Bibliografie tematiche / HSMath

Letteratura scientifica selezionata sul tema "HSMath"

Autore: Grafiati
Pubblicato: 25 luglio 2024

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Articoli di riviste sul tema "HSMath"

1

Marquez, Raymond M., Matthew A. Singer, Norma T. Takaesu, W. Ross Waldrip, Yevgenya Kraytsberg e Stuart J. Newfeld. "Transgenic Analysis of the Smad Family of TGF-β Signal Transducers in Drosophila melanogaster Suggests New Roles and New Interactions Between Family Members". Genetics 157, n. 4 (1 aprile 2001): 1639–48. http://dx.doi.org/10.1093/genetics/157.4.1639.

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Abstract Smad signal transducers are required for transforming growth factor-β-mediated developmental events in many organisms including humans. However, the roles of individual human Smad genes (hSmads) in development are largely unknown. Our hypothesis is that an hSmad performs developmental roles analogous to those of the most similar Drosophila Smad gene (dSmad). We expressed six hSmad and four dSmad transgenes in Drosophila melanogaster using the Gal4/UAS system and compared their phenotypes. Phylogenetically related human and Drosophila Smads induced similar phenotypes supporting the hypothesis. In contrast, two nearly identical hSmads generated distinct phenotypes. When expressed in wing imaginal disks, hSmad2 induced oversize wings while hSmad3 induced cell death. This observation suggests that a very small number of amino acid differences, between Smads in the same species, confer distinct developmental roles. Our observations also suggest new roles for the dSmads, Med and Dad, in dActivin signaling and potential interactions between these family members. Overall, the study demonstrates that transgenic methods in Drosophila can provide new information about non-Drosophila members of developmentally important multigene families.
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2

Campbell, M. S., G. K. Chan e T. J. Yen. "Mitotic checkpoint proteins HsMAD1 and HsMAD2 are associated with nuclear pore complexes in interphase". Journal of Cell Science 114, n. 5 (1 marzo 2001): 953–63. http://dx.doi.org/10.1242/jcs.114.5.953.

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Mad1 was first identified in budding yeast as an essential component of the checkpoint system that monitors spindle assembly in mitosis and prevents premature anaphase onset. Using antibodies to the human homologue of Mad1 (HsMAD1), we have begun to characterize this protein in mammalian cells. HsMad1 is found localized at kinetochores in mitosis. The labeling is brightest in prometaphase and is absent from kinetochores at metaphase and anaphase. In cells where most chromosomes have reached the metaphase plate, those aligned at the plate show no labeling while remaining, unaligned chromosomes are still brightly labeled. We find HsMad1 associated with HsMad2. Association with p55CDC, a protein previously shown to bind HsMad2, was not detected. Surprisingly, unlike any other known mitotic checkpoint proteins, HsMad1 and HsMAD2 were found localized at nuclear pores throughout interphase. This was confirmed by co-labeling with an antibody to known nuclear pore complex proteins and by their co-purification with enriched nuclear envelope fractions. HsMad1 was identified serendipitously by its binding to a viral protein, HTLV-1 Tax, which affects transcription of viral and human proteins. The localization of HsMad1 to nuclear pore complexes suggests an alternate, non-mitotic role for the Mad1/Tax interaction in the viral transformation of cells.
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3

Iwanaga, Yoichi, Takefumi Kasai, Karen Kibler e Kuan-Teh Jeang. "Characterization of Regions in hsMAD1 Needed for Binding hsMAD2". Journal of Biological Chemistry 277, n. 34 (31 maggio 2002): 31005–13. http://dx.doi.org/10.1074/jbc.m110666200.

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4

Hogea, Bogdan Gheorghe, Mugurel Constantin Rusu, Adelina Maria Jianu, Bogdan Adrian Manta e Adrian Cosmin Ilie. "Rare Anatomic Variation: The Hepatosplenomesentericophrenic Trunk". Medicina 57, n. 2 (15 febbraio 2021): 170. http://dx.doi.org/10.3390/medicina57020170.

