المؤلفون: Mulić Bilsana, Peco-Antić Amira, Ozaltin Fatih

المصدر: Srpski Arhiv za Celokupno Lekarstvo, Vol 152, Iss 1-2, Pp 81-84 (2024)

مصطلحات موضوعية: nphs1 gene, nephrin, hereditary nephrotic syndrome, infant, Medicine

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/0370-8179Test; https://doaj.org/toc/2406-0895Test

الوصول الحر: https://doaj.org/article/498b39466bca4ace8d7f411b4b0a9a60Test

المساهمون: College of Medicine, Dept. of Pharmacology, Markus M Rinschen, Markus Godel, Florian Grahammer, Stefan Zschiedrich, Martin Helmstadter, Oliver Kretz, Mostafa Zarei, Daniela A Braun, Sebastian Dittrich, Caroline Pahmeyer, Patricia Schroder, Carolin Teetzen, HeonYung Gee, Ghaleb Daouk, Martin Pohl, Elisa Kuhn, Bernhard Schermer, Victoria Kuttner, Melanie Boerries, Hauke Busch, Mario Schiffer, Carsten Bergmann, Marcus Kruger, Friedhelm Hildebrandt, Joern Dengjel, Thomas Benzing, Tobias B Huber, Gee, Heon Yung

مصطلحات موضوعية: end-stage renal disease, focal segmental glomerulosclerosis, hereditary nephrotic syndrome, kinase, metabolism, proteinuria, proteostasis, pulse SILAC, slit diaphragm, systems biology

العلاقة: CELL REPORTS; J00488; OAK-2018-02771; https://ir.ymlib.yonsei.ac.kr/handle/22282913/162592Test; T201801954; CELL REPORTS, Vol.23(8) : 2495-2508, 2018

الإتاحة: https://doi.org/10.1016/j.celrep.2018.04.059Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/162592Test

المؤلفون: Hirono Suzuki, Takuji Yamada, 山田 拓司, 鈴木 博乃

المصدر: 日本小児腎臓病学会雑誌 / Japanese journal of pediatric nephrology. 2019, 32(1):37

المؤلفون: Akiko KINOSHITA, Atsuo OGURA, Hajime MIYAMOTO, Kozue UCHIO, Makoto MIYAMOTO, Noboru MANABE, Yoshie YAMAMOTO, otaro KTAMURA

المصدر: Journal of Veterinary Medical Science. 1999, 61(7):769

المؤلفون: 崔洁媛, 张宏文

المساهمون: 河北省儿童医院肾脏免疫科 河北石家庄 050031, 北京大学第一医院儿科 北京 100034

المصدر: CSCD ; 万方 ; 知网 ; http://d.g.wanfangdata.com.cn/Periodical_lcekzz201612018.aspxTest

مصطلحات موضوعية: 遗传性肾病综合征, NPHS2基因, 临床特点, 儿童, hereditary nephrotic syndrome, NPHS2 gene, clinical feature, child

العلاقة: 临床儿科杂志. 2016, 34(12), 933-935.; 1914088; http://hdl.handle.net/20.500.11897/478174Test

الإتاحة: https://doi.org/20.500.11897/478174Test
https://doi.org/10.3969/j.issn.1000-3606.2016.12.013Test
https://hdl.handle.net/20.500.11897/478174Test

المؤلفون: Paolo Mene', Giorgio Punzo, Nicola Pirozzi

المساهمون: Mene', Paolo, Punzo, Giorgio, Pirozzi, Nicola

مصطلحات موضوعية: autosomic dominant polycystic kidney disease, hereditary nephrotic syndrome, trp channel, familial focal glomerulosclerosi, receptor-operated ca2+ channel, store-operated ca2+ channels

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23432067; info:eu-repo/semantics/altIdentifier/wos/WOS:000316941300013; volume:13; issue:3; firstpage:386; lastpage:397; numberofpages:12; journal:CURRENT TOPICS IN MEDICINAL CHEMISTRY; http://hdl.handle.net/11573/672020Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84876712900

الإتاحة: https://doi.org/10.2174/1568026611313030013Test
http://hdl.handle.net/11573/672020Test

المؤلفون: Giorgio Punzo, Paolo Menè, Nicola Pirozzi

المصدر: Current topics in medicinal chemistry. 13(3)

