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*  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/
*  High incidence of t(11;18)(q21;q21) in Helicobacter pylori-negative gastric MALT lymphoma.
Chromosomes, Human, Pair 18*. Female. Helicobacter pylori* / isolation & purification. Humans. Incidence. Lymphoma, B-Cell, ... 0/Adaptor Proteins, Signal Transducing; 0/BCL10 protein, human; 0/Carrier Proteins ... BCL10 nuclear expression was observed in 7 of 8 t(11;18)(q21;q21)-positive cases and 4 of 7 t(11;18)(q21;q21)-negative cases, ... We reviewed the clinical data and histology, and we examined t(11;18)(q21;q21) and BCL10 expression pattern in 17 such cases. ...
http://www.biomedsearch.com/nih/High-incidence-in-Helicobacter-pylori/12517817.html
*  Detection of errors in dinucleotide repeat typing by nondenaturing electrophoresis.
Chromosomes, Human, Pair 11*. DNA / analysis*. Dinucleotide Repeats*. Electrophoresis, Polyacrylamide Gel / methods. Genotype. ... n repeats located on human chromosome 11p15. To investigate the utility of our approach, a large population sample of 405 ... 8242059 - The human d11s554 locus: four distinct families of repeat pattern alleles at one locus.. 1301149 - Isolation and ... Humans. Nucleic Acid Denaturation. Nucleic Acid Heteroduplexes. Pedigree. Polymerase Chain Reaction / methods. ...
http://www.biomedsearch.com/nih/Detection-errors-in-dinucleotide-repeat/11545389.html
*  Expression of H19, CDKNIC and 1GF1 in mature human dopa | Open-i
CDKNIC and 1GF1 in mature human dopaminergic neurons.(A) Amplification plot for tyrosine hydroxylase copy RNA from neuromelanin ... Chromosomes, Human, Pair 11*. *Dopamine/metabolism*. *Embryonic Stem Cells/cytology*. *Gene Expression Profiling* ... IGF2 and CDKN1C were also found to be highly expressed in mature human TH-positive dopamine neurons isolated from human brain ... IGF2 and CDKN1C were also found to be highly expressed in mature human TH-positive dopamine neurons isolated from human brain ...
https://openi.nlm.nih.gov/detailedresult.php?img=PMC2170519_pone.0001422.g005&req=4
*  HKU Scholars Hub: Identification of tumor suppressive activity by irradiation microcell-mediated chromosome transfer and...
Chromosomes, Human, Pair 11. -. dc.subject.mesh. DNA Methylation. -. dc.subject.mesh. alpha-Crystallin B Chain - physiology. - ... Chromosome 11q. Irradiation microcell-mediated chromosome transfer. Microcell hybrid. Nasopharyngeal carcinoma. Issue Date. ... The chromosome 11 fragment containing the 1.8 Mb NPC CR at 11q13 (CR1), the CR at 11q22.3 mapped near D11S2000 (CR2), part of ... The chromosome 11 fragment containing the 1.8 Mb NPC CR at 11q13 (CR1), the CR at 11q22.3 mapped near D11S2000 (CR2), part of ...
http://hub.hku.hk/handle/10722/58245
*  acinic cell tumor salivary gland 2005:2010 - BioMedLib™ search engine
Chromosomes, Human, Pair 19. Female. Humans. Immunohistochemistry. In Situ Hybridization, Fluorescence. Kaplan-Meier Estimate. ... Human-caused Phenomenon or Process. B2.1.1. Environmental Effect of Humans. B2.2. Natural Phenomenon or Process. B2.2.1. ... Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / KRT5 protein, human; 0 / KRT7 protein, human; 0 / Keratin-5; 0 / Keratin-7 ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ...
http://bmlsearch.com/?kwr=acinic%20cell%20tumor%20salivary%20gland%202005:2010
*  adult acute myeloid leukemia cellular diagnosis 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 11 / genetics. Chromosomes, Human, Pair 9 / genetics. Leukemia, Myeloid / pathology. Myeloid-Lymphoid ... Chromosome Aberrations. Female. Gene Silencing. Humans. Karyotyping. Male. Middle Aged. Prognosis. Risk Factors ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ... Cites] Genes Chromosomes Cancer. 2003 Aug;37(4):396-405 [12800151.001]. *[Cites] Int J Oncol. 2004 Feb;24(2):305-12 [ ...
http://www.bmlsearch.com/?kwr=adult+acute+myeloid+leukemia+cellular+diagnosis+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  askin's tumor morphologic abnormality 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 22 / genetics. Humans. Male. Oncogene Proteins, Fusion / genetics. Proto-Oncogene Protein c-fli-1 / ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ... Using a human peripheral primitive neuroectodermal tumor cell line, SK-N-MC, we demonstrated FGF2 stimulated phosphorylation of ... Humans. Immunohistochemistry. In Situ Hybridization, Fluorescence. Middle Aged. Phosphopyruvate Hydratase / analysis. *[Email] ...