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The rare anatomic variants of the celiac trunk and superior mesenteric artery include the hepatosplenic, hepatosplenomesenteric (HSMT), celiacomesenteric, hepatomesenteric and gastrosplenic trunks. We report a 72-year-old female patient whose computed tomography angiograms indicated a rare anatomic feature whereby the right inferior phrenic artery was inserted in the origin of an HSMT, thus modifying it into a hepatosplenomesentericophrenic trunk (HSMPT). Above the HSMPT, the insertion of the left inferior phrenic artery in the origin of the left gastric artery determined a left gastrophrenic trunk (GPT). Proper identification of this type of rare anatomic variant is of utmost importance prior to different surgical procedures. For example, an HSMT origin of the right inferior phrenic artery is surgically relevant if this artery is an extrinsic pedicle of a hepatocellular carcinoma and is used for embolization of the tumor.
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Miskey, Csaba, Balázs Papp, Lajos Mátés, Ludivine Sinzelle, Heiko Keller, Zsuzsanna Izsvák e Zoltán Ivics. "The Ancient mariner Sails Again: Transposition of the Human Hsmar1 Element by a Reconstructed Transposase and Activities of the SETMAR Protein on Transposon Ends". Molecular and Cellular Biology 27, n. 12 (2 aprile 2007): 4589–600. http://dx.doi.org/10.1128/mcb.02027-06.

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Abstract (sommario):
ABSTRACT Hsmar1, one of the two subfamilies of mariner transposons in humans, is an ancient element that entered the primate genome lineage ∼50 million years ago. Although Hsmar1 elements are inactive due to mutational damage, one particular copy of the transposase gene has apparently been under selection. This transposase coding region is part of the SETMAR gene, in which a histone methylatransferase SET domain is fused to an Hsmar1 transposase domain. A phylogenetic approach was taken to reconstruct the ancestral Hsmar1 transposase gene, which we named Hsmar1-Ra. The Hsmar1-Ra transposase efficiently mobilizes Hsmar1 transposons by a cut-and-paste mechanism in human cells and zebra fish embryos. Hsmar1-Ra can also mobilize short inverted-repeat transposable elements (MITEs) related to Hsmar1 (MiHsmar1), thereby establishing a functional relationship between an Hsmar1 transposase source and these MITEs. MiHsmar1 excision is 2 orders of magnitude more efficient than that of long elements, thus providing an explanation for their high copy numbers. We show that the SETMAR protein binds and introduces single-strand nicks into Hsmar1 inverted-repeat sequences in vitro. Pathway choices for DNA break repair were found to be characteristically different in response to transposon cleavage mediated by Hsmar1-Ra and SETMAR in vivo. Whereas nonhomologous end joining plays a dominant role in repairing excision sites generated by the Hsmar1-Ra transposase, DNA repair following cleavage by SETMAR predominantly follows a homology-dependent pathway. The novel transposon system can be a useful tool for genome manipulations in vertebrates and for investigations into the transpositional dynamics and the contributions of these elements to primate genome evolution.
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6

Moosa, Aminath Shiwaza, Alvin Jia Hao Ngeow, Yuhan Yang, Zhimin Poon, Ding Xuan Ng, Eileen Koh Yi Ling e Ngiap Chuan Tan. "A Novel Smartphone App for Self-Monitoring of Neonatal Jaundice Among Postpartum Mothers: Qualitative Research Study". JMIR mHealth and uHealth 11 (22 dicembre 2023): e53291-e53291. http://dx.doi.org/10.2196/53291.

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Abstract (sommario):
Abstract Background Neonatal jaundice (NNJ) or hyperbilirubinemia is a ubiquitous condition in newborn infants. Currently, the transcutaneous bilirubinometer is used to screen for NNJ in health care facilities, where neonates need to be physically present (ie, a centralized model of care for NNJ screening). Mobile health (mHealth) apps present a low-cost, home-based, and noninvasive system that could facilitate self-monitoring of NNJ and could allow mothers the convenience of screening for NNJ remotely. However, end users’ acceptability of such mHealth apps is of fundamental importance before the incorporation of such apps into clinical practice. Objective The study aimed to explore the perception of postpartum mothers toward self-monitoring of NNJ using a novel mHealth app. Methods Mothers attending video consultations for early postpartum care at 2 Singapore primary care clinics watched an instructional video for a hyperbilirubinemia-screening mHealth app (HSMA). An independent researcher used a semistructured topic guide to conduct in-depth interviews with 25 mothers, assessing their views on HSMAs. All interviews were audio recorded, transcribed verbatim, and checked for accuracy before data analysis. Two researchers independently analyzed the transcripts via thematic analysis. Data were managed using NVivo qualitative data management software. Results The identified themes were grouped under perceived usability and utility. Mothers valued the convenience and utility of HSMAs for remote monitoring of NNJ. They appreciated the objectivity the app readings provided compared to visual inspection. However, they perceived that the app’s applicability would be restricted to severe jaundice, were concerned about its accuracy and restriction to the English language, and lacked confidence in using it. Nevertheless, they were willing to use it once its accuracy was proven and when they received adequate guidance from health care professionals. They also suggested including an action plan for the measured readings and clinical signs within the app. Mothers proposed pairing teleconsultations with HSMAs to boost their confidence and enhance adoption. Conclusions Mothers were receptive to using HSMAs but had concerns. Multiple languages, proof of accuracy, and resources to guide users should be incorporated into the app in the next phase to increase its successful adoption. Complementing such apps with a teleconsultation service presents a plausible and pragmatic NNJ care delivery model in general practice.
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Gemma, Akihiko, Koichi Hagiwara, Francoise Vincent, Yang Ke, Amy R. Hancock, Makoto Nagashima, William P. Bennett e Curtis C. Harris. "hSmad5 gene, a human hSmad family member: its full length cDNA, genomic structure, promoter region and mutation analysis in human tumors". Oncogene 16, n. 7 (febbraio 1998): 951–56. http://dx.doi.org/10.1038/sj.onc.1201614.

