Iskani rezultati za avtorja

1

Reassessing carrier status for dystrophinopathies od Newcomb, Tara M., Flanigan, Kevin M.

Izdano 2016

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2

N-terminal α Dystroglycan (αDG-N): A Potential Serum Biomarker for Duchenne Muscular Dystrophy od Crowe, Kelly E., Shao, Guohong, Flanigan, Kevin M., Martin, Paul T.

Izdano 2016

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3

Comparison of Serum rAAV Serotype-Specific Antibodies in Patients with Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, Inclusion Body Myositis, or GNE Myopathy od Zygmunt, Deborah A., Crowe, Kelly E., Flanigan, Kevin M., Martin, Paul T.

Izdano 2017

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4

DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6 od Gurvich, Olga, Maiti, Baijayanta, Weiss, Robert B., Howard, Michael T., Flanigan, Kevin M.

Izdano 2009

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5

Clinico-pathological Conference: A hypotonic newborn with cleft palate, micrognathia and bilateral club feet od Waldrop, Megan A., Boue, Daniel R., Sites, Emily, Flanigan, Kevin M., Shell, Richard

Izdano 2017

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6

Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in Duchenne muscular dystrophy od Weiss, Robert B., Vieland, Veronica J., Dunn, Diane M., Kaminoh, Yuuki, Flanigan, Kevin M.

Izdano 2018

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7

Automated immunofluorescence analysis for sensitive and precise dystrophin quantification in muscle biopsies od Vetter, Tatyana A., Nicolau, Stefan, Bradley, Adrienne J., Frair, Emma C., Flanigan, Kevin M.

Izdano 2021

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8

Recoding elements located adjacent to a subset of eukaryal selenocysteine-specifying UGA codons od Howard, Michael T, Aggarwal, Gaurav, Anderson, Christine B, Khatri, Shikha, Flanigan, Kevin M, Atkins, John F

Izdano 2005

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9

204th ENMC international workshop on biomarkers in Duchenne Muscular Dystrophy 24–26 January 2014, Naarden, The Netherlands od Ferlini, Alessandra, Flanigan, Kevin M., Lochmuller, Hanns, Muntoni, Francesco, ‘t Hoen, Peter AC, McNally, Elizabeth

Izdano 2014

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10

Becker Muscular Dystrophy Due to an Inversion of Exons 23 and 24 of the DMD Gene od Flanigan, Kevin M., Dunn, Diane, Larsen, C. Aaron, Medne, Livija, Bönnemann, Carsten B., Weiss, Robert B.

Izdano 2011

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11

Natural history of echocardiographic abnormalities in mucopolysaccharidosis III od Wilhelm, Carolyn M., Truxal, Kristen V., McBride, Kim L., Kovalchin, John P., Flanigan, Kevin M.

Izdano 2018

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12

Pre-clinical dose-escalation studies establish a therapeutic range for U7snRNA-mediated DMD exon 2 skipping od Simmons, Tabatha R., Vetter, Tatyana A., Huang, Nianyuan, Vulin-Chaffiol, Adeline, Wein, Nicolas, Flanigan, Kevin M.

Izdano 2021

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13

Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment od McDonald, Craig M., Wei, Lee‐Jen, Flanigan, Kevin M., Elfring, Gary, Trifillis, Panayiota, Muntoni, Francesco

Izdano 2021

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14

Rapid Direct Sequence Analysis of the Dystrophin Gene od Flanigan, Kevin M., Niederhausern, Andrew von, Dunn, Diane M., Alder, Jonathan, Mendell, Jerry R., Weiss, Robert B.

Izdano 2003

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15

Identification of New Dystroglycan Complexes in Skeletal Muscle od Johnson, Eric K., Li, Bin, Yoon, Jung Hae, Flanigan, Kevin M., Martin, Paul T., Ervasti, James, Montanaro, Federica

Izdano 2013

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16

Anti-Dystrophin T Cell Responses in Duchenne Muscular Dystrophy: Prevalence and a Glucocorticoid Treatment Effect od Flanigan, Kevin M., Campbell, Katie, Viollet, Laurence, Wang, Wei, Gomez, Ana Maria, Walker, Christopher M., Mendell, Jerry R.

Izdano 2013

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17

Utility of Cystatin C to monitor renal function in Duchenne muscular dystrophy od Viollet, Laurence, Gailey, Susan, Thornton, David J., Friedman, Neil R., Flanigan, Kevin M., Mahan, John D., Mendell, Jerry R.

Izdano 2009

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18

Cryptic MHC class I-binding peptides are revealed by aminoglycoside-induced stop codon read-through into the 3′ UTR od Goodenough, Elliot, Robinson, Tara M., Zook, Matthew B., Flanigan, Kevin M., Atkins, John F., Howard, Michael T., Eisenlohr, Laurence C.

Izdano 2014

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19

Early Progressive Dilated Cardiomyopathy in a Family with Becker Muscular Dystrophy Related to a Novel Frameshift Mutation in the Dystrophin Gene Exon 27 od Tsuda, Takeshi, Fitzgerald, Kristi, Scavena, Mena, Gidding, Samuel, Cox, Mary O., Marks, Harold, Flanigan, Kevin M., Moore, Steven A.

