Результати пошуку - Sandesh C.S. Nagamani
- Показ 1 - 20 результатів із 42
- На наступну сторінку
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Argininosuccinate lyase deficiency за авторством Sandesh C.S. Nagamani, Ayelet Erez, Brendan Lee
Опубліковано 2012Revisão -
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Argininosuccinate lyase deficiency—Argininosuccinic aciduria and beyond за авторством Ayelet Erez, Sandesh C. Sreenath Nagamani, Brendan Lee
Опубліковано 2011Revisão -
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Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders за авторством Lindsay C. Burrage, Sandesh C.S. Nagamani, Philippe M. Campeau, Brendan H. Lee
Опубліковано 2014Revisão -
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Argininosuccinic aciduria: Recent pathophysiological insights and therapeutic prospects за авторством Julien Baruteau, Carmen Dı́ez-Fernández, Shaul Lerner, Giusy Ranucci, Paul Gissen, Carlo Dionisi‐Vici, Sandesh C.S. Nagamani, Ayelet Erez, Johannes Häberle
Опубліковано 2019Revisão -
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Early prediction of phenotypic severity in Citrullinemia Type 1 за авторством Matthias Zielonka, Stefan Kölker, Florian Gleich, Nicolas Stützenberger, Sandesh C.S. Nagamani, Andrea Gropman, Georg F. Hoffmann, Sven F. Garbade, Roland Posset
Опубліковано 2019Artigo -
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Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders за авторством Sandesh C.S. Nagamani, Ayelet Erez, Bruria Ben‐Zeev, Moshe Frydman, Susan Winter, Robert S. Zeller, Dima El‐Khechen, Luis Escobar, Paweł Stankiewicz, Ankita Patel, Sau Wai Cheung
Опубліковано 2012Artigo -
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Evaluation of teriparatide treatment in adults with osteogenesis imperfecta за авторством Eric Orwoll, Jay R. Shapiro, Sandra Veith, Ying Wang, Jodi Lapidus, Chaim Vanek, Jan L. Reeder, Tony M. Keaveny, David C. Lee, Mary A. Mullins, Sandesh C.S. Nagamani, Brendan Lee
Опубліковано 2014Artigo -
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Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation за авторством Zixue Jin, Jordan Kho, Brian Dawson, Ming‐Ming Jiang, Yuqing Chen, Saima Ali, Lindsay C. Burrage, Monica Grover, Donna Palmer, Dustin L. Turner, Philip Ng, Sandesh C.S. Nagamani, Brendan Lee
Опубліковано 2020Artigo -
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Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency за авторством Lindsay C. Burrage, Qin Sun, Sarah H. Elsea, Ming‐Ming Jiang, Sandesh C.S. Nagamani, Arthur E. Frankel, Everett Stone, Susan E. Alters, Dale E. Johnson, Scott W. Rowlinson, George Georgiou, Brendan Lee
Опубліковано 2015Artigo -
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Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 за авторством Sandesh C. Sreenath Nagamani, Ayelet Erez, Joseph Shen, Chumei Li, Elizabeth Roeder, Sarah K. Cox, Lefkothea Karaviti, Margret Pearson, Sung‐Hae Kang, Trilochan Sahoo, Seema R. Lalani, Paweł Stankiewicz, V. Reid Sutton, Sau Wai Cheung
Опубліковано 2009Artigo -
14
Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes за авторством Susan A. Berry, Uta Lichter‐Konecki, George A. Díaz, Shawn E. McCandless, William J. Rhead, Wendy E. Smith, Cynthia LeMons, Sandesh C.S. Nagamani, Dion F. Coakley, Masoud Mokhtarani, Bruce F. Scharschmidt, Brendan Lee
Опубліковано 2014Artigo -
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Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3 за авторством Shen Gu, Bo Yuan, Ian M. Campbell, Christine R. Beck, Claudia M.B. Carvalho, Sandesh C.S. Nagamani, Ayelet Erez, Ankita Patel, Carlos A. Bacino, Chad A. Shaw, Paweł Stankiewicz, Sau Wai Cheung, Weimin Bi, James R. Lupski
Опубліковано 2015Artigo -
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Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis за авторством Shiran Rabinovich, Lital N. Adler, Keren Yizhak, Alona Sarver, Alon Silberman, Shani Agron, Noa Stettner, Qin Sun, Alexander Brandis, Daniel Helbling, Stanley H. Korman, Shalev Itzkovitz, David Dimmock, Igor Ulitsky, Sandesh C.S. Nagamani, Eytan Ruppin, Ayelet Erez
Опубліковано 2015Artigo -
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Untargeted metabolomic profiling reveals multiple pathway perturbations and new clinical biomarkers in urea cycle disorders за авторством Lindsay C. Burrage, Lillian R Thistlethwaite, Bridget M. Stroup, Qin Sun, Marcus J. Miller, Sandesh C.S. Nagamani, William Craigen, Fernando Scaglia, V. Reid Sutton, Brett H. Graham, Adam D. Kennedy, Aleksandar Milosavljević, Brendan Lee, Sarah H. Elsea
Опубліковано 2019Artigo -
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Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an <i>IFITM</i> <i>5</i> Mutation за авторством Jay R. Shapiro, Caressa Lietman, Monica Grover, James T. Lu, Sandesh C.S. Nagamani, Brian C. Dawson, Dustin Baldridge, Matthew N. Bainbridge, D.H. Cohn, Maria Blazo, Timothy T. Roberts, Feng-Shu Brennen, Yimei Wu, Richard A. Gibbs, Pamela Melvin, Philippe M. Campeau, Brendan Lee
Опубліковано 2013Artigo -
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Next-generation sequencing for disorders of low and high bone mineral density за авторством Gautam Sule, Philippe M. Campeau, V. W. Zhang, Sandesh C.S. Nagamani, Brian C. Dawson, Monica Grover, Carlos A. Bacino, V. Reid Sutton, Nicola Brunetti‐Pierri, James T. Lu, Edmond G. Lemire, Richard A. Gibbs, Daniel H. Cohn, Hong Cui, L. Wong, Brendan H. Lee
Опубліковано 2013Artigo -
20
A cross‐sectional multicenter study of osteogenesis imperfecta in North America – results from the linked clinical research centers за авторством Ruchita Patel, Sandesh C.S. Nagamani, David Cuthbertson, Philippe M. Campeau, J. Krischer, Jay R. Shapiro, Robert D. Steiner, Peter A. Smith, Michael B. Bober, Peter H. Byers, Melanie Pepin, Michaela Durigova, Francis H. Glorieux, Frank Rauch, B.H. Lee, Tracy Hart, V. Reid Sutton
Опубліковано 2014Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Medicine
Internal medicine
Gene
Genetics
Biochemistry
Amino acid
Arginine
Chemistry
Urea cycle
Endocrinology
Pathology
Phenotype
Osteogenesis imperfecta
Arginase
Argininosuccinate synthase
Chromosome
Comparative genomic hybridization
Genome
Pediatrics
Argininosuccinate lyase
Copy-number variation
Gene duplication
Hyperammonemia
Bone mineral
Cell biology
Cohort
Disease
Osteoporosis
Psychiatry