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Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma.

AJP reports

Sur A, Manraj H, Lavoie PM, Lim K, Courtemanche D, Brooks P, Albersheim S.
PMID: 26929881
AJP Rep. 2016 Mar;6(1):e99-e103. doi: 10.1055/s-0035-1570342. Epub 2016 Jan 04.

Rapidly involuting congenital hemangiomas (RICH) are the commonest variety of congenital hemangioma, often diagnosed antenatally as high-flow arteriovenous shunts causing hemodynamic compromise to the fetus. The postnatal management of such patients is often challenging. We present the case of...

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Sur A, Manraj H, Lavoie PM, et al. Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma. AJP Rep. 2016;6(1):e99-e103doi: 10.1055/s-0035-1570342.
Sur, A., Manraj, H., Lavoie, P. M., Lim, K., Courtemanche, D., Brooks, P., & Albersheim, S. (2016). Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma. AJP reports, 6(1), e99-e103. https://doi.org/10.1055/s-0035-1570342
Sur, Amitava, et al. "Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma." AJP reports vol. 6,1 (2016): e99-e103. doi: https://doi.org/10.1055/s-0035-1570342
Sur A, Manraj H, Lavoie PM, Lim K, Courtemanche D, Brooks P, Albersheim S. Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma. AJP Rep. 2016 Mar;6(1):e99-e103. doi: 10.1055/s-0035-1570342. Epub 2016 Jan 04. PMID: 26929881; PMCID: PMC4737636.
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Immunogold localization of xyloglucan and rhamnogalacturonan I in the cell walls of suspension-cultured sycamore cells.

Plant physiology

Moore PJ, Darvill AG, Albersheim P, Staehelin LA.
PMID: 16665111
Plant Physiol. 1986 Nov;82(3):787-94. doi: 10.1104/pp.82.3.787.

PLANT CELL WALLS SERVE SEVERAL FUNCTIONS: they impart rigidity to the plant, provide a physical and chemical barrier between the cell and its environment, and regulate the size and shape of each cell. Chemical studies have provided information on...

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Moore PJ, Darvill AG, Albersheim P, et al. Immunogold localization of xyloglucan and rhamnogalacturonan I in the cell walls of suspension-cultured sycamore cells. Plant Physiol. 1986;82(3):787-94doi: 10.1104/pp.82.3.787.
Moore, P. J., Darvill, A. G., Albersheim, P., & Staehelin, L. A. (1986). Immunogold localization of xyloglucan and rhamnogalacturonan I in the cell walls of suspension-cultured sycamore cells. Plant physiology, 82(3), 787-94. https://doi.org/10.1104/pp.82.3.787
Moore, P J, et al. "Immunogold localization of xyloglucan and rhamnogalacturonan I in the cell walls of suspension-cultured sycamore cells." Plant physiology vol. 82,3 (1986): 787-94. doi: https://doi.org/10.1104/pp.82.3.787
Moore PJ, Darvill AG, Albersheim P, Staehelin LA. Immunogold localization of xyloglucan and rhamnogalacturonan I in the cell walls of suspension-cultured sycamore cells. Plant Physiol. 1986 Nov;82(3):787-94. doi: 10.1104/pp.82.3.787. PMID: 16665111; PMCID: PMC1056208.
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The Structure of Plant Cell Walls: IV. A Structural Comparison of the Wall Hemicellulose of Cell Suspension Cultures of Sycamore (Acer PseudoPlatAnus) and of Red Kidney Bean (Phaseolus Vulgaris).

Plant physiology

Wilder BM, Albersheim P.
PMID: 16658434
Plant Physiol. 1973 May;51(5):889-93. doi: 10.1104/pp.51.5.889.

The molecular structure and chemical properties of the hemicellulose present in the isolated cell walls of suspension cultures of sycamore (Acer pseudoplatanus) cells has recently been described by Bauer et al. (Plant Physiol. 51: 174-187). The hemicellulose of the...

