Angiotensin II early regulated genes in H295R human adrenocortical cells von Romero, Damian G, Plonczynski, Maria, Vergara, Gaston R, Gomez-Sanchez, Elise P, Gomez-Sanchez, Celso E

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β-Thalassemia in Southwestern Iran von Merat, A., Haghshenas, M., Pour, Z. Mostafavi, Plonczynski, M. W., Harrell, A. N., Coleman, M. B., Steinberg, M. H.

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Double Heterozygosity for the Codon β 39 C-to-T Nonsense Mutation and a Triplicate α-Globin Gene Locus Can Cause "Dominantly" Inherited β-Thalassemia Intermedia von Rhodes, S.L., Plonczynski, M., Harrell, A., Li, J., Safaya, S., Files, J.C., Steinberg, M.H.

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Interleukin-8 Synthesis, Regulation, and Steroidogenic Role in H295R Human Adrenocortical Cells von Romero, Damian G, Vergara, Gaston R, Zhu, Zheng, Covington, Gina S, Plonczynski, Maria W, Yanes, Licy L, Gomez-Sanchez, Elise P, Gomez-Sanchez, Celso E

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β-Thalassemia Intermedia with Exceptionally High Hemoglobin A2: Relationship to Mutations in the β-Gene Promoter von Coleman, Mary B., Adams, Junius G., Plonczynski, Maria W., Harrell, Audrey H., Walker, Alice M., Fairbanks, Virgil, Steinberg, Martin H.

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Genetic studies suggest a multicentric origin for Hb G-coushatta [β22(B4)Glu→Ala] von Li, J., Wilson, D., Plonczynski, M., Harrell, A., Cook, C. B., Scheer, W. D., Zeng, Y-T., Coleman, M. B., Steinberg, M. H.

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The -87 (C→A) β+-Thalassemia Mutation in a Black Family von Coleman, M. B., Steinberg, M. H., Harrell, A. H., Plonczynski, M. W., Walker, A. M., Adams, J. G.

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Severe Hb S-β+ Thalassemia Caused by IVS-I Splice Site Mutations von Li, J., Plonczynski, M., Steinberg, M. H., Kheradpour, A., Alter, B. P.

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New state record for Libellula cyanea Fabr. from Wisconsin, United States (Anisoptera: Libellulidae) von Plonczynski, M

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HB San Diego [β109(G11)VAL→MET] in an Iranian: Further Evidence for a Mutational Hot Spot at Position 109 of the β-Globin Gene von Coleman, M. B., Adams, J. G., Walker, A. M., Plonczynski, M. W., Harrell, A. H., Kark, J. A., Schechter, G. P.

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GγAγ(β+) hereditary persistence of fetal hemoglobin: The Gγ – 158 C → T mutation in cis to the − 175 T → C mutation of the Aγ‐globin gene results in increased Gγ‐globin synthesis... von Coleman, M. B., Adams, J. G., Steinberg, M. H., Plonczynski, M. W., Harrell, A. H., Castro, O., Winter, W. P.

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Gene Expression Profiling during Erythroid Differentiation of K562 Cells von Mitchell, Tim, Plonczynski, Maria, McCollum, Amy, Hardy, Cheryl L., Safaya, Surinder, Steinberg, Martin H.

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Fetal Hemoglobin in Sickle Cell Anemia: Examination of Phylogenetically Conserved Sequences Within the Locus Control Region but Outside the Cores of Hypersensitive Sites 2 and 3 von Plonczynski, Maria, Figueiredo, Maria Stella, Steinberg, Martin H.

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Induction of Globin Synthesis in K562 Cells Is Associated with Differential Expression of Transcription Factor Genes von Plonczynski, Maria, Hardy, Cheryl L, Safaya, Surinder, Harrell, Audrey, McCoy, Lakeyra, Brinson, Alisha, Agwarangbo, Lovell, Steinberg, Martin H

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Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine) von Coleman, M B, Lu, Z H, Smith, 2nd, C M, Adams, 3rd, J G, Harrell, A, Plonczynski, M, Steinberg, M H

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Double Heterozygosity for the Codon ?? 39 C-to-T Nonsense Mutation and a Triplicate ??-Globin Gene Locus Can Cause ???Dominantly??? Inherited ??-Thalassemia Intermedia von Rhodes, S. L., Plonczynski, M., Harrell, A., Li, J., Safaya, S., Files, J. C., Steinberg, M. H.

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β‐Globin gene haplotype in Hb SC disease von Steinberg, Martin H., Nagel, Ronald L., Lawrence, Christine, Swaminathan, Venkataramani, Lu, Zhi‐Hong, Plonczynski, Maria, Harrell, Audrey

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GγAγ(β+) hereditary persistence of fetal hemoglobin : the Gγ-158C→T mutation in cis to the -175T→C mutation of the Aγ-globin gene results in increased Gγ-globin synthesis von COLEMAN, M. B, ADAMS, J. G, STEINBERG, M. H, PLONCZYNSKI, M. W, HARRELL, A. H, CASTRO, O, WINTER, W. P

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Slowly exchanging ca-binding sites unique to the cardiac/slow muscle variant of troponin C von Pan, Bo-Sheng, Plonczynski, Maria, Solaro, R. John

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Slowly exchanging calcium binding sites unique to cardiac/slow muscle troponin C von Pan, Bo-Sheng, Palmiter, Kimberly A., Plonczynski, Maria, Solaro, R.John

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