Izdano 2014

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20

A Comparative Study of N-glycolylneuraminic Acid (Neu5Gc) and Cytotoxic T Cell (CT) Carbohydrate Expression in Normal and Dystrophin-Deficient Dog and Human Skeletal Muscle od Martin, Paul T., Golden, Bethannie, Okerblom, Jonathan, Camboni, Marybeth, Chandrasekharan, Kumaran, Xu, Rui, Varki, Ajit, Flanigan, Kevin M., Kornegay, Joe N.

Izdano 2014

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Rezultati - Flanigan, Kevin M

Reassessing carrier status for dystrophinopathies od Newcomb, Tara M., Flanigan, Kevin M.

N-terminal α Dystroglycan (αDG-N): A Potential Serum Biomarker for Duchenne Muscular Dystrophy od Crowe, Kelly E., Shao, Guohong, Flanigan, Kevin M., Martin, Paul T.

Comparison of Serum rAAV Serotype-Specific Antibodies in Patients with Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, Inclusion Body Myositis, or GNE Myopathy od Zygmunt, Deborah A., Crowe, Kelly E., Flanigan, Kevin M., Martin, Paul T.

DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6 od Gurvich, Olga, Maiti, Baijayanta, Weiss, Robert B., Howard, Michael T., Flanigan, Kevin M.

Clinico-pathological Conference: A hypotonic newborn with cleft palate, micrognathia and bilateral club feet od Waldrop, Megan A., Boue, Daniel R., Sites, Emily, Flanigan, Kevin M., Shell, Richard

Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in Duchenne muscular dystrophy od Weiss, Robert B., Vieland, Veronica J., Dunn, Diane M., Kaminoh, Yuuki, Flanigan, Kevin M.

Automated immunofluorescence analysis for sensitive and precise dystrophin quantification in muscle biopsies od Vetter, Tatyana A., Nicolau, Stefan, Bradley, Adrienne J., Frair, Emma C., Flanigan, Kevin M.

Recoding elements located adjacent to a subset of eukaryal selenocysteine-specifying UGA codons od Howard, Michael T, Aggarwal, Gaurav, Anderson, Christine B, Khatri, Shikha, Flanigan, Kevin M, Atkins, John F

204th ENMC international workshop on biomarkers in Duchenne Muscular Dystrophy 24–26 January 2014, Naarden, The Netherlands od Ferlini, Alessandra, Flanigan, Kevin M., Lochmuller, Hanns, Muntoni, Francesco, ‘t Hoen, Peter AC, McNally, Elizabeth

Becker Muscular Dystrophy Due to an Inversion of Exons 23 and 24 of the DMD Gene od Flanigan, Kevin M., Dunn, Diane, Larsen, C. Aaron, Medne, Livija, Bönnemann, Carsten B., Weiss, Robert B.

Natural history of echocardiographic abnormalities in mucopolysaccharidosis III od Wilhelm, Carolyn M., Truxal, Kristen V., McBride, Kim L., Kovalchin, John P., Flanigan, Kevin M.

Pre-clinical dose-escalation studies establish a therapeutic range for U7snRNA-mediated DMD exon 2 skipping od Simmons, Tabatha R., Vetter, Tatyana A., Huang, Nianyuan, Vulin-Chaffiol, Adeline, Wein, Nicolas, Flanigan, Kevin M.

Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment od McDonald, Craig M., Wei, Lee‐Jen, Flanigan, Kevin M., Elfring, Gary, Trifillis, Panayiota, Muntoni, Francesco

Rapid Direct Sequence Analysis of the Dystrophin Gene od Flanigan, Kevin M., Niederhausern, Andrew von, Dunn, Diane M., Alder, Jonathan, Mendell, Jerry R., Weiss, Robert B.

Identification of New Dystroglycan Complexes in Skeletal Muscle od Johnson, Eric K., Li, Bin, Yoon, Jung Hae, Flanigan, Kevin M., Martin, Paul T., Ervasti, James, Montanaro, Federica

Anti-Dystrophin T Cell Responses in Duchenne Muscular Dystrophy: Prevalence and a Glucocorticoid Treatment Effect od Flanigan, Kevin M., Campbell, Katie, Viollet, Laurence, Wang, Wei, Gomez, Ana Maria, Walker, Christopher M., Mendell, Jerry R.

Utility of Cystatin C to monitor renal function in Duchenne muscular dystrophy od Viollet, Laurence, Gailey, Susan, Thornton, David J., Friedman, Neil R., Flanigan, Kevin M., Mahan, John D., Mendell, Jerry R.

Cryptic MHC class I-binding peptides are revealed by aminoglycoside-induced stop codon read-through into the 3′ UTR od Goodenough, Elliot, Robinson, Tara M., Zook, Matthew B., Flanigan, Kevin M., Atkins, John F., Howard, Michael T., Eisenlohr, Laurence C.

Early Progressive Dilated Cardiomyopathy in a Family with Becker Muscular Dystrophy Related to a Novel Frameshift Mutation in the Dystrophin Gene Exon 27 od Tsuda, Takeshi, Fitzgerald, Kristi, Scavena, Mena, Gidding, Samuel, Cox, Mary O., Marks, Harold, Flanigan, Kevin M., Moore, Steven A.

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