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Wilder BM, Albersheim P. The Structure of Plant Cell Walls: IV. A Structural Comparison of the Wall Hemicellulose of Cell Suspension Cultures of Sycamore (Acer PseudoPlatAnus) and of Red Kidney Bean (Phaseolus Vulgaris). Plant Physiol. 1973;51(5):889-93doi: 10.1104/pp.51.5.889.
Wilder, B. M., & Albersheim, P. (1973). The Structure of Plant Cell Walls: IV. A Structural Comparison of the Wall Hemicellulose of Cell Suspension Cultures of Sycamore (Acer PseudoPlatAnus) and of Red Kidney Bean (Phaseolus Vulgaris). Plant physiology, 51(5), 889-93. https://doi.org/10.1104/pp.51.5.889
Wilder, B M, and Albersheim, P. "The Structure of Plant Cell Walls: IV. A Structural Comparison of the Wall Hemicellulose of Cell Suspension Cultures of Sycamore (Acer PseudoPlatAnus) and of Red Kidney Bean (Phaseolus Vulgaris)." Plant physiology vol. 51,5 (1973): 889-93. doi: https://doi.org/10.1104/pp.51.5.889
Wilder BM, Albersheim P. The Structure of Plant Cell Walls: IV. A Structural Comparison of the Wall Hemicellulose of Cell Suspension Cultures of Sycamore (Acer PseudoPlatAnus) and of Red Kidney Bean (Phaseolus Vulgaris). Plant Physiol. 1973 May;51(5):889-93. doi: 10.1104/pp.51.5.889. PMID: 16658434; PMCID: PMC366370.
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Characterization of a H Efflux from Suspension-cultured Plant Cells.

Plant physiology

Fisher ML, Albersheim P.
PMID: 16658725
Plant Physiol. 1974 Mar;53(3):464-8. doi: 10.1104/pp.53.3.464.

A readily assayed H(+) efflux from sycamore (Acer pseudoplatanus), rye (Lolium perenne), and bean (Phaseolus vulgaris cultivars Red Kidney and Small White) suspension-cultured cells has been detected and partially characterized. The H(+) efflux has been shown to require a...

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Fisher ML, Albersheim P. Characterization of a H Efflux from Suspension-cultured Plant Cells. Plant Physiol. 1974;53(3):464-8doi: 10.1104/pp.53.3.464.
Fisher, M. L., & Albersheim, P. (1974). Characterization of a H Efflux from Suspension-cultured Plant Cells. Plant physiology, 53(3), 464-8. https://doi.org/10.1104/pp.53.3.464
Fisher, M L, and Albersheim, P. "Characterization of a H Efflux from Suspension-cultured Plant Cells." Plant physiology vol. 53,3 (1974): 464-8. doi: https://doi.org/10.1104/pp.53.3.464
Fisher ML, Albersheim P. Characterization of a H Efflux from Suspension-cultured Plant Cells. Plant Physiol. 1974 Mar;53(3):464-8. doi: 10.1104/pp.53.3.464. PMID: 16658725; PMCID: PMC543253.
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Host-Pathogen Interactions: VII. Plant Pathogens Secrete Proteins which Inhibit Enzymes of the Host Capable of Attacking the Pathogen.

Plant physiology

Albersheim P, Valent BS.
PMID: 16658768
Plant Physiol. 1974 May;53(5):684-7. doi: 10.1104/pp.53.5.684.

The results presented demonstrate that microbial pathogens of plants have the ability to secrete proteins which effectively inhibit an enzyme synthesized by the host; an enzyme whose substrate is a constituent of the cell wall of the pathogen. The...

