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  1. Article ; Online: Why is motilin active in some studies with mice, rats, and guinea pigs, but not in others? Implications for functional variability among rodents.

    Sanger, Gareth J

    Pharmacology research & perspectives

    2022  Volume 10, Issue 2, Page(s) e00900

    Abstract: ... e.g., "Sprague-Dawley") or were inbred strains. It is speculated that variation in source/type ... in rodents (e.g., to dimerize with GPCRs and create different pharmacological profiles). Is the absence ...

    Abstract The gastrointestinal (GI) hormone motilin helps control human stomach movements during hunger and promotes hunger. Although widely present among mammals, it is generally accepted that in rodents the genes for motilin and/or its receptor have undergone pseudonymization, so exogenous motilin cannot function. However, several publications describe functions of low concentrations of motilin, usually within the GI tract and CNS of mice, rats, and guinea pigs. These animals were from institute-held stocks, simply described with stock names (e.g., "Sprague-Dawley") or were inbred strains. It is speculated that variation in source/type of animal introduces genetic variations to promote motilin-sensitive pathways. Perhaps, in some populations, motilin receptors exist, or a different functionally-active receptor has a good affinity for motilin (indicating evolutionary pressures to retain motilin functions). The ghrelin receptor has the closest sequence homology, yet in non-rodents the receptors have a poor affinity for each other's cognate ligand. In rodents, ghrelin may substitute for certain GI functions of motilin, but no good evidence suggests rodent ghrelin receptors are highly responsive to motilin. It remains unknown if motilin has functional relationships with additional bioactive molecules formed from the ghrelin and motilin genes, or if a 5-TM motilin receptor has influence in rodents (e.g., to dimerize with GPCRs and create different pharmacological profiles). Is the absence/presence of responses to motilin in rodents' characteristic for systems undergoing gene pseudonymization? What are the consequences of rodent supplier-dependent variations in motilin sensitivity (or other ligands for receptors undergoing pseudonymization) on gross physiological functions? These are important questions for understanding animal variation.
    MeSH term(s) Animals ; Gastrointestinal Tract/physiology ; Genetic Variation ; Ghrelin/metabolism ; Guinea Pigs ; Humans ; Mice ; Motilin/metabolism ; Rats ; Receptors, Gastrointestinal Hormone/metabolism ; Receptors, Ghrelin/metabolism ; Receptors, Neuropeptide/metabolism ; Rodentia ; Species Specificity
    Chemical Substances Ghrelin ; Receptors, Gastrointestinal Hormone ; Receptors, Ghrelin ; Receptors, Neuropeptide ; motilin receptor ; Motilin (52906-92-0)
    Language English
    Publishing date 2022-02-21
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2740389-0
    ISSN 2052-1707 ; 2052-1707
    ISSN (online) 2052-1707
    ISSN 2052-1707
    DOI 10.1002/prp2.900
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The relationship between symptom improvement and gastric emptying in the treatment of gastroparesis: remember the pharmacology.

    Sanger, G J

    The American journal of gastroenterology

    2014  Volume 109, Issue 3, Page(s) 444–445

    MeSH term(s) Diabetes Mellitus, Type 2/complications ; Gastric Emptying/drug effects ; Gastrointestinal Agents/therapeutic use ; Gastroparesis/drug therapy ; Humans
    Chemical Substances Gastrointestinal Agents
    Language English
    Publishing date 2014-03-04
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 390122-1
    ISSN 1572-0241 ; 0002-9270
    ISSN (online) 1572-0241
    ISSN 0002-9270
    DOI 10.1038/ajg.2013.432
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Ghrelin and motilin receptor agonists: time to introduce bias into drug design.

    Sanger, G J

    Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society

    2014  Volume 26, Issue 2, Page(s) 149–155

    Abstract: ... e.g., camicinal, under development for patients with gastric hypo-motility)? For ghrelin, additional ... relief: e.g., low-dose erythromycin), would low doses of ghrelin and motilin agonists relieve symptoms ...

