Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rajanikanth J Maganti"'
Autor:
Kimberly A Coughlan, Rajanikanth J Maganti, Andrea Frassetto, Christine M DeAntonis, meredith Wolfrom, Anne-Renee Graham, Shawn M Hillier, Steven Fortucci, Hoor Al Jandal, Sue-Jean Hong, Paloma H Giangrande, Paolo GV Martini
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 2, Iss 1, Pp 28-39 (2019)
Background: Primary Hyperoxaluria Type 1 (PH1) is an inborn error of metabolism caused by mutations in the AGXT gene, which encodes for the hepatocyte-specific enzyme alanine: glyoxylate aminotransferase (AGT). AGT catalyzes the conversion of glyoxyl
Externí odkaz:
https://doaj.org/article/34d2d66e91a546d3a80cafe65ab1b4dd
Autor:
Rajanikanth J. Maganti, Xiaoping L. Hronowski, Dunstan, Robert W., Wipke, Brian T., Xueli Zhang, Jandreski, Luke, Hamann, Stefan, Juhasz, Peter
Supplemental material, DS_10.1369_0022155418815860 for Defining Changes in the Spatial Distribution and Composition of Brain Lipids in the Shiverer and Cuprizone Mouse Models of Myelin Disease by Rajanikanth J. Maganti, Xiaoping L. Hronowski, Robert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdbe59843cbff7792b4c65d7d45fdca
Autor:
June E. Olds, Jeremiah A. Lyons, Rajanikanth J. Maganti, Jennifer E. Flower, Michael Stone, Phillip C. Gauger, Kathryn C. Gamble, Michele A. Sims, Allison D. Tuttle, Pamela A. Tuomi
Publikováno v:
Journal of Zoo and Wildlife Medicine. 45:620-631
Six cases of esophageal squamous cell carcinoma were identified in six captive adult Pacific (Phoca vitulina richardsii; n = 2) and Atlantic (Phoca vitulina concolor; n = 4) harbor seals. These seals presented with intermittent dysphagia, regurgitati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910d82accf4e7d5bb98f973e1c0fc589
https://doi.org/10.1638/2012-0218r1.1
https://doi.org/10.1638/2012-0218r1.1
Autor:
Martin Junhong Wang, Glenn Deng, Sairam V. Jabba, Philine Wangemann, Nurith Kurn, Joe Don Heath, Rajanikanth J Maganti, Ruchira Singh
Publikováno v:
American Journal of Physiology-Cell Physiology. 288:C1179-C1189
Gene expression profiling using microarrays requires microgram amounts of RNA, which limits its direct application for the study of nanogram RNA samples obtained using microdissection, laser capture microscopy, or needle biopsy. A novel system based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::166d68a3250d8d6c0125c1cf4baa9a0b
https://doi.org/10.1152/ajpcell.00258.2004
https://doi.org/10.1152/ajpcell.00258.2004
Autor:
Tao Wu, Joel D. Sanneman, Rajanikanth J Maganti, Kazuhiro Nakaya, Donald G. Harbidge, Philine Wangemann, Sara E. Billings, Erin M Itza, Daniel C. Marcus
Publikováno v:
American journal of physiology. Renal physiology. 292(5)
Pendred syndrome, characterized by childhood deafness and postpuberty goiter, is caused by mutations of SLC26A4, which codes for the anion exchanger pendrin. The goal of the present study was to determine how loss of pendrin leads to hair cell degene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebbf7529e4e074ccd355d2f5989fed6e
https://pubmed.ncbi.nlm.nih.gov/17299139
https://pubmed.ncbi.nlm.nih.gov/17299139
Publikováno v:
The FASEB Journal. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dce50c53410bae11c1d7459507b16873
https://doi.org/10.1096/fasebj.20.5.a1163-d
https://doi.org/10.1096/fasebj.20.5.a1163-d
Autor:
Eric D. Green, Lorraine A. Everett, Ruchira Singh, Sairam V. Jabba, Susan M. Wall, Alisha Oelke, Sherry D. Fleming, Rajanikanth J Maganti, Philine Wangemann
Publikováno v:
BMC Medicine
BMC Medicine, Vol 4, Iss 1, p 37 (2006)
BMC Medicine, Vol 4, Iss 1, p 37 (2006)
Background Pendred syndrome, an autosomal-recessive disorder characterized by deafness and goiter, is caused by a mutation of SLC26A4, which codes for the anion exchanger pendrin. We investigated the relationship between pendrin expression and deafne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acbe6e0edbd8f5c9b89d8f493f254d3b
http://europepmc.org/articles/PMC1796619
http://europepmc.org/articles/PMC1796619
Autor:
Erin M Itza, Philine Wangemann, Lorraine A. Everett, Beatrice Albrecht, Daniel C. Marcus, Tao Wu, Eric D. Green, Ines E. Royaux, Rajanikanth J Maganti, Sairam V. Jabba, Susan M. Wall, Jun Ho Lee
Publikováno v:
BMC Medicine
BMC Medicine, Vol 2, Iss 1, p 30 (2004)
BMC Medicine, Vol 2, Iss 1, p 30 (2004)
Background Pendred syndrome, a common autosomal-recessive disorder characterized by congenital deafness and goiter, is caused by mutations of SLC26A4, which codes for pendrin. We investigated the relationship between pendrin and deafness using mice t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2183c940a5516b8866153966af726f41