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8

Nabokina, Svetlana M., Veedamali S. Subramanian e Hamid M. Said. "Association of PDZ-containing protein PDZD11 with the human sodium-dependent multivitamin transporter". American Journal of Physiology-Gastrointestinal and Liver Physiology 300, n. 4 (aprile 2011): G561—G567. http://dx.doi.org/10.1152/ajpgi.00530.2010.

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Abstract (sommario):
Intestinal absorption of biotin is mediated via the sodium-dependent multivitamin transporter (SMVT). Studies from our laboratory and others have characterized different aspects of the human SMVT (hSMVT), but nothing is currently known about protein(s) that may interact with hSMVT and affect its physiology/biology. In this study, a PDZ-containing protein PDZD11 was identified as an interacting partner with hSMVT using yeast two-hybrid screen of a human intestinal cDNA library. The interaction between hSMVT and PDZD11 was confirmed by in vitro GST-pull-down assay and in vivo in a mammalian cell environment by a two-hybrid luciferase and coimmunoprecipitation assays. Furthermore, confocal imaging of live human intestinal epithelial HuTu-80 cells expressing hSMVT-GFP and DsRed-PDZD11 demonstrated colocalization of these two proteins. We also examined the functional consequence of the interaction between hSMVT and PDZD11 in HuTu-80 cells and observed significant induction in [3H]biotin uptake upon coexpression of hSMVT and PDZD11. In contrast, knocking down of PDZD11 with gene-specific small interfering RNA led to a significant decrease in biotin uptake; biotinylation assay showed this to be associated with a marked decrease in level of expression of hSMVT at the cell membrane. By truncation approach, we also demonstrated that the PDZ binding domain that is located in the COOH-terminal tail of hSMVT polypeptide is involved in the interaction with PDZD11. These results demonstrate for the first time that PDZD11 is an interacting partner with hSMVT in intestinal epithelial cells and that this interaction affects hSMVT function and cell biology.
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Reidling, Jack C., e Hamid M. Said. "Regulation of the human biotin transporter hSMVT promoter by KLF-4 and AP-2: confirmation of promoter activity in vivo". American Journal of Physiology-Cell Physiology 292, n. 4 (aprile 2007): C1305—C1312. http://dx.doi.org/10.1152/ajpcell.00360.2006.

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Abstract (sommario):
The mechanism of biotin uptake in human intestine has been well characterized and involves the human sodium-dependent multivitamin transporter (hSMVT), yet little is known about the molecular/transcriptional regulation of the system. Previous investigations cloned the 5′ regulatory region of the hSMVT gene and identified the minimal promoter. To expand these investigations, we compared activity of the hSMVT promoter in three human intestinal epithelial cell lines (NCM460, Caco-2, and HuTu-80) and contrasted a renal epithelial cell line (HEK-293). We analyzed the role of putative cis-elements in regulating promoter activity and confirmed activity of the cloned hSMVT promoter in vivo. In vitro studies demonstrated that all cell lines utilized the same minimal promoter region, and mutation of specific cis-regulatory elements [Kruppel-like factor 4 (KLF-4) and activator protein-2 (AP-2)] led to a decrease in promoter activity in all intestinal cell types but not in renal cells. Using electrophoretic mobility shift assays, we identified two specific DNA/protein complexes. Using oligonucleotide competition and antibody supershift analysis, we determined that KLF-4 and AP-2 were involved in forming the complexes. In HEK-293 cells, overexpressing KLF-4 increased the endogenous hSMVT message levels threefold and activated a cotransfected hSMVT promoter-reporter construct. In vivo studies using hSMVT promoter-luciferase transgenic mice established physiological relevance and showed the pattern of hSMVT promoter expression to be similar to endogenous mouse SMVT mRNA expression. The results demonstrate, for the first time, the importance of KLF-4 and AP-2 in regulating the activity of the hSMVT promoter in the intestine and provide direct in vivo confirmation of hSMVT promoter activity.
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10