    Abstract Ghrelin and motilin receptor agonists increase gastric motility and are attractive drug targets. However, 14 years after the receptors were described (18-24 years since ligands became available) the inactivity of the ghrelin agonist TZP-102 in patients with gastroparesis joins the list of unsuccessful motilin agonists. Fundamental questions must be asked. Pustovit et al., have now shown that the ghrelin agonist ulimorelin evokes prolonged increases in rat colorectal propulsion yet responses to other ghrelin agonists fade. Similarly, different motilin agonists induce short- or long-lasting effects in a cell-dependent manner. Together, these and other data create the hypothesis that the receptors can be induced to preferentially signal ('biased agonism') via particular pathways to evoke different responses with therapeutic advantages/disadvantages. Biased agonism has been demonstrated for ghrelin. Are motilin agonists which cause long-lasting facilitation of human stomach cholinergic function (compared with motilin) biased agonists (e.g., camicinal, under development for patients with gastric hypo-motility)? For ghrelin, additional complications exist because the therapeutic aims/mechanisms of action are uncertain, making it difficult to select the best (biased) agonist. Will ghrelin agonists be useful treatments of nausea and/or as suggested by Pustovit et al., chronic constipation? How does ghrelin increase gastric motility? As gastroparesis symptoms poorly correlate with delayed gastric emptying (yet gastro-prokinetic drugs can provide relief: e.g., low-dose erythromycin), would low doses of ghrelin and motilin agonists relieve symptoms simply by restoring neuromuscular rhythm? These questions on design and functions need addressing if ghrelin and motilin agonists are to reach patients as drugs.
    MeSH term(s) Animals ; Drug Design ; Gastrointestinal Motility/drug effects ; Humans ; Rats ; Receptors, Gastrointestinal Hormone/agonists ; Receptors, Ghrelin/agonists ; Receptors, Neuropeptide/agonists
    Chemical Substances Receptors, Gastrointestinal Hormone ; Receptors, Ghrelin ; Receptors, Neuropeptide ; motilin receptor
    Language English
    Publishing date 2014-01-20
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1186328-6
    ISSN 1365-2982 ; 1350-1925
    ISSN (online) 1365-2982
    ISSN 1350-1925
    DOI 10.1111/nmo.12300
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Ghrelin and motilin receptor agonists: a long and winding misconception.

    Sanger, G J

    Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society

    2013  Volume 25, Issue 12, Page(s) 1002

    MeSH term(s) Diabetes Mellitus, Type 1/complications ; Diabetes Mellitus, Type 2/complications ; Female ; Gastric Emptying/drug effects ; Gastroparesis/drug therapy ; Humans ; Macrocyclic Compounds/therapeutic use ; Male ; Receptors, Ghrelin/agonists
    Chemical Substances Macrocyclic Compounds ; Receptors, Ghrelin
    Language English
    Publishing date 2013-10-01
    Publishing country England
    Document type Letter ; Comment
    ZDB-ID 1186328-6
    ISSN 1365-2982 ; 1350-1925
    ISSN (online) 1365-2982
    ISSN 1350-1925
    DOI 10.1111/nmo.12241
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Comparative evaluation of somatostatin and CXCR4 receptor expression in different types of thyroid carcinoma using well-characterised monoclonal antibodies.

    Czajkowski, Max / Kaemmerer, Daniel / Sänger, Jörg / Sauter, Guido / Wirtz, Ralph M / Schulz, Stefan / Lupp, Amelie

    BMC cancer

    2022  Volume 22, Issue 1, Page(s) 740

    Abstract: Background: Papillary and follicular thyroid carcinomas can be treated surgically and with radioiodine therapy, whereas therapeutic options for advanced stage IV medullary and for anaplastic tumours are limited. Recently, somatostatin receptors (SSTs) ... ...

    Abstract Background: Papillary and follicular thyroid carcinomas can be treated surgically and with radioiodine therapy, whereas therapeutic options for advanced stage IV medullary and for anaplastic tumours are limited. Recently, somatostatin receptors (SSTs) and the chemokine receptor CXCR4 have been evaluated for the treatment of thyroid carcinomas, however, with contradictory results.
    Methods: The expression of the five SSTs and of CXCR4 was assessed in 90 samples from 56 patients with follicular, papillary, medullary, or anaplastic thyroid carcinoma by means of immunohistochemistry using well-characterised monoclonal antibodies. The stainings were evaluated using the Immunoreactivity Score (IRS) and correlated to clinical data. In order to further substantiate the immunohistochemistry results, in serial sections of a subset of the samples receptor expression was additionally examined at the mRNA level using qRT-PCR.
    Results: Overall, SST and CXCR4 protein expression was low in all four entities. In single cases, however, very high IRS values for SST2 and CXCR4 were observed. SST2 was the most frequently expressed receptor, found in 38% of cases, followed by SST5 and SST4, found in 14 and 9% of tumours, respectively. SST1 and SST3 could not be detected to any significant extent. CXCR4 was present in 12.5% of medullary and 25% of anaplastic carcinomas. Expression SST3, SST4, SST5 and CXCR4 was positively correlated with expression of the proliferation marker Ki-67. Additionally, a negative interrelationship between SST4 or SST5 expression and patient survival and a positive association between SST3 expression and tumour diameter were observed. qRT-PCR revealed a similar receptor expression pattern to that seen at the protein level. However, probably due to the low overall expression, no correlation was found for the SSTs or the CXCR4 between the IRS and the mRNA values.
    Conclusions: SST- or CXCR4-based diagnostics or therapy in thyroid carcinomas should not be considered in general but may be feasible in single cases with high levels of expression of these receptors.
    MeSH term(s) Antibodies, Monoclonal ; Humans ; Iodine Radioisotopes ; RNA, Messenger/metabolism ; Receptors, CXCR4/genetics ; Receptors, CXCR4/metabolism ; Receptors, Somatostatin/genetics ; Receptors, Somatostatin/metabolism ; Thyroid Neoplasms/genetics
    Chemical Substances Antibodies, Monoclonal ; CXCR4 protein, human ; Iodine Radioisotopes ; RNA, Messenger ; Receptors, CXCR4 ; Receptors, Somatostatin
    Language English
    Publishing date 2022-07-07
    Publishing country England
    Document type Journal Article
    ZDB-ID 2041352-X
    ISSN 1471-2407 ; 1471-2407
    ISSN (online) 1471-2407
    ISSN 1471-2407
    DOI 10.1186/s12885-022-09839-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: On the causes, consequences, and avoidance of PCR duplicates: Towards a theory of library complexity.

    Rochette, Nicolas C / Rivera-Colón, Angel G / Walsh, Jessica / Sanger, Thomas J / Campbell-Staton, Shane C / Catchen, Julian M

    Molecular ecology resources

    2023  Volume 23, Issue 6, Page(s) 1299–1318

    Abstract: Library preparation protocols for most sequencing technologies involve PCR amplification of the template DNA, which open the possibility that a given template DNA molecule is sequenced multiple times. Reads arising from this phenomenon, known as PCR ... ...

    Abstract Library preparation protocols for most sequencing technologies involve PCR amplification of the template DNA, which open the possibility that a given template DNA molecule is sequenced multiple times. Reads arising from this phenomenon, known as PCR duplicates, inflate the cost of sequencing and can jeopardize the reliability of affected experiments. Despite the pervasiveness of this artefact, our understanding of its causes and of its impact on downstream statistical analyses remains essentially empirical. Here, we develop a general quantitative model of amplification distortions in sequencing data sets, which we leverage to investigate the factors controlling the occurrence of PCR duplicates. We show that the PCR duplicate rate is determined primarily by the ratio between library complexity and sequencing depth, and that amplification noise (including in its dependence on the number of PCR cycles) only plays a secondary role for this artefact. We confirm our predictions using new and published RAD-seq libraries and provide a method to estimate library complexity and amplification noise in any data set containing PCR duplicates. We discuss how amplification-related artefacts impact downstream analyses, and in particular genotyping accuracy. The proposed framework unites the numerous observations made on PCR duplicates and will be useful to experimenters of all sequencing technologies where DNA availability is a concern.
    MeSH term(s) Reproducibility of Results ; Polymerase Chain Reaction/methods ; Sequence Analysis, DNA/methods ; DNA/genetics ; Gene Library ; High-Throughput Nucleotide Sequencing/methods
    Chemical Substances DNA (9007-49-2)
    Language English
    Publishing date 2023-04-16
    Publishing country England
    Document type Journal Article
    ZDB-ID 2406833-0
    ISSN 1755-0998 ; 1755-098X
    ISSN (online) 1755-0998
    ISSN 1755-098X
    DOI 10.1111/1755-0998.13800
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Conference proceedings: HLA-G levels in human seminal plasma depend on male abstinence time and are not correlated with male serum progesterone

    Schallmoser, A / Bakjaji, F / Färber, C / Einenkel, R / Allam, J-P / Sänger, N

    Geburtshilfe und Frauenheilkunde

    2022  Volume 82, Issue 10

    Event/congress 64. Kongress der Deutschen Gesellschaft für Gynäkologie und Geburtshilfe e. V., München, 2022-10-12
    Language German
    Publishing date 2022-10-01
    Publisher Georg Thieme Verlag
    Publishing place Stuttgart ; New York
    Document type Article ; Conference proceedings
    ZDB-ID 80111-2
    ISSN 1438-8804 ; 0016-5751 ; 1615-3359
    ISSN (online) 1438-8804
    ISSN 0016-5751 ; 1615-3359
    DOI 10.1055/s-0042-1757031
    Database Thieme publisher's database

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  8. Article ; Online: Evaluation of the Ph. Eur. anti-A and anti-B assay on a pipetting robot in combination with a camera guided reading mode.

    Hausammann, G J / Bellac, C L / Sänger, M / Gilgen, M

    Biologicals : journal of the International Association of Biological Standardization

    2017  Volume 47, Page(s) 76–80

    Abstract: The main objective of this study was the standardization of the direct anti-A, anti-B haemagglutination assay for immunoglobulin products in microtitre plates and gelcards by automation on a liquid handling robot. In addition, the evaluation of the ... ...

    Abstract The main objective of this study was the standardization of the direct anti-A, anti-B haemagglutination assay for immunoglobulin products in microtitre plates and gelcards by automation on a liquid handling robot. In addition, the evaluation of the pipetted microtitre plates with a computer-controlled camera was investigated and these results were related to titres from visual live reading. The titres obtained with the automated and the manual assay in microtitre plates and gelcards were compared. They were in excellent agreement: the titres of samples processed with the automated method varied maximally one titre step relative to the median titres of the same sample analysed with the manual method. The implementation of a camera guided test plate reading further increased the repeatability of the reported titres. In summary, the automated haemagglutination assay combined with a camera improved the consistency plus the traceability of the results and reduced the required hands-on time.
    Language English
    Publishing date 2017-05
    Publishing country England
    Document type Journal Article
    ZDB-ID 1017370-5
    ISSN 1095-8320 ; 1045-1056
    ISSN (online) 1095-8320
    ISSN 1045-1056
    DOI 10.1016/j.biologicals.2017.03.004
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Sixteen capillary electrophoresis applications for viral vaccine analysis.

    Geurink, Lars / van Tricht, Ewoud / van der Burg, Debbie / Scheppink, Gerard / Pajic, Bojana / Dudink, Justin / Sänger-van de Griend, Cari

    Electrophoresis

    2021  Volume 43, Issue 9-10, Page(s) 1068–1090

    Abstract: ... verifications, and identity testing (e.g., CZE for intact virus particles, CE-SDS application for hemagglutinin ...

    Abstract A broad range of CE applications from our organization is reviewed to give a flavor of the use of CE within the field of vaccine analyses. Applicability of CE for viral vaccine characterization, and release and stability testing of seasonal influenza virosomal vaccines, universal subunit influenza vaccines, Sabin inactivated polio vaccines (sIPV), and adenovirus vector vaccines were demonstrated. Diverse CZE, CE-SDS, CGE, and cIEF methods were developed, validated, and applied for virus, protein, posttranslational modifications, DNA, and excipient concentration determinations, as well as for the integrity and composition verifications, and identity testing (e.g., CZE for intact virus particles, CE-SDS application for hemagglutinin quantification and influenza strain identification, chloride or bromide determination in process samples). Results were supported by other methods such as RP-HPLC, dynamic light scattering (DLS), and zeta potential measurements. Overall, 16 CE methods are presented that were developed and applied, comprising six adenovirus methods, five viral protein methods, and methods for antibodies determination of glycans, host cell-DNA, excipient chloride, and process impurity bromide. These methods were applied to support in-process control, release, stability, process- and product characterization and development, and critical reagent testing. Thirteen methods were validated. Intact virus particles were analyzed at concentrations as low as 0.8 pmol/L. Overall, CE took viral vaccine testing beyond what was previously possible, improved process and product understanding, and, in total, safety, efficacy, and quality.
    MeSH term(s) Bromides ; Chlorides ; Electrophoresis, Capillary/methods ; Excipients ; Humans ; Influenza, Human ; Viral Proteins/analysis ; Viral Vaccines/analysis
    Chemical Substances Bromides ; Chlorides ; Excipients ; Viral Proteins ; Viral Vaccines
    Language English
    Publishing date 2021-11-21
    Publishing country Germany
    Document type Journal Article ; Review
    ZDB-ID 619001-7
    ISSN 1522-2683 ; 0173-0835
    ISSN (online) 1522-2683
    ISSN 0173-0835
    DOI 10.1002/elps.202100269
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: A program quality framework: a collaborative teaching team approach to quality assurance, quality enhancement and staff capacity building.

    van de Mortel, Thea / Mitchell, Creina / Shuker, Mary-Ann / Needham, Judith / Kain, Victoria / Sanger, Georgina / Pierce, Beth

    Frontiers in medicine

    2023  Volume 10, Page(s) 1242408

    Abstract: A global shortage of registered nurses provides a further impetus to retain nursing students and graduate safe nurses. While various frameworks support curriculum design and describe the need for ongoing curriculum evaluation and monitoring, there is ... ...

    Abstract A global shortage of registered nurses provides a further impetus to retain nursing students and graduate safe nurses. While various frameworks support curriculum design and describe the need for ongoing curriculum evaluation and monitoring, there is little in the literature to support the enactment and ongoing quality enhancement of curricula. Translation of the curriculum plan into the delivered curriculum relies on academics who may or may not be adequately prepared for course writing and teaching in higher education settings, despite their discipline expertise. Additionally, there are well recognized issues of curriculum drift where curriculum innovations and changes are whittled away over time by incremental changes to courses that interfere with the integrity of the accredited curriculum. We propose an evidence-based Program Quality (ProQual) Framework that takes a holistic, collaborative, and systematic approach to monitoring and enhancing curriculum quality and program delivery over the life of the curriculum while developing staff capability and scholarship.
    Language English
    Publishing date 2023-08-31
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2023.1242408
    Database MEDical Literature Analysis and Retrieval System OnLINE

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