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Papers authored by Sprenkle J

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Structure of the EMMPRIN N-terminal domain 1: Dimerization via beta-strand swapping.

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Luo J, Teplyakov A, Obmolova G, Malia T, Wu SJ, Beil E, Baker A, Swencki-Underwood B, Zhao Y, Sprenkle J, Dixon K, Sweet R, and Gilliland GL

Proteins 77(4):1009-14, 2009 Dec - Who cited this? | PubMed ID: 19768682 | Fulltext

Device for rapid quantification of human carotid baroreceptor-cardiac reflex responses.

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Sprenkle JM, Eckberg DL, Goble RL, Schelhorn JJ, and Halliday HC

Journal of applied physiology (Bethesda, Md. : 1985) 60(2):727-32, 1986 Feb - Who cited this? | PubMed ID: 3949673 | Fulltext

Mechanism of origin of complete hydatidiform moles.

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Jacobs PA, Wilson CM, Sprenkle JA, Rosenshein NB, and Migeon BR

Nature 286(5774):714-6, 1980 Aug 14 - Who cited this? | PubMed ID: 6447836 | Fulltext

Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.

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Pai GS, Sprenkle JA, Do TT, Mareni CE, and Migeon BR

Proceedings of the National Academy of Sciences of the United States of America 77(5):2810-3, 1980 May - Who cited this? | PubMed ID: 6930669 | Fulltext

Stability of the "two active X" phenotype in triploid somatic cells.

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Migeon BR, Sprenkle JA, and Do TT

Cell 18(3):637-41, 1979 Nov - Who cited this? | PubMed ID: 229959 | Fulltext

Studies of human-mouse cell hybrids with respect to X-chromosome inactivation.

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Migeon BR, Sprenkle JA, and Do TT

Basic life sciences 12:329-37, 1978 - Who cited this? | PubMed ID: 752324 | Fulltext

X-linked Hunter syndrome: the heterozygous phenotype in cell culture.

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Migeon BR, Sprenkle JA, Liebaers I, Scott JF, and Neufeld EF

American journal of human genetics 29(5):448-54, 1977 Sep - Who cited this? | PubMed ID: 409283 | Fulltext

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