*  Common genetic variants on chromosome 9p21 predict perioperative myocardial injury after coronary artery bypass graft surgery.
Chromosomes, Human, Pair 9 / genetics*. Coronary Artery Bypass / adverse effects*. Female. Genetic Variation*. Humans. Linkage ... identified an association between myocardial infarction in nonsurgical populations and common genetic variants on chromosome ...
  http://www.biomedsearch.com/nih/Common-genetic-variants-chromosome-9p21/19819472.html
*  Frequent genetic alterations in simple urothelial hyperplasias of the bladder in patients with papillary urothelial carcinoma ...
Chromosomes, Human, Pair 9/genetics. MESH. Female. MESH. Gene Deletion. MESH. Humans. MESH. ... Six out of 12 samples of microdissected normal urothelium also showed genetic alterations on chromosome 9. Microdissection of ... showed deletions of chromosome 9. In 7 out of 8 patients with genetic alterations in the hyperplasias the genetic change was ... in situ hybridization was done using a dual color staining technique of biotinylated centromeric probes of chromosomes 9 and 17 ...
  https://epub.uni-regensburg.de/15355/
*  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
*  Chromosome 9 (human) - Wikipedia
Gilbert F, Kauff N (2001). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 9". Genet Test. 5 (2): ... People normally have two copies of this chromosome, as they normally do with all chromosomes. Chromosome 9 spans about 138 ... million base pairs of nucleic acids (the building blocks of DNA) and represents between 4 and 4.5 percent of the total DNA in ... See also: Category:Genes on human chromosome 9. The following is a partial list of genes on human chromosome 9. For complete ...
  https://en.wikipedia.org/wiki/Chromosome_9_(human)
*  Loss of heterozygosity at chromosome 9p in ductal carcinoma in situ and invasive carcinoma of the breast. - The Christie...
Chromosomes, Human, Pair 9. -. dc.subject.mesh. DNA, Neoplasm. -. dc.subject.mesh. Female. - ... Loss of heterozygosity at chromosome 9p in ductal carcinoma in situ and invasive carcinoma of the breast.. Authors:. Marsh, K L ... In addition to the gene encoding p16, chromosome 9p is also thought to contain other putative tumour-suppressor genes. If the ... In addition to the gene encoding p16, chromosome 9p is also thought to contain other putative tumour-suppressor genes. If the ...
  http://christie.openrepository.com/christie/handle/10541/92916
*  Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. -...
BACKGROUND: Chromosome 9p21 variants have been robustly associated with coronary heart disease, but questions remain on the ... Chromosomes, Human, Pair 9, Coronary Angiography, Coronary Artery Disease, Genetic Loci, Humans, Myocardial Infarction, ... Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. ... Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis. ...
  https://www.rdm.ox.ac.uk/publications/375736
*  Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
Case-Control Studies, Chromosomes, Human, Pair 9, Genes, p16, Genetic Predisposition to Disease, Genome-Wide Association Study ... Chromosomes, Human, Pair 9,Genes, p16,Genetic Predisposition to Disease,Genome-Wide Association Study,Humans,Precursor Cell ... Humans, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Journal Article, Research Support, Non-U.S. Gov't. in Nature Genetics. ...
  https://lup.lub.lu.se/search/publication/20c09338-9512-40ce-a42f-69179ad044c3
*  acute promyelocytic leukemia childhood 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 8. Core Binding Factor Alpha 2 Subunit / genetics. Female. Humans. Infant ... Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 17. Humans. Prognosis. Translocation, Genetic ... MeSH-major] Chromosomes, Human, Pair 15. Chromosomes, Human, Pair 17. Leukemia, Promyelocytic, Acute / genetics. Oncogene ... MeSH-major] Chromosomes, Human, Pair 4. Chromosomes, Human, Pair 5. Leukemia, Promyelocytic, Acute / genetics. Leukemia, ...
  http://www.bmlsearch.com/?kwr=acute+promyelocytic+leukemia+childhood+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. - Nuffield Department of Orthopaedics,...
... on chromosome 9q that had previously been linked to AS. We replicated these associations in a study of 730 AS patients compared ... in caspase recruitment domain-containing protein 9 (CARD9) and small nuclear RNA-activating complex polypeptide 4 (SNAPC4) ... Chromosomes, Human, Pair 9, Humans, Spondylitis, Ankylosing, DNA-Binding Proteins, Transcription Factors, Case-Control Studies ... Elucidating the chromosome 9 association with AS; CARD9 is a candidate gene. Share Share Share Share ...
