... pair is the sex chromosomes, X and Y. If this pair is made up of an X and Y chromosome, then the pair of chromosomes is not ... So humans have two homologous chromosome sets in each cell, meaning humans are diploid organisms. Homologous chromosomes are ... Therefore, when two chromosomes of the exact structure exist, they are able to pair together to form homologous chromosomes. ...
  https://en.wikipedia.org/wiki/Homologous_chromosome
*  HKU Scholars Hub: Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in...
Chromosomes, human, pair 7. en_HK. dc.subject.mesh. Adipose tissue - chemistry. en_HK. ... Article: Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human. * ... Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human. en_HK. ... Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in human. ...
  http://hub.hku.hk/handle/10722/44303
*  Michael Cascio - Publications - Oregon Health & Science University
Chromosomes, Human, Pair 21 Precursor Cell Lymphoblastic Leukemia-Lymphoma Cytogenetics Genetic Markers ... Mouse chromosome 7 harbors a quantitative trait locus for isoflurane minimum alveolar concentration. Cascio, M., Xing, Y., Gong ... Cytogenetic Variation of B-Lymphoblastic Leukemia with Intrachromosomal Amplification of Chromosome 21 (iAMP21): A Multi- ... Cascio, M. J., O'Donnell, R. J. & Horvai, A. E. Apr 2010 In : Modern Pathology. 23, 4, p. 574-580 7 p.. Research output: ...
  https://ohsu.pure.elsevier.com/en/persons/michael-cascio/publications/
*  anlage tumor retinal 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 1. Chromosomes, Human, Pair 7. Comparative Genomic Hybridization. Etoposide / administration & dosage ... Chromosomes, Human, Pair 17. Epithelium / pathology. Epithelium / ultrastructure. Glial Fibrillary Acidic Protein / metabolism ... Chromosome Aberrations. Endothelin-3 / pharmacology. Female. Fluorescent Antibody Technique. Humans. Immunohistochemistry. ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ...
  http://www.bmlsearch.com/?kwr=anlage+tumor+retinal+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  adenocarcinoma in situ of thyroid 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 2. Chromosomes, Human, Pair 20. Chromosomes, Human, Pair 3. Female. Gene Rearrangement. Humans. In ... Chromosomes, Human, Pair 7 / genetics. DNA Mutational Analysis. Genes, ras / genetics. Genetic Markers. Humans. In Situ ... human; EC 2.7.11.1 / BRAF protein, human; EC 2.7.11.1 / Proto-Oncogene Proteins B-raf; EC 3.6.5.2 / HRAS protein, human; EC 3.6 ... Chromosome Deletion. Cytogenetics. Diagnosis, Differential. Disease-Free Survival. Female. Humans. Immunophenotyping. In Situ ...
  http://www.bmlsearch.com/?kwr=adenocarcinoma+in+situ+of+thyroid+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  acute basophilic leukemia morphologic abnormality 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
MeSH-major] Chromosomes, Human, Pair 7. Chromosomes, Human, Pair 8. Leukemia, Basophilic, Acute / genetics. Leukemia, ... MeSH-major] Chromosomes, Human, Pair 7 / genetics. Leukemia, Basophilic, Acute / genetics. Monosomy / diagnosis. Monosomy / ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ... Humans. Immunophenotyping. Male. Phenotype. *[Email] Email this result item Email the results to the following email address: [ ...
  http://www.bmlsearch.com/?kwr=acute+basophilic+leukemia+morphologic+abnormality+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  In situ hybridization localization of SPAM1 transcripts | Open-i
In situ hybridization localization of SPAM1 transcripts in human corpus epididymal epithelium. Histological sections were ... Chromosomes, Human, Pair 7/genetics. *Humans. *Hyaluronoglucosaminidase/metabolism. *Hydrogen-Ion Concentration. *In Situ ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC184449_1477-7827-1-54-3&req=4
*  Chromosome 7 (human) - Wikipedia
A ring chromosome occurs when both ends of a broken chromosome are reunited. G-banding ideograms of human chromosome 7 In the ... See also: Category:Genes on human chromosome 7. The following is a partial list of genes on human chromosome 7. For complete ... The following are some of the gene count estimates of human chromosome 7. Because researchers use different approaches to ... People normally have two copies of this chromosome. Chromosome 7 spans about 159 million base pairs (the building material of ...
  https://en.wikipedia.org/wiki/Chromosome_7_(human)
*  Effects of modulation of HIPK2 protein levels on Gal-3 | Open-i
Chromosomes, Human, Pair 7. *Female. *Gene Expression. *Humans. *Immunohistochemistry. *Loss of Heterozygosity ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Health and Human Services • 8600 Rockville Pike,Bethesda,MD 20894 Privacy • Accessibility • Freedom of Information Act • ... Open-i® and the Open i logo are service marks of U.S. Department of Health and Human Services. ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC3117790_pone.0020665.g005&req=4
*  HASGE analysis at pH 7.0 of protein extracts from testi | Open-i
... vas deferens and sperm of human and macaque. Equal amounts (60 μg) of protein were loaded ... Chromosomes, Human, Pair 7/genetics. *Humans. *Hyaluronoglucosaminidase/metabolism. *Hydrogen-Ion Concentration. *In Situ ... 5). In samples from the human caput, human sperm and macaque corpus there was also a narrow band with a higher MW (,114 kDa, as ... 5). In samples from the human caput, human sperm and macaque corpus there was also a narrow band with a higher MW (,114 kDa, as ...
