المؤلفون: Chiara Traini, Eglantina Idrizaj, Cristina Biagioni, Maria Caterina Baccari, Maria Giuliana Vannucchi

المصدر: International Journal of Molecular Sciences, Vol 24, Iss 8, p 7440 (2023)

مصطلحات موضوعية: mucus secretion, choline acetyl transferase, muscarinic receptors, protein gene product 9.5, tetrodotoxin, atropine, Biology (General), QH301-705.5, Chemistry, QD1-999

العلاقة: https://www.mdpi.com/1422-0067/24/8/7440Test; https://doaj.org/toc/1661-6596Test; https://doaj.org/toc/1422-0067Test; https://doaj.org/article/0522692bc1aa404db1bf837201215495Test

الإتاحة: https://doi.org/10.3390/ijms24087440Test
https://doaj.org/article/0522692bc1aa404db1bf837201215495Test

المؤلفون: Iván Díaz, Ana Cecilia Colmenárez-Raga, David Pérez-González, Venezia G. Carmona, Ignacio Plaza Lopez, Miguel A. Merchán

المصدر: Frontiers in Neuroscience, Vol 15 (2021)

مصطلحات موضوعية: corti organ, auditory brainstem responses, quantitative immunocytochemistry, choline acetyl transferase, epidural anodal direct current stimulation, cochlear inflammatory response, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

العلاقة: https://www.frontiersin.org/articles/10.3389/fnins.2021.642047/fullTest; https://doaj.org/toc/1662-453XTest

الوصول الحر: https://doaj.org/article/42b75f08ac6c446c8df7a173e21264f1Test

المؤلفون: Schwartz, Mathias, Sternberg, Damien, Whalen, Sandra, Afenjar, Alexandra, Isapof, Arnaud, Chabrol, Brigitte, Portnoï, Marie-France, Heide, Solveig, Keren, Boris, Chantot-Bastaraud, Sandra, Siffroi, Jean-Pierre

المساهمون: CHU Trousseau APHP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Maladies génétiques d'expression pédiatrique (U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau APHP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), CHU Pitié-Salpêtrière AP-HP, Hôpital de la Timone CHU - APHM (TIMONE)

المصدر: ISSN: 1552-4825.

مصطلحات موضوعية: choline acetyl-transferase, compound heterozygoty, single nucleotide polymorphisms array, vesicular acetyl-choline transporter, MESH: Amino Acid Sequence, MESH: Choline O-Acetyltransferase, MESH: Mutation, MESH: Myasthenic Syndromes, Congenital, MESH: Oligonucleotide Array Sequence Analysis, MESH: Phenotype, MESH: Polymorphism, Single Nucleotide, MESH: Vesicular Acetylcholine Transport Proteins, MESH: Chromosome Deletion, MESH: Chromosomes, Human, Pair 10, MESH: Female, MESH: Genes, Recessive, MESH: Genetic Association Studies, MESH: Humans, MESH: In Situ Hybridization, Fluorescence, MESH: Infant, MESH: Male, [SDV]Life Sciences [q-bio], [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/29130637; inserm-03851530; https://inserm.hal.science/inserm-03851530Test; https://inserm.hal.science/inserm-03851530/documentTest; https://inserm.hal.science/inserm-03851530/file/American%20J%20of%20Med%20Genetics%20Pt%20A%20-%202017%20-%20Schwartz%20-%20How%20chromosomal%20deletions%20can%20unmask%20recessive%20mutations%20Deletions%20in.pdfTest; PUBMED: 29130637; WOS: 000417872600019

الإتاحة: https://doi.org/10.1002/ajmg.a.38515Test
https://inserm.hal.science/inserm-03851530Test
https://inserm.hal.science/inserm-03851530/documentTest
https://inserm.hal.science/inserm-03851530/file/American%20J%20of%20Med%20Genetics%20Pt%20A%20-%202017%20-%20Schwartz%20-%20How%20chromosomal%20deletions%20can%20unmask%20recessive%20mutations%20Deletions%20in.pdfTest

المؤلفون: Philippe De Deurwaerdère, Roxanne A. Vaughan, Silvana Gaetani

المصدر: Journal of Neurochemistry. 152:623-626

مصطلحات موضوعية: Male, 0301 basic medicine, DA, ChaT, choline acetyl transferase, COMT, catechol-O-methyl transferase, DA, dopamine, DAT, dopamine transporter, DOPAC, 3,4-dihydroxyphenyl acetic acid, GABA, gamma-aminobutyric acid, HVA, homovanillic acid, MAO, monoamine oxidase, 5-HT, serotonin, 5-HIAA, 5-hydroxyindoleacetic acid, 5-HT, Caudate nucleus, Striatum, Biochemistry, DOPAC, GABA, chemistry.chemical_compound, 0302 clinical medicine, monoamine oxidase, Neurotransmitter, dopamine transporter, Neurotransmitter Agents, Putamen, 5-HIAA, homovanillic acid, Human brain, serotonin, medicine.anatomical_structure, MAO, 4-dihydroxyphenyl acetic acid, Female, dopamine, 5-hydroxyindoleacetic acid, Correlative, gamma-aminobutyric acid, Biology, 03 medical and health sciences, Cellular and Molecular Neuroscience, Neurochemical, ChaT, catechol-O-methyl transferase, medicine, Humans, Motor activity, Aged, DAT, COMT, HVA, 030104 developmental biology, choline acetyl transferase, chemistry, Postmortem Changes, Caudate Nucleus, Neuroscience, Biomarkers, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5490db6766d8d0d52958e3e9cdc5df8dTest
https://doi.org/10.1111/jnc.14929Test

المؤلفون: Michela Ferrucci, Alida Spalloni, Alessia Bartalucci, Emanuela Cantafora, Federica Fulceri, Michele Nutini, Patrizia Longone, Antonio Paparelli, Francesco Fornai

المصدر: Neurobiology of Disease, Vol 37, Iss 2, Pp 370-383 (2010)

مصطلحات موضوعية: Amyotrophic lateral sclerosis, Transgenic G93A mouse, Brainstem motor neurons, Synaptic boutons, Choline acetyl transferase, Lithium, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

العلاقة: http://www.sciencedirect.com/science/article/pii/S0969996109003039Test; https://doaj.org/toc/1095-953XTest

الوصول الحر: https://doaj.org/article/fc0a6f47a78348cb820d15c3bf9bb377Test

المؤلفون: Miguel A. Merchán, Ignacio López, Iván Díaz, David Pérez-González, Ana Cecilia Colmenárez-Raga, Venezia G Carmona

المصدر: Frontiers in Neuroscience, Vol 15 (2021)
Frontiers in Neuroscience

مصطلحات موضوعية: 0301 basic medicine, Efferent, Neurosciences. Biological psychiatry. Neuropsychiatry, Stimulation, Auditory cortex, 03 medical and health sciences, 0302 clinical medicine, medicine, quantitative immunocytochemistry, Original Research, corti organ, business.industry, General Neuroscience, Efferent Neuron, medicine.disease, Choline acetyltransferase, 030104 developmental biology, medicine.anatomical_structure, auditory brainstem responses, choline acetyl transferase, cochlear inflammatory response, Cholinergic, epidural anodal direct current stimulation, sense organs, Hair cell, business, cochleotopy, Neuroscience, 030217 neurology & neurosurgery, Noise-induced hearing loss, RC321-571

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0073e3aa98b63087fb6c52a548632ceaTest
https://doi.org/10.3389/fnins.2021.642047Test

المؤلفون: Semo, M, Gias, C, Ahmado, A, Vugler, A

المصدر: Exp Eye Res , 119 pp. 8-18. (2014)

مصطلحات موضوعية: atropine, choline acetyl transferase (ChAT), ciliary body, ciliary marginal zone (CMZ), intrinsic pupillary light reflex (iPLR), intrinsically photosensitive retinal ganglion cell (ipRGC), ipRGC, iris, melanopsin, melanopsin knockout (MKO), olivary pretectal nucleus (OPN), stem cells

وصف الملف: application/pdf

العلاقة: https://discovery.ucl.ac.uk/id/eprint/1416470/1/1-s2.0-S0014483513003400-main.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1416470Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/1416470/1/1-s2.0-S0014483513003400-main.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1416470Test/

المؤلفون: I. Rinner, P. Felsner, P. M. Liebmann, D. Hofer, A. Wölfler, A. Globerson, K. Schauenstein

المصدر: Clinical and Developmental Immunology, Vol 6, Iss 3-4, Pp 245-252 (1998)

مصطلحات موضوعية: Neuroimmunomodulation, catecholamines, acetylcholine, lymphocytes, thymic epithelial cells, apoptosis, choline-acetyl transferase, dopamine-beta-hydroxylase., Immunologic diseases. Allergy, RC581-607

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1740-2522Test; https://doaj.org/toc/1740-2530Test

الوصول الحر: https://doaj.org/article/f0a155dd54e34ec49df4ee78f9ea60ceTest

المؤلفون: De Deurwaerdere P., Gaetani S., Vaughan R. A.

المساهمون: De Deurwaerdere, P., Gaetani, S., Vaughan, R. A.

مصطلحات موضوعية: ChaT, choline acetyl transferase, COMT, catechol-O-methyl transferase, DA, dopamine, DAT, dopamine transporter, DOPAC, 3,4-dihydroxyphenyl acetic acid, GABA, gamma-aminobutyric acid, HVA, homovanillic acid, MAO, monoamine oxidase, 5-HT, serotonin, 5-HIAA, 5-hydroxyindoleacetic acid

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31917872; info:eu-repo/semantics/altIdentifier/wos/WOS:000506293300001; volume:152; issue:6; firstpage:623; lastpage:626; numberofpages:4; journal:JOURNAL OF NEUROCHEMISTRY; http://hdl.handle.net/11573/1402425Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85078036773

الإتاحة: https://doi.org/10.1111/jnc.14929Test
http://hdl.handle.net/11573/1402425Test

المؤلفون: Jean-Pierre Siffroi, Solveig Heide, Alexandra Afenjar, Damien Sternberg, Arnaud Isapof, Mathias Schwartz, Sandra Whalen, Marie-France Portnoï, Boris Keren, Sandra Chantot-Bastaraud, Brigitte Chabrol

المساهمون: Service de génétique et embryologie médicales [CHU Trousseau], CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Institut du Cerveau = Paris Brain Institute (ICM), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Service de Biochimie Métabolique et Centre de Génétique moléculaire et chromosomique [CHU Pitié Salpêtrière], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), Service de Neuropédiatrie [CHU Trousseau], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Trousseau [APHP], Hôpital de la Timone [CHU - APHM] (TIMONE), Service de Génétique médicale [CHU Pitié-Salpêtrière], CHU Pitié-Salpêtrière [AP-HP], Couvet, Sandrine, UF de Génétique chromosomique [CHU Trousseau], Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], UF Neurométabolique Bioclinique et Génétique [CHU Pitié-Salpêtrière]

المصدر: American Journal of Medical Genetics Part A
American Journal of Medical Genetics Part A, 2018, 176 (1), pp.151-155. ⟨10.1002/ajmg.a.38515⟩

مصطلحات موضوعية: Male, 0301 basic medicine, choline acetyl-transferase, [SDV]Life Sciences [q-bio], Vesicular Acetylcholine Transport Proteins, MESH: Amino Acid Sequence, single nucleotide polymorphisms array, Congenital myasthenia, 0302 clinical medicine, MESH: In Situ Hybridization, Fluorescence, In Situ Hybridization, Fluorescence, Genetics (clinical), MESH: Genetic Association Studies, Oligonucleotide Array Sequence Analysis, MESH: Choline O-Acetyltransferase, Genetics, MESH: Polymorphism, Single Nucleotide, Congenital myasthenic syndrome, MESH: Infant, Choline acetyltransferase, Phenotype, [SDV] Life Sciences [q-bio], Female, Chromosome Deletion, compound heterozygoty, MESH: Myasthenic Syndromes, Congenital, vesicular acetyl-choline transporter, MESH: Mutation, MESH: Chromosome Deletion, Genes, Recessive, Locus (genetics), Single-nucleotide polymorphism, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, MESH: Phenotype, Polymorphism, Single Nucleotide, DNA sequencing, Choline O-Acetyltransferase, 03 medical and health sciences, medicine, Humans, Amino Acid Sequence, Gene, MESH: Genes, Recessive, Genetic Association Studies, Myasthenic Syndromes, Congenital, MESH: Humans, MESH: Vesicular Acetylcholine Transport Proteins, Chromosomes, Human, Pair 10, Infant, medicine.disease, MESH: Male, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH: Chromosomes, Human, Pair 10, MESH: Oligonucleotide Array Sequence Analysis, Mutation, MESH: Female, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3b0c2dd902139a6e400d91b29aabb5Test
https://doi.org/10.1002/ajmg.a.38515Test