*  The region 3′ to Xist mediates X chromosome counting and H3 Lys‐4 dimethylation within the Xist gene | The EMBO Journal
Open triangles indicate the primer pair (DC651Up‐Del1Lo) used for the PCR screening of the deleted clones. Arrowheads represent ... Interestingly, comparative sequence analysis has identified a 2 kb region of mouse/human conservation (80610-82632 of Genbank ... A counting process senses the X chromosome/autosome ratio and ensures that X chromosome inactivation (XCI) initiates in the ... Rastan S, Robertson EJ, Rasmussen TP, Mastrangelo MA, Eden A, Pehrson JR, Jaenisch R (1985) X‐chromosome deletions in embryo‐ ...
  http://emboj.embopress.org/content/23/3/594
*  Her-2 immunohistochemical expression in oral squamous cell carcinomas is associated with polysomy of chromosome 17, not Her-2...
Chromosome Aberrations. Chromosomes, Human, Pair 17 / genetics*. Female. Gene Amplification. Humans. Immunohistochemistry. In ... Previous Document: Phosphocreatine recovery overshoot after high intensity exercise in human skeletal muscle is associa.... ... As in invasive breast carcinomas Her-2 overexpression has been related to an increased number of chromosome 17 copies, a common ... Her-2 immunohistochemical expression in oral squamous cell carcinomas is associated with polysomy of chromosome 17, not Her-2 ...
  http://www.biomedsearch.com/nih/Her-2-Immunohistochemical-Expression-in/20596843.html
*  benign deep fibrous histiocytoma 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
MeSH-major] Chromosomes, Human, Pair 16. Chromosomes, Human, Pair 17. Histiocytoma, Benign Fibrous / genetics. Karyotyping / ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ... Humans. Male. Radiotherapy, Adjuvant. Vimentin / metabolism. Young Adult. *[Email] Email this result item Email the results to ... Humans. Immunohistochemistry. Microscopy, Electron, Scanning. *MedlinePlus Health Information. consumer health - Breast Cancer. ...
  http://www.bmlsearch.com/?kwr=benign+deep+fibrous+histiocytoma+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  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
*  anlage tumor retinal 2005:2010[pubdate] *count=100 - BioMedLib™ search engine
Chromosomes, Human, Pair 1. Chromosomes, Human, Pair 7. Comparative Genomic Hybridization. Etoposide / administration & dosage ... Chromosomes, Human, Pair 17. Epithelium / pathology. Epithelium / ultrastructure. Glial Fibrillary Acidic Protein / metabolism ... Chromosome Aberrations. Endothelin-3 / pharmacology. Female. Fluorescent Antibody Technique. Humans. Immunohistochemistry. ... Humans Animals + Gender. And for: Male Female + Age. And for these age groups: Newborn: birth to 1 month. Infant: 1 to 23 ...
  http://www.bmlsearch.com/?kwr=anlage+tumor+retinal+2005:2010%5Bpubdate%5D&cxts=100&stmp=b0
*  Laser microdissection and microsatellite analyses of breast cancer reveal a high degree of tumor heterogeneity -...
Chromosomes, Human, Pair 17/genetics. MESH. Dissection/methods. MESH. Female. MESH. Genetic Heterogeneity. MESH. ...
  https://epub.uni-regensburg.de/15369/
*  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 9. Cytogenetics. Humans. In Situ Hybridization, Fluorescence. Infant. ... 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
*  Chromosome 17 (human) - Wikipedia
Gilbert F (1998). "Disease genes and chromosomes: disease maps of the human genome. Chromosome 17". Genet Test. 2 (4): 357-81. ... The following is a partial list of genes on human chromosome 17. For complete list, see the link in the infobox on the right. ... The following are some of the gene count estimates of human chromosome 17. Because researchers use different approaches to ... People normally have two copies of this chromosome. Chromosome 17 spans more than 83 million base pairs (the building material ...
  https://en.wikipedia.org/wiki/Chromosome_17_(human)
*  The human ROX gene: genomic structure and mutation analysis in human breast tumors. - The Christie Research Publications...
Chromosomes, Human, Pair 17. -. dc.subject.mesh. DNA Mutational Analysis. -. dc.subject.mesh. DNA-Binding Proteins. - ... The human ROX gene: genomic structure and mutation analysis in human breast tumors.. Authors:. Lo Nigro, C; Venesio, T; Reymond ... The ROX gene maps to chromosome 17p13.3, a region frequently deleted in human malignancies. Here we report the genomic ... The ROX gene maps to chromosome 17p13.3, a region frequently deleted in human malignancies. Here we report the genomic ...
  http://christie.openrepository.com/christie/handle/10541/92932
*  Allelic imbalance in the region of the BRCA1 gene in ductal carcinoma in situ of the breast. - The Christie Research...
Chromosomes, Human, Pair 17. -. dc.subject.mesh. Female. -. dc.subject.mesh. Genes, erbB-2. - ... Frequent alterations of chromosome 1 in ductal carcinoma in situ of the breast.Authors: Munn KE, Walker RA, Varley JM. Issue ... Mutation of the TP53 gene and allelic imbalance at chromosome 17p13 in ductal carcinoma in situ.Authors: Munn KE, Walker RA, ... Amplification units and translocation at chromosome 17q and c-erbB-2 overexpression in the pathogenesis of breast cancer. ...
  http://christie.openrepository.com/christie/handle/10541/95600
*  A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22...