مصطلحات موضوعية: medicine.medical_specialty, TRPV5, Autosomal dominant polycystic kidney disease, TRPP, TRPV, Transient receptor potential channel, Transient Receptor Potential Channels, Internal medicine, Drug Discovery, medicine, Animals, Humans, Distal convoluted tubule, Molecular Targeted Therapy, education, education.field_of_study, Reabsorption, Chemistry, autosomic dominant polycystic kidney disease, hereditary nephrotic syndrome, trp channels, familial focal glomerulosclerosis, receptor-operated ca2+ channels, store-operated ca2+ channels, General Medicine, medicine.disease, medicine.anatomical_structure, Polycystin 2, Endocrinology, Hypertension, Kidney Diseases

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50ac4c34434c42b4adb067251a5d6d87Test
https://pubmed.ncbi.nlm.nih.gov/23432067Test

المؤلفون: Sandalio Durán Álvarez

المصدر: Revista Cubana de Pediatría, Vol 80, Iss 3, p 0 (2008)

مصطلحات موضوعية: Síndrome nefrótico hereditario, lesión mínima familiar, tratamiento, treatment, Hereditary nephrotic syndrome, lcsh:RJ1-570, lcsh:Pediatrics, mutaciones genéticas, genetic mutations, family minimal lesion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doajarticles::6f4fceb2d2c190df8f63a4bfbfc90170Test
http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0034-75312008000300010Test

المؤلفون: Caroline Pahmeyer, Markus M. Rinschen, Mario Schiffer, Melanie Boerries, Martin Pohl, Marcus Krüger, Elisa Kuhn, Bernhard Schermer, Florian Grahammer, Ghaleb Daouk, Carsten Bergmann, Friedhelm Hildebrandt, Martin Helmstädter, Joern Dengjel, Heon Yung Gee, Daniela A. Braun, Patricia Schroder, Oliver Kretz, Carolin Teetzen, Sebastian Dittrich, Thomas Benzing, Victoria Küttner, Tobias B. Huber, Markus Gödel, Hauke Busch, Stefan Zschiedrich, Mostafa Zarei

المصدر: Cell Reports
Rinschen, M M, Gödel, M, Grahammer, F, Zschiedrich, S, Helmstädter, M, Kretz, O, Zarei, M, Braun, D A, Dittrich, S, Pahmeyer, C, Schroder, P, Teetzen, C, Gee, H Y, Daouk, G, Pohl, M, Kuhn, E, Schermer, B, Küttner, V, Boerries, M, Busch, H, Schiffer, M, Bergmann, C, Krüger, M, Hildebrandt, F, Dengjel, J, Benzing, T & Huber, T B 2018, ' A Multi-layered Quantitative In Vivo Expression Atlas of the Podocyte Unravels Kidney Disease Candidate Genes ', Cell Reports, vol. 23, no. 8, pp. 2495-2508 . https://doi.org/10.1016/j.celrep.2018.04.059Test
Cell Reports, Vol 23, Iss 8, Pp 2495-2508 (2018)

مصطلحات موضوعية: 0301 basic medicine, Candidate gene, Proteome, kinase, hereditary nephrotic syndrome, 030232 urology & nephrology, Computational biology, Proteomics, General Biochemistry, Genetics and Molecular Biology, Article, End stage renal disease, Podocyte, 03 medical and health sciences, Mice, 0302 clinical medicine, medicine, pulse SILAC, Animals, Humans, Zebrafish, lcsh:QH301-705.5, Cells, Cultured, Genetic Association Studies, focal segmental glomerulosclerosis, Gene knockdown, end-stage renal disease, proteostasis, biology, Base Sequence, Podocytes, systems biology, biology.organism_classification, 3. Good health, slit diaphragm, 030104 developmental biology, MRNA Sequencing, medicine.anatomical_structure, lcsh:Biology (General), Gene Expression Regulation, Slit diaphragm, Kidney Diseases, proteinuria, Transcriptome, metabolism

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::add740ae482b4186337ce6f069435eb5Test

المؤلفون: Desmond, Michael James

مصطلحات موضوعية: proteinuria, hereditary nephrotic syndrome, action myoclonus renal failure syndrome

العلاقة: Desmond, M. J. (2011). The lysosomal pathway to proteinuria. PhD thesis, Faculty of Medicine, Dentistry & Health Sciences, Department of Medicine (Austin & Northern Health), The University of Melbourne.; http://hdl.handle.net/11343/35987Test

الإتاحة: http://hdl.handle.net/11343/35987Test