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/
Clinical significance of the translocation (11;14)(q13;q32) in multiple myeloma.
We have identified 24 patients at our institution who had t(11;14 ... 14)(q13;q32). Here, we describe the clinical characteristics of ... Chromosomes, Human, Pair 11 / genetics, ultrastructure*. Chromosomes, Human, Pair 14 / genetics, ultrastructure*. Creatinine / ... Humans. Leukemia, Plasma Cell / genetics, mortality, pathology. Multiple Myeloma / drug therapy, genetics*, mortality, ... 2004308 - Extramedullary blast crisis in a patient with philadelphia chromosome-positive chronic .... 12506758 - Prognostic ...http://www.biomedsearch.com/nih/Clinical-significance-translocation-in-multiple/10609798.html
ZFIN Publication: Risinger et al., 1998
Chromosomes/genetics*; Chromosomes, Human, Pair 14/genetics; Chromosomes, Human, Pair 20/genetics; Cloning, Molecular; ... The two zebrafish snap25 loci are located in paralogous linkage groups that seem to correspond to human chromosome 20, which ... and human chromosome 14. Because no additional Snap25 homologue has been reported for any mammal or chicken, snap25.2 may have ... Amino Acid Sequence; Animals; Base Sequence; Chickens/genetics*; Chromosome Mapping (all 27) Amino Acid Sequence; Animals; Base ...https://zfin.org/ZDB-PUB-981209-14
"Familial and sporadic Alzheimer's disease: neuropathology cannot exclu" by Carol F. Lippa, Ann M. Saunders et al.
... six AD patients with mutations of chromosome 21 (codon 717 of the beta-amyloid percursor protein gene), and 11 sporadic AD (SAD ... Chromosomes, Human, Pair 21; Gene Frequency; Humans; Linkage (Genetics); Middle Aged; Mutation; Neurites; Neurofibrillary ... six AD patients with mutations of chromosome 21 (codon 717 of the beta-amyloid percursor protein gene), and 11 sporadic AD (SAD ... Chromosomes, Human, Pair 14; ...https://escholarship.umassmed.edu/neuro_pp/300/
Chromosome 14 (human) - Wikipedia
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 14". Genet Test. 3 (4): 379-91. ... The following is a partial list of genes on human chromosome 5. For complete list, see the link in the infobox on the right. ... Kamnasaran D, Cox DW (2002). "Current status of human chromosome 14". J Med Genet. 39 (2): 81-90. doi:10.1136/jmg.39.2.81. PMC ... The following are some of the gene count estimates of human chromosome 14. Because researchers use different approaches to ...https://en.wikipedia.org/wiki/Chromosome_14_(human)
SOX11 as a minimal residual disease marker for Mantle cell lymphoma - Danish National Research Database
Aged; Aged, 80 and over; Case-Control Studies; Chromosomes, Human, Pair 11; Chromosomes, Human, Pair 14; Female; Gene ... Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 14, Female, Gene Expression Regulation, Neoplastic, Humans, Lymphoma, ... Expression Regulation, Neoplastic; Humans; Lymphoma, Mantle-Cell; Male; Middle Aged; Monitoring, Physiologic; Neoplasm Staging ...http://www.forskningsdatabasen.dk/en/catalog/266969816
Akkari, P. A.<...
Chromosomes, Human, Pair 14 Medicine & Life Sciences Muscular Diseases Medicine & Life Sciences ... Production of human skeletal α-actin proteins by the baculovirus expression system. Akkari, P. A., Nowak, K., Beckman, S. K., ... Early onset chromosome 14-linked distal myopathy (Laing). Mastaglia, F., Phillips, B. A., Cala, L., Meredith, C., Egli, S., ... Adjunct Senior Teaching Fellow, Faculty of Science, School of Human Sciences. *Contractor / Visitor, Faculty of Health and ...https://research-repository.uwa.edu.au/en/persons/anthony-akkari
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/
DECLARATION of Emanuel Petricoin, Ph for Association For Molecular Pathology et al v. United States Patent and Trademark Office...
