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J M Puck

Showing results (61-70 of 99) with videos related to

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The EMBO Journal|September 2, 1996
Interleukin-4-specific signal transduction events are driven by homotypic interactions of the interleukin-4 receptor alpha subunitS Y Lai, J Molden, K D Liu, et al.
Nature Genetics|July 1, 1996
Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiencyR Hirschhorn, D R Yang, J M Puck, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Localization of the 75-kDa inositol polyphosphate-5-phosphatase (INPP5B) to human chromosome band 1p34P A Jänne, A S Dutra, N C Dracopoli, et al.
Nature|May 22, 1986
Isolation of cDNA clones encoding the 20K non-glycosylated polypeptide chain of the human T-cell receptor/T3 complexD P Gold, J M Puck, C L Pettey, et al.
Genomics|September 1, 1994
IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human diseaseP S Henthorn, R L Somberg, V M Fimiani, et al.
Genomics|September 1, 1994
Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiencyS M Deschênes, J M Puck, A S Dutra, et al.
American Journal of Human Genetics|August 23, 2001
An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single familyT P Atkinson, A A Schäffer, B Grimbacher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Analphoid marker chromosome in a patient with hyper-IgE syndrome, autism, and mild mental retardationB Grimbacher, A S Dutra, S M Holland, et al.
Oral Diseases|January 5, 2008
Novel intraoral phenotypes in hyperimmunoglobulin-E syndromeD L Domingo, A F Freeman, J Davis, et al.
Pageof 10

Showing results (61-70 of 99) with videos related to

Sort By:
Pageof 10
The EMBO Journal|September 2, 1996
Interleukin-4-specific signal transduction events are driven by homotypic interactions of the interleukin-4 receptor alpha subunitS Y Lai, J Molden, K D Liu, et al.
Nature Genetics|July 1, 1996
Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiencyR Hirschhorn, D R Yang, J M Puck, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Report of the committee on the genetic constitution of the X chromosomeJ L Mandel, H F Willard, R L Nussbaum, et al.
Cytogenetics and Cell Genetics|January 1, 1994
Localization of the 75-kDa inositol polyphosphate-5-phosphatase (INPP5B) to human chromosome band 1p34P A Jänne, A S Dutra, N C Dracopoli, et al.
Nature|May 22, 1986
Isolation of cDNA clones encoding the 20K non-glycosylated polypeptide chain of the human T-cell receptor/T3 complexD P Gold, J M Puck, C L Pettey, et al.
Genomics|September 1, 1994
IL-2R gamma gene microdeletion demonstrates that canine X-linked severe combined immunodeficiency is a homologue of the human diseaseP S Henthorn, R L Somberg, V M Fimiani, et al.
Genomics|September 1, 1994
Comparative mapping of canine and human proximal Xq and genetic analysis of canine X-linked severe combined immunodeficiencyS M Deschênes, J M Puck, A S Dutra, et al.
American Journal of Human Genetics|August 23, 2001
An immune defect causing dominant chronic mucocutaneous candidiasis and thyroid disease maps to chromosome 2p in a single familyT P Atkinson, A A Schäffer, B Grimbacher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 21, 2001
Analphoid marker chromosome in a patient with hyper-IgE syndrome, autism, and mild mental retardationB Grimbacher, A S Dutra, S M Holland, et al.
Oral Diseases|January 5, 2008
Novel intraoral phenotypes in hyperimmunoglobulin-E syndromeD L Domingo, A F Freeman, J Davis, et al.
Pageof 10