James W. Nagle

Biochemistry, Genetics and Molecular Biology · Life Sciences

28h-index9.1kcitations48works0.02yr avg
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Research Topics

RNA Research and Splicing(8), Genomics and Chromatin Dynamics(5), Lysosomal Storage Disorders Research(5), RNA modifications and cancer(5), T-cell and B-cell Immunology(4)

Publications48 total

A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing
Cell·2007· 3.6k citedOpen Access
Thymic output generates a new and diverse TCR repertoire after autologous stem cell transplantation in multiple sclerosis patients
The Journal of Experimental Medicine·2005· 495 citedOpen Access
Blockade of Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand Exacerbates Type 1 Diabetes in NOD Mice
Diabetes·2003· 102 citedOpen Access
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c‐terminal α‐helical segment
Muscle & Nerve·2003· 62 cited
Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations
Neuromuscular Disorders·2003· 66 cited
Identification of novel Drosophila neural precursor genes using a differential embryonic head cDNA screen
Mechanisms of Development·2002· 55 cited
Rapid identification of local T cell expansion in inflammatory organ diseases by flow cytometric T cell receptor Vβ analysis
Journal of Immunological Methods·2000· 46 cited
The Genomic Organization and Polymorphism Analysis of the Human Niemann-Pick C1 Gene
Biochemical and Biophysical Research Communications·1999· 86 cited
Novel exon 3B proteolipid protein gene mutation causing late-onset spastic paraplegia type 2 with variable penetrance in female family members
Annals of Neurology·1999· 43 cited
Novel exon 3B proteolipid protein gene mutation causing late‐onset spastic paraplegia type 2 with variable penetrance in female family members
Annals of Neurology·1999· 5 cited
Missense mutations in desmin associated with familial cardiac and skeletal myopathy
Nature Genetics·1998· 503 cited
Regulation of POU genes by <i>castor</i> and<i>hunchback</i> establishes layered compartments in the<i>Drosophila</i> CNS
Genes & Development·1998· 273 citedOpen Access
C2H2‐171 : A novel human cDNA representing a developmentally regulated poz domain/zinc finger protein preferentially expressed in brain
International Journal of Developmental Neuroscience·1997· 17 cited
Myelin transcription factor 1 (Myt1) of the oligodendrocyte lineage, along with a closely related CCHC zinc finger, is expressed in developing neurons in the mammalian central nervous system
Journal of Neuroscience Research·1997· 106 citedOpen Access
Immunodominance of a low-affinity major histocompatibility complex-binding myelin basic protein epitope (residues 111-129) in HLA-DR4 (B1*0401) subjects is associated with a restricted T cell receptor repertoire.
Journal of Clinical Investigation·1997· 101 citedOpen Access
Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis
Science·1997· 1.5k cited
Molecular Cloning and Mapping of a Novel Human KRAB Domain-Containing C2H2-Type Zinc Finger to Chromosome 7q36.1
Genomics·1997· 5 cited
Molecular cloning and mapping of a novel developmentally regulated human C2H2-type zinc finger
Mammalian Genome·1997· 1 cited
Short Communication: C2H2-546: A zinc finger protein differentially expressed in HTLV-1 infected T cells
Journal of NeuroVirology·1997· 1 cited
Molecular Cloning of the Mouse Apolipoprotein D Gene and Its Upregulated Expression in Niemann-Pick Disease Type C Mouse Model
DNA and Cell Biology·1996· 31 cited
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Frequent Co-authors

Lev G. Goldfarb(8), William E. Biddison(7), David Filpula(6), Kevin G. Becker(6), Rachel D. Canning(6), Larisa Červen̆áková(5), Kumaraswamy Sivakumar(5), Marinos C. Dalakas(5), Paul D. Drew(5), Olavo M. Vasconcelos(4), Toshio Ohshima(4), Ameer Gado(4), Roscoe O. Brady(3), Peter G. Pentchev(3), Mark Dubnick(3), Paolo A. Muraro(3), Roland Martinꝉ(3), Lynn D. Hudson(3), Nyamkhishig Sambuughin(3), Christine A. Kozak(3)