Errors in chromosome segregation during oogenesis and early embryogenesis   - WRAP: Warwick Research Archive Portal  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, ...
more infohttp://wrap.warwick.ac.uk/3796/
Interdisciplinary Program of Integrated OMICS for Biomedical Sciences<...  Interdisciplinary Program of Integrated OMICS for Biomedical Sciences<...
200+ Protein Concentrations in Healthy Human Blood Plasma: Targeted Quantitative SRM SIS Screening of Chromosomes 18, 13, Y, ... and the Mitochondrial Chromosome Encoded Proteome. Kopylov, A. T., Ponomarenko, E. A., Ilgisonis, E. V., Pyatnitskiy, M. A., ...
more infohttps://yonsei.pure.elsevier.com/en/organisations/interdisciplinary-program-of-integrated-omics-for-biomedical-scie
Find Research Outputs
             - Yonsei University  Find Research Outputs - Yonsei University
200+ Protein Concentrations in Healthy Human Blood Plasma: Targeted Quantitative SRM SIS Screening of Chromosomes 18, 13, Y, ... and the Mitochondrial Chromosome Encoded Proteome. Kopylov, A. T., Ponomarenko, E. A., Ilgisonis, E. V., Pyatnitskiy, M. A., ... Park, J., Ryu, J. & Yang, S-B., 2019 May 1, In : Wireless Networks. 25, 4, p. 1519-1531 13 p.. Research output: Contribution to ... tissue-derived mesenchymal stem cells cultured at high density express IFN-β and TRAIL and suppress the growth of H460 human ...
more infohttps://yonsei.pure.elsevier.com/en/publications/
Chromosome 13 (human) - Wikipedia  Chromosome 13 (human) - Wikipedia
The following is a partial list of genes on human chromosome 5. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 13. Because researchers use different approaches to ... People normally have two copies of this chromosome. Chromosome 13 spans about 114 million base pairs (the building material of ... International Standing Committee on Human Cytogenetic Nomenclature (2013). ISCN 2013: An International System for Human ...
more infohttps://en.wikipedia.org/wiki/Chromosome_13_(human)
SONIA LARACH  WALTERS - Resultado de la investigación
     - Universidad Andrés Bello  SONIA LARACH WALTERS - Resultado de la investigación - Universidad Andrés Bello
Significant evidence for a schizophrenia susceptibility locus in the centromeric region of human chromosome. Shaw, S. H., ... A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder. ... Lack of evidence for linkage to chromosomes 13 and 8 for schizophrenia and schizoaffective disorder. Delisi, L. E., Shaw, S., ... Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder. DeLisi, L. E ...
more infohttps://researchers.unab.cl/es/persons/sonia-larach-walters-3/publications/?type=%2Fdk%2Fatira%2Fpure%2Fresearchoutput%2Fresearchoutputtypes%2Fcontributiontojournal%2Farticle
SONIA LARACH  WALTERS - Resultado de la investigación
     - Universidad Andrés Bello  SONIA LARACH WALTERS - Resultado de la investigación - Universidad Andrés Bello
Significant evidence for a schizophrenia susceptibility locus in the centromeric region of human chromosome. Shaw, S. H., ... A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder. ... Lack of evidence for linkage to chromosomes 13 and 8 for schizophrenia and schizoaffective disorder. Delisi, L. E., Shaw, S., ... Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder. DeLisi, L. E ...
more infohttps://researchers.unab.cl/es/persons/sonia-larach-walters-3/publications/
Fonseca, R.<...  Fonseca, R.<...
Chromosome Aberrations Multiple Myeloma Fluorescence In Situ Hybridization Chromosomes, Human, Pair 13 ...
more infohttps://mayoclinic.pure.elsevier.com/en/persons/rafael-fonseca
Array-MLPA analysis of chromosome X monosomy mosaicism. | Open-i  Array-MLPA analysis of chromosome X monosomy mosaicism. | Open-i
The average copy number on chromosome X was 0.71. (B) G-bandi ... Array-MLPA analysis of chromosome X monosomy mosaicism. (A) A ... Chromosomes, Human, Pair 18. *Chromosomes, Human, Pair 21. *Chromosomes, Human, X. *Chromosomes, Human, Y ... Background: Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well as sex chromosome aneuploidy, are ... Background: Chromosome abnormalities, especially trisomy of chromosome 21, 13, or 18 as well as sex chromosome aneuploidy, are ...
more infohttps://openi.nlm.nih.gov/detailedresult.php?img=PMC3111339_1471-2350-12-68-4&req=4
CHEILOGNATO URANO STAFILOSCHISI ASSOCIATA A T (Y;13)<...  CHEILOGNATO URANO STAFILOSCHISI ASSOCIATA A T (Y;13)<...
Q band determination of the karyotype showed an unbalanced translocation of the luminous part of the Y chromosome on to the ... Q band determination of the karyotype showed an unbalanced translocation of the luminous part of the Y chromosome on to the ... Q band determination of the karyotype showed an unbalanced translocation of the luminous part of the Y chromosome on to the ... Q band determination of the karyotype showed an unbalanced translocation of the luminous part of the Y chromosome on to the ...
more infohttps://moh-it.pure.elsevier.com/en/publications/a-case-of-harelip-and-cleft-palate-associated-with-y-13-transloca
RMMG - Revista Médica de Minas Gerais  RMMG - Revista Médica de Minas Gerais
Keywords Chromosomes, Human, Pair 13; Abnormalities; Ring Chromosomes; Genetic Counseling. Artigos de Revisão 10 - Memória de ... We describe an individual with ring chromosome 13, whose clinical picture concern at the group 2 of Brown's et al. ... The characterization of the clinical and cytogenetical aspects involving structural abnormalities of chromosome 13 contributes ... Descreve-se um indivíduo portador de cromossomo 13 em anel, cujo quadro clínico é compatível com o grupo 2 de Brown et al. ( ...