http://www.bmlsearch.com/?kwr=askin
*  Chromosome 11 (human) - Wikipedia
... paired box 6 PCNX3 encoding protein Pecanex homolog 3 PGA3 encoding protein Pepsinogen 3, group I (pepsinogen A) PIWIL4 ... Humans normally have two copies of this chromosome. Chromosome 11 spans about 135 million base pairs (the building material of ... chromosomes in the human genome. More than 40% of the 856 olfactory receptor genes in the human genome are located in 28 single ... The following is a partial list of genes on human chromosome 11. For complete list, see the link in the infobox on the right. ...
https://en.wikipedia.org/wiki/Chromosome_11_(human)
*  A single ataxia telangiectasia gene with a product similar to PI-3 kinase.
Chromosome Mapping. *Chromosomes, Artificial, Yeast. *Chromosomes, Human, Pair 11. *Cloning, Molecular. *DNA, Complementary/ ... U.S. Department of Health & Human Services National Institutes of Health National Center for Advancing Translational Sciences ... was identified by positional cloning on chromosome 11q22-23. AT is characterized by cerebellar degeneration, immunodeficiency, ...
https://publications.ncats.nih.gov/publications/7792600
*  SOX11 as a minimal residual disease marker for Mantle cell lymphoma - Danish National Research Database
Chromosomes, Human, Pair 14; Female; Gene Expression Regulation, Neoplastic; Humans; Lymphoma, Mantle-Cell; Male; Middle Aged; ... Chromosomes, Human, Pair 14, Female, Gene Expression Regulation, Neoplastic, Humans, Lymphoma, Mantle-Cell, Male, Middle Aged, ... Aged; Aged, 80 and over; Case-Control Studies; Chromosomes, Human, Pair 11; ... Chromosomes, Human, Pair 11, ...
http://www.forskningsdatabasen.dk/en/catalog/266969816
*  QIMR Genetic Epidemiology Laboratory Home Page
Chromosomes, Human, Pair 20. genetics. Chromosomes, Human, Pair 5. genetics. Cytokines. genetics. ... Chromosomes, Human, Pair 11. genetics. ... 2010 May;11(5):331-44. 20395968. Cites. N Engl J Med. 2010 Sep ...
https://keppel.qimr.edu.au/general/publicationsfulllisting.cgi?pmid=22197932
*  OPUS at UTS: Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. - Open...
Chromosomes, Human, Pair 5. en_US. dc.subject.mesh. Chromosomes, Human, Pair 11. en_US. ... Chromosomes, Human, Pair 20. en_US. dc.subject.mesh. Chromosomes, Human, Pair 5. en_US. ... Chromosomes, Human, Pair 11. en_US. dc.subject.mesh. ... Chromosomes, Human, Pair 20. en_US. dc.subject.mesh. Humans. en ...
https://opus.lib.uts.edu.au/handle/10453/113594
*  Finer linkage mapping of primary hip osteoarthritis susceptibility on chromosome 11q in a cohort of affected female sibling...
... interval of chromosome 11q that we had previously identified as harboring susceptibility to hip OA in a female sibling-pair ... CONCLUSION: Dense linkage mapping has highlighted the presence of 2 loci on chromosome 11q, each conferring susceptibility to ... microsatellite markers with a mean marker interval of 1.4 cM were genotyped in 146 families containing female sibling pairs who ... Chromosomes, Human, Pair 11, Humans, Osteoarthritis, Hip, Disease Susceptibility, Chromosome Mapping, Microsatellite Repeats, ...
https://www.ndorms.ox.ac.uk/publications/107292
*  MEN1 gene mutations in 12 MEN1 families and their associated tumors
Adenoma, Chromosomes, Human, Pair 11, Gastrinoma, Germ-Line Mutation, Humans, Insulinoma, Loss of Heterozygosity, Multiple ... Chromosomes, Human, Pair 11,Gastrinoma,Germ-Line Mutation,Humans,Insulinoma,Loss of Heterozygosity,Multiple Endocrine Neoplasia ... analysis and DNA sequence analysis as well as for loss of heterozygosity on chromosome 11q13. We identified nine different ... analysis and DNA sequence analysis as well as for loss of heterozygosity on chromosome 11q13. We identified nine different ...
https://lup.lub.lu.se/search/publication/20bc6a2f-288e-4767-a9e9-0f34f73ba229
*  Chromosome 11 - Genetics Home Reference
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 11, one copy inherited from ... Ring chromosomes occur when a chromosome breaks in two places and the ends of the chromosome arms fuse together to form a ... chromosome consisting of a piece of chromosome 22 attached to a piece of chromosome 11. The extra chromosome is known as a ... Human chromosome 11 DNA sequence and analysis including novel gene identification. Nature. 2006 Mar 23;440(7083):497-500. (PDF) ...
