Robust Processes for Polymer Modification and Pharmaceutical Synthesis by Ahlqvist, Grace Putka

Get full text

Continuous dimethyldioxirane generation for polymer epoxidation by Ahlqvist, Grace P, Burke, Eileen G, Johnson, Jeremiah A, Jamison, Timothy F

Get full text

Continuous dimethyldioxirane generation for polymer epoxidation by Ahlqvist, Grace P., Burke, Eileen G, Johnson, Jeremiah A., Jamison, Timothy F

Get full text

The Genetic Landscape of Renal Complications in Type 1 Diabetes by Sandholm, N, van Zuydam, N, Ahlqvist, E, Rayner, N, Juliusdottir, T, McCarthy, M, SUMMIT Consortium

Progress Toward a Large-Scale Synthesis of Molnupiravir (MK-4482, EIDD-2801) from Cytidine by Ahlqvist, Grace P., McGeough, Catherine P., Senanayake, Chris, Armstrong, Joseph D., Yadaw, Ajay, Roy, Sarabindu, Ahmad, Saeed, Snead, David R., Jamison, Timothy F

Get full text

High-resolution mapping of a complex disease, a model for rheumatoid arthritis, using heterogeneous stock mice. by Ahlqvist, E, Ekman, D, Lindvall, T, Popovic, M, Förster, M, Hultqvist, M, Klaczkowska, D, Teneva, I, Johannesson, M, Flint, J, Valdar, W, Nandakumar, K, Holmdahl, R

A concise route to MK-4482 (EIDD-2801) from cytidine by Vasudevan, N, Ahlqvist, Grace P, McGeough, Catherine P, Paymode, Dinesh J, Cardoso, Flavio SP, Lucas, Tobias, Dietz, Jule-Phillip, Opatz, Till, Jamison, Timothy F, Gupton, Frank B, Snead, David R

Get full text

A concise route to MK-4482 (EIDD-2801) from cytidine by Vasudevan, N., Ahlqvist, Grace P., McGeough, Catherine P., Paymode, Dinesh J., Cardoso, Flavio S. P., Lucas, Tobias, Dietz, Jule-Phillip, Opatz, Till, Jamison, Timothy F., Gupton, Frank B., Snead, David R.

Get full text

Heritability of variation in glycaemic response to metformin: a genome-wide complex trait analysis. by Zhou, K, Donnelly, L, Yang, J, Li, M, Deshmukh, H, Van Zuydam, N, Ahlqvist, E, Spencer, C, Groop, L, Morris, A, Colhoun, H, Sham, P, McCarthy, M, Palmer, C, Pearson, E

Diastereoselectivity is in the Details: Minor Changes Yield Major Improvements to the Synthesis of Bedaquiline** by Mear, Sarah Jane, Lucas, Tobias, Ahlqvist, Grace P, Robey, Juliana MS, Dietz, Jule‐Philipp, Khairnar, Pankaj V, Maity, Sanjay, Williams, Corshai L, Snead, David R, Nelson, Ryan C, Opatz, Till, Jamison, Timothy F

Get full text

Heritability of variation in glycaemic response to metformin: A genome-wide complex trait analysis by Zhou, K, Donnelly, L, Yang, J, Li, M, Deshmukh, H, Van Zuydam, N, Ahlqvist, E, Spencer, C, Groop, L, Morris, A, Colhoun, H, Sham, P, McCarthy, M, McCarthy, M, McCarthy, M, Palmer, C, Pearson, E

A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes by Taira, M, Imamura, M, Takahashi, A, Kamatani, Y, Yamauchi, T, Araki, S, Tanaka, N, van Zuydam, N, Ahlqvist, E, Toyoda, M, Umezono, T, Kawai, K, Imanishi, M, Watada, H, Suzuki, D, Maegawa, H, Babazono, T, Kaku, K, Kawamori, R, Summit Consortium, Groop, L, McCarthy, M, Kadowaki, T, Maeda, S

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. by Strawbridge, R, Dupuis, J, Prokopenko, I, Barker, A, Ahlqvist, E, Rybin, D, Petrie, JR, Travers, M, Bouatia-Naji, N, Dimas, A, Nica, A, Wheeler, E, Chen, H, Voight, B, Taneera, J, Kanoni, S, Peden, J, Turrini, F, Gustafsson, S, Zabena, C, Almgren, P, Barker, D, Barnes, D, Dennison, E, Eriksson, J

Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. by Strawbridge, R, Dupuis, J, Prokopenko, I, Barker, A, Ahlqvist, E, Rybin, D, Petrie, JR, Travers, M, Bouatia-Naji, N, Dimas, A, Nica, A, Wheeler, E, Chen, H, Voight, B, Taneera, J, Kanoni, S, Peden, J, Turrini, F, Gustafsson, S, Zabena, C, Almgren, P, Barker, D, Barnes, D, Dennison, E, Eriksson, J

A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria by Ahluwalia, T, Schulz, C, Waage, J, Skaaby, T, Sandholm, N, Van Zuydam, N, Charmet, R, Bork-Jensen, J, Almgren, P, Thuesen, B, Bedin, M, Brandslund, I, Christensen, C, Linneberg, A, Ahlqvist, E, Groop, P, Hadjadj, S, Tregouet, D, Jørgensen, M, Grarup, N, Pedersen, O, Simons, M, Groop, L, Orho-Melander, M, McCarthy, M, Melander, O, Rossing, P, Kilpeläinen, T, Hansen, T

Genome-wide association study of peripheral artery disease by van Zuydam, NR, Stiby, A, Abdalla, M, Austin, E, Dahlström, EH, Dahlström, EH, McLachlan, S, Vlachopoulou, E, Ahlqvist, E, Di Liao, C, Sandholm, N, Forsblom, C, Mahajan, A, Robertson, NR, Rayner, NW, Lindholm, E, Sinisalo, J, Perola, M, Kallio, M, Weiss, E, Price, J, Paterson, A, Klein, B, Salomaa, V, Palmer, CNA, Groop, P-H, Groop, L, McCarthy, MI, de Andrade, M, Morris, AP, Hopewell, JC, Colhoun, HM, Kullo, IJ

Genetic discrimination between LADA and childhood-onset type 1 diabetes within the MHC by Mishra, Rajashree, Åkerlund, Mikael, Cousminer, Diana L., Ahlqvist, Emma, Bradfield, Jonathan P., Chesi, Alessandra, Hodge, Kenyaita M., Guy, Vanessa C., Brillon, David J., Pratley, Richard E., Rickels, Michael R., Vella, Adrian, Ovalle, Fernando, Harris, Ronald I., Melander, Olle, Varvel, Stephen, Hakonarson, Hakon, Froguel, Phillippe, Lonsdale, John T., Mauricio, Didac, Schloot, Nanette C., Khunti, Kamlesh, Greenbaum, Carla J., Yderstræde, Knud B., Tuomi, Tiinamaija, Voight, Benjamin F., Schwartz, Stanley, Boehm, Bernhard Otto, Groop, Leif, Leslie, Richard David, Grant, Struan F. A.

Get full text

Loss of ZnT8 function protects against diabetes by enhanced insulin secretion by Dwivedi, O, Lehtovirta, M, Hastoy, B, Chandra, V, Krentz, N, Kleiner, S, Jain, D, Richard, A, Abaitua, F, Beer, N, Grotz, A, Prasad, R, Hansson, O, Ahlqvist, E, Krus, U, Artner, I, Suoranta, A, Gomez, D, Baras, A, Champon, B, Payne, A, Moralli, D, Thomsen, S, Kramer, P, Spiliotis, I, Ramracheya, R, Chabosseau, P, Theodoulou, A, Cheung, R, Van De Bunt, M, Flannick, J, Trombetta, M, Bonora, E, Wolheim, C, Sarelin, L, Bonadonna, R, Rorsman, P, Davies, B, Brosnan, J, McCarthy, M, Otonkoski, T, Lagerstedt, J, Rutter, G, Gromada, J, Gloyn, A, Tuomi, T, Groop, L

The genetic landscape of renal complications in type 1 diabetes. by Sandholm, N, Van Zuydam, N, Ahlqvist, E, Juliusdottir, T, Deshmukh, H, Rayner, N, Di Camillo, B, Forsblom, C, Fadista, J, Ziemek, D, Salem, R, Hiraki, L, Pezzolesi, M, Trégouët, D, Dahlström, E, Valo, E, Oskolkov, N, Ladenvall, C, Marcovecchio, M, Cooper, J, Sambo, F, Malovini, A, Manfrini, M, McKnight, A, Lajer, M, Harjutsalo, V, Gordin, D, Parkkonen, M, Tuomilehto, J, Lyssenko, V, McKeigue, P, Rich, S, Brosnan, M, Fauman, E, Bellazzi, R, Rossing, P, Hadjadj, S, Krolewski, A, Paterson, A, Florez, J, Hirschhorn, J, Maxwell, A, Dunger, D, Cobelli, C, Colhoun, H, Groop, L, McCarthy, M, Groop, P

A central role for GRB10 