Subramanian, Veedamali S., Jonathan S. Marchant, Michael J. Boulware, Thomas Y. Ma e Hamid M. Said. "Membrane targeting and intracellular trafficking of the human sodium-dependent multivitamin transporter in polarized epithelial cells". American Journal of Physiology-Cell Physiology 296, n. 4 (aprile 2009): C663—C671. http://dx.doi.org/10.1152/ajpcell.00396.2008.

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Abstract (sommario):
The human sodium-dependent multivitamin transporter (hSMVT) mediates sodium-dependent uptake of biotin in renal and intestinal epithelia. To date, however, there is nothing known about the structure-function relationship or targeting sequences in the hSMVT polypeptide that control its polarized expression within epithelia. Here, we focused on the role of the COOH-terminal tail of hSMVT in the targeting and functionality of this transporter. A full-length hSMVT-green fluorescent protein (GFP) fusion protein was functional and expressed at the apical membrane in renal and intestinal cell lines. Microtubule disrupting agents disrupted the mobility of trafficking vesicles and impaired cell surface delivery of hSMVT, which was also prevented in cells treated with dynamitin (p50), brefeldin, or monensin. Progressive truncation of the COOH-terminal tail impaired the functionality and targeting of the transporter. First, biotin transport decreased by approximately 20–30% on deletion of up to 15 COOH-terminal amino acids of hSMVT, a decrease mimicked solely by deletion of the terminal PDZ motif (TSL). Second, deletions into the COOH-terminal tail (between residues 584-612, containing a region of predicted high surface accessibility) resulted in a further drop in hSMVT transport (to ∼40% of wild-type). Third, apical targeting was lost on deletion of a helical-prone region between amino acids 570-584. We conclude that the COOH tail of hSMVT contains several determinants important for polarized targeting and biotin transport.
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Più fonti

Tesi sul tema "HSMath"

1

Claeys, Bouuaert Corentin. "The mechanism of mariner transposition : a molecular analysis of the human Hsmar1 transposon". Thesis, University of Nottingham, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555257.

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Abstract (sommario):
Transposons are specialized genetic elements that mobilize and amplify within a host genome. They are disruptive by nature and are therefore considered as molecular parasites, but they are also important evolutionary forces. The Tc1-mariner superfamily of transposons is particularly widespread in eukaryotes. These elements transpose via a cut-and-paste mechanism and are unusual in that double-strand cleavage of the transposon ends does not rely on the formation of a hairpin intermediate. This suggests that Tc1-mariner elements use a fundamentally different mechanism of transposition, yet it remains poorly understood. A highly tractable in vitro reaction provided by a resurrected transposase, Hsmar 1, has presented an opportunity to investigate the mechanism adopted by mariners. Transposition relies on the formation of a synaptic complex which, unusually, is assembled asymmetrically. A transposase dimer binds one end of the transposon and recruits a naked end within this complex. Binding of the second end is slow and can be accelerated by juxtaposition of the ends in the right-handed geometry of negative supercoiling nodes. This provides mariner with topological selectivity towards the configuration of recombining partners. In the presence of an excess of transposase the slow rate of synapsis also introduces a competition between transposases dimers for recruiting a free transposon end. This is the basis of a characteristic auto-regulatory mechanism which mariner elements probably take advantage of to limit the extent of a genomic invasion. Within the transpososome, the two strands of a transposon end are cleaved by the same active site. First, the non-transferred strands are cleaved at both ends. Then, a structural transition which is coordinated at the two ends of the complex relocates the active sites onto the transferred strands. Cleavage of the transferred strands exposes 3' -hydroxyls which are transferred 5' of a target TA dinucleotide. The tightly coupled sequence of events, dictated by the architecture of the transpososome, allows a single transposase dimer to complete transposition without recourse to the hairpin mechanism. This provides the first example of a DDE/D enzyme where the active site performs two sequential hydrolyses of DNA strands of opposite polarity. Biological implications of the strategy adopted by mariner elements are discussed.
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2

Kalibjian, Jeff. "Securing Telemetry Post Processing Applications with Hardware Based Security". International Foundation for Telemetering, 2004. http://hdl.handle.net/10150/605052.