  https://www.ndorms.ox.ac.uk/publications/108782
*  adult acute non lymphocytic leukemia in remission 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
MeSH-major] Chromosomes, Human, Pair 20. Chromosomes, Human, Pair 22. Chromosomes, Human, Pair 9. Leukemia, B-Cell / genetics. ... MeSH-major] Chromosome Deletion. Chromosomes, Human, Pair 17. Gene Expression Regulation, Leukemic. Hematopoietic Stem Cell ... Humans. Male. Recurrence. Sex Chromosomes / genetics. Sex Chromosomes / physiology. Transplantation Conditioning. Young Adult ... Chromosome Banding. Chromosome Mapping. Female. Humans. In Situ Hybridization, Fluorescence. Karyotyping. Male ...
  http://www.bmlsearch.com/?kwr=adult+acute+non+lymphocytic+leukemia+in+remission+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  Wellcome Sanger Institute - Wikipedia
The Institute was engaged in collaborations to sequence 8 of the 23 human pairs of chromosomes (1, 6, 9, 10, 13, 20, 22, and X ... "International Human Genome Sequencing Consortium Announces "Working Draft" of Human Genome". National Human Genome Research ... Human Genome Sequencing Consortium (2004). "Finishing the euchromatic sequence of the human genome". Nature. 431 (7011): 931- ... The Institute's research in human genetics focuses on the characterisation of human genetic variation in health and disease. ...
  https://en.wikipedia.org/wiki/Wellcome_Sanger_Institute
*  A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort...
Chromosomes, Human, Pair 9. *Cohort Studies. *European Continental Ancestry Group/genetics*. *Female ... Center for Human Genetics, Duke University Medical Center, Durham, NC, USA.. 4. NIHR Biomedical Research Centre at Moorfields ... analyses of the significantly associated SNPs were performed using data from the Multiple Tissue Human Expression Resource ( ...
  https://www.ncbi.nlm.nih.gov/pubmed/24518671
*  Aldolase B - Wikipedia
In humans, aldolase B is encoded by the ALDOB gene located on chromosome 9. The gene is 14,500 base pairs long and contains 9 ... Mutant alleles are a result of a number different types of mutations including base pair substitutions and small deletions. The ... 1988). "Human aldolase B gene: characterization of the genomic aldolase B gene and analysis of sequences required for multiple ... Ali M, Sebastio G, Cox TM (1994). "Identification of a novel mutation (Leu 256→Pro) in the human aldolase B gene associated ...
  https://en.wikipedia.org/wiki/Aldolase_B
*  Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. - PubMed - NCBI
Chromosomes, Human, Pair 9*. *DNA Repeat Expansion*. *Female. *Frontotemporal Dementia/genetics*. *Genetic Predisposition to ... Expanded GGGGCC hexanucleotide repeat in C9ORF72 causes FTD and ALS linked to chromosome 9p in family VSM-20 ... Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS.. DeJesus- ... Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked frontotemporal dementia and ...
  https://www.ncbi.nlm.nih.gov/pubmed/21944778?access_num=21944778&link_type=MED&dopt=Abstract
*  Exome sequencing reveals VCP mutations as a cause of familial ALS. - PubMed - NCBI
2010 Dec 9;68(5):857-64. doi: 10.1016/j.neuron.2010.11.036. Multicenter Study; Research Support, N.I.H., Extramural; Research ... Chromosomes, Human, Pair 9/genetics*. *Cohort Studies. *Exons/genetics*. *Female. *Humans. *Male ... An ideogram of chromosome 9 is shown at the top. The 17 exons of VCP are numbered. Mutations detected in familial ALS cases are ... Neuron. 2010 Dec 9;68(5):857-64. doi: 10.1016/j.neuron.2010.11.036. ...
  https://www.ncbi.nlm.nih.gov/pubmed/21145000
*  C9orf72 - Wikipedia
More precisely, the C9orf72 gene is located from base pair 27,546,542 to base pair 27,573,863 on chromosome 9. The mutation of ... The human C9orf72 gene is located on the short (p) arm of chromosome 9 open reading frame 72, from base pair 27,546,542 to base ... base pairs 27,546,542 to 27,573,863 The C9orf72 gene is located on the short (p) arm of chromosome 9 at position 21.2. ... "Human PubMed Reference:". "Mouse PubMed Reference:". C9orf72 chromosome 9 open reading frame 72 [Homo sapiens] - Gene - NCBI ...
  https://en.wikipedia.org/wiki/C9orf72
*  Heterogeneous multi-core computer architectures and - PDF
24 Human resources Human resources: HPC group (CAPA-SiPS): 4 PhD s 11 PhD Students Many MSc Students Currently working on these ... Human DNA has 3x10 9 base pairs organized in 23 chromosome pairs; High-Throughput Short Read (HTSR) sequencing technologies ... 9 Heterogeneous any-core processing 9. 10 Heterogeneous any-core processing Specialized processors - Dedicated cores: ... Portugal 9 th Workshop on Algorithms, Models and Tools for Parallel ...
