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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 .
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 ...
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.
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 ...
15433 Ensembl ENSG00000128714 ENSMUSG00000001819 UniProt P35453 P70217 RefSeq (mRNA) NM_000523 NM_008275 RefSeq (protein) NP_000514 NP_032301 Location (UCSC) Chr 2: 176.09 – 176.1 Mb Chr 2: 74.5 – 74.5 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Homeobox protein Hox-D13 is a protein that in humans is encoded by the HOXD13 gene. This gene belongs to the homeobox family of ...
The protein encoded by the gene belongs to a solute carrier family, numbered as 13. [6] It was discovered in 2002 that it binds preferentially to and transports citrate anions . [ 7 ] It is known as Na + -coupled citrate transporter (NaCT), and is also referred to by the gene name SLC13A5.
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.
268379 Ensembl ENSG00000179869 ENSMUSG00000004668 UniProt Q86UQ4 Q5SSE9 RefSeq (mRNA) NM_152701 NM_152555 NM_178259 RefSeq (protein) NP_689914 NP_839990 Location (UCSC) Chr 7: 48.17 – 48.65 Mb Chr 11: 9.14 – 9.63 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse ATP-binding cassette sub-family A member 13 also known as ABCA13 is a protein that in humans is encoded by the ABCA13 ...