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Albersheim P, Valent BS. Host-Pathogen Interactions: VII. Plant Pathogens Secrete Proteins which Inhibit Enzymes of the Host Capable of Attacking the Pathogen. Plant Physiol. 1974;53(5):684-7doi: 10.1104/pp.53.5.684.
Albersheim, P., & Valent, B. S. (1974). Host-Pathogen Interactions: VII. Plant Pathogens Secrete Proteins which Inhibit Enzymes of the Host Capable of Attacking the Pathogen. Plant physiology, 53(5), 684-7. https://doi.org/10.1104/pp.53.5.684
Albersheim, P, and Valent, B S. "Host-Pathogen Interactions: VII. Plant Pathogens Secrete Proteins which Inhibit Enzymes of the Host Capable of Attacking the Pathogen." Plant physiology vol. 53,5 (1974): 684-7. doi: https://doi.org/10.1104/pp.53.5.684
Albersheim P, Valent BS. Host-Pathogen Interactions: VII. Plant Pathogens Secrete Proteins which Inhibit Enzymes of the Host Capable of Attacking the Pathogen. Plant Physiol. 1974 May;53(5):684-7. doi: 10.1104/pp.53.5.684. PMID: 16658768; PMCID: PMC541424.
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Host-Pathogen Interactions: XII. Response of Suspension-cultured Soybean Cells to the Elicitor Isolated from Phytophthora megasperma var. sojae, a Fungal Pathogen of Soybeans.

Plant physiology

Ebel J, Ayers AR, Albersheim P.
PMID: 16659568
Plant Physiol. 1976 May;57(5):775-9. doi: 10.1104/pp.57.5.775.

The glucan elicitor isolated from the mycelial walls of Phytophthora megasperma var. sojae, the fungus which causes stem and root rot in soybeans, stimulates the activity of phenylalanine ammonia-lyase and the accumulation of glyceollin in suspension-cultured soybean cells. Nigeran,...

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Ebel J, Ayers AR, Albersheim P. Host-Pathogen Interactions: XII. Response of Suspension-cultured Soybean Cells to the Elicitor Isolated from Phytophthora megasperma var. sojae, a Fungal Pathogen of Soybeans. Plant Physiol. 1976;57(5):775-9doi: 10.1104/pp.57.5.775.
Ebel, J., Ayers, A. R., & Albersheim, P. (1976). Host-Pathogen Interactions: XII. Response of Suspension-cultured Soybean Cells to the Elicitor Isolated from Phytophthora megasperma var. sojae, a Fungal Pathogen of Soybeans. Plant physiology, 57(5), 775-9. https://doi.org/10.1104/pp.57.5.775
Ebel, J, et al. "Host-Pathogen Interactions: XII. Response of Suspension-cultured Soybean Cells to the Elicitor Isolated from Phytophthora megasperma var. sojae, a Fungal Pathogen of Soybeans." Plant physiology vol. 57,5 (1976): 775-9. doi: https://doi.org/10.1104/pp.57.5.775
Ebel J, Ayers AR, Albersheim P. Host-Pathogen Interactions: XII. Response of Suspension-cultured Soybean Cells to the Elicitor Isolated from Phytophthora megasperma var. sojae, a Fungal Pathogen of Soybeans. Plant Physiol. 1976 May;57(5):775-9. doi: 10.1104/pp.57.5.775. PMID: 16659568; PMCID: PMC542116.
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Host-Pathogen Interactions: XIII. Extracellular Invertases Secreted by Three Races of a Plant Pathogen Are Glycoproteins Which Possess Different Carbohydrate Structures.

Plant physiology

Ziegler E, Albersheim P.
PMID: 16660002
Plant Physiol. 1977 Jun;59(6):1104-10. doi: 10.1104/pp.59.6.1104.

The invertase present in the culture fluid of races 1, 2, and 3 of Phytophthora megasperma Drechs. var. sojae A. A. Hildebrand (Pms) were purified until they gave but a single band, whether stained for protein or carbohydrate, after...