This meta-analysis has led to identification of a novel region on chromosome 17 linked to type 2 diabetes; this region has not ... The analysis provided evidence for linkage of type 2 diabetes to six regions, with the strongest evidence on chromosome 17p11.2 ... Chromosome Mapping, Chromosomes, Human, Pair 17, Diabetes Mellitus, Type 2, Europe, Genome, Human, Humans, Lod Score ... This meta-analysis has led to identification of a novel region on chromosome 17 linked to type 2 diabetes; this region has not ...
  https://www.rdm.ox.ac.uk/publications/23425
*  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 15. Chromosomes, Human, Pair 17. Leukemia, Myeloid, Acute / genetics. Leukemia, ... MeSH-major] Chromosomes, Human, Pair 16 / genetics. Chromosomes, Human, Pair 22 / 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
*  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}, ...
  https://lup.lub.lu.se/search/publication/4a5b78be-d49a-4e06-839f-d72bc6485291
*  Chromosome 17 - Genetics Home Reference
Humans normally have 46 chromosomes in each cell, divided into 23 pairs. Two copies of chromosome 17, one copy inherited from ... Ensembl Human Map View. *. Gilbert F. Disease genes and chromosomes: disease maps of the human genome. Chromosome 17. Genet ... Ring chromosomes occur when a chromosome breaks in two places and the ends of the chromosome arms fuse together to form a ... DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage. Nature. 2006 Apr 20;440(7087):1045-9. ( ...
  https://ghr.nlm.nih.gov/chromosome/17
*  DNA - New World Encyclopedia
For instance, the largest human chromosome, chromosome number 1, is 220 million base pairs long.[17] ... The set of chromosomes in a cell makes up its genome. The human genome has approximately 3 billion base pairs of DNA arranged ... The GC base pair is therefore stronger than the AT base pair. As a result, it is both the percentage of GC base pairs and the ... and in human cells the different chromosomes even occupy separate areas in the nucleus called "chromosome territories."[105] ...
  http://www.newworldencyclopedia.org/entry/DNA
*  NAVER Academic > Search...
Alleles, Base Pairing, Base Sequence, Case-Control Studies, Chromosomes, Human, Pair 4, genetics, Consensus Sequence, Female, ... Adult, Aged, Autopsy, Chromosome Deletion, Chromosomes, Human, Pair 17, genetics, Diabetes Mellitus, Epilepsy, complications, ... Australia, Body Height, genetics, Chromosomes, Human, Databases, Genetic, Female, Genetic Variation, Genome, Human, Humans, ... Genome partitioning of genetic variation for height from 11,214 sibling pairs.. Peter M Visscher et al. American Journal of ...
  https://academic.naver.com/search.naver?field=3&query=American+Journal+of+Human+Genetics+81%EA%B6%8C+5%ED%98%B8
*  Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated...
We replicated published associations in the 4q22/SNCA and 17q21/MAPT chromosome regions (P, 10(-10)) and found evidence for an ... Age of Onset, Case-Control Studies, Chromosomes, Human, Pair 17, European Continental Ancestry Group, Genetic Predisposition to ... We replicated published associations in the 4q22/SNCA and 17q21/MAPT chromosome regions (P, 10(-10)) and found evidence for an ... Disease, Genome-Wide Association Study, Haplotypes, Humans, Parkinson Disease, Polymorphism, Single Nucleotide, Sample Size, ...
  https://www.rdm.ox.ac.uk/publications/110431
*  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
*  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, ... Aged, Chromosomes, Human, Pair 6, Humans, Karyotyping, Male, Ring Chromosomes, Thymoma, genetics, pathology, Thymus Neoplasms ...
  https://academic.naver.com/search.naver?field=3&query=Genes%2C+Chromosomes+and+Cancer+6%EA%B6%8C+4%ED%98%B8
*  Common variants at 6q22 and 17q21 are associated with intracranial volume. - Nuffield Department of Orthopaedics, Rheumatology...
... localized to the inversion on chromosome 17q21. We replicated the associations of these loci with intracranial volume in a ... a known height-associated locus on chromosome 6q22, and rs9915547 (P = 1.5 × 10(-12)), ... Chromosomes, Human, Pair 6, Chromosomes, Human, Pair 17, Humans, Genetic Markers, Polymorphism, Single Nucleotide, Aged, Aged, ... a known height-associated locus on chromosome 6q22, and rs9915547 (P = 1.5 × 10(-12)), localized to the inversion on chromosome ...
  https://www.ndorms.ox.ac.uk/publications/325293
*  Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2. - Nuffield...
On the other hand, Sillence OI type I segregated with both COL1A1 (17 pedigrees) and COL1A2 (7 pedigrees). The concordant locus ... with 13 of the 17 COL1A1 segregants and none of the 7 COL1A2 segregants showing this feature. ... Chromosomes, Human, Pair 7, Chromosomes, Human, Pair 17, Humans, Osteogenesis Imperfecta, Collagen, DNA Restriction Enzymes, ... On the other hand, Sillence OI type I segregated with both COL1A1 (17 pedigrees) and COL1A2 (7 pedigrees). The concordant locus ...
  https://www.ndorms.ox.ac.uk/publications/108615
*  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
*  M33 (gene) - Wikipedia
... from base pair 119,022,962 to base pair 119,031,270 (Build GRCm38/mm10)(Map). Human homolog of M33, Chromobox homolog 2 (CBX2 ... is located on Chromosome 17, from base pair 79,777,188 to base pair 79,787,650(Build GRCh38.p2 )(Map). This protein contains ... In human ortholog CBX2, synonyms CDCA6, M33, SRXY5 from orthology source HGNC. M33 was isolated by means of the structural ... In humans, the mutations in this gene are also associated with gonadal dysgenesis. Compound heterozygous mutations in M33 were ...
  https://en.wikipedia.org/wiki/M33_(gene)
*  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 ...
  https://www.slideshare.net/InvestingTips/stock-options-profits-from-low-cost-gene-sequencing