J. Nagle

发表

A Mammalian microRNA Expression Atlas Based on Small RNA Library Sequencing

C. Sander, N. Socci, M. Palkovits, 2007, Cell.

Sequence identification of 2,375 human brain genes

J. Craig Venter, Mark Dubnick, Mark D. Adams, 1992, Nature.

Molecular cloning of human ornithine aminotransferase mRNA.

J. Nagle, N. Katunuma, E. Kominami, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Characterization and Sequencing of Prototypic Human T-Lymphotropic Virus Type 1 (HTLV-1) from an HTLV-1/2 Seroindeterminate Patient

J. Nagle, S. Jacobson, A. Waziri, 2000, Journal of Virology.

Blockade of tumor necrosis factor-related apoptosis-inducing ligand exacerbates type 1 diabetes in NOD mice.

J. Nagle, D. Ly, YOUHAI H. Chen, 2003, Diabetes.

Is hereditary inclusion body myopathy a “Familial prion disease”?

J. Nagle, M. Dalakas, K. Sivakumar, 1996, Annals of neurology.

Missense mutations in desmin associated with familial cardiac and skeletal myopathy

J. Nagle, M. Dalakas, S. Gorokhova, 1998, Nature Genetics.

Identification of fifteen novel mutations and genotype–phenotype relationship in Fabry disease

R. Schiffmann, J. Nagle, L. Goldfarb, 2001, Clinical genetics.

Genetic and phylogenetic analyses of hantaviral sequences amplified from archival tissues of deer mice (Peromyscus maniculatus nubiterrae) captured in the eastern United States

J. Nagle, R. Yanagihara, L. Baek, 2005, Archives of Virology.

Genetic evidence for a hantavirus enzootic in deer mice (Peromyscus maniculatus) captured a decade before the recognition of hantavirus pulmonary syndrome.

J. Nagle, B. Hjelle, V. Nerurkar, 1994, Virology.

CHAPTER 11 – Structure and evolution of the streptococcal genes encoding protein G

P. Alexander, J. Nagle, D. Filpula, 1990 .

Production of engineered IgM-binding single-chain antibodies inEscherichia coli

Timothy K Lee, J. Nagle, M. Rollence, 1995, Journal of Industrial Microbiology.

Nonsense mutation in the phosphofructokinase muscle subunit gene associated with retention of intron 10 in one of the isolated transcripts in Ashkenazi Jewish patients with Tarui disease.

M. Dubnick, J. Nagle, M. Dalakas, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Molecular cloning of the mouse apolipoprotein D gene and its upregulated expression in Niemann-Pick disease type C mouse model.

A. Kulkarni, J. Nagle, R. Brady, 1996, DNA and cell biology.

Low-incidence latent infection with variant B or roseola type human herpesvirus 6 in leukocytes of healthy adults

J. Nagle, J. Rajčáni, D. Asher, 2005, Archives of Virology.

Structural organization and expression of the mouse gene encoding α-galactosidase A

A. Kulkarni, J. Nagle, R. Brady, 1995 .

Cloning and expression analysis of a human cDNA homologous to Xenopus TFIIIA.

K. Becker, J. Nagle, K. Ozato, 1995, Gene.

Infectious amyloid precursor gene sequences in primates used for experimental transmission of human spongiform encephalopathy

M. Dubnick, K. Pettrone, J. Nagle, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Exons 16 and 17 of the amyloid precursor protein gene in familial inclusion body myopathy

J. Nagle, M. Dalakas, K. Sivakumar, 1995, Annals of neurology.

Rapid isolation and characterization of 118 novel C2H2-type zinc finger cDNAs expressed in human brain.

K. Becker, J. Nagle, K. Ozato, 1995, Human Molecular Genetics.

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

J. Nagle, R. Armstrong, D. Agoston, 1997, Journal of neuroscience research.

Selection of transduced CD34+ progenitors and enzymatic correction of cells from Gaucher patients, with bicistronic vectors.

S. Karlsson, J. Nagle, J. Medin, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis.

K. G. Coleman, M. Polymeropoulos, W. Pavan, 1997, Science.

Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel.