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International Telemetering Conference Proceedings / October 18-21, 2004 / Town & Country Resort, San Diego, California
The use of hardware security for telemetry in satellites utilized for intelligence and defense applications is well known. Less common is the use of hardware security in ground-based computers hosting applications that post process telemetry data. Analysis reveals vulnerabilities in software only security solutions that can result in the compromise of telemetry data housed on ground-based computer systems. Such systems maybe made less susceptible to compromise with the use of hardware based security.
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3

Chen, Qiujia. "A role for SETMAR in gene regulation: insights from structural analysis of the dna-binding domain in complex with dna". Diss., 2016. http://hdl.handle.net/1805/10895.

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Indiana University-Purdue University Indianapolis (IUPUI)
SETMAR is a chimeric protein that originates from the fusion of a SET domain to the mariner Hsmar1 transposase. This fusion event occurred approximately 50 million years ago, after the split of an anthropoid primate ancestor from the prosimians. Thus, SETMAR is only expressed in anthropoid primates, such as humans, apes, and New World monkeys. Evolutionary sequence analyses have revealed that the DNA-binding domain, one of the two functional domains in the Hsmar1 transposase, has been subjected to a strong purifying selection. Consistent with these analyses, SETMAR retains robust binding specificity to its ancestral terminal inverted repeat (TIR) DNA. In the human genome, this TIR sequence is dispersed in over 1500 perfect or nearly perfect sites. Given that many DNA-binding domains of transcriptional regulators are derived from transposases, we hypothesized that SETMAR may play a role in gene regulation. In this thesis, we determined the crystal structures of the DNA-binding domain bound to both its ancestral TIR DNA and a variant TIR DNA sequence at 2.37 and 3.07 Å, respectively. Overall, the DNA-binding domain contains two helix-turn-helix (HTH) motifs linked by two AT-hook motifs and dimerizes through its HTH1 motif. In both complexes, minor groove interactions with the AT-hook motifs are similar, and major groove interactions with HTH1 involve a single residue. However, four residues from HTH2 participate in nucleobase-specific interactions with the TIR and only two with the variant DNA sequence. Despite these differences in nucleobase-specific interactions, the DNA-binding affinities of SETMAR to TIR or variant TIR differ by less than two-fold. From cell-based studies, we found that SETMAR represses firefly luciferase gene expression while the DNA-binding deficient mutant does not. A chromatin immunoprecipitation assay further confirms that SETMAR binds the TIR sequence in cells. Collectively, our studies suggest that SETMAR functions in gene regulation.
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Capitoli di libri sul tema "HSMath"

1

Pardasani, R. T., e P. Pardasani. "Effective magnetic moment of [Fe(Hsmt)(smt)]". In Magnetic Properties of Paramagnetic Compounds, 2161. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23675-4_1924.

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Pardasani, R. T., e P. Pardasani. "Effective magnetic moment of Fe(Hsmt)Cl2". In Magnetic Properties of Paramagnetic Compounds, 2159. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23675-4_1922.

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Pardasani, R. T., e P. Pardasani. "Effective magnetic moment of [Fe(Hsmt)2]Cl". In Magnetic Properties of Paramagnetic Compounds, 2160. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-23675-4_1923.

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4

Heuer, Anna. "Die Hotellerie im Wandel in Richtung New Work – eine Reflexion aus HSMA-Verbandsperspektive". In New Work, Leadership und Human Resources Management im Tourismus, 71–74. Wiesbaden: Springer Fachmedien Wiesbaden, 2024. http://dx.doi.org/10.1007/978-3-658-42932-4_5.

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5

Suzuki, K. "Human Sensory Measurement Application Technology (HSMAT)". In International Encyclopedia of Ergonomics and Human Factors, Second Edition - 3 Volume Set. CRC Press, 2006. http://dx.doi.org/10.1201/9780849375477.ch620.

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"Human Sensory Measurement Application Technology (HSMAT)". In International Encyclopedia of Ergonomics and Human Factors - 3 Volume Set, 3260–63. CRC Press, 2006. http://dx.doi.org/10.1201/9780849375477-639.

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Atti di convegni sul tema "HSMath"

1

Zhang, Jingnan, Anna Ström e Ingrid Undeland. "Creating functional protein ingredients by cross-processing herring co-products with lingonberry press-cake, shrimp shells or green seaweed". In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/xogq1535.