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Ziegler E, Albersheim P. Host-Pathogen Interactions: XIII. Extracellular Invertases Secreted by Three Races of a Plant Pathogen Are Glycoproteins Which Possess Different Carbohydrate Structures. Plant Physiol. 1977;59(6):1104-10doi: 10.1104/pp.59.6.1104.
Ziegler, E., & Albersheim, P. (1977). Host-Pathogen Interactions: XIII. Extracellular Invertases Secreted by Three Races of a Plant Pathogen Are Glycoproteins Which Possess Different Carbohydrate Structures. Plant physiology, 59(6), 1104-10. https://doi.org/10.1104/pp.59.6.1104
Ziegler, E, and Albersheim, P. "Host-Pathogen Interactions: XIII. Extracellular Invertases Secreted by Three Races of a Plant Pathogen Are Glycoproteins Which Possess Different Carbohydrate Structures." Plant physiology vol. 59,6 (1977): 1104-10. doi: https://doi.org/10.1104/pp.59.6.1104
Ziegler E, Albersheim P. Host-Pathogen Interactions: XIII. Extracellular Invertases Secreted by Three Races of a Plant Pathogen Are Glycoproteins Which Possess Different Carbohydrate Structures. Plant Physiol. 1977 Jun;59(6):1104-10. doi: 10.1104/pp.59.6.1104. PMID: 16660002; PMCID: PMC542515.
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Host-Pathogen Interactions : XX. BIOLOGICAL VARIATION IN THE PROTECTION OF SOYBEANS FROM INFECTION BY PHYTOPHTHORA MEGASPERMA F. SP. GLYCINEA.

Plant physiology

Desjardins AE, Ross LM, Spellman MW, Darvill AG, Albersheim P.
PMID: 16662342
Plant Physiol. 1982 May;69(5):1046-50. doi: 10.1104/pp.69.5.1046.

Phytophthora megasperma f.sp. glycinea, which causes soybean (Glycine max) root and stem rot, exists as several races which differ in their ability to infect a range of soybean cultivars. A glycoprotein-rich fraction (Fraction I) isolated from fungal culture fluid...

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Desjardins AE, Ross LM, Spellman MW, et al. Host-Pathogen Interactions : XX. BIOLOGICAL VARIATION IN THE PROTECTION OF SOYBEANS FROM INFECTION BY PHYTOPHTHORA MEGASPERMA F. SP. GLYCINEA. Plant Physiol. 1982;69(5):1046-50doi: 10.1104/pp.69.5.1046.
Desjardins, A. E., Ross, L. M., Spellman, M. W., Darvill, A. G., & Albersheim, P. (1982). Host-Pathogen Interactions : XX. BIOLOGICAL VARIATION IN THE PROTECTION OF SOYBEANS FROM INFECTION BY PHYTOPHTHORA MEGASPERMA F. SP. GLYCINEA. Plant physiology, 69(5), 1046-50. https://doi.org/10.1104/pp.69.5.1046
Desjardins, A E, et al. "Host-Pathogen Interactions : XX. BIOLOGICAL VARIATION IN THE PROTECTION OF SOYBEANS FROM INFECTION BY PHYTOPHTHORA MEGASPERMA F. SP. GLYCINEA." Plant physiology vol. 69,5 (1982): 1046-50. doi: https://doi.org/10.1104/pp.69.5.1046
Desjardins AE, Ross LM, Spellman MW, Darvill AG, Albersheim P. Host-Pathogen Interactions : XX. BIOLOGICAL VARIATION IN THE PROTECTION OF SOYBEANS FROM INFECTION BY PHYTOPHTHORA MEGASPERMA F. SP. GLYCINEA. Plant Physiol. 1982 May;69(5):1046-50. doi: 10.1104/pp.69.5.1046. PMID: 16662342; PMCID: PMC426356.
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Host-Pathogen Interactions: XVI. PURIFICATION AND CHARACTERIZATION OF A beta-GLUCOSYL HYDROLASE/TRANSFERASE PRESENT IN THE WALLS OF SOYBEAN CELLS.

Plant physiology

Cline K, Albersheim P.
PMID: 16661872
Plant Physiol. 1981 Jul;68(1):207-20. doi: 10.1104/pp.68.1.207.

The fact that fungal glucans will stimulate soybeans to accumulate phytoalexins prompted an investigation of soybean cell beta-1,3-glucanases and beta-glucosidases, as well as the ability of these enzymes to hydrolyze the fungal glucans. Several beta-1,3-glucanases and beta-glucosidases can be...