  http://docplayer.com.br/9769267-Heterogeneous-multi-core-computer-architectures-and.html
*  HOXB1 (Human) Matched Antibody Pair - (H00003211-AP51) - Products - Abnova
This antibody pair set comes with matched antibody pair to detect and quantify protein level of human HOXB1. (H00003211-AP51 ... This gene is one of several homeobox HOXB genes located in a cluster on chromosome 17. [provided by RefSeq ... This antibody pair set comes with matched antibody pair to detect and quantify protein level of human HOXB1. ... Antibody pair set content:. 1. Capture antibody: mouse monoclonal anti-HOXB1 (100 ug). 2. Detection antibody: rabbit purified ...
  http://www.abnova.com/products/products_detail.asp?catalog_id=H00003211-AP51
*  Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis. - Oxford...
In a third OS case, WGS revealed paternal isodisomy for chromosome 9, leading to identification of the causal homozygous ... WGS500 Consortium, Chromosomes, Human, Pair 9, Humans, Epilepsy, Uniparental Disomy, Genetic Predisposition to Disease, ... In a third OS case, WGS revealed paternal isodisomy for chromosome 9, leading to identification of the causal homozygous ...
  https://www.bdi.ox.ac.uk/publications/447735
*  PAX7 - Wikipedia
Schäfer BW, Mattei MG (July 1993). "The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2". Genomics. 17 (1 ... Paired box protein Pax-7 is a protein that in humans is encoded by the PAX7 gene. Pax-7 plays a role in neural crest ... Pilz AJ, Povey S, Gruss P, Abbott CM (March 1993). "Mapping of the human homologs of the murine paired-box-containing genes". ... PAX7 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) PAX7 human gene location in the UCSC ...
  https://en.wikipedia.org/wiki/PAX7
*  HOXC8 (Human) Matched Antibody Pair - (H00003224-AP51) - Products - Abnova
This antibody pair set comes with matched antibody pair to detect and quantify protein level of human HOXC8. (H00003224-AP51 ... This gene is one of several homeobox HOXC genes located in a cluster on chromosome 12. The product of this gene may play a role ... This antibody pair set comes with matched antibody pair to detect and quantify protein level of human HOXC8. ... Antibody pair set content:. 1. Capture antibody: mouse monoclonal anti-HOXC8 (100 ug). 2. Detection antibody: rabbit purified ...
  http://www.abnova.com/products/products_detail.asp?catalog_id=H00003224-AP51
*  The Role of Osteoclast-Associated Receptor in Osteoimmunology | The Journal of Immunology
Murine Oscar is localized to chromosome 7, adjacent to a region where the paired Ig-like receptors family resides. The human ... OSCAR and human diseases. Knowledge about the role of OSCAR for human disease is limited to reports on skeletal and joint ... Structure-function relationship of human OSCAR. Human OSCAR contains two Ig-like motifs and one transmembrane domain, which ... Ligation of the FcR gamma chain-associated human osteoclast-associated receptor enhances the proinflammatory responses of human ...
  http://www.jimmunol.org/content/186/1/13
*  Coiled-Coil Domain Containing 142 - Wikipedia
The CCDC142 gene is located on chromosome 2 (at 2p13), spans 4339 base pairs and contains 9 exons. The gene codes for the ... "Microarray Data :: Allen Brain Atlas: Human Brain". human.brain-map.org. Retrieved 2016-05-01. "EST Profile - Hs.430199". www. ... Allen Human Brain Atlas Expression of CCDC142 Lateral View Red=Low Expression11 Frontal View Green=High Expression11 Above are ... The coding region is 8292 base pairs long, encoding for two protein isoforms 743 to 665 amino acids in length. On the telomeric ...
  https://en.wikipedia.org/wiki/Coiled-Coil_Domain_Containing_142
*  CD300C - Wikipedia
... gene structure predicts for an independently expressed member of an ITIM/ITAM pair of molecules localized to human chromosome ... "The gene encoding the immunoregulatory signaling molecule CMRF-35A localized to human chromosome 17 in close proximity to other ... CMRF35-like molecule 6 (CLM-6) also known as CD300 antigen-like family member C (CD300c) is a protein that in humans is encoded ... "Entrez Gene: CD300C CD300c molecule". Human CD300C genome location and CD300C gene details page in the UCSC Genome Browser. ...
  https://en.wikipedia.org/wiki/CD300C
*  CD300A - Wikipedia
... gene structure predicts for an independently expressed member of an ITIM/ITAM pair of molecules localized to human chromosome ... CD300A protein, human at the US National Library of Medicine Medical Subject Headings (MeSH) CD300a, Bernholtz - The Possible ... Alvarez Y, Tang X, Coligan JE, Borrego F (2007). "The CD300a (IRp60) inhibitory receptor is rapidly up-regulated on human ... 2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci ...
  https://en.wikipedia.org/wiki/CD300A