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1
In vivo molecular analysis of lymphokines involved in the murine immune response during Schistosoma mansoni infection. I. IL-4 mRNA, not IL-2 mRNA, is abundant in the granulomatous livers, mesenteric lymph nodes, and spleens of infected mice
In vivo molecular analysis of lymphokines involved in the murine immune response during Schistosoma mansoni infection. I. IL-4 mRNA, not IL-2 mRNA, is abundant in the granulomatous livers, mesenteric lymph nodes, and spleens of infected mice
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In vivo molecular analysis of lymphokines involved in the murine immune response during Schistosoma mansoni infection. I. IL-4 mRNA, not IL-2 mRNA, is abundant in the granulomatous livers, mesenteric lymph nodes, and spleens of infected mice

Henderson, GS ; Conary, JT ; Summar, M ; McCurley, TL ; Colley, DG

The Journal of immunology (1950), 1991-08, Vol.147 (3), p.992-997 [Periódico revisado por pares]

United States: Am Assoc Immnol

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2
The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci
The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci
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The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci

Summar, M L

Progress in brain research, 1992, Vol.93, p.309-317 [Periódico revisado por pares]

Netherlands

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3
Chapter 22 The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci
Chapter 22 The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci
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Chapter 22 The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci

Summar, Marshall L.

Progress in Brain Research, 1992, Vol.93, p.309-317

Elsevier Science & Technology

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4
The CEPH consortium linkage map of human chromosome 2
The CEPH consortium linkage map of human chromosome 2
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The CEPH consortium linkage map of human chromosome 2

Spurr, Nigel K. ; Cox, Simon ; Bryant, Stephen P. ; Attwood, John ; Robson, Elizabeth B. ; Shields, Denis C. ; Steinbrueck, Todd ; Jenkins, Trefor ; Murray, Jeffrey C. ; Kidd, Kenneth K. ; Summar, Marshall L. ; Tsipouras, Petros ; Retief, Andries E. ; Kruse, Torben A. ; Bale, Allen E. ; Vergnaud, Gilles ; Weber, James L. ; McBride, O.W. ; Donis-Keller, Helen ; White, Raymond L.

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.1055-1063 [Periódico revisado por pares]

SAN DIEGO: Elsevier Inc

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5
Genes regulating glutathione concentration in X-ray transformed rat embryo fibroblasts: Changes in γ-glutamylcysteine synthetase and γ-glutamyl transpeptidase expression
Genes regulating glutathione concentration in X-ray transformed rat embryo fibroblasts: Changes in γ-glutamylcysteine synthetase and γ-glutamyl transpeptidase expression
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Genes regulating glutathione concentration in X-ray transformed rat embryo fibroblasts: Changes in γ-glutamylcysteine synthetase and γ-glutamyl transpeptidase expression

Smith, Michael D. ; Sierra-Rivera, Elaine ; Meredith, Michael J. ; Summar, Marshall L. ; Stoffel, Christine M. ; Freeman, Michael L.

Free radical biology & medicine, 1993-11, Vol.15 (5), p.546-546 [Periódico revisado por pares]

Elsevier Inc

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6
Linkage Mapping of the Gene for Type III Collagen (COL3A1) to Human Chromosome 2q Using a VNTR Polymorphism
Linkage Mapping of the Gene for Type III Collagen (COL3A1) to Human Chromosome 2q Using a VNTR Polymorphism
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Linkage Mapping of the Gene for Type III Collagen (COL3A1) to Human Chromosome 2q Using a VNTR Polymorphism

Tiller, George E. ; Polumbo, Paula A. ; Summar, Marshall L.

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.275-277 [Periódico revisado por pares]

San Diego, CA: Elsevier Inc

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7
Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient
Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient
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Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient

LEWANDA, A. F ; GREEN, E. D ; CLARREN, S. K ; JABS, E. W ; WEISSENBACH, J ; JERALD, H ; TAYLOR, E ; SUMMAR, M. L ; PHILLIPS, J. A ; COHEN, M ; FEINGOLD, M ; MOURADIAN, W

American journal of human genetics, 1994-12, Vol.55 (6), p.1195-1201 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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8
Molecular Cloning, Sequencing, Chromosomal Localization, and Tissue Distribution of the Human Na+/H+Exchanger (SLC9A2)
Molecular Cloning, Sequencing, Chromosomal Localization, and Tissue Distribution of the Human Na+/H+Exchanger (SLC9A2)
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Molecular Cloning, Sequencing, Chromosomal Localization, and Tissue Distribution of the Human Na+/H+Exchanger (SLC9A2)

GHISHAN, FAYEZ K. ; KNOBEL, SUSAN M. ; SUMMAR, MARSHALL

Genomics (San Diego, Calif.), 1995-11, Vol.30 (1), p.25-30 [Periódico revisado por pares]

San Diego, CA: Elsevier Inc

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9
Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia
Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia
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Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia

Van Hove, Johan L. K. ; Kishnani, Priya ; Muenzer, Joseph ; Wenstrup, Richard J. ; Summar, Marshall L. ; Brummond, Michael R. ; Lachiewicz, Ave M. ; Millington, David S. ; Kahler, Stephen G.

American journal of medical genetics, 1995-12, Vol.59 (4), p.444-453 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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10
Effective hemodialysis and hemofiltration driven by an extracorporeal membrane oxygenation pump in infants with hyperammonemia
Effective hemodialysis and hemofiltration driven by an extracorporeal membrane oxygenation pump in infants with hyperammonemia
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Effective hemodialysis and hemofiltration driven by an extracorporeal membrane oxygenation pump in infants with hyperammonemia

Summar, Marshall ; Pietsch, John ; Deshpande, Jayant ; Schulman, Gerald

The Journal of pediatrics, 1996-03, Vol.128 (3), p.379-382 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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Deste Autor:

  1. Patil, S
  2. Paththinige, C
  3. Shotelersuk, V
  4. Sokunbi, O
  5. Muenke, M

Neste Assunto:

  1. Science & Technology
  2. Life Sciences & Biomedicine
  3. Humans
  4. Genetics & Heredity
  5. Female

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