  https://openi.nlm.nih.gov/detailedresult.php?img=PMC184449_1477-7827-1-54-5&req=4
*  Genetics and Genomics - Research Output - Experts@Minnesota
Assignment of linkage groups to turkey chromosome 1 (MGA1). Reed, K., Sullivan, L. R., Foster, L. K., Chaves, L. D. & Ponce De ... Functional expression of IgA receptor FcαRI on human platelets. Qian, K., Xie, F., Gibson, A. W., Edberg, J. C., Kimberly, R. P ... Characterization of the turkey MHC chromosome through genetic and physical mapping. Chaves, L. D., Krueth, S. B. & Reed, K., ... Recombination is suppressed over a large region of the rainbow trout y chromosome. Phillips, R. B., Dekoning, J. J., Ventura, A ...
  https://experts.umn.edu/en/organisations/genetics-and-genomics/publications/
*  Chromosome 7: Human Genomics: Collection: Supplement: Nature
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Osborne L. R. et al. ... Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31. ... The DNA sequence of human chromosome 7. Hillier L. W. et al. ... HUMAN. A physical map of the human genome. The International ... Initial sequencing and analysis of the human genome. International Human Genome Sequencing Consortium ...
  http://www.nature.com/nature/supplements/collections/humangenome/chromosomes/7.html?error=cookies_not_supported&code=a3d312e2-18d3-41a4-b359-84867cdea7c4
*  Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias. - Radcliffe...
Cell Nucleus, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 7, Female, Homeodomain Proteins, Humans, Infant, Leukemia, ... Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias. ... Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias. ... Ectopic expression of the HLXB9 gene is associated with an altered nuclear position in t(7;12) leukaemias. ...
  https://www.rdm.ox.ac.uk/publications/57927
*  acute myelogenous leukemia without maturation fab m1 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 11 / genetics. Chromosomes, Human, Pair 5 / genetics. Chromosomes, Human, Pair 7 / genetics. Gene ... MeSH-major] Chromosome Aberrations. Chromosomes, Human, Pair 12. Chromosomes, Human, Pair 7. Leukemia, Myeloid, Acute / ... MeSH-major] Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 17. Leukemia, Myeloid, Acute / genetics. Leukemia, ... MeSH-major] Chromosomes, Human, Pair 16 / genetics. Chromosomes, Human, Pair 22 / genetics. Leukemia, Myeloid, Acute / genetics ...
  http://www.bmlsearch.com/?kwr=acute+myelogenous+leukemia+without+maturation+fab+m1+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  OriGene - YAE1D1 (NM 020192) qPCR Primer Pair
... qSTAR qPCR primer pairs against Homo sapiens gene YAE1D1 available for purchase from OriGene - Your Gene Company. ... Recombinant protein of human chromosome 7 open reading frame 36 (C7orf36), full length, with N-terminal HIS tag, expressed in E ... Lenti ORF particles, YAE1D1 (Myc-DDK tagged) - Human chromosome 7 open reading frame 36 (C7orf36) , 200ul, >10^7 TU/mL ... Lenti ORF particles, YAE1D1 (Myc-DDK tagged) - Human chromosome 7 open reading frame 36 (C7orf36) , 200ul, >10^7 TU/mL ...
  http://www.origene.com/qPCR/primer_pair/HP213546.aspx
*  Creationist Confusion, page 7
Humans have 23 pairs of chromosomes while chimpanzees have 24. Some evolutionists believe that one of the human chromosomes has ... Random assortment in humans produces 223 (8,388,608) different combinations of chromosomes. . ., none of these chromosomes is " ... two sets of Chromosomes). It is estimated that from 10 20% of all human fertilized eggs contain chromosome abnormalities, and ... two sets of Chromosomes). quote: It is estimated that from 10 20% of all human fertilized eggs contain chromosome abnormalities ...
  http://www.abovetopsecret.com/forum/thread95780/pg7
*  Restriction site-specific methylation studies of imprinted genes with quantitative real-time PCR. - Nuffield Department of...
The imprinted loci on chromosome 7 behaved as expected in maternal UPD7 (100% methylation) and paternal UPD7 (,10% methylation ... quantitative real-time PCR analyses with 6 unique PCR assays to investigate 4 imprinting control regions on chromosomes 7 and ... 11 in individuals with uniparental disomy of chromosome 7 (UPD7) and in control individuals. RESULTS: Our validation of the ... Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 7, DNA Methylation, Female, Genetic Diseases, Inborn, Genomic Imprinting ...
  https://www.ndph.ox.ac.uk/publications/6441
*  Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita). - Nuffield Department of Clinical Neurosciences
... has recently been linked to chromosome 7q35 in the region of the human skeletal muscle chloride channel gene (HUMCLC). Single ... Amino Acid Sequence, Animals, Base Sequence, Chloride Channels, Chromosome Mapping, Chromosomes, Human, Pair 7, DNA, DNA ... has recently been linked to chromosome 7q35 in the region of the human skeletal muscle chloride channel gene (HUMCLC). Single ... Primers, Exons, Female, Humans, Male, Molecular Sequence Data, Muscles, Mutation, Myotonia Congenita, Pedigree, Polymerase ...
  https://www.ndcn.ox.ac.uk/publications/35760
*  Stem and progenitor cells in myelodysplastic syndromes show aberrant stage-specific expansion and harbor genetic and epigenetic...
Antigens, CD, Azacitidine, Case-Control Studies, Cell Lineage, Chromosome Aberrations, Chromosomes, Human, Pair 7, DNA ... Karpe Group - Human fat distribution and metabolic disease * Kerr-Cai Group - Tumour microenvironment and colorectal cancer ... cross-talk between adipose tissue and the cardiovascular system in humans ... Methylation, Epigenesis, Genetic, Flow Cytometry, Gene Expression, Hematopoietic Stem Cells, Humans, Karyotyping, ...
  https://www.rdm.ox.ac.uk/publications/341226