Kent Bradford

Dr. Kent Bradford


Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 January 2022 in Heredity
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Journal Article
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RRReagan C. Reed
Reagan C. Reed
KBKent Bradford
Kent Bradford
IKIMTIYAZ KHANDAY
IMTIYAZ KHANDAY

1 March 2002 in Weed Science
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Journal Article
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KBKent Bradford
Kent Bradford
Applications of hydrothermal time to quantifying and modeling seed germination and dormancy - Volume 50 Issue 2 - Kent J. Bradford

18 July 2002 in Plant, Cell & Environment
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Journal Article
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VAV. Alvarado
V. Alvarado
KBKent Bradford
Kent Bradford

1 January 2018 in Trends in Food Science & Technology
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Journal Article
Open access
KBKent Bradford
Kent Bradford
PDPeetambar Dahal
Peetambar Dahal
JAJohan Van Asbrouck
Johan Van Asbrouck
KKKeshavulu Kunusoth
Keshavulu Kunusoth
PBPedro Bello
Pedro Bello
FWFelicia Wu
Felicia Wu

28 March 2016 in Proceedings of the National Academy of Sciences
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HHHeqiang Huo
Heqiang Huo
SWShouhui Wei
Shouhui Wei
KBKent Bradford
Kent Bradford
Significance: Annual plants adapt to their environments by matching their life cycles, particularly seed germination and flowering, to the appropriate seasons. Although genetic evidence has suggested connections among genes regulating seed dormancy and flowering, specific mechanisms for such coordination are unknown. We report that a gene [ DELAY OF GERMINATION1 ( DOG1 )] involved in determining the depth of seed dormancy, and therefore the seasonal timing of germination, also influences the timing of flowering in Arabidopsis and lettuce. We further show that this gene acts through influencing the production of microRNAs that govern the progression of developmental phase transitions through the plant life cycle, providing a molecular genetic mechanism for the coordinate adaptation of seed dormancy and flowering phenotypes to environmental conditions.

1 August 2000 in Plant Physiology
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Journal Article
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HNHiroyuki Nonogaki
Hiroyuki Nonogaki
OGOliver H. Gee
Oliver H. Gee
KBKent Bradford
Kent Bradford
Endo-β-mannanase (EC 3.2.1.78) is involved in hydrolysis of the mannan-rich cell walls of the tomato (Lycopersicon esculentum Mill.) endosperm during germination and post-germinative seedling growth. Different electrophoretic isoforms of endo-β-mannanase are expressed sequentially in different parts of the endosperm, initially in the micropylar endosperm cap covering the radicle tip and subsequently in the remaining lateral endosperm surrounding the rest of the embryo. We have isolated a cDNA from imbibed tomato seeds (LeMAN2) that shares 77% deduced amino acid sequence similarity with a post-germinative tomato mannanase (LeMAN1). When expressed in Escherichia coli, the protein encoded by LeMAN2 cDNA was recognized by anti-mannanase antibody and exhibited endo-β-mannanase activity, confirming the identity of the gene. LeMAN2was expressed exclusively in the endosperm cap tissue of tomato seeds prior to radicle emergence, whereas LeMAN1 was expressed only in the lateral endosperm after radicle emergence.LeMAN2 mRNA accumulation and mannanase activity were induced by gibberellin in gibberellin-deficient gib-1mutant seeds but were not inhibited by abscisic acid in wild-type seeds. Distinct mannanases are involved in germination and post-germinative growth, with LeMAN2 being associated with endosperm cap weakening prior to radicle emergence, whereasLeMAN1 mobilizes galactomannan reserves in the lateral endosperm.