Kranz anatomy is not essential for terrestrial C4 plant photosynthesis. - Test2 - elhamkhani - TriplyDB

Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

http://www.wikidata.org/entity/Q30666643

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Greater efficiency of photosynthetic carbon fixation due to single amino-acid substitution Germination of dimorphic seeds of the desert annual halophyte Suaeda aralocaspica (Chenopodiaceae), a C4 plant without Kranz anatomy Nature's green revolution: the remarkable evolutionary rise of C4 plants The Road to C4 Photosynthesis: Evolution of a Complex Trait via Intermediary States Evolution of C4 plants: a new hypothesis for an interaction of CO2 and water relations mediated by plant hydraulics The function of the aerenchyma in arborescent lycopsids: evidence of an unfamiliar metabolic strategy Transit peptide elements mediate selective protein targeting to two different types of chloroplasts in the single-cell C4 species Bienertia sinuspersici The unique structural and biochemical development of single cell C4 photosynthesis along longitudinal leaf gradients in Bienertia sinuspersici and Suaeda aralocaspica (Chenopodiaceae)Isolation of dimorphic chloroplasts from the single-cell C4 species Bienertia sinuspersici New evidence for grain specific C4 photosynthesis in wheat Tree stem phosphoenolpyruvate carboxylase (PEPC): lack of biochemical and localization evidence for a C4-like photosynthesis system.One decade after the discovery of single-cell C4 species in terrestrial plants: what did we learn about the minimal requirements of C4 photosynthesis?Identification of C4 photosynthesis metabolism and regulatory-associated genes in Eleocharis vivipara by SSH.C(4) photosynthesis: principles of CO(2) concentration and prospects for its introduction into C(3) plants.Proof of C4 photosynthesis without Kranz anatomy in Bienertia cycloptera (Chenopodiaceae).C4 cycles: past, present, and future research on C4 photosynthesis.Evidence of coexistence of C₃ and C₄ photosynthetic pathways in a green-tide-forming alga, Ulva prolifera.Rubisco evolution in C₄ eudicots: an analysis of Amaranthaceae sensu lato.Overexpression of C(4)-cycle enzymes in transgenic C(3) plants: a biotechnological approach to improve C(3)-photosynthesis.Strategies for engineering a two-celled C(4) photosynthetic pathway into rice.CO2-concentrating mechanisms in Egeria densa, a submersed aquatic plant.Identification and preliminary characterization of two cDNAs encoding unique carbonic anhydrases from the marine alga Emiliania huxleyi.Single-cell C(4) photosynthesis: efficiency and acclimation of Bienertia sinuspersici to growth under low light.Deep evolutionary comparison of gene expression identifies parallel recruitment of trans-factors in two independent origins of C4 photosynthesis.Structural and biochemical characterization of the C₃-C₄ intermediate Brassica gravinae and relatives, with particular reference to cellular distribution of Rubisco The Fatty Acid Profile Analysis of Cyperus laxus Used for Phytoremediation of Soils from Aged Oil Spill-Impacted Sites Revealed That This Is a C18:3 Plant Species.The nature of the CO2 -concentrating mechanisms in a marine diatom, Thalassiosira pseudonana.Effects of salinity on the growth, physiology and relevant gene expression of an annual halophyte grown from heteromorphic seeds.Diversity of CO2 concentrating mechanisms and responses to CO2 concentration in marine and freshwater diatoms.Responses of Ottelia alismoides, an aquatic plant with three CCMs, to variable CO2 and light.Ecological imperatives for aquatic carbon dioxide-concentrating mechanisms.Can improvement in photosynthesis increase crop yields?Physiological and photosynthetic characteristics of indica Hang2 expressing the sugarcane PEPC gene The role of proteins in C(3) plants prior to their recruitment into the C(4) pathway.Eukaryotic metabolism: measuring compartment fluxes.The recurrent assembly of C4 photosynthesis, an evolutionary tale.Evolution of the C4 photosynthetic pathway: events at the cellular and molecular levels.Environmental and physiological determinants of carbon isotope discrimination in terrestrial plants.Diversity, distribution and roles of osmoprotective compounds accumulated in halophytes under abiotic stress.Walking the C4 pathway: past, present, and future.

P2860

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P2860

Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

http://www.wikidata.org/entity/Q30666643

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2001 nî lūn-bûn

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2001 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2001 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2001年の論文

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Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

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Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

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Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

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Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

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Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

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Kranz anatomy is not essential for terrestrial C4 plant photosynthesis.

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Edwards GE

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Franceschi VR

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Freitag H

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Kiirats O

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Voznesenskaya EV

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P2860

What does it take to be C4? Lessons from the evolution of C4 photosynthesis

MOLECULAR ENGINEERING OF C4 PHOTOSYNTHESIS.

Occurrence of C(3) and C(4) photosynthesis in cotyledons and leaves of Salsola species (Chenopodiaceae).

Regulation of Soybean Net Photosynthetic CO(2) Fixation by the Interaction of CO(2), O(2), and Ribulose 1,5-Diphosphate Carboxylase.

A Remarkable New Leaf Type With Unusual Photosynthetic Tissue in a Central Asiatic Genus of Chenopodiaceae

Utilization of O2 in the metabolic optimization of C4 photosynthesis

Expansion and emergence of C4 plants

P2888

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