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*  Sex chromosome | genetics | Britannica.com
In humans the sex chromosomes comprise one pair of the total of 23 pairs of chromosomes. The other ... either of a pair of chromosomes that determine whether an individual is male or female. The sex chromosomes of human beings and ... In humans the sex chromosomes comprise one pair of the total of 23 pairs of chromosomes. The other 22 pairs of chromosomes are ... Sex chromosome, either of a pair of chromosomes that determine whether an individual is male or female. The sex chromosomes of ...
https://www.britannica.com/science/sex-chromosome
*  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/
*  The Process of Meiosis- Online Textbook Chapters - Alyvea.com
... where n is the number of chromosomes per set. Humans have 23 chromosome pairs, which results in over eight million (223) ... Recall that, in mitosis, homologous chromosomes do not pair together. In mitosis, homologous chromosomes line up end-to-end so ... there is just one of each pair of the homologous chromosomes. Therefore, only one full set of the chromosomes is present. This ... in which homologous chromosomes are paired and exchange non-sister chromatid segments. The homologous chromosomes separate into ...
http://alyvea.com/biology-textbook/meiosis.php
*  Isolated trisomy 15: a clonal chromosome abnormality in bone marrow with doubtful hematologic significance.
... trisomy 15 (with or without -Y), who did not have any morphologic or clinical features of hematologic disease at initial ... Chromosome Deletion. Chromosomes, Human, Pair 15 / genetics*. Chromosomes, Human, Y / genetics. Female. Humans. In Situ ... a clonal chromosome abnormality in bone marrow with doubtful hematologic significance. ... Clonal trisomy 15 in isolation or in combination with -Y is an uncommon cytogenetic finding that does not seem to be associated ...
http://www.biomedsearch.com/nih/Isolated-trisomy-15-clonal-chromosome/18285273.html
*  Assessment of hyperphagia in Prader-Willi syndrome.
Chromosome Mapping. Chromosomes, Human, Pair 15. Factor Analysis, Statistical. Female. Humans. Hyperphagia / epidemiology*. ... Vanderbilt Kennedy Center for Research on Human Development, 230 Appleton Place, Peabody Box 40, Vanderbilt University, ... Title: Obesity (Silver Spring, Md.) Volume: 15 ISSN: 1930-7381 ISO Abbreviation: Obesity (Silver Spring) Publication Date: 2007 ...
http://www.biomedsearch.com/nih/Assessment-hyperphagia-in-Prader-Willi/17636101.html
*  QIMR Genetic Epidemiology Laboratory Home Page
Chromosomes, Human, Pair 15. genetics. Cohort Studies. genetics. Endometriosis. genetics. Female. genetics. ...
https://genepi.qimr.edu.au/general/publicationsfulllisting.cgi?pmid=21151130
*  Protein kinase profiling in miscarriage: implications for the pathogenesis of trisomic pregnancy. | CureHunter
Chromosomes, Human, Pair 15 (genetics) *Chromosomes, Human, Pair 16 (genetics) *Female. *Gene Amplification ... including dosage-dependent over-expression of the chromosome 16-encoded ERK1 in trisomy 16. This supports a role for chromosome ... with trisomy 16 the most common trisomy in human conceptions. The pathogenesis and protein expression profiles in trisomic ... trisomy 16 or trisomy 15) and compared to chromosomally normal (euploid) miscarriages (n = 4). ...
http://www.curehunter.com/public/pubmed23231796.do
*  acute promyelocytic leukemia childhood 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
MeSH-major] Chromosomes, Human, Pair 4. Chromosomes, Human, Pair 5. Leukemia, Promyelocytic, Acute / genetics. Leukemia, ... Chromosomes, Human, Pair 17. Humans. Prognosis. Translocation, Genetic. *Genetic Alliance. consumer health - Acute ... Chromosomes, Human, Pair 8. Core Binding Factor Alpha 2 Subunit / genetics. Female. Humans. Infant. Kaplan-Meier Estimate. Male ... Chromosomes, Human, Pair 9. Cytogenetics. Humans. In Situ Hybridization, Fluorescence. Infant. Molecular Sequence Data. Reverse ...
http://www.bmlsearch.com/?kwr=acute+promyelocytic+leukemia+childhood+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  FEV1 by CHRNA3 genotype (rs1051730) in the AAT Genetic | Open-i
Chromosomes, Human, Pair 15/genetics. *Female. *Humans. *Male. *Middle Aged. *Polymorphism, Single Nucleotide ... 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=PMC3306733_1465-9921-13-16-1&req=4
*  Chromosome 15 (human) - Wikipedia
Gilbert F (1999). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 15". Genet Test. 3 (3): 309-322 ... The human leukocyte antigen gene for β2-microglobulin is found at chromosome 15. The following are some of the gene count ... The following is a partial list of genes on human chromosome 15. For complete list, see the link in the infobox on the right. ... The program...recounts how one scientist determined how the deletion of a key sequence of DNA on human chromosome 15 could lead ...
https://en.wikipedia.org/wiki/Chromosome_15_(human)
*  Angelman syndrome in Denmark. birth incidence, genetic findings, and age at diagnosis - Danish National Research Database
Chromosome Deletion; Chromosome Duplication; Chromosomes, Human, Pair 15; Denmark; Female; Humans; Incidence; Male Main ... Five patients had paternal uniparental disomy (pUPD) of chromosome 15, and four had a verified UBE3A mutation. Additional ... is a neurogenetic disorder caused by loss of expression of the maternal imprinted gene UBE3A on chromosome 15q11.2-q13. ...
http://www.forskningsdatabasen.dk/en/catalog/244254215
*  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 16 / genetics. Chromosomes, Human, Pair 22 / genetics. Leukemia, Myeloid, Acute / genetics ... MeSH-major] Chromosomes, Human, Pair 10 / genetics. Chromosomes, Human, Pair 17 / 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
*  Dorsal and ventral stream mediated visual processing in genetic subtypes of Prader-Willi syndrome. - PSY
Adolescent, Analysis of Variance, Child, Chromosome Deletion, Chromosomes, Human, Pair 15, Female, Fragile X Mental Retardation ... Protein, Humans, Male, Neuropsychological Tests, Pattern Recognition, Visual, Photic Stimulation, Prader-Willi Syndrome, ...
https://www.psy.ox.ac.uk/publications/311493
*  VNTR polymorphism in the hepatic lipase gene (LIPC). - Radcliffe Department of Medicine
Base Sequence, Chromosomes, Human, Pair 15, European Continental Ancestry Group, Humans, Lipase, Liver, Molecular Sequence Data ...
https://www.rdm.ox.ac.uk/publications/165114
*  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 ...
https://en.wikipedia.org/wiki/Robertsonian_translocation
*  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
*  Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families. - Radcliffe Department of Medicine
Body Height, Body Mass Index, Chromosome Mapping, Chromosomes, Human, Pair 11, Chromosomes, Human, Pair 15, Chromosomes, Human ... Pair 16, Chromosomes, Human, Pair 3, Eye Diseases, Female, Genetic Linkage, Growth Disorders, Humans, Kidney, Laurence-Moon ...
https://www.rdm.ox.ac.uk/publications/826713
*  Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypes. - PubMed - NCBI
Chromosome Deletion*. *Chromosomes, Human, Pair 15. *Cohort Studies. *DNA Copy Number Variations ... identified from this study are shown in solid lines with base pair positions of BPs confirmed by aCGH. These base pair ... have maternal-only expression in mouse and humans, and this imprinted expression is limited to certain tissue-specific regions ...
https://www.ncbi.nlm.nih.gov/pubmed/22045295
*  Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2. -...
Chromosome Deletion*. *Chromosomes, Human, Pair 15/genetics*. *DNA Copy Number Variations/genetics* ... The proximal region of chromosome 15 is one of the genomic hotspots for copy number variants (CNVs). Among the rearrangements ... Transmission disequilibrium test revealed significant preferential transmission only for the duplicated chromosome in probands ...
https://www.ncbi.nlm.nih.gov/pubmed/24821083
*  Identification of a novel proinsulin-associated SNP and demonstration that proinsulin is unlikely to be a causal factor in...
An 11-SNP score, including the previously identified and the chromosome 15 proinsulin-associated loci, was significantly and ... Linear regression was used to identify proinsulin-associated genetic variants.We identified a proinsulin locus on chromosome 15 ... IMPROVE study group, Chromosomes, Human, Pair 15, Humans, Carotid Artery Diseases, Genetic Predisposition to Disease, ... Linear regression was used to identify proinsulin-associated genetic variants.We identified a proinsulin locus on chromosome 15 ...
https://www.bdi.ox.ac.uk/publications/737221
*  Longer leukocyte telomere length is associated with smaller hippocampal volume among non-demented APOE ε3/ε3 subjects
They consist of tandemly repeated non-coding short nucleotide sequences (TTAGGG in all vertebrates), in humans spanning over ... Telomeres are the outermost parts of linear chromosomes. ... the last 2 to 15 kilobase pairs of the chromosome. Due to the ...
http://umu.diva-portal.org/smash/record.jsf?pid=diva2:516681
*  https://www.medicalnewstoday.com/articles/182287.php
All human genes come in pairs, except for those related to sex characteristics. One copy is from the father, called the ... In PWS, it is thought that the paternal genes on chromosome 15 are either missing or faulty. ... It remains unclear which genes are involved, but the abnormality is found on chromosome 15. ... People with PWS have seven genes on chromosome 15 that are deleted or unexpressed. ...
https://www.medicalnewstoday.com/articles/182287.php
*  Genetic polymorphisms in 15q25 and 19q13 loci, cotinine levels, and risk of lung cancer in EPIC. - Oxford Big Data Institute
Chromosomes, Human, Pair 19, Humans, Adenocarcinoma, Carcinoma, Large Cell, Carcinoma, Squamous Cell, Lung Neoplasms, Cotinine ... Chromosomes, Human, Pair 15, ...
https://www.bdi.ox.ac.uk/publications/175151
*  March 1996 Senate Hearing on NIH Revitalization, Cancer and Genetics - National Human Genome Research Institute (NHGRI)
... statement before the Senate Labor and Human Resources Committee's March 6-7, 1996 hearing on NIH revitalization, cancer and ... National Center for Human Genome Research Director Francis Collins' ... detailed maps of the 23 pairs of human chromosomes and sequencing the 3 billion nucleotide bases that make up the human genome ... Director, National Center for Human Genome Research. March 6-7, 1996. The Human Genome Project. The Human Genome Project is a ...
https://www.genome.gov/10002350/march-1996-senate-hearing-on-nih-revitalization-cancer-and-genetics/