machine learning trained milliken population charge model Search Results


milliken ga 1980  (Milliken)
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Milliken milliken ga 1980
Milliken Ga 1980, supplied by Milliken, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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duplan corp v deering milliken  (Milliken)
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li milliken  (Milliken)
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mannaway  (Novozymes limited)
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Novozymes limited mannaway
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u.s. pat  (Milliren Technologies Inc)
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milligen 9050 synthesizer  (Rapp Polymere GmbH)
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koncepcji dretskego i millikan  (Analiza Inc)
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Analiza Inc koncepcji dretskego i millikan
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rendell  (Milliken)
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Milliken rendell
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myb5  (Milliken)
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Milliken myb5
Deletion of <t>MYB5</t> , JAZ3 and FYPP3 on chromosome A1 is likely associated with high protein and low ADF in DP125410314. (A) Differential expression analysis of MYB5 , JAZ3 and FYPP3 , located within the deleted A1 chromosomal region, identified these genes as potential causal regulators in the DP125410314 mutant. MYB5 is associated with lignification, while JAZ3 and FYPP3 are implicated in seed storage protein accumulation. Expression profiles are shown for seed coat (S1–S5) and embryo (E1–E5) stages from DP125410314 compared to the NRCDH4079 control. (B) Expression patterns of lignin biosynthesis‐related transcription factors ( MYB7 , MYB32 , MYB85 , ANAC018 ) and seed storage protein genes ( CRU1 , CRU2 , CRU3 , SESA4 ) highlight altered regulatory networks in DP125410314. (C) Overview of the phenylpropanoid pathway showing genes that are significantly upregulated or downregulated in the DP125410314 seed coat relative to the NRCDH4079 control. Fold change values relative to wild type are shown only for differentially expressed genes. (D) Schematic pathway depicting normal seed development with proper MYB5 , JAZ3 and FYPP3 function, and the resulting phenotypic changes in DP125410314 due to their downregulation or deletion, specifically reduced ADF and enhanced seed storage protein content.
Myb5, supplied by Milliken, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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littell  (Milliken)
86
Milliken littell
Deletion of <t>MYB5</t> , JAZ3 and FYPP3 on chromosome A1 is likely associated with high protein and low ADF in DP125410314. (A) Differential expression analysis of MYB5 , JAZ3 and FYPP3 , located within the deleted A1 chromosomal region, identified these genes as potential causal regulators in the DP125410314 mutant. MYB5 is associated with lignification, while JAZ3 and FYPP3 are implicated in seed storage protein accumulation. Expression profiles are shown for seed coat (S1–S5) and embryo (E1–E5) stages from DP125410314 compared to the NRCDH4079 control. (B) Expression patterns of lignin biosynthesis‐related transcription factors ( MYB7 , MYB32 , MYB85 , ANAC018 ) and seed storage protein genes ( CRU1 , CRU2 , CRU3 , SESA4 ) highlight altered regulatory networks in DP125410314. (C) Overview of the phenylpropanoid pathway showing genes that are significantly upregulated or downregulated in the DP125410314 seed coat relative to the NRCDH4079 control. Fold change values relative to wild type are shown only for differentially expressed genes. (D) Schematic pathway depicting normal seed development with proper MYB5 , JAZ3 and FYPP3 function, and the resulting phenotypic changes in DP125410314 due to their downregulation or deletion, specifically reduced ADF and enhanced seed storage protein content.
Littell, supplied by Milliken, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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milligen synthesizer model 9050  (PerSeptive Biosystems Inc)
90
PerSeptive Biosystems Inc milligen synthesizer model 9050
Deletion of <t>MYB5</t> , JAZ3 and FYPP3 on chromosome A1 is likely associated with high protein and low ADF in DP125410314. (A) Differential expression analysis of MYB5 , JAZ3 and FYPP3 , located within the deleted A1 chromosomal region, identified these genes as potential causal regulators in the DP125410314 mutant. MYB5 is associated with lignification, while JAZ3 and FYPP3 are implicated in seed storage protein accumulation. Expression profiles are shown for seed coat (S1–S5) and embryo (E1–E5) stages from DP125410314 compared to the NRCDH4079 control. (B) Expression patterns of lignin biosynthesis‐related transcription factors ( MYB7 , MYB32 , MYB85 , ANAC018 ) and seed storage protein genes ( CRU1 , CRU2 , CRU3 , SESA4 ) highlight altered regulatory networks in DP125410314. (C) Overview of the phenylpropanoid pathway showing genes that are significantly upregulated or downregulated in the DP125410314 seed coat relative to the NRCDH4079 control. Fold change values relative to wild type are shown only for differentially expressed genes. (D) Schematic pathway depicting normal seed development with proper MYB5 , JAZ3 and FYPP3 function, and the resulting phenotypic changes in DP125410314 due to their downregulation or deletion, specifically reduced ADF and enhanced seed storage protein content.
Milligen Synthesizer Model 9050, supplied by PerSeptive Biosystems Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/machine+learning+trained+milliken+population+charge+model/9050+plus+pepsynthesizer/pmc02199041-25-33-37
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milliren, evans  (Milliren Technologies Inc)
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Milliren Technologies Inc milliren, evans
Deletion of <t>MYB5</t> , JAZ3 and FYPP3 on chromosome A1 is likely associated with high protein and low ADF in DP125410314. (A) Differential expression analysis of MYB5 , JAZ3 and FYPP3 , located within the deleted A1 chromosomal region, identified these genes as potential causal regulators in the DP125410314 mutant. MYB5 is associated with lignification, while JAZ3 and FYPP3 are implicated in seed storage protein accumulation. Expression profiles are shown for seed coat (S1–S5) and embryo (E1–E5) stages from DP125410314 compared to the NRCDH4079 control. (B) Expression patterns of lignin biosynthesis‐related transcription factors ( MYB7 , MYB32 , MYB85 , ANAC018 ) and seed storage protein genes ( CRU1 , CRU2 , CRU3 , SESA4 ) highlight altered regulatory networks in DP125410314. (C) Overview of the phenylpropanoid pathway showing genes that are significantly upregulated or downregulated in the DP125410314 seed coat relative to the NRCDH4079 control. Fold change values relative to wild type are shown only for differentially expressed genes. (D) Schematic pathway depicting normal seed development with proper MYB5 , JAZ3 and FYPP3 function, and the resulting phenotypic changes in DP125410314 due to their downregulation or deletion, specifically reduced ADF and enhanced seed storage protein content.
Milliren, Evans, supplied by Milliren Technologies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Deletion of MYB5 , JAZ3 and FYPP3 on chromosome A1 is likely associated with high protein and low ADF in DP125410314. (A) Differential expression analysis of MYB5 , JAZ3 and FYPP3 , located within the deleted A1 chromosomal region, identified these genes as potential causal regulators in the DP125410314 mutant. MYB5 is associated with lignification, while JAZ3 and FYPP3 are implicated in seed storage protein accumulation. Expression profiles are shown for seed coat (S1–S5) and embryo (E1–E5) stages from DP125410314 compared to the NRCDH4079 control. (B) Expression patterns of lignin biosynthesis‐related transcription factors ( MYB7 , MYB32 , MYB85 , ANAC018 ) and seed storage protein genes ( CRU1 , CRU2 , CRU3 , SESA4 ) highlight altered regulatory networks in DP125410314. (C) Overview of the phenylpropanoid pathway showing genes that are significantly upregulated or downregulated in the DP125410314 seed coat relative to the NRCDH4079 control. Fold change values relative to wild type are shown only for differentially expressed genes. (D) Schematic pathway depicting normal seed development with proper MYB5 , JAZ3 and FYPP3 function, and the resulting phenotypic changes in DP125410314 due to their downregulation or deletion, specifically reduced ADF and enhanced seed storage protein content.