R. Schiffmann, J. Nagle, S. Slaugenhaupt, 2000, Human molecular genetics.

Genes for alkaline protease and neutral protease from Bacillus amyloliquefaciens contain a large open reading frame between the regions coding for signal sequence and mature protein

J. Nagle, D. Filpula, N. Vasantha, 1984, Journal of bacteriology.

Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations

J. Nagle, M. Dalakas, Kye-yoon Park, 2003, Neuromuscular Disorders.

Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c‐terminal α‐helical segment

J. Nagle, W. Squier, L. Goldfarb, 2003, Muscle & nerve.

C2H2-171 : A novel human cDNA representing a developmentally regulated poz domain/zinc finger protein preferentially expressed in brain

M. Polymeropoulos, K. Becker, J. Nagle, 1997, International Journal of Developmental Neuroscience.

Sequence of the chicken delta 2 crystallin gene and its intergenic spacer. Extreme homology with the delta 1 crystallin gene.

J. Nagle, J. Piatigorsky, E. Wawrousek, 1986, The Journal of biological chemistry.

Thymic output generates a new and diverse TCR repertoire after autologous stem cell transplantation in multiple sclerosis patients

D. Douek, J. Nagle, Roland Martin, 2005, The Journal of experimental medicine.

The genomic organization and polymorphism analysis of the human Niemann-Pick C1 gene.

K. G. Coleman, J. Nagle, E. Carstea, 1999, Biochemical and biophysical research communications.

Structural organization, expression and chromosomal mapping of the mouse cystatin-C-encoding gene (Cst3)

C. Huh, S. Karlsson, J. Nagle, 1995, Gene.

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.

D E Banks, J. Nagle, H. McFarland, 1997, The Journal of clinical investigation.

Rapid identification of local T cell expansion in inflammatory organ diseases by flow cytometric T cell receptor Vbeta analysis.

W. Oertel, J. Nagle, B. Hemmer, 2000, Journal of immunological methods.

Identification of novel Drosophila neural precursor genes using a differential embryonic head cDNA screen

T. Brody, J. Nagle, W. Odenwald, 2002, Mechanisms of Development.

A systematic survey of the intergenic region between the murine oxytocin- and vasopressin-encoding genes.

H. Gainer, B. Venkatesh, J. Nagle, 1996, Gene.

Gene for an immunoglobulin-binding protein from a group G streptococcus

P. Alexander, J. Nagle, D. Filpula, 1986, Journal of bacteriology.

Regulation of POU genes by castor and hunchback establishes layered compartments in the Drosophila CNS.

J. Nagle, S. Poole, W. Odenwald, 1998, Genes & development.

Molecular cloning and chromosomal mapping of the mouse cyclin-dependent kinase 5 gene.

A. Kulkarni, J. Nagle, R. Brady, 1995, Genomics.

C2H2-546: a zinc finger protein differentially expressed in HTLV-1 infected T cells.

A. Dehejia, M. Polymeropoulos, K. Becker, 1997, Journal of neurovirology.

Novel exon 3B proteolipid protein gene mutation causing late‐onset spastic paraplegia type 2 with variable penetrance in female family members

J. Nagle, L. Hudson, N. Sambuughin, 1999, Annals of neurology.

Molecular cloning of human ornithine aminotransferase mRNA (gyrate atrophy/cDNA/Xgtll/plaque immunoscreening/tryptic peptide microsequencing)

J. Nagle, N. Katunuma, T. Shiono, 2016 .

Molecular cloning and mapping of a novel developmentally regulated human C2H2-type zinc finger

A. Dehejia, M. Polymeropoulos, K. Becker, 1997, Mammalian Genome.

Molecular cloning and chromosomal mapping of the mouse gene encoding cyclin-dependent kinase 5 regulatory subunit p35.

A. Kulkarni, J. Nagle, R. Brady, 1996, Genomics.

Molecular cloning and mapping of a novel human KRAB domain-containing C2H2-type zinc finger to chromosome 7q36.1.

A. Dehejia, M. Polymeropoulos, K. Becker, 1997, Genomics.

Urinary myelin basic protein‐like material as a correlate of the progression of multiple sclerosis

J. Nagle, MD Larisa Cervenikovi, MD Kumaraswamy Sivakumar, 1996, Annals of neurology.

Structural organization and expression of the mouse gene encoding alpha-galactosidase A.

A. Kulkarni, J. Nagle, R. Brady, 1995, Gene.