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Cline K, Albersheim P. Host-Pathogen Interactions: XVI. PURIFICATION AND CHARACTERIZATION OF A beta-GLUCOSYL HYDROLASE/TRANSFERASE PRESENT IN THE WALLS OF SOYBEAN CELLS. Plant Physiol. 1981;68(1):207-20doi: 10.1104/pp.68.1.207.
Cline, K., & Albersheim, P. (1981). Host-Pathogen Interactions: XVI. PURIFICATION AND CHARACTERIZATION OF A beta-GLUCOSYL HYDROLASE/TRANSFERASE PRESENT IN THE WALLS OF SOYBEAN CELLS. Plant physiology, 68(1), 207-20. https://doi.org/10.1104/pp.68.1.207
Cline, K, and Albersheim, P. "Host-Pathogen Interactions: XVI. PURIFICATION AND CHARACTERIZATION OF A beta-GLUCOSYL HYDROLASE/TRANSFERASE PRESENT IN THE WALLS OF SOYBEAN CELLS." Plant physiology vol. 68,1 (1981): 207-20. doi: https://doi.org/10.1104/pp.68.1.207
Cline K, Albersheim P. Host-Pathogen Interactions: XVI. PURIFICATION AND CHARACTERIZATION OF A beta-GLUCOSYL HYDROLASE/TRANSFERASE PRESENT IN THE WALLS OF SOYBEAN CELLS. Plant Physiol. 1981 Jul;68(1):207-20. doi: 10.1104/pp.68.1.207. PMID: 16661872; PMCID: PMC425917.
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Host-Pathogen Interactions : XXIII. The Mechanism of the Antibacterial Action of Glycinol, a Pterocarpan Phytoalexin Synthesized by Soybeans.

Plant physiology

Weinstein LI, Albersheim P.
PMID: 16663042
Plant Physiol. 1983 Jun;72(2):557-63. doi: 10.1104/pp.72.2.557.

The biochemical basis for the ability of the pterocarpan phytoalexin glycinol (3,6a,9-trihydroxypterocarpan) to inhibit the growth of bacteria was examined. Glycinol at bacteriostatic concentrations (e.g. 50 micrograms per milliliter) inhibits the ability of Erwinia carotovora to incorporate [(3)H]leucine, [(3)H]thymidine,...

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Weinstein LI, Albersheim P. Host-Pathogen Interactions : XXIII. The Mechanism of the Antibacterial Action of Glycinol, a Pterocarpan Phytoalexin Synthesized by Soybeans. Plant Physiol. 1983;72(2):557-63doi: 10.1104/pp.72.2.557.
Weinstein, L. I., & Albersheim, P. (1983). Host-Pathogen Interactions : XXIII. The Mechanism of the Antibacterial Action of Glycinol, a Pterocarpan Phytoalexin Synthesized by Soybeans. Plant physiology, 72(2), 557-63. https://doi.org/10.1104/pp.72.2.557
Weinstein, L I, and Albersheim, P. "Host-Pathogen Interactions : XXIII. The Mechanism of the Antibacterial Action of Glycinol, a Pterocarpan Phytoalexin Synthesized by Soybeans." Plant physiology vol. 72,2 (1983): 557-63. doi: https://doi.org/10.1104/pp.72.2.557
Weinstein LI, Albersheim P. Host-Pathogen Interactions : XXIII. The Mechanism of the Antibacterial Action of Glycinol, a Pterocarpan Phytoalexin Synthesized by Soybeans. Plant Physiol. 1983 Jun;72(2):557-63. doi: 10.1104/pp.72.2.557. PMID: 16663042; PMCID: PMC1066273.
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Host-Pathogen Interactions : XXV. Endopolygalacturonic Acid Lyase from Erwinia carotovora Elicits Phytoalexin Accumulation by Releasing Plant Cell Wall Fragments.

Plant physiology

Davis KR, Lyon GD, Darvill AG, Albersheim P.
PMID: 16663385
Plant Physiol. 1984 Jan;74(1):52-60. doi: 10.1104/pp.74.1.52.