more infohttp://www.rmmg.org/Sumario/49
Search Articles | University of Toronto Libraries  Search Articles | University of Toronto Libraries
Human, X , Pregnancy , Chromosomes, Human, Y , Trisomy - diagnosis , Sex Chromosome Aberrations , Chromosomes, Human, Pair 18 ... Chromosomes, Human, Pair 18 , Sensitivity and Specificity , Chromosomes, Human, Pair 13 , Adult , Female , Down Syndrome - ... Chromosomes, Human, Pair 18 , Epidemiologic Methods , Adolescent , Chromosomes, Human, Pair 13 , Turner Syndrome - genetics , ... Chromosomes, Human, Pair 18 , Adolescent , Chromosomes, Human, Pair 13 , Index Medicus ...
more infohttps://query.library.utoronto.ca/index.php/search/q?kw=SubjectTerms:Trisomy%2013%20Syndrome%20-%20blood
Genetic predisposition to breast cancer  Genetic predisposition to breast cancer
Breast Neoplasms, Chromosomes, Human, Pair 13, Chromosomes, Human, Pair 17, Female, Genes, Tumor Suppressor, Genes, p53, ... Chromosomes, Human, Pair 13,Chromosomes, Human, Pair 17,Female,Genes, Tumor Suppressor,Genes, p53,Genetic Linkage,Genetic ... Genetic Linkage, Genetic Markers, Genetic Predisposition to Disease, Genetic Testing, Humans, Mutation. in Acta oncologica ( ... Markers,Genetic Predisposition to Disease,Genetic Testing,Humans,Mutation}, language = {eng}, number = {1}, pages = {1--8}, ...
more infohttps://lup.lub.lu.se/search/publication/4a5b78be-d49a-4e06-839f-d72bc6485291
WikiPremed MCAT Course - Human Genetics  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 ...
more infohttps://www.wikipremed.com/mcat_course.php?code=040406
What Is the Difference Between Chromosomes and Genes? | Reference.com  What Is the Difference Between Chromosomes and Genes? | Reference.com
Each chromosome contains one DNA molecule and each DNA molecule contains several genes or... ... Genes are individual segments of DNA and chromosomes are structures which contain many genes packed together. ... while a human being has 46 chromosomes, or 23 pairs. Human chromosomes range from 300 genes to 8,000 genes in size. ... Do Homologous Pairs of Chromosomes Carry the Same Genes?. A: Homologous pairs of chromosomes carry the same genes. Although the ...
more infohttps://www.reference.com/science/difference-between-chromosomes-genes-5e2283fb1be45eaa
miRNA Search Results  miRNA Search Results
... that are located within an 800-base pair region of human chromosome 13. [score:1] ... The human chromosome 13 MIR17HG cluster (800bp) encodes six tightly grouped miRNAs with four distinct "seed" sequences 31, 50: ... The human miR-17 family consists of eight miRNAs (miR-17, miR-18a/b, miR-20a/b, miR-93, and miR-106a/b), with three of these ( ... In human BCL2, we identified 13 binding sites for miR-17∼19b miRNAs (five sites for miR-17, six sites for miR-18a and two sites ...
more infohttp://www.mirbase.org/cgi-bin/sentences.pl?acc=MI0000072
Chromosome 13 - Genetics Home Reference  Chromosome 13 - Genetics Home Reference
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 13, one copy inherited from ... The DNA sequence and analysis of human chromosome 13. Nature. 2004 Apr 1;428(6982):522-8. (PDF) ... The DNA sequence and analysis of human chromosome 13. Nature. 2004 Apr 1;428(6982):522-8. ... Can changes in the number of chromosomes affect health and development?. *Can changes in the structure of chromosomes affect ...
more infohttps://ghr.nlm.nih.gov/chromosome/13
Stock Options Profits from Low Cost Gene Sequencing  Stock Options Profits from Low Cost Gene Sequencing
There is a race going on to lower the cost human gene sequencing to a level of a comprehensive battery of blood tests. The ... called chromosomes. These strands are paired, connected side to side along their lengths. Humans have 23 pairs of chromosomes. ... These strands are paired, connected side to side along their lengths. Humans have 23 pairs of chromosomes. www.Options-Trading- ... The human genome is the sum total of all human genes.Human genes are present on long strands of DNA (complex molecules) called ...
more infohttps://www.slideshare.net/InvestingTips/stock-options-profits-from-low-cost-gene-sequencing
science - Revision Cards in GCSE Biology  science - Revision Cards in GCSE Biology
... names of chromosomes and order of chromosomes (A B X Y). each human has 26 pairs of chromosomes. 13 from each parent. defaults ... the human genome project was set up to identify all of the genes and chromosomes in the human body, therefore increasing the ... this is the structure of the human body. the order goes like this. cells - nucleus - genes - chromosomes - ... in chromosomes cause illnesses like sickle cell anemia and down syndrome.. ...
more infohttps://getrevising.co.uk/revision-cards/science_51
Robertsonian translocation - Wikipedia  Robertsonian translocation - Wikipedia
In humans, Robertsonian translocations generally occur in the five acrocentric chromosome pairs, namely 13, 14, 15, 21 and 22. ... or non-homologous chromosomes (i.e. two different chromosomes, not belonging to a homologous pair). A feature of chromosomes ... This type of translocation is cytologically visible, and can reduce chromosome number (from 23 to 22 pairs, in humans) if the ... In humans, when a Robertsonian translocation joins the long arm of chromosome 21 with the long arm of chromosomes 14 or 15, the ...
more infohttps://en.wikipedia.org/wiki/Robertsonian_translocation