Papers with the keyword osteosacoma | Read by QxMD
The FISH study of the numerical aberrations in chromosomes 1 and 17 or the structural aberrations in chromosome arm 1p or 17p ... with one pair consisting of 1q12 and 1p36 and the other pair consisting of the 17 cemtromere and 17p13.3. There was no ... METHODS: Using the isolated total RNA from osteosacoma cell line MG63 as a template, the cDNA encoding region of human OPG was ... METHODS: To obtain the purified cathepsin K, we cloned the target fragment from the mRNA of human osteosacoma cell line MG63 ...https://www.readbyqxmd.com/keyword/111010
Endotoxin-tolerant Mice Have Mutations in Toll-like Receptor 4 (Tlr4) | JEM
Human PAPPA had previously been mapped to chromosome 9q33.1, a region known to be homologous to a portion of mouse chromosome 4 ... 1992) Cloning and stable maintenance of 300-kilobase-pair fragments of human DNA in Escherichia coliusing an F-factor-based ... and comparative mapping of ESTs and genes that had been assigned to regions of human chromosome 9 syntenic with mouse ... was recently identified as a direct downstream element of the human Toll signaling pathway ((36)). Human Toll and IL-1R ...http://jem.rupress.org/content/189/4/615
Identification of a novel gene (ECM2) encoding a putative extracellular matrix protein expressed predominantly in adipose and...
Chromosome Mapping. Chromosomes, Human, Pair 9 / genetics*. Cloning, Molecular. Extracellular Matrix Proteins / chemistry*, ... Previous Document: Human genes for KNSL4 and MAZ are located close to one another on chromosome 16p11.2.. Next Document: ... and uterus among 20 human adult tissues examined. We assigned the gene to chromosome 9q22.3 by means of fluorescence in situ ... Humans. In Situ Hybridization, Fluorescence. Molecular Sequence Data. RNA, Messenger / genetics. Sequence Analysis, DNA. von ...http://www.biomedsearch.com/nih/Identification-novel-gene-ECM2-encoding/9790758.html
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
HKU Scholars Hub: Isolated lymph node T lymphoblastic transformation of chronic myeloid leukemia during interferon treatment
Chromosomes, Human, Pair 22. en_US. dc.subject.mesh. Chromosomes, Human, Pair 9. en_US. ...http://hub.hku.hk/handle/10722/162287
"Linkage and association study of late-onset Alzheimer disease families" by S Züchner, J R Gilbert et al.
We conclude that CDKN2A is a promising new candidate gene potentially contributing to AD susceptibility on chromosome 9p. ... Age of Onset; Aged; Aged, 80 and over; Alzheimer Disease; Chromosomes, Human, Pair 9; Family; Genes, p16; Genetic Linkage; ... We conclude that CDKN2A is a promising new candidate gene potentially contributing to AD susceptibility on chromosome 9p. ... Annals of Human Genetics, 72 (Pt 6). http://dx.doi.org/10.1111/j.1469-1809.2008.00474.x ...https://hsrc.himmelfarb.gwu.edu/smhs_neuro_facpubs/457/
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/
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)
Welcome to LibAge, the ageing reference resource
Entries tagged Chromosomes, Human, Pair 9/genetics (6). Sort:. Number of citations. Author. Title. Year. PubMed ID. ... 2010) "Preliminary evidence of a genetic association between chromosome 9p21.3 and human longevity." Rejuvenation Res 13(1):23- ... 2002) "AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34." Nat. Genet. 31(1):21-23 (PubMed) ... A curated database of candidate human ageing-related genes and genes associated with longevity and/or ageing in model organisms ...http://libage.ageing-map.org/entries/tags/4249/
Kamens, H. M.<...
Chromosomes, Human, Pair 9 Quantitative Trait Loci Nicotinic Receptors Cholinergic Agents Substance-Related Disorders ...https://pennstate.pure.elsevier.com/en/persons/helen-m-kamens
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
QIMR Genetic Epidemiology Laboratory Home Page
Chromosomes, Human, Pair 22. genetics. Chromosomes, Human, Pair 9. genetics. Genetic Predisposition to Disease. genetics. ...https://keppel.qimr.edu.au/general/publicationsfulllisting.cgi?pmid=19578365
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
Jacksonville, FL - Research Output - Mayo Clinic
Chromosomes, Human, Pair 9 An alternative transcript of the Alzheimer's disease risk gene SORL1 encodes a truncated receptor. ... Distinct cytokine profiles in human brains resilient to Alzheimer's pathology. Barroeta-Espar, I., Weinstock, L. D., Perez- ... The Cancer Genome Atlas Research Network, Apr 9 2018, In : Cancer Cell. 33, 4, p. 690-705.e9. Research output: Contribution to ... Rea, I. M., Gibson, D. S., McGilligan, V., McNerlan, S. E., Denis Alexander, H. & Ross, O. A., Apr 9 2018, In : Frontiers in ...https://mayoclinic.pure.elsevier.com/en/organisations/jacksonville-fl/publications/
QIMR Genetic Epidemiology Laboratory Home Page
Chromosomes, Human, Pair 9. genetics. DNA-Binding Proteins. genetics. Facial Neoplasms. genetics. ... Polymorphisms in the syntaxin 17 gene are not associated with human cutaneous malignant melanoma.. ...https://keppel.qimr.edu.au/general/publicationsfulllisting.cgi?pmid=19209086
DI-fusion Dek-can rearrangement in translocation (6;9)(p23;q34).
Chromosome Fragility. Chromosome Mapping. Chromosomes, Human, Pair 6. Chromosomes, Human, Pair 9. ... Dek-can rearrangement in translocation (6;9)(p23;q34).. par Soekarman, D;von Lindern, M;van der Plas, D C;Selleri, L;Bartram, C ...http://difusion.ulb.ac.be/vufind/Record/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/59430/Details
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
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
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
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
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD. - PubMed - NCBI
Chromosomes, Human, Pair 9*. *Female. *Finland. *Frontotemporal Dementia/genetics*. *Genetic Predisposition to Disease ... A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD.. Renton AE1, Majounie E, Waite A, ... The chromosome 9p21 amyotrophic lateral sclerosis-frontotemporal dementia (ALS-FTD) locus contains one of the last major ... A) Physical map of the chromosome 9p21 ALS/FTD locus showing the p-values for SNPs genotyped in the previous GWAs (), the ...https://www.ncbi.nlm.nih.gov/pubmed/21944779?dopt=Abstract
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