Zobrazeno 1 - 10
of 1 161
pro vyhledávání: '"Deletion mapping"'
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Loss of heterozygosity (LOH) on chromosome 10 frequently occurs in gliomas. Whereas genetic loci with allelic deletion often implicate tumor suppressor genes, a putative tumor suppressor Adducin3 (ADD3) mapped to chromosome 10q25.2 was found to be pr
Externí odkaz:
https://doaj.org/article/b2f5c96529514e67ab65c9d64b6ce528
Autor:
Rayla Greenberg Temin
Publikováno v:
Genetics. 215:1085-1105
Segregation Di st orter (SD) is a naturally occurring male meiotic drive system in Drosophila melanogaster, characterized by almost exclusive transmission of the SD chromosome owing to dysfunction of sperm receiving the SD+ homolog. Previous studies
Autor:
Pritesh Vyas, Imran Sheikh, Ajar Nath Yadav, Harcharan Singh Dhaliwal, Sewa Ram, Sunil Kumar, Krishan Kumar, Yogesh Sharma, Parveen Chhuneja, Ambika Sharma
Publikováno v:
Journal of Plant Biochemistry and Biotechnology. 29:407-417
Bread wheat sustains genes for grain softness on “Ha” locus of short arm of 5D chromosome. Pina-D1 and Pinb-D1 alleles of “Ha” locus together are responsible for soft grain texture of wheat. The wheat cultivar WL711 had wild type Pinb-D1a and
Autor:
Daniela M. Lichtblau, Dibin Baby, Christopher Endres, Christin Sieberg, Birte Schwarz, Petra Bauer
Plants use the micronutrient iron (Fe) efficiently to balance the requirements for Fe during growth with its potential cytotoxic effects. A cascade of basic helix-loop-helix (bHLH) transcription factors is initiated by bHLH proteins of the subgroups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c56bfd3f63830a4ac47f4439c6451b7a
https://doi.org/10.1101/2021.10.07.463536
https://doi.org/10.1101/2021.10.07.463536
Akademický článek
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Autor:
Joel S. Shore, Andrew G. McCubbin, Hasan J Hamam, Jonathan D J Labonne, Paul D J Chafe, Paige M Henning
Publikováno v:
New Phytologist. 224:1316-1329
Distyly is an intriguing floral adaptation that increases pollen transfer precision and restricts inbreeding. It has been a model system in evolutionary biology since Darwin. Although the S-locus determines the long- and short-styled morphs, the gene
Publikováno v:
Archives of Oral Biology. 96:243-248
Objectives Runt-related transcription factor 2 (RUNX2) gene is known to cause rare autosomal dominant skeletal disorder Cleidocranial dysplasia (CCD). Here, we explored a novel, large deletion in RUNX2 gene in a Chinese patient with CCD and the funct
Autor:
Culiat, Cymbeline T., Stubbs, Lisa, Nicholls, Robert D., Montgomery, Clyde S., Russell, Liane B., Johnson, Dabney K., Rinchik, Eugene M.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1993 Jun 01. 90(11), 5105-5109.
Externí odkaz:
https://www.jstor.org/stable/2362231
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1978 Dec 01. 75(12), 6182-6186.
Externí odkaz:
https://www.jstor.org/stable/68925
Autor:
Rosenwasser, Lanny J., Webb, Andrew C., Clark, Burton D., Irie, Shinkichi, Chang, Lauren, Dinarello, Charles A., Gehrke, Lee, Wolff, Sheldon M., Rich, Alexander, Auron, Philip E.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1986 Jul . 83(14), 5243-5246.
Externí odkaz:
https://www.jstor.org/stable/27898