Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis von Papanikolaou, George, Babakaiff, Ryan, Goldberg, Y Paul, Franchini, Patrick L, Dubé, Marie-Pierre, MacFarlane, Julie, Pape, Terry D, Radomski, Christopher C, Davidas, Owen, Risler, Jenni K, Nemeth, Elizabeta, Zaborowska, Catherine, Politou, Marianna, Lockitch, Gillian, Brissot, Pierre, Thompson, Jay, Ludwig, Erwin H, MacDonald, Marcia L E, Samuels, Mark E, Sakellaropoulos, Nikos, Ganz, Tomas, Hayden, Michael R, Andres, Lisa, Christakis, John

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A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro von Inoue, I, Nakajima, T, Williams, C S, Quackenbush, J, Puryear, R, Powers, M, Cheng, T, Ludwig, E H, Sharma, A M, Hata, A, Jeunemaitre, X, Lalouel, J M

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High-level lipoprotein [a] expression in transgenic mice: evidence for oxidized phospholipids in lipoprotein [a] but not in low density lipoproteins von Schneider, Matthias, Witztum, Joseph L., Young, Stephen G., Ludwig, Erwin H., Miller, Elizabeth R., Tsimikas, Sotirios, Curtiss, Linda K., Marcovina, Santica M., Taylor, John M., Lawn, Richard M., Innerarity, Thomas L., Pitas, Robert E.

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Hypervariability in a minisatellite 3' of the apolipoprotein B gene in patients with coronary heart disease compared with normal controls von Friedl, W, Ludwig, EH, Paulweber, B, Sandhofer, F, McCarthy, BJ

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Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region von Afshar-Kharghan, Vahid, Diz-Küçükkaya, Reyhan, Ludwig, Erwin H., Marian, Ali J., López, José A.

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DGAT1 promoter polymorphism associated with alterations in body mass index, high density lipoprotein levels and blood pressure in Turkish women von Ludwig, EH, Mahley, RW, Palaoglu, E, Özbayrakçı, S, Balestra, ME, Borecki, IB, Innerarity, TL, Farese Jr, RV

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Association between a Specific Apolipoprotein B Mutation and Familial Defective Apolipoprotein B-100 von Soria, Luis F., Ludwig, Erwin H., Howard R. G. Clarke, Vega, Gloria L., Grundy, Scott M., McCarthy, Brian J.

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Polymorphism of human glycoprotein Ib alpha results from a variable number of tandem repeats of a 13-amino acid sequence in the mucin-like macroglycopeptide region. Structure/funct... von LOPEZ, J. A, LUDWIG, E. H, MCCARTHY, B. J

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Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics von Williams, Roger R., Hunt, Steven C., Schumacher, M.Catherine, Hegele, Robert A., Leppert, Mark F., Ludwig, Erwin H., Hopkins, Paul N.

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High-resolution analysis of a hypervariable region in the human apolipoprotein B gene von LUDWIG, E. H, FRIEDL, W, MCCARTHY, B. J

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Associations of candidate loci angiotensinogen and angiotensin-converting enzyme with severe hypertension: The NHLBI family heart study von Borecki, I.B., Province, M.A., Ludwig, E.H., Ellison, R.C., Folsom, A.R., Heiss, G., Lalouel, J.M., Higgins, M., Rao, D.C.

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Haplotype analysis of the human apolipoprotein B mutation associated with familial defective apolipoprotein B100 von LUDWIG, E. H, MCCARTHY, B. J

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Association of genetic variations in apolipoprotein B with hypercholesterolemia, coronary artery disease, and receptor binding of low density lipoproteins von Ludwig, E H, Hopkins, P N, Allen, A, Wu, L L, Williams, R R, Anderson, J L, Ward, R H, Lalouel, J M, Innerarity, T L

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Associations between candidate loci angiotensin-converting enzyme and angiotensinogen with coronary heart disease and myocardial infarction: The NHLBI family heart study von Ludwig, E.H., Borecki, I.B., Ellison, R.C., Folsom, A.R., Heiss, G., Higgins, M., Lalouel, J.M., Province, M.A., Rao, D.C.

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Analysis of two different tandem repetitive elements within the human apolipoprotein B gene von Ludwig, EH, Haubold, K, McCarthy, BJ

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Angiotensin-converting enzyme genotypes and risk for myocardial infarction in women von ANDERSON, J. L, CARLQUIST, J. F, KING, G. J, MORRISON, L, THOMSON, M. J, LUDWIG, E. H, MUHLESTEIN, J. B, BAIR, T. L, WARD, R. H

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Genetic Basis of Familial Dyslipidemia and Hypertension: 15-Year Results From Utah von Williams, R.R., Hunt, S.C., Hopkins, P.N., Wu, L.L., Hasstedt, S.J., Berry, T.D., Barlow, G.K., Stults, B.M., Schumacher, M.C., Ludwig, E.H., Elbein, S.C., Wilson, D.E., Lifton, R.P., Lalouel, J.M.

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A polymorphism in a region with enhancer activity in the second intron of the human apolipoprotein B gene von Levy-Wilson, B, Soria, L, Ludwig, EH, Argyres, M, Brooks, AR, Blackhart, BD, Friedl, W, McCarthy, BJ

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Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: The atherosclerosis risk in communities and the NHLBI family heart studies von Arnett, Donna K, Borecki, Ingrid B, Ludwig, Erwin H, Pankow, James S, Myers, Richard, Evans, Greg, Folsom, Aaron R, Heiss, Gerardo, Higgins, Millicent

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DNA sequence of the human apolipoprotein B gene von Ludwig, E H, Blackhart, B D, Pierotti, V R, Caiati, L, Fortier, C, Knott, T, Scott, J, Mahley, R W, Levy-Wilson, B, McCarthy, B J

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