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