المؤلفون: Tomas-Roca, L., Qiu, Z., Fransén, Erik, 1962, Gokhale, R., Bulovaite, E., Price, D. J., Komiyama, N. H., Grant, S. G. N.

المصدر: Nature Communications. 13(1)

مصطلحات موضوعية: pentobarbital, transcription factor PAX6, PAX6 protein, human, Pax6 protein, mouse, brain, developmental biology, disease prevalence, nervous system disorder, protein, rodent, trajectory, turnover, animal experiment, animal model, animal tissue, Article, Bayes theorem, brain function, brain region, cognition, computer model, confocal microscopy, connectome, controlled study, disease model, electrophysiology, excitatory postsynaptic potential, functional magnetic resonance imaging, genetic disorder, genotype, haploinsufficiency, hippocampal CA1 region, mental disease, Monte Carlo method, nerve cell network, nonhuman, phenotype, postnatal development, protein metabolism, synapse, synaptic transmission, animal, genetics, metabolism, preschool child, Animals, Child, Preschool, Humans, Mice, Neurodevelopmental Disorders, PAX6 Transcription Factor, Synapses

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-329015Test
https://doi.org/10.1038/s41467-022-34131-wTest

المؤلفون: Vasilyeva T.A., Voskresenskaya A.A., Khlebnikova O.V., Pozdeyeva N.A., Marakhonov A.V., Zinchenko R.A.

المساهمون: Российский научный фонд (грант №17-15-01051)

المصدر: Annals of the Russian academy of medical sciences; Vol 72, No 4 (2017); 233-241 ; Вестник Российской академии медицинских наук; Vol 72, No 4 (2017); 233-241 ; 2414-3545 ; 0869-6047 ; 10.15690/vramn724

مصطلحات موضوعية: congenital aniridia, WAGR syndrome, anterior segment mesenchymal dysgenesis, PAX6 protein, deletion 11p13, врожденная аниридия, WAGR-синдром, дисгенезии переднего отрезка глаза, PAX6, 11p13

وصف الملف: application/pdf

العلاقة: https://vestnikramn.spr-journal.ru/jour/article/view/834/823Test; https://vestnikramn.spr-journal.ru/jour/article/downloadSuppFile/834/303Test; https://vestnikramn.spr-journal.ru/jour/article/downloadSuppFile/834/304Test; https://vestnikramn.spr-journal.ru/jour/article/view/834Test

الإتاحة: https://doi.org/10.15690/vramn834Test
https://doi.org/10.15690/vramn724Test
https://vestnikramn.spr-journal.ru/jour/article/view/834Test

المؤلفون: Kyoung Hee Han, Hye Jin Lee, Il-Soo Ha, Hee Gyung Kang, Hae Il Cheong

المصدر: Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S1-S4 (2016)

مصطلحات موضوعية: Congenital aniridia, WAGR syndrome, Gene, Wilms tumor, PAX6 protein, Pediatrics, RJ1-570

وصف الملف: electronic resource

العلاقة: http://kjp.or.kr/upload/pdf/kjped-59-S1.pdfTest; https://doaj.org/toc/1738-1061Test; https://doaj.org/toc/2092-7258Test

الوصول الحر: https://doaj.org/article/6bd7f7b8dad64c97ac756e262ff78178Test

المؤلفون: Kyoung Hee, Han, Hye Jin, Lee, Il-Soo, Ha, Hee Gyung, Kang, Hae Il, Cheong

المصدر: Korean Journal of Pediatrics

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, WAGR syndrome, Wilms tumor, Case Report, Congenital aniridia, sense organs, PAX6 protein, Gene, eye diseases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::c10d56d0dbd08ae5ea770d566574eae7Test
https://pubmed.ncbi.nlm.nih.gov/28018434Test

المؤلفون: Gessler, M

المساهمون: Department of Physiological Chemistry I, Theodor-Boveri-Institute (Biocenter), University of Wuerzburg, Wuerzburg, Germany

مصطلحات موضوعية: Chromosome 11, Cancer Prone Diseases Section, PAX6 protein, WT1 Proteins, Kidney Diseases, Kidney Neoplasms, Neoplasms, Complex and Mixed, Neoplastic Syndromes, Hereditary, Urogenital Neoplasms, Urologic Diseases, Urologic Neoplasms, Wilms Tumor

العلاقة: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org//Kprones/WAGRID10032.htmlTest; Atlas of Genetics and Cytogenetics in Oncology and Haematology; 1999, Vol. 3, N° 4; p. 217-218; http://hdl.handle.net/2042/37572Test; https://doi.org/10.4267/2042/37572Test

الإتاحة: https://doi.org/10.4267/2042/37572Test
http://hdl.handle.net/2042/37572Test

مصطلحات الفهرس: pentobarbital, transcription factor PAX6, PAX6 protein, human, Pax6 protein, mouse, brain, developmental biology, disease prevalence, nervous system disorder, protein, rodent, trajectory, turnover, animal experiment, animal model, animal tissue, Article, Bayes theorem, brain function, brain region, cognition, computer model, confocal microscopy, connectome, controlled study, disease model, electrophysiology, excitatory postsynaptic potential, functional magnetic resonance imaging, genetic disorder, genotype, haploinsufficiency, hippocampal CA1 region, mental disease, Monte Carlo method, nerve cell network, nonhuman, phenotype, postnatal development, protein metabolism, synapse, synaptic transmission, animal, genetics, metabolism, preschool child, Animals, Child, Preschool, Humans, Mice, Neurodevelopmental Disorders, PAX6 Transcription Factor, Synapses, Neurosciences, Neurovetenskaper, Article in journal, info:eu-repo/semantics/article, text

URL: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-329015Test
Nature Communications, 2022, 13:1

المؤلفون: Dr Steve Wilson

المصدر: B0001155

المؤلفون: Dr Steve Wilson

المصدر: B0001092

المؤلفون: Dr Steve Wilson

المصدر: B0001106

المؤلفون: Dr Steve Wilson

المصدر: B0001154