Výsledky vyhledávání - Sandesh C.S. Nagamani
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Argininosuccinate lyase deficiency Autor Sandesh C.S. Nagamani, Ayelet Erez, Brendan Lee
Vydáno 2012Revisão -
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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 Autor 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
Vydáno 2012Artigo -
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Evaluation of teriparatide treatment in adults with osteogenesis imperfecta Autor 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
Vydáno 2014Artigo -
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Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation Autor 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
Vydáno 2020Artigo -
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Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency Autor 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
Vydáno 2015Artigo -
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Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 Autor 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
Vydáno 2009Artigo -
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Glycerol phenylbutyrate treatment in children with urea cycle disorders: Pooled analysis of short and long-term ammonia control and outcomes Autor 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
Vydáno 2014Artigo -
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Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3 Autor 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
Vydáno 2015Artigo -
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Diversion of aspartate in ASS1-deficient tumours fosters de novo pyrimidine synthesis Autor 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
Vydáno 2015Artigo -
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Untargeted metabolomic profiling reveals multiple pathway perturbations and new clinical biomarkers in urea cycle disorders Autor 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
Vydáno 2019Artigo -
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Phenotypic Variability of Osteogenesis Imperfecta Type V Caused by an <i>IFITM</i> <i>5</i> Mutation Autor 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
Vydáno 2013Artigo -
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Next-generation sequencing for disorders of low and high bone mineral density Autor 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
Vydáno 2013Artigo -
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A cross‐sectional multicenter study of osteogenesis imperfecta in North America – results from the linked clinical research centers Autor 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
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
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