المؤلفون: Jupri Mustofa, Simon Bambang Widjanarko, Ahmad Zaki Mubarok

المصدر: Jurnal Teknologi Pertanian, Vol 25, Iss 1, Pp 77-92 (2024)

مصطلحات موضوعية: glukomanan porang, gula aren, mocd, stabilitas, susu kedelai, Agriculture (General), S1-972

وصف الملف: electronic resource

Relation: https://jtp.ub.ac.id/index.php/jtp/article/view/1318/1153; https://doaj.org/toc/1411-5131; https://doaj.org/toc/2528-2794

URL الوصول: https://doaj.org/article/92ed963216f34cc3922f9b377feb9ebb

المؤلفون: Jamal Sayed, Abdallah Nasir, Ahmed Gamal Sayed, Omar A. Alghamdi, Elaf Jameel Alsharif

المصدر: Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)

مصطلحات موضوعية: MoCD, MoCS2, neonate, seizures, Medicine, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2050-0904

URL الوصول: https://doaj.org/article/ea46557dd19a4ce48bc8a8640aea1f7e

المؤلفون: Jakub Piotr Adamus, Anna Ruszczyńska, Aleksandra Wyczałkowska-Tomasik

المصدر: Biomolecules, Vol 14, Iss 7, p 869 (2024)

مصطلحات موضوعية: molybdenum (Mo), molybdenum cofactor (MoCo), molybdenum cofactor deficiency (MoCD), xanthine oxidase (XO), aldehyde oxidase (AO), sulfite oxidase (SOX), Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2218-273X/14/7/869; https://doaj.org/toc/2218-273X

URL الوصول: https://doaj.org/article/6428ec0ca9b446b4b18d0bc7366e23c0

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المؤلفون: Yu Abe, Yu Aihara, Wakaba Endo, Hiroshi Hasegawa, Kimiyoshi Ichida, Mitsugu Uematsu, Shigeo Kure

المصدر: Molecular Genetics and Metabolism Reports, Vol 26, Iss , Pp 100716- (2021)

مصطلحات موضوعية: Molybdenum cofactor deficiency (MoCD), Molybdenum cofactor (Moco), MOCS1, Dietary protein restriction, Sulfocysteine (SSC), Electroencephalogram, Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2214426921000100; https://doaj.org/toc/2214-4269

URL الوصول: https://doaj.org/article/60548ca8070b433194fe13225fcad0ce

لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.

المؤلفون: Maxime Fuduche, Sylvain Davidson, Céline Boileau, Long-Fei Wu, Yannick Combet-Blanc

المصدر: Frontiers in Microbiology, Vol 10 (2019)

مصطلحات موضوعية: microaerobes, MOCD, magnetotactic bacteria, Magnetospirillum gryphiswaldense MSR-1, Magnetospira sp. QH- 2, Microbiology, QR1-502

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fmicb.2019.00534/full; https://doaj.org/toc/1664-302X

URL الوصول: https://doaj.org/article/3ce8e4eb65dc490690fbfaced5adb24b

المؤلفون: Yu, Abe, Yu, Aihara, Wakaba, Endo, Hiroshi, Hasegawa, Kimiyoshi, Ichida, Mitsugu, Uematsu, Shigeo, Kure

المصدر: Molecular Genetics and Metabolism Reports

مصطلحات موضوعية: Electroencephalogram, Molybdenum cofactor (Moco), MOCS1, Dietary protein restriction, Sulfocysteine (SSC), Molybdenum cofactor deficiency (MoCD), Research Paper

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::6daa4f724b7445990e0a71d14482880f
https://pubmed.ncbi.nlm.nih.gov/33552910

المؤلفون: Alex Veldman, Linda C. Meiners, Terry G J Derks, Roelineke J. Lunsing, Charlotte M A Lubout, Francjan J. van Spronsen, Jan Jaap H. M. Erwich, Guenter Schwarz, Klasien A. Bergman

المساهمون: Center for Liver, Digestive and Metabolic Diseases (CLDM), Reproductive Origins of Adult Health and Disease (ROAHD)

المصدر: European Journal of Paediatric Neurology, 22(3), 536-540. ELSEVIER SCI LTD

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Cyclic pyranopterin monophosphate, 030105 genetics & heredity, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Pregnancy, Prenatal Diagnosis, Internal medicine, prenatal Magnetic Resonance Imaging, medicine, Journal Article, Humans, MoCD-A, Molybdenum cofactor deficiency, Cyclic pyranopterin mono-phosphate, Metal Metabolism, Inborn Errors, medicine.diagnostic_test, Brain, Magnetic resonance imaging, General Medicine, medicine.disease, Magnetic Resonance Imaging, Molybdenum cofactor deficiency type A, Endocrinology, chemistry, Inborn error of metabolism, Pediatrics, Perinatology and Child Health, Female, cPMP, Neurology (clinical), 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::655417bca318e60699982a2935f7a9c5
https://research.rug.nl/en/publications/9dcb7cb5-b850-405f-a021-ae63147f6092

المؤلفون: Shigeo Kure, Hiroshi Hasegawa, Wakaba Endo, Yu Aihara, Yu Abe, Kimiyoshi Ichida, Mitsugu Uematsu

المصدر: Molecular Genetics and Metabolism Reports, Vol 26, Iss, Pp 100716-(2021)

مصطلحات موضوعية: medicine.medical_specialty, Molybdenum cofactor (Moco), Urinary system, medicine.medical_treatment, Sulfocysteine (SSC), Urine, chemistry.chemical_compound, Endocrinology, Low-protein diet, Internal medicine, Dietary protein restriction, Genetics, medicine, Missense mutation, lcsh:QH301-705.5, Molecular Biology, Molybdenum cofactor deficiency, lcsh:R5-920, business.industry, MOCS1, Molybdenum cofactor deficiency (MoCD), medicine.disease, Electroencephalogram, lcsh:Biology (General), chemistry, Inborn error of metabolism, Uric acid, lcsh:Medicine (General), Molybdenum cofactor, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::397167bbabf8416681bf9a4f898ac6aa
https://doi.org/10.1016/j.ymgmr.2021.100716