نتایج جستجو برای: eya1
تعداد نتایج: 222 فیلتر نتایج به سال:
In eyes absent (eya) mutants, eye progenitor cells undergo cell death early in development. Whereas the phenotype of eya1 is limited to the eye, other mutations are lethal. Genetic and molecular analysis reveals that mutations in one region of the gene cause embryonic lethality, whereas mutations throughout the gene cause defects in eye development. Mosaic analysis indicates that the eya requir...
Drosophila regulatory factor X is an embryonic type I sensory neuron marker also expressed in spermatids and in the brain of Drosophila 159 Preferential expression of Mdm2 oncogene during the development of neural crest and its derivatives in mouse early embryo-genesis 163 Wnt receptors and Wnt inhibitors are expressed in gradients in the developing telencephalon 167 Localization of the netrin ...
Tyr142, the C-terminal amino acid of histone variant H2A.X is phosphorylated by WSTF (Williams-Beuren syndrome transcription factor), a component of the WICH complex (WSTF-ISWI chromatin-remodeling complex), under basal conditions in the cell. In response to DNA double-strand breaks (DSBs), H2A.X is instantaneously phosphorylated at Ser139 by the kinases ATM and ATR and is progressively dephosp...
Hu, Kriz and May recently reexamined ideas implicit in Priddy's elegant homotopy theoretic construction of the Brown-Peterson spectrum at a prime p. They discussed May's notions of nuclear complexes and of cores of spaces, spectra, and commutative S-algebras. Their most striking conclusions, due to Hu and Kriz, were negative: cores are not unique up to equivalence, and BP is not a core of M U c...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید