يعرض 1 - 10 نتائج من 107 نتيجة بحث عن '"Cation Transport Proteins/genetics"', وقت الاستعلام: 1.01s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Coexistence of Ammonium Transporter and Channel Mechanisms in Amt-Mep-Rh Twin-His Variants Impairs the Filamentation Signaling Capacity of Fungal Mep2 Transceptors.

    المؤلفون: Williamson, Gordon, Brito, Ana Sofia, Bizior, Adriana, Tamburrino, Giulia, Dias Mirandela, Gaëtan, Harris, Thomas, Hoskisson, Paul A, Zachariae, Ulrich, Marini, Anna Maria, Boeckstaens, Mélanie, Javelle, Arnaud

    المصدر: mBio, 13 (2

    مصطلحات موضوعية: Sciences bio-médicales et agricoles, Ammonium Compounds, Cation Transport Proteins -- genetics, Escherichia coli, Escherichia coli Proteins -- genetics, Fungal Proteins -- genetics, Humans, Membrane Transport Proteins -- genetics, Saccharomyces cerevisiae -- genetics, Saccharomyces cerevisiae Proteins -- genetics, Signal Transduction, Translocation, Genetic, Candida albicans, Saccharomyces cerevisiae, ammonium assimilation, fungal filamentation, secondary transporter mechanism

    وصف الملف: 2 full-text file(s): application/pdf | application/pdf

    العلاقة: uri/info:doi/10.1128/mbio.02913-21; uri/info:pmid/35196127; uri/info:scp/85129086126; uri/info:pmcid/PMC9040831; https://dipot.ulb.ac.be/dspace/bitstream/2013/344216/1/PMC9040831.pdfTest; https://dipot.ulb.ac.be/dspace/bitstream/2013/344216/5/Williamson_Boeckstaens_2022_mBio.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/344216Test

    الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/344216Test
    https://dipot.ulb.ac.be/dspace/bitstream/2013/344216/1/PMC9040831.pdfTest
    https://dipot.ulb.ac.be/dspace/bitstream/2013/344216/5/Williamson_Boeckstaens_2022_mBio.pdfTest

    View record in BASE

    أضف إلى المفضلة
  2. 2
    دورية أكاديمية
    Bi-allelic loss of function variants in SLC30A5 as cause of perinatal lethal cardiomyopathy

    المؤلفون: Lieberwirth, Johann Kaspar, Joset, Pascal, Heinze, Anja, Hentschel, Julia, Stein, Anja, Iannaccone, Antonella, Steindl, Katharina, Kuechler, Alma, Abou Jamra, Rami

    المصدر: http://lobid.org/resources/99370671030206441Test#!, 29(5):808-815.

    مصطلحات موضوعية: Homozygote [MeSH], Infant, Newborn [MeSH], Female [MeSH], Development, Adult [MeSH], Humans [MeSH], Cardiomyopathies/pathology [MeSH], Medical genetics, Medical genomics, Loss of Function Mutation [MeSH], Article, Pedigree [MeSH], Male [MeSH], Cation Transport Proteins/genetics [MeSH], Fatal Outcome [MeSH], Cardiovascular diseases, Cardiomyopathies/genetics [MeSH]

    العلاقة: https://repository.publisso.de/resource/frl:6442796Test; https://doi.org/10.1038/s41431-020-00803-8Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110774Test/

    الإتاحة: https://doi.org/10.1038/s41431-020-00803-8Test
    https://repository.publisso.de/resource/frl:6442796Test
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110774Test/

    View record in BASE

    أضف إلى المفضلة
  3. 3
    دورية أكاديمية
    De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures.

    المؤلفون: Royer-Bertrand, B., Jequier Gygax, M., Cisarova, K., Rosenfeld, J.A., Bassetti, J.A., Moldovan, O., O'Heir, E., Burrage, L.C., Allen, J., Emrick, L.T., Eastman, E., Kumps, C., Abbas, S., Van Winckel, G., Chabane, N., Zackai, E.H., Lebon, S., Keena, B., Bhoj, E.J., Umair, M., Li, D., Donald, K.A., Superti-Furga, A.

    المساهمون: Undiagnosed Diseases Network

    المصدر: Molecular autism, vol. 12, no. 1, pp. 69

    مصطلحات موضوعية: Autism Spectrum Disorder/genetics, Calcium Channels, R-Type/genetics, Cation Transport Proteins/genetics, Child, Developmental Disabilities, Humans, Intellectual Disability/genetics, Phenotype, Seizures/genetics, Social Cognition, Autism spectrum disorder, CACNA1E, Developmental regression, Epilepsy, Exome sequencing, Global developmental delay, Intellectual disability, Neurodevelopmental disorders, Seizures, Topiramate

    وصف الملف: application/pdf

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34702355; info:eu-repo/semantics/altIdentifier/eissn/2040-2392; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_665170C145262; https://serval.unil.ch/notice/serval:BIB_665170C14526Test; https://serval.unil.ch/resource/serval:BIB_665170C14526.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_665170C145262Test

    الإتاحة: https://doi.org/10.1186/s13229-021-00473-3Test
    https://serval.unil.ch/notice/serval:BIB_665170C14526Test
    https://serval.unil.ch/resource/serval:BIB_665170C14526.P001/REF.pdfTest
    http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_665170C145262Test

    View record in BASE

    أضف إلى المفضلة
  4. 4
    دورية أكاديمية
    Zinc transporter 8 autoantibody testing requires age-related cut-offs

    المؤلفون: Grace, S. L., Cooper, A., Jones, A. G., McDonald, T. J.

    مصطلحات موضوعية: Adolescent, Adult, Aged, 80 and over, Autoantibodies, Cation Transport Proteins/genetics, Child, Preschool, Diabetes Mellitus, Type 1/diagnosis, Type 2, Humans, Infant, Newborn, Middle Aged, Young Adult, Zinc Transporter 8, autoantibodies, autoimmunity, biomarkers, type 1

    العلاقة: https://drc.bmj.com/lookup/pmidlookup?view=long&pmid=34348918Test; BMJ Open Diabetes Res Care. 2021 Aug;9(1):e002296. doi:10.1136/bmjdrc-2021-002296.; https://rde.dspace-express.com/handle/11287/622144Test; BMJ open diabetes research & care; PMC8340275

    الإتاحة: https://doi.org/10.1136/bmjdrc-2021-002296Test
    https://rde.dspace-express.com/handle/11287/622144Test

    View record in BASE

    أضف إلى المفضلة
  5. 5
    دورية أكاديمية
    Tooth loss and adiposity: possible role of carnitine transporter (OCTN1/2) polymorphisms in women but not in men

    المؤلفون: Meisel, Peter, Pagels, Stefanie, Grube, Markus, Jedlitschky, Gabriele, Völzke, Henry, Kocher, Thomas

    المصدر: http://lobid.org/resources/99370672697806441Test#!, 25(2):701-709.

    مصطلحات موضوعية: Aged, 80 and over [MeSH], OCTN1/2, Aged [MeSH], Polymorphism, Single Nucleotide [MeSH], Organic Cation Transport Proteins/genetics [MeSH], Original Article, Tooth loss, Male [MeSH], Carnitine, Carnitine [MeSH], Obesity/genetics [MeSH], Tooth Loss/genetics [MeSH], Genetic Predisposition to Disease [MeSH], Obesity, Symporters/genetics [MeSH], Female [MeSH], Follow-Up Studies [MeSH], Adult [MeSH], Humans [MeSH], Adiposity/genetics [MeSH], Middle Aged [MeSH], Solute Carrier Family 22 Member 5 [MeSH], Sex, Genotype [MeSH]

    العلاقة: https://repository.publisso.de/resource/frl:6467930Test; https://doi.org/10.1007/s00784-020-03594-wTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208909Test/

    الإتاحة: https://doi.org/10.1007/s00784-020-03594-wTest
    https://repository.publisso.de/resource/frl:6467930Test
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8208909Test/

    View record in BASE

    أضف إلى المفضلة
  6. 6
    دورية أكاديمية
    The Connective Tissue Disorder Associated with Recessive Variants in the SLC39A13 Zinc Transporter Gene (Spondylo-Dysplastic Ehlers-Danlos Syndrome Type 3): Insights from Four Novel Patients and Follow-Up on Two Original Cases.

    المؤلفون: Kumps, C., Campos-Xavier, B., Hilhorst-Hofstee, Y., Marcelis, C., Kraenzlin, M., Fleischer, N., Unger, S., Superti-Furga, A.

    المصدر: Genes, vol. 11, no. 4, pp. 420

    مصطلحات موضوعية: Adolescent, Adult, Case-Control Studies, Cation Transport Proteins/genetics, Child, Ehlers-Danlos Syndrome/genetics, Ehlers-Danlos Syndrome/pathology, Female, Follow-Up Studies, Humans, Male, Mutation, Osteochondrodysplasias/genetics, Osteochondrodysplasias/pathology, Prognosis, Young Adult, DeepGestalt technology, Ehlers–Danlos syndrome, SLC39A13, connective tissue, dysmorphology, short stature

    وصف الملف: application/pdf

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32295219; info:eu-repo/semantics/altIdentifier/eissn/2073-4425; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_DA412F996FF00; https://serval.unil.ch/notice/serval:BIB_DA412F996FF0Test; urn:issn:2073-4425; https://serval.unil.ch/resource/serval:BIB_DA412F996FF0.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_DA412F996FF00Test

    الإتاحة: https://doi.org/10.3390/genes11040420Test
    https://serval.unil.ch/notice/serval:BIB_DA412F996FF0Test
    https://serval.unil.ch/resource/serval:BIB_DA412F996FF0.P001/REF.pdfTest
    http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_DA412F996FF00Test

    View record in BASE النص الكامل

    أضف إلى المفضلة
  7. 7
    دورية أكاديمية
    Characterization of the molecular properties of KtrC, a second RCK domain that regulates a Ktr channel in Bacillus subtilis

    المؤلفون: Rocha, R, Teixeira-Duarte, CM, JMP, J, Morais-Cabral, JH

    المساهمون: Instituto de Investigação e Inovação em Saúde

    المصدر: http://creativecommons.org/licenses/by-nc-nd/4.0Test/.

    مصطلحات موضوعية: Adenosine Diphosphate / chemistry, Adenosine Diphosphate / metabolism, Adenosine Triphosphate / chemistry, Adenosine Triphosphate / metabolism, Amino Acid Motifs, Bacillus subtilis / chemistry, Bacillus subtilis / metabolism, Bacterial Proteins / chemistry, Bacterial Proteins / genetics, Bacterial Proteins / metabolism, Binding Sites, Cation Transport Proteins / chemistry, Cation Transport Proteins / genetics, Cation Transport Proteins / metabolism, Cations, Monovalent, Cloning, Molecular, Crystallography, X-Ray, Dinucleoside Phosphates / chemistry, Dinucleoside Phosphates / metabolism, Escherichia coli / genetics, Escherichia coli / metabolism, Gene Expression, Genetic Complementation Test, Genetic Vectors / chemistry, Genetic Vectors / metabolism, Ion Transport, Models

    وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

    العلاقة: Journal of structural biology, vol. 205(3) pag. 34-43; https://www.sciencedirect.com/science/article/pii/S1047847719300255?via%3DihubTest; https://hdl.handle.net/10216/127799Test

    الإتاحة: https://doi.org/10.1016/j.jsb.2019.02.002Test
    https://hdl.handle.net/10216/127799Test

    View record in BASE

    أضف إلى المفضلة
  8. 8
    دورية أكاديمية
    Activation of a nucleotide-dependent RCK domain requires binding of a cation cofactor to a conserved site

    المؤلفون: Teixeira-Duarte, CM, Fonseca, F, Morais-Cabral, JH

    المساهمون: Instituto de Investigação e Inovação em Saúde

    مصطلحات موضوعية: Adenosine Triphosphate / chemistry, Bacillus subtilis / chemistry, Bacillus subtilis / genetics, Bacterial Proteins / chemistry, Bacterial Proteins / genetics, Bacterial Proteins / ultrastructure, Binding Sites / genetics, Calcium / metabolism, Cation Transport Proteins / chemistry, Cation Transport Proteins / genetics, Cation Transport Proteins / ultrastructure, Cations / chemistry, Crystallography, X-Ray, Kv1.6 Potassium Channel / chemistry, Kv1.6 Potassium Channel / ultrastructure, Nucleotides / chemistry, Nucleotides / genetics, Potassium / chemistry, Potassium / metabolism, Potassium Channels / chemistry, Potassium Channels / genetics, Potassium Channels / ultrastructure, Protein Conformation, Protein Domains / genetics, Protein Structure, Tertiary, Ribosomal Proteins

    وصف الملف: application/pdf

    العلاقة: eLife, vol.8:e50661; https://elifesciences.org/articles/50661Test; https://hdl.handle.net/10216/138997Test

    الإتاحة: https://doi.org/10.7554/eLife.50661Test
    https://hdl.handle.net/10216/138997Test

    View record in BASE النص الكامل

    أضف إلى المفضلة
  9. 9
    دورية أكاديمية
    Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study.

