Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment von Nho, K, Corneveaux, J J, Kim, S, Lin, H, Risacher, S L, Shen, L, Swaminathan, S, Ramanan, V K, Liu, Y, Foroud, T, Inlow, M H, Siniard, A L, Reiman, R A, Aisen, P S, Petersen, R C, Green, R C, Jack, C R, Weiner, M W, Baldwin, C T, Lunetta, K, Farrer, L A, Furney, S J, Lovestone, S, Simmons, A, Mecocci, P, Vellas, B, Tsolaki, M, Kloszewska, I, Soininen, H, McDonald, B C, Farlow, M R, Ghetti, B, Huentelman, M J, Saykin, A J

Volltext

New Insights into the Structural Characteristics of the Arabinogalactan−Protein (AGP) Fraction of Gum Arabic von Mahendran, T, Williams, P. A, Phillips, G. O, Al-Assaf, S, Baldwin, T. C

Volltext

apoplastic chitinase CpCHT1 isolated from the corolla of wintersweet exhibits both antifreeze and antifungal activities von Zhang, S. -H, Wei, Y, Liu, J. -L, Yu, H. -M, Yin, J. -H, Pan, H. -Y, Baldwin, T. C

Volltext

Inflammation and metabolism gene sets in subcutaneous abdominal adipose tissue are altered 1 hour after exercise in adults with obesity von Ludzki, A. C., Schleh, M. W., Krueger, E. M., Taylor, N. M., Ryan, B. J., Baldwin, T. C., Gillen, J. B., Ahn, C., Varshney, P., Horowitz, J. F.

Volltext

Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics von Nho, K, Corneveaux, J J, Kim, S, Lin, H, Risacher, S L, Shen, L, Swaminathan, S, Ramanan, V K, Liu, Y, Foroud, T, Inlow, M H, Siniard, A L, Reiman, R A, Aisen, P S, Petersen, R C, Green, R C, Jack, C R, Weiner, M W, Baldwin, C T, Lunetta, K, Farrer, L A, Furney, S J, Lovestone, S, Simmons, A, Mecocci, P, Vellas, B, Tsolaki, M, Kloszewska, I, Soininen, H, McDonald, B C, Farlow, M R, Ghetti, B, Huentelman, M J, Saykin, A J

Volltext

Genetic association between endothelial nitric oxide synthase and Alzheimer disease von Akomolafe, A, Lunetta, KL, Erlich, PM, Cupples, LA, Baldwin, CT, Huyck, M, Green, RC, Farrer, LA

Volltext

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia von Sebastiani, P., Farrell, J.J., Alsultan, A., Wang, S., Edward, H.L., Shappell, H., Bae, H., Milton, J.N., Baldwin, C.T., Al-Rubaish, A.M., Naserullah, Z., Al-Muhanna, F., Alsuliman, A., Patra, P.K., Farrer, L.A., Ngo, D., Vathipadiekal, V., Chui, D.H.K., Al-Ali, A.K., Steinberg, M.H.

Volltext

Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea von Ma, Q, Wyszynski, D F, Farrell, J J, Kutlar, A, Farrer, L A, Baldwin, C T, Steinberg, M H

Volltext

Evidence for Linkage Between Essential Hypertension and a Putative Locus on Human Chromosome 17 von Baima, Jader, Nicolaou, Michael, Schwartz, Faina, DeStefano, Anita L, Manolis, Athanasios, Gavras, Irene, Laffer, Cheryl, Elijovich, Fernando, Farrer, Lindsay, Baldwin, Clinton T, Gavras, Haralambos

Volltext

Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3 von BONNE-TAMIR, B, DESTEFANO, A. L, BRIGGS, C. E, ADAIR, R, FRANKLYN, B, WEISS, S, KOROSTISHEVSKY, M, FRYDMAN, M, BALDWIN, C. T, FARRER, L. A

Volltext

Maternal component in the familial aggregation of hypertension von DeStefano, AL, Gavras, H, Heard-Costa, N, Bursztyn, M, Manolis, A, Farrer, LA, Baldwin, CT, Gavras, I, Schwartz, F

Volltext

Identification and Characterization of GONST1, a Golgi-Localized GDP-Mannose Transporter in Arabidopsis von Baldwin, T. C.

Volltext

Genetic predisposition to stroke in relatives of hypertensives von NICOLAOU, M, DESTEFANO, A. L, GAVRAS, I, CUPPLES, L. A, MANOLIS, A. J, BALDWIN, C. T, GAVRAS, H, FARRER, L. A

Volltext

Single Base Mutation in the Type II Procollagen Gene (COL2A1) as a Cause of Primary Osteoarthritis Associated with a Mild Chondrodysplasia von Ala-Kokko, Leena, Baldwin, Clinton T., Moskowitz, Roland W., Prockop, Darwin J.

Volltext

Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population von Baldwin, Clinton T., Weiss, Sari, Farrer, Lindsay A., De Stefano, Anita L., Adair, Ronald, Franklyn, Barbara, Kidd, Kenneth K., Korostishevsky, Michael, Bonné-Tamir, Batsheva

Volltext

Identification and Characterization of GONST1, a Golgi-Localized GDP-Mannose Transporter in Arabidopsis von Baldwin, Timothy C., Handford, Michael G., Yuseff, Maria-Isabel, Orellana, Ariel, Dupree, Paul

Volltext

Association of Polymorphisms in the Angiotensin-Converting Enzyme Gene with Alzheimer Disease in an Israeli Arab Community von Meng, Yan, Baldwin, Clinton T., Bowirrat, Abdalla, Waraska, Kristin, Inzelberg, Rivka, Friedland, Robert P., Farrer, Lindsay A.

Volltext

Clinical and genetic correlates of soluble P‐selectin in the community von LEE, D. S., LARSON, M. G., LUNETTA, K. L., DUPUIS, J., RONG, J., KEANEY, J. F., LIPINSKA, I., BALDWIN, C. T., VASAN, R. S., BENJAMIN, E. J.

Volltext

Structure of cDNA clones coding for the entire preproα1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codo... von Ala-Kokko, L, Kontusaari, S, Baldwin, C T, Kuivaniemi, H, Prockop, D J

Volltext

A new epidermal growth factor-like domain in the human core protein for the large cartilage-specific proteoglycan. Evidence for alternative splicing of the domain von BALDWIN, C. T, REGINATO, A. M, PROCKOP, D. J

Volltext