https://ghr.nlm.nih.gov/chromosome/11
*  Fc epsilon RI-beta polymorphism and risk of atopy in a general population sample. - Nuffield Department of Population Health
To establish the prevalence of Fc epsilon RI-beta polymorphisms Leu181 and Leu181/Leu183 on chromosome 11q13 in the general ... Adolescent, Adult, Base Sequence, Bronchial Hyperreactivity, Child, Chromosomes, Human, Pair 11, Female, Genetic Linkage, ... OBJECTIVE: To establish the prevalence of Fc epsilon RI-beta polymorphisms Leu181 and Leu181/Leu183 on chromosome 11q13 in the ... Heterozygote, Humans, Hypersensitivity, Immediate, Male, Molecular Sequence Data, Polymorphism, Genetic, Receptors, IgE, Risk ...
https://www.ndph.ox.ac.uk/publications/631921
*  What percentage of DNA do humans share with a dog
They also have a different number of chromosomes. Humans have 23 pairs of chromosomes and dogs have 39 pairs. ... of human DNA - the answer depends on what proportion of theremaining 98% is the same. Humans have 23… pairs of chromosomes ... chromosomes 4, 9, 12, 21, and y). Some specific examples of differences include: 1) Humans have 23 pairs of chromosomes in ... Humans and cats have similar x and y chromosomes and have the sameancestor from the past. Cats and humans share 90 percent ...
http://www.answers.com/Q/What_percentage_of_DNA_do_humans_share_with_a_dog
*  NAVER Academic > Search...
Animals, Chimera, Chromosome Mapping, Chromosomes, Human, Pair 21, Chromosomes, Human, Pair 8, Cloning, Molecular, Core Binding ... Aging, Alleles, Child, Child, Preschool, Chromosome Mapping, Chromosomes, Human, Pair 11, DNA Primers, Diabetes Mellitus, Type ... Adipose Tissue, Brown, metabolism, Animals, Carrier Proteins, genetics, Chromosome Mapping, Chromosomes, Human, Pair 11, Gene ... Alternative Splicing, Base Sequence, Cells, Cultured, Chromosome Mapping, Chromosomes, Artificial, Yeast, Chromosomes, Human, ...
https://academic.naver.com/search.naver?field=3&query=Nature+Genetics+15%EA%B6%8C+3%ED%98%B8
*  What Is PGD? - Embryo Screening & Surrogacy | CSP
Each cell has a nucleus that contains chromosomes. Humans have 23 pairs of chromosomes (Compared to chimps that have 24 pairs ... and chromosomes X and Y (the sex chromosomes). Sperm and eggs only contain 23 single chromosomes (one from each chromosome pair ... Most cells contain 23 pairs or 46 chromosomes. These include chromosomes 1 to 22 (the autosomes) ... Chromosome 17: Charcot-Marie-Tooth Disease Chromosome 18: Niemann-Pick Disease, pancreatic cancer Chromosome 21: Down syndrome ...
https://www.creatingfamilies.com/parents/?should-we-do-pgd-187
*  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 ... 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 method ... Chromosomes, Human, Pair 7, DNA Methylation, Female, Genetic Diseases, Inborn, Genomic Imprinting, Humans, Male, Polymerase ...
https://www.ndph.ox.ac.uk/publications/6441
*  Common genetic determinants of vitamin D insufficiency: a genome-wide association study. - The Kennedy Institute of Rheumatology
Canada, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 4, Cohort Studies, Dietary Supplements, Europe, European ... Kennedy Institute joins global Human Cell Atlas initiative * Professor Michael Dustin reviews innovative work for Nature ... Pengjun Xi * Bin Xie * Chun-Yao Yang * Shamsideen Yusuf * Izma Abdul Zani ... Continental Ancestry Group, Genetic Predisposition to Disease, Genome-Wide Association Study, Heterozygote, Homozygote, Humans ...
https://www.kennedy.ox.ac.uk/publications/66229
*  Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11. - Radcliffe...
18 cloned human DNA sequences from chromosome 11 were then used to identify restriction-fragment-length polymorphisms. A loss ... We conclude that a single inherited locus on chromosome 11, band q13, causes MEN-1 and that the monoclonal development of ... Pancreatic tumors have previously been shown to be associated with the loss of alleles on chromosome 11; we therefore looked ... the MEN-1 gene was thus mapped to the pericentromeric region of the long arm of chromosome 11 (11q13). Our location of the MEN- ...
https://www.rdm.ox.ac.uk/publications/28147
*  Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13...
Chromosome Mapping, Chromosomes, Artificial, Yeast, Chromosomes, Human, Pair 11, Gene Library, Humans, Multiple Endocrine ... Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 ... Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 ... Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 ...
https://www.rdm.ox.ac.uk/publications/28095