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Benjamin Lewin is a molecular biologist who founded the journal Cell [1] and authored the textbook Genes. [2] He is credited with building Cell into a recognized journal of cellular biology in a short period of time to rival Nature and Science .
Researchers have not determined which other genes are located in the deleted region, but a loss of several genes is likely responsible for these developmental problems. Trisomy 13: Trisomy 13 occurs when each cell in the body has three copies of chromosome 13 instead of the usual two copies. Trisomy 13 can also result from an extra copy of ...
13q deletion syndrome is a rare genetic disease caused by the deletion of some or all of the large arm of human chromosome 13. Depending upon the size and location of the deletion on chromosome 13, the physical and mental manifestations will vary. It has the potential to cause intellectual disability and congenital malformations that affect a ...
•List of human protein-coding genes page 2 covers genes EPHA1–MTMR3 •List of human protein-coding genes page 3 covers genes MTMR4–SLC17A7 •List of human protein-coding genes page 4 covers genes SLC17A8–ZZZ3 NB: Each list page contains 5000 human protein-coding genes, sorted alphanumerically by the HGNC-approved gene symbol.
Human chromosome 13 gene stubs (132 P) Pages in category "Genes on human chromosome 13" The following 200 pages are in this category, out of approximately 214 total.
As introduced by Kurt Lewin, genidentity is an existential relationship underlying the genesis of an object from one moment to the next. What we usually consider to be an object really consists of multiple entities, which are the phases of the object at various times.
Interleukin 13 (IL-13) is a protein that in humans is encoded by the IL13 gene. [ 4 ] [ 5 ] [ 6 ] IL-13 was first cloned in 1993 and is located on chromosome 5q31.1 with a length of 1.4kb. [ 4 ] It has a mass of 13 kDa and folds into 4 alpha helical bundles. [ 7 ]
Trisomy 13 was first described by Thomas Bartholin in 1657, [11] [12] but the chromosomal nature of the disease was ascertained by Dr. Klaus Patau and Dr. Eeva Therman in 1960. [13] The disease is named in Patau's honor. In England and Wales during 2008–09, there were 172 diagnoses of Patau syndrome (trisomy 13), with 91% of diagnoses made ...