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Cross-processing herring co-products with lingonberry press-cake, shrimp shells and green seaweed (hereafter referred to as €œhelpers€) was recently reported to mitigate lipid oxidation during pH-shift-based protein isolation but had the drawback to reduce protein yield. Here, four strategies to counteract this yield-reduction were studied; optimized solubilization and precipitation pHs, increased water to raw material ratio as well as application of high shear mechanical homogenization (HSMH) and ultrasonication (US). Beyond effects on protein yield, the impacts of the process conditions on the structural, rheological and functional properties of the recovered proteins were also investigated.Increasing solubilization pH from 11.5 to 12 and decreasing precipitation pH from 5.5 to 5.0 or 4.5, as well as increasing the water-to-raw material ratio significantly improved protein yield with all helpers. Rotor-stator (RS)-HSMH and US also improved protein yield by 5-12% with a more marked effect of the type of helper. Cross-processing herring co-products with antioxidant-rich helpers substantially improved water solubility and emulsification capacity of the protein isolates but the effects of RS-HSMH and US were highly dependent on the type of helper. RS-HSMH helped in mitigating the observed negative impact of cross-processing on gel-forming capacity of protein isolates produced in presence of all three helpers; results with lingonberry press-cake were particularly promising. Altogether, tuning processing conditions as well as adding RS-HSMH and US can help in maximizing protein yield during cross-processing of herring co-products with antioxidant-containing helpers. However, the effects of processing conditions on protein functionality are intimately linked to the type of helpers. The combination of herring co-products with lingonberry press-cake was the most promising and will be subject for further studies.
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2

Yadava, Girijesh K., Stephen Rudin, Andrew T. Kuhls-Gilcrist e Daniel R. Bednarek. "Generalized objective performance assessment of a new high-sensitivity microangiographic fluoroscopic (HSMAF) imaging system". In Medical Imaging, a cura di Jiang Hsieh e Ehsan Samei. SPIE, 2008. http://dx.doi.org/10.1117/12.769808.

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Böker, KO, S. Siegk, JH Wagner, M. Remling, X. Shang, W. Lehmann e AF Schilling. "Evaluation of different hydrogels (PEGDA, CSMA, HSMA, Fibrin) for 3D-Bone-Tissue Engineering". In Deutscher Kongress für Orthopädie und Unfallchirurgie. Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1717318.

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4

Sharma, Kamaldeep, Vikram Kamboj e Sanjay Marwaha. "Optimum assortment of gear ratio of hybrid electric vehicles via hSMA-PS algorithm". In 14TH INTERNATIONAL CONFERENCE ON MATERIALS PROCESSING AND CHARACTERIZATION 2023. AIP Publishing, 2024. http://dx.doi.org/10.1063/5.0196509.

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Kalaivaani, P. T., e A. Rajeswari. "An analysis of H-MAC, HSMAC and H-MAC based AOMDV for wireless sensor networks to achieve energy efficiency using spatial correlation concept". In 2015 2nd International Conference on Electronics and Communication Systems (ICECS). IEEE, 2015. http://dx.doi.org/10.1109/ecs.2015.7125021.

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6

Li, Pinna. "Research on Protection of Intellectual Property Rights of Intangible Cultural Heritage". In 2017 International Conference on Humanities Science, Management and Education Technology (HSMET 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/hsmet-17.2017.1.

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Li, Tao. "Research on the Talent Demand of Industrial Clusters and the Transformation of Newly Established Undergraduate Colleges". In 2017 International Conference on Humanities Science, Management and Education Technology (HSMET 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/hsmet-17.2017.10.

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Jiang, Hong, e Hong Zhao. "Apply MQ Group Discussion to TJPU Tertiary Large Class Teaching in China". In 2017 International Conference on Humanities Science, Management and Education Technology (HSMET 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/hsmet-17.2017.100.

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Li, Haoqin. "Research on Reform Directions of Physical Education in Universities from Sunshine Sports Perspective". In 2017 International Conference on Humanities Science, Management and Education Technology (HSMET 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/hsmet-17.2017.101.

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Li, Changjian, e Yaqun Wang. "Coordinated Development of Community Rights and Land Rights: Realization and Development of Farmland Expropriation Intergenerational Equity". In 2017 International Conference on Humanities Science, Management and Education Technology (HSMET 2017). Paris, France: Atlantis Press, 2017. http://dx.doi.org/10.2991/hsmet-17.2017.102.

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