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*  Chromosomal Dynamics in Meiosis | Centro de Investigaciones Biológicas - CIB
Differential cohesin loading marks paired and unpaired regions of platypus sex chromosomes at prophase I. Sci. Rep. 7(1):4217. ... and infertility in humans. A key protagonist in this control is the cohesin complex, which are composed essentially by four ... MOLECULAR BASIS OF ANEUPLOIDY IN CANCER:CHROMOSOME SEGREGATION CONTROL AND CHROMOSOME STABILITY. FUNDACIÓN DE INVESTIGACIÓN ... Chromosome segregation control in mammalian meiosis: Cohesins and cohesin-regulators. Head: José Luis Barbero Esteban ...
http://cib.csic.es/research/cellular-and-molecular-biology/chromosomal-dynamics-meiosis
*  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/
*  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
*  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)
*  Find Research Outputs - Albert Einstein College of Medicine
Chromosomes, Human, Pair 7 Glioblastoma Fluorescence In Situ Hybridization Immunohistochemistry Chromosomes, Human, Pair 20 ... "Development of temporal lobe epilepsy during maintenance electroconvulsive therapy: A case of human kindling?". Moshe, S. L. & ... CHAPTER 9: Structure, Function and Regulation of Human Heme-based Dioxygenases. Lewis-Ballester, A., Pham, K. N., Liao, M., ... Barriers to Allogeneic Hematopoietic Stem Cell Transplantation for Human T Cell Lymphotropic Virus 1-Associated Adult T Cell ...
https://einstein.pure.elsevier.com/en/publications/?format=&page=1
*  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
*  HKU Scholars Hub: Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patients
Chromosome deletion. en_HK. dc.subject.mesh. Chromosomes, human, pair 7. en_HK. ... A detailed physical map consisting of cosmid, P1 artificial chromosomes, and yeast artificial chromosomes was constructed and ... A detailed physical map consisting of cosmid, P1 artificial chromosomes, and yeast artificial chromosomes was constructed and ...
http://hub.hku.hk/handle/10722/44304
*  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
*  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
*  Localisation of a gene implicated in a severe speech and language disorder. - Wellcome Centre for Integrative Neuroimaging
We initiated a genome-wide search for linkage in the KE family and have identified a region on chromosome 7 which co-segregates ... Chromosome Mapping, Chromosomes, Human, Pair 7, Female, Genetic Linkage, Genetic Markers, Genotype, Humans, Language Disorders ... We initiated a genome-wide search for linkage in the KE family and have identified a region on chromosome 7 which co-segregates ...
https://www.win.ox.ac.uk/publications/25077
*  MMTAG2 - PCR Primer Pair - SYBR | PrimePCR | Bio-Rad
Bos taurus chromosome 7 open reading frame, human C1orf35 (C7H1orf35), mRNA.. Aliases:. Not Available. ...
http://www.bio-rad.com/en-us/prime-pcr-assays/assay/qbtaced0015468-primepcr-sybr-green-assay-mmtag2-cow
*  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
*  NAVER Academic > Search...
Adult, Chromosomes, Human, Pair 12, ultrastructure, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 14, Dysgerminoma, ... Adult, Chromosomes, Human, Pair 12, ultrastructure, Chromosomes, Human, Pair 22, Clone Cells, Diagnosis, Differential, ... Chromosome Aberrations, Chromosome Banding, Chromosomes, Human, Pair 22, Clone Cells, ultrastructure, Humans, Karyotyping, ... Animals, Base Sequence, Chromosome Mapping, Chromosomes, Human, Pair 17, Genes, Tumor Suppressor, Humans, Mice, Molecular ...
https://academic.naver.com/search.naver?field=3&query=Genes%2C+Chromosomes+and+Cancer+6%EA%B6%8C+4%ED%98%B8
*  HUMAN OBESITY SUSCEPTIBILITY GENE ENCODING A MEMBER OF THE NEUREXIN FAMILY AND USES THEREOF - Patent application
... of the chromosome (p-ter). TABLE-US-00003 TABLE 2 Proportion of Human informative chromosome Clones Start End pairs p-value 7 ... 144 736 618 base pairs to 150 314 820 base pairs on human chromosome 7. The p-value 2×10-5 corresponding to the significance ... chromosome 2p21, chromosome 6p21, chromosome 10 and chromosome 20q13 (Chagnon et al., 2003). SUMMARY OF THE INVENTION [0026]The ... Mega base pairs between clones representing the whole human genome were tested for linkage using GenomeHIP. Each point ...
http://www.patentsencyclopedia.com/app/20090208482
*  Diagnosis | Leukemia and Lymphoma Society
Most humans have 23 pairs of chromosomes, for a total of 46 chromosomes. In some cases of CMML, a copy of chromosome 7 is ... Abnormal Chromosomes. Twenty to forty percent of people with CMML have chromosomes that are abnormal in structure or number ( ... a piece of one chromosome breaks off and attaches to another chromosome, which can lead to the development of an "oncogene" ( ... A chromosome translocation involving the PDGFR-β and TEL genes. About 1 to 4 percent of CMML patients have an abnormality ...
http://www.lls.org/leukemia/chronic-myelomonocytic-leukemia/diagnosis