The human genome comprises about 3 billion nucleotides organized into 23 chromosome pairs. Each chromosome comprises DNA and ... The isolated sequences are no longer located on a human chromosome and therefore are not necessarily assembled in the native ... While a human body does transcribe a gene into mRNA, which is then translated into a protein, the human body does not isolate ... Genes and human genetic sequences are comprised of DNA. The term DNA is an acronym for a chemical compound which is also known ...https://docs.justia.com/cases/federal/district-courts/new_york/nysdce/1:2009cv04515/345544/203
ZIP9 - Wikipedia
... in the SLC39A9 gene can occur due to genetic deletion of the q24.1-24.3 band of base pairs within the human chromosome 14. This ... ZIP9 influxes zinc ions into the cytosol and its gene is expressed almost in every tissue of human body. The sub-cellular ... Role of human ZIP9 in testosterone-induced prostate and breast cancer cell apoptosis". Endocrinology. 155 (11): 4250-65. doi: ... A study in 2014, elucidated the intermediary role of ZIP9 in causing human breast and prostate cancer, as it induced the ...https://en.wikipedia.org/wiki/ZIP9
Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE). - Nuffield Department of...
Cell Line, Chromosomes, Human, Pair 14, Cytokines, GPI-Linked Proteins, Gene Expression Regulation, Genetic Linkage, Genetic ... Loci, Genetic Predisposition to Disease, Humans, Lupus Erythematosus, Systemic, Monocytes, Neural Cell Adhesion Molecules, Odds ...https://www.ndph.ox.ac.uk/publications/7820
Chromosome 14 - Genetics Home Reference
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 14, one copy inherited from ... Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 14. Genet Test. 1999;3(4):379-91. ... Ensembl Human Map View. *. Falk MJ, Curtis CA, Bass NE, Zinn AB, Schwartz S. Maternal uniparental disomy chromosome 14: case ... The DNA Sequence and Analysis of Human Chromosome 14. Nature. 2003 Feb 6;421(6923):601-7. (PDF) ...https://ghr.nlm.nih.gov/chromosome/14
Big data allows computer engineers to find genetic clues in humans - McKelvey School of Engineering at Washington University...
Applied Science tackled some big data about an important protein and discovered its connection in human history as well as ... Humans carry pairs of chromosomes, and 30 percent of Japanese individuals carry two yin haplotypes or two yang haplotypes. ... Louis showed a massive yin-yang haplotype pair encompassing the gene gephyrin on human chromosome 14. ... Big data finds genetic clues in humans - Science Codex. * Mining public big data yields genetic clues in complex human diseases ...https://engineering.wustl.edu/news/Pages/Big-data-allows-computer-engineers-to-find-genetic-clues-in-humans.aspx
Expression of the bcl-2 oncogene product and chromosomal translocation t(14;18) in Hodgkin's disease. - Radcliffe Department of...
In a smaller number of cases this expression of bcl-2 could be explained by the presence of the translocation t(14;18). ... The reciprocal chromosomal translocation t(14;18), leading to overexpression of this oncogene, can be found in the majority of ... 14;18) translocation. We were particularly interested to determine whether nodular paragranuloma (lymphocyte-predominant, ... Chromosomes, Human, Pair 18, Gene Expression, Hodgkin Disease, Humans, Immunoenzyme Techniques, Polymerase Chain Reaction, ...https://www.rdm.ox.ac.uk/publications/486737
WikiPremed MCAT Course - Human Genetics
... translocation is a common form of chromosomal rearrangement that occurs in the five acrocentric human chromosome pairs, namely ... Human Y-chromosome DNA haplogroups. Human Y-chromosome DNA haplogroups are large groups of haplotypes defined by differences in ... XYY syndrome is an aneuploidy of the sex chromosomes in which a human male receives an extra Y chromosome. ... Y-chromosomal Adam is the patrilineal human most recent common ancestor from whom all Y chromosomes in living men are descended ...https://www.wikipremed.com/mcat_course.php?code=040406
The mechanism of chromosome 14 inversion in a human T cell lymphoma. - Radcliffe Department of Medicine
Therefore, chromosome inversion and IgT formation were mediated by two sequential VH-J alpha joining events. Moreover, ... a cell line derived from a human T cell lymphoma. Here, we report that the centromeric breakpoint in SUP-T1 constitutes the ... The chromosome 14 inversion produces cytogenetic breakpoints at either end of the long arm of this chromosome. Previous studies ... Chromosome Inversion, Chromosome Mapping, Chromosomes, Human, Pair 14, DNA Restriction Enzymes, Humans, Immunoglobulin Heavy ...https://www.rdm.ox.ac.uk/publications/601879
