complementation group वाक्य
उदाहरण वाक्य
मोबाइल
- The FANCG gene is responsible for complementation group G.
- This gene encodes the protein for complementation group E.
- The clinical phenotype of all Fanconi anemia ( FA ) complementation groups is similar.
- These patients are classified as XP complementation group F ( XP-F ).
- This gene encodes a member of the Fanconi anemia, complementation group A protein.
- GSTP1 has been shown to interact with Fanconi anemia, complementation group C and MAPK8.
- The clinical phenotype of mutational defects in all Fanconi anemia ( FA ) complementation groups is similar.
- FA patients with ERCC4 mutations have been classified as belonging to Fanconi anemia complementation group P ( FANCP ).
- FANCF has been shown to interact with Fanconi anemia, complementation group C, FANCG, FANCA and FANCE.
- This gene encodes the protein for complementation group I . Alternative splicing results in two transcript variants encoding different isoforms.
- Mutations in the gene are the cause of vitamin B 12-dependent methylmalonic aciduria linked to the cblB complementation group.
- Mutations in the MTR gene have been identified as the underlying cause of methylcobalamin deficiency complementation group G, or methylcobalamin deficiency cblG-type.
- Mutations in this gene have been associated with complementation group 1 peroxisomal disorders such as neonatal adrenoleukodystrophy, infantile Refsum disease, and Zellweger syndrome.
- The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex.
- Multiple independent complementation groups of Chinese hamster ovary ( CHO ) cells were isolated, and this gene restored UV resistance to cells of complementation group 1.
- Multiple independent complementation groups of Chinese hamster ovary ( CHO ) cells were isolated, and this gene restored UV resistance to cells of complementation group 1.
- Defects in this gene can result in three different disorders : the cancer-prone syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy, and Cockayne syndrome.
- Multiple independent complementation groups of Chinese hamster ovary ( CHO ) cells have been isolated, and this gene restored UV resistance to cells of complementation group 4.
- Multiple independent complementation groups of Chinese hamster ovary ( CHO ) cells have been isolated, and this gene restored UV resistance to cells of complementation group 4.
- This cellular phenotype is shared by yeast'pex'mutants, and human orthologs of yeast PEX genes defective in some PBD complementation groups ( CGs ).
- अधिक वाक्य: 1 2
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