    المؤلفون: Luo, Q., Chen, Q., Wang, W., Desrivières, S., Quinlan, E.B., Jia, T., Macare, C., Robert, G.H., Cui, J., Guedj, M., Palaniyappan, L., Kherif, F., Banaschewski, T., Bokde, ALW, Büchel, C., Flor, H., Frouin, V., Garavan, H., Gowland, P., Heinz, A., Ittermann, B., Martinot, J.L., Artiges, E., Paillère-Martinot, M.L., Nees, F., Orfanos, D.P., Poustka, L., Fröhner, J.H., Smolka, M.N., Walter, H., Whelan, R., Callicott, J.H., Mattay, V.S., Pausova, Z., Dartigues, J.F., Tzourio, C., Crivello, F., Berman, K.F., Li, F., Paus, T., Weinberger, D.R., Murray, R.M., Schumann, G., Feng, J.

    المساهمون: IMAGEN consortium

    المصدر: JAMA psychiatry, vol. 76, no. 4, pp. 435-445

    مصطلحات موضوعية: Adolescent, Adult, Case-Control Studies, Cation Transport Proteins/biosynthesis, Cation Transport Proteins/genetics, Female, Genetic Predisposition to Disease/genetics, Genome-Wide Association Study, Gray Matter/pathology, Humans, Hypertrophy/genetics, Hypertrophy/pathology, Magnetic Resonance Imaging, Male, Mutation, Missense/genetics, Neuroimaging, Putamen/pathology, Schizophrenia/genetics, Schizophrenia/pathology, Siblings

    وصف الملف: application/pdf

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30649180; info:eu-repo/semantics/altIdentifier/eissn/2168-6238; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_B785772057372; https://serval.unil.ch/notice/serval:BIB_B78577205737Test; urn:issn:2168-622X; https://serval.unil.ch/resource/serval:BIB_B78577205737.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B785772057372Test

    الإتاحة: https://doi.org/10.1001/jamapsychiatry.2018.4126Test
    https://serval.unil.ch/notice/serval:BIB_B78577205737Test
    https://serval.unil.ch/resource/serval:BIB_B78577205737.P001/REF.pdfTest
    http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B785772057372Test

    View record in BASE

    أضف إلى المفضلة
  10. 10
    دورية أكاديمية
    Using a semi-mechanistic model to identify the main sources of variability of metformin pharmacokinetics

    المؤلفون: Stage, Tore Bjerregaard, Wellhagen, Gustaf, Christensen, Mette Marie Hougaard, Guiastrennec, Benjamin, Brøsen, Kim, Kjellsson, Maria C

    المصدر: Stage , T B , Wellhagen , G , Christensen , M M H , Guiastrennec , B , Brøsen , K & Kjellsson , M C 2019 , ' Using a semi-mechanistic model to identify the main sources of variability of metformin pharmacokinetics ' , Basic & Clinical Pharmacology & Toxicology , vol. 124 , no. 1 , pp. 105-114 . https://doi.org/10.1111/bcpt.13139Test

    مصطلحات موضوعية: Acidosis, Lactic/chemically induced, Administration, Oral, Adult, Biological Availability, Biological Variation, Individual, Population/physiology, Clinical Trials as Topic, Gastrointestinal Absorption/physiology, Gastrointestinal Transit/physiology, Healthy Volunteers, Humans, Hypoglycemic Agents/administration & dosage, Metformin/administration & dosage, Middle Aged, Models, Biological, Organic Cation Transport Proteins/genetics, Pharmacogenomic Variants, Polymorphism, Single Nucleotide, Time Factors, Young Adult

    وصف الملف: application/pdf

    العلاقة: https://portal.findresearcher.sdu.dk/da/publications/a1815011-6077-4490-9fa7-b37e5f715afbTest

    الإتاحة: https://doi.org/10.1111/bcpt.13139Test
    https://portal.findresearcher.sdu.dk/da/publications/a1815011-6077-4490-9fa7-b37e5f715afbTest
    https://findresearcher.sdu.dk/ws/files/146453151/Using_a_semi_mechanistic_model_to_identify_the_main_sources_of_variability_of_metformin_pharmacokinetics.pdfTest

    View record in BASE

    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS — أرسل هذا البحث بالبريد الإلكتروني — حفظ البحث