Heat-labile elicitors of phytoalexin accumulation in soybeans (Glycine max L. Merr. cv Wayne) were detected in culture filtrates of Erwinia carotovora grown on a defined medium containing citrus pectin as the sole carbon source. The heat-labile elicitors were highly...

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Davis KR, Lyon GD, Darvill AG, et al. Host-Pathogen Interactions : XXV. Endopolygalacturonic Acid Lyase from Erwinia carotovora Elicits Phytoalexin Accumulation by Releasing Plant Cell Wall Fragments. Plant Physiol. 1984;74(1):52-60doi: 10.1104/pp.74.1.52.
Davis, K. R., Lyon, G. D., Darvill, A. G., & Albersheim, P. (1984). Host-Pathogen Interactions : XXV. Endopolygalacturonic Acid Lyase from Erwinia carotovora Elicits Phytoalexin Accumulation by Releasing Plant Cell Wall Fragments. Plant physiology, 74(1), 52-60. https://doi.org/10.1104/pp.74.1.52
Davis, K R, et al. "Host-Pathogen Interactions : XXV. Endopolygalacturonic Acid Lyase from Erwinia carotovora Elicits Phytoalexin Accumulation by Releasing Plant Cell Wall Fragments." Plant physiology vol. 74,1 (1984): 52-60. doi: https://doi.org/10.1104/pp.74.1.52
Davis KR, Lyon GD, Darvill AG, Albersheim P. Host-Pathogen Interactions : XXV. Endopolygalacturonic Acid Lyase from Erwinia carotovora Elicits Phytoalexin Accumulation by Releasing Plant Cell Wall Fragments. Plant Physiol. 1984 Jan;74(1):52-60. doi: 10.1104/pp.74.1.52. PMID: 16663385; PMCID: PMC1066623.
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Host-Pathogen Interactions : XXIX. Oligogalacturonides Released from Sodium Polypectate by Endopolygalacturonic Acid Lyase Are Elicitors of Phytoalexins in Soybean.

Plant physiology

Davis KR, Darvill AG, Albersheim P, Dell A.
PMID: 16664663
Plant Physiol. 1986 Feb;80(2):568-77. doi: 10.1104/pp.80.2.568.

Recent studies have demonstrated that an apparently homogeneous preparation of an alpha-1,4-d-endopolygalacturonic acid lyase (EC 4.2.2.2) isolated from the phytopathogenic bacterium Erwinia carotovora induced phytoalexin accumulation in cotyledons of soybean (Glycine max [L.] Merr. cv Wayne) and that this...

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Davis KR, Darvill AG, Albersheim P, et al. Host-Pathogen Interactions : XXIX. Oligogalacturonides Released from Sodium Polypectate by Endopolygalacturonic Acid Lyase Are Elicitors of Phytoalexins in Soybean. Plant Physiol. 1986;80(2):568-77doi: 10.1104/pp.80.2.568.
Davis, K. R., Darvill, A. G., Albersheim, P., & Dell, A. (1986). Host-Pathogen Interactions : XXIX. Oligogalacturonides Released from Sodium Polypectate by Endopolygalacturonic Acid Lyase Are Elicitors of Phytoalexins in Soybean. Plant physiology, 80(2), 568-77. https://doi.org/10.1104/pp.80.2.568
Davis, K R, et al. "Host-Pathogen Interactions : XXIX. Oligogalacturonides Released from Sodium Polypectate by Endopolygalacturonic Acid Lyase Are Elicitors of Phytoalexins in Soybean." Plant physiology vol. 80,2 (1986): 568-77. doi: https://doi.org/10.1104/pp.80.2.568
Davis KR, Darvill AG, Albersheim P, Dell A. Host-Pathogen Interactions : XXIX. Oligogalacturonides Released from Sodium Polypectate by Endopolygalacturonic Acid Lyase Are Elicitors of Phytoalexins in Soybean. Plant Physiol. 1986 Feb;80(2):568-77. doi: 10.1104/pp.80.2.568. PMID: 16664663; PMCID: PMC1075156.
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