Journal: Plant Biotechnology Journal

Article Title: Haploid Mutation Mapping Identifies a Homoeologous Non‐Reciprocal Translocation Linked to Reduced Fibre and Enhanced Protein in Brassica napus

doi: 10.1111/pbi.70535

Figure Lengend Snippet: Deletion of MYB5 , JAZ3 and FYPP3 on chromosome A1 is likely associated with high protein and low ADF in DP125410314. (A) Differential expression analysis of MYB5 , JAZ3 and FYPP3 , located within the deleted A1 chromosomal region, identified these genes as potential causal regulators in the DP125410314 mutant. MYB5 is associated with lignification, while JAZ3 and FYPP3 are implicated in seed storage protein accumulation. Expression profiles are shown for seed coat (S1–S5) and embryo (E1–E5) stages from DP125410314 compared to the NRCDH4079 control. (B) Expression patterns of lignin biosynthesis‐related transcription factors ( MYB7 , MYB32 , MYB85 , ANAC018 ) and seed storage protein genes ( CRU1 , CRU2 , CRU3 , SESA4 ) highlight altered regulatory networks in DP125410314. (C) Overview of the phenylpropanoid pathway showing genes that are significantly upregulated or downregulated in the DP125410314 seed coat relative to the NRCDH4079 control. Fold change values relative to wild type are shown only for differentially expressed genes. (D) Schematic pathway depicting normal seed development with proper MYB5 , JAZ3 and FYPP3 function, and the resulting phenotypic changes in DP125410314 due to their downregulation or deletion, specifically reduced ADF and enhanced seed storage protein content.

Article Snippet: MYB5 , a transcription factor involved in seed coat development (Li, Milliken, et al. ; Xu et al. ), could play a key role in lignin deposition, and its loss may contribute to reduced ADF levels (Figure ).

Techniques: Quantitative Proteomics, Mutagenesis, Expressing, Control