Active RNA polymerases: mobile or immobile molecular machines? - Oxford Neuroscience
We test this using chromosome conformation capture and human genes switched on rapidly and synchronously by tumour necrosis ... Base Pairing, Cells, Cultured, Chromosomes, Human, Pair 14, DNA-Directed RNA Polymerases, Enzyme Activation, Humans, In Situ ... We test this using chromosome conformation capture and human genes switched on rapidly and synchronously by tumour necrosis ...https://www.neuroscience.ox.ac.uk/publications/65905
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes. - PubMed - NCBI
Chromosomes, Human, Pair 14/genetics*. *Diabetes Mellitus, Type 1/genetics*. *Family Health ... The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.. Wallace C1, Smyth DJ, ... The imprinted region on chromosome 14q32.2. The region shown is delimited by the most distant genes known to be imprinted 8 ... Our meta-analysis also provided support at genome-wide significance for a T1D locus at chromosome 19p13.2. The highest ...https://www.ncbi.nlm.nih.gov/pubmed/19966805
Using an experimentally acquired dataset for human chromosome 14, tandem repeats > 200 bp were assembled. Alignment of the ... is derived from an identity-based protocol without pairing. Moreover, this proposed protocol is provably secure in the CK model ... for the assembly of repetitive sequences by constructing contigs directly from paired-end reads. ... contigs to the human genome reference (GRCh38) revealed that 84.3% of tandem repetitive regions were correctly covered. For ...https://www.inderscience.com/info/ingeneral/forthcoming.php?jcode=ijhpcn
Comparison of familial and sporadic chronic lymphocytic leukaemia using high resolution array comparative genomic hybridization...
Chromosomes, Human, Pair 11/genetics. *Chromosomes, Human, Pair 13/genetics. *Chromosomes, Human, Pair 14/genetics ...https://www.ncbi.nlm.nih.gov/pubmed/20812997
S182: from worm sperm to Alzheimer's disease. - Wellcome Centre for Integrative Neuroimaging
Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 21, Genes, Humans, Membrane Proteins, Mutation, Presenilin-1 ... Alzheimer Disease, Amyloid beta-Protein Precursor, Apolipoproteins E, Chromosome Mapping, Chromosomes, Human, Pair 14, ...https://www.win.ox.ac.uk/publications/657628
Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and hedgehog signaling pathways...
Because BMP4 interacts with HH signaling genes in animals, we evaluated gene expression in human embryos and demonstrate ... of low-penetrant variants in BMP4 and HH signaling partners is suggestive of an interaction between the two pathways in humans. ... Using in situ hybridization in human embryos, we demonstrate expression of BMP4 in optic vesicle, developing retina and lens, ... Bone Morphogenetic Protein 4, Bone Morphogenetic Proteins, Chromosome Aberrations, Chromosomes, Human, Pair 14, Cohort Studies ...https://www.ndcn.ox.ac.uk/publications/186522
PACE - Doc. 14328 (2017) - The use of new genetic technologies in human beings
The human genome is the complete set of DNA within the 23 chromosome pairs in cell nuclei and in a small DNA molecule found ... including the Universal Declaration on the Human Genome and Human Rights in 1997, the International Declaration on Human ... 5. The 1997 Council of Europe Convention for the Protection of Human Rights and Dignity of the Human Being with regard to the ... Indeed, the 1997 Council of Europe Convention for the Protection of Human Rights and Dignity of the Human Being with regard to ...http://assembly.coe.int/nw/xml/XRef/Xref-XML2HTML-en.asp?fileid=23730&lang=en
PAX1 - Wikipedia
... a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ ... Paired box protein Pax-1 is a protein that in humans is encoded by the PAX1 gene. This gene is a member of the paired box (PAX ... 1989). "Conservation of the paired domain in metazoans and its structure in three isolated human genes". EMBO J. 8 (4): 1183-90 ... 2002). "The DNA sequence and comparative analysis of human chromosome 20". Nature. 414 (6866): 865-71. doi:10.1038/414865a. ...https://en.wikipedia.org/wiki/PAX1
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