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Chromosome 17 - Wikipedia
WEBchromosome 17 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. chromosome 17 spans more than 84 million base pairs (the building material of DNA) and represents between 2.5 and 3% of the total DNA in cells. chromosome 17 contains the Homeobox B gene cluster.
En.wikipedia.orgChromosome 17 - MedlinePlus
WEBchromosome 17 spans about 83 million DNA building blocks (base pairs) and represents between 2.5 and 3 percent of the total DNA in cells. Learn about health implications of genetic changes.
Medlineplus.govChromosome 17: an evolutionary black sheep? | Broad Institute
WEBApr 27, 2006 — In the April 20 issue of Nature, an international scientific team led by Broad Institute researchers reports the full sequence and analysis of chromosome 17, revealing an unusual history that may help to illuminate the …
Broadinstitute.orgDNA sequence of human chromosome 17 and analysis of
WEBApr 1, 2006 — chromosome 17 is unusual among the human chromosomes in many respects. It is the largest human autosome with orthology to only a single mouse chromosome 1, mapping entirely to the distal half
Nature.comChromosome 17 - an overview | ScienceDirect Topics
WEBchromosome 17 is defined as a human chromosome enriched with protein-coding genes and a complex rearrangement architecture, predisposing it to non-allelic homologous recombination (NAHR) and responsible for various human CNV disorders like Smith-Magenis Syndrome (SMS) and Potocki-Lupski Syndrome (PTLS).
Sciencedirect.comChromosome 17 | Human Genome Project
WEBThe chromosome image below is the online version of chromosome 17 depicted on the Human Genome Landmarks poster. Click Here for Printable Image. Legend: Magenta and green. These regions reflect the unique patterns of light and dark bands seen on human chromosomes that have been stained to allow viewing through a light microscope. Red.
Doe-humangenomeproject.ornl.govDNA sequence of human chromosome 17 and analysis of …
WEBApr 4, 2006 — Human chromosome 17 is implicated in a wide range of human genetic diseases. It is home to genes involved in early-onset breast cancer (BRCA1), neurofibromatosis (NF1) and the DNA damage response (TP53 encoding the p53 protein).
Ncbi.nlm.nih.govChromosome 17 - an overview | ScienceDirect Topics
WEBchromosome 17 (Chr17) harbors crucial genes that encode proteins implicated in a variety of cancers, including some that guard cancer cells from genomic instability and others that interfere with metastasis.
Sciencedirect.comThe Important Molecular Markers on Chromosome 17 and Their …
WEBSep 5, 2011 — Abnormalities of chromosome 17 are important molecular genetic events in human breast cancers. Several famous oncogenes (HER2, TOP2A and TAU), tumor suppressor genes (p53, BRCA1 and HIC-1) or DNA double-strand break repair gene (RDM1) are located on chromosome 17.
Ncbi.nlm.nih.govNeurofibromatosis type I - Wikipedia
WEBNeurofibromatosis type I (NF-1), or von Recklinghausen syndrome, is a complex multi-system human disorder caused by the mutation of neurofibromin 1 (NF-1), a gene on chromosome 17 that is responsible for production of a protein (neurofibromin) which is needed for normal function in many human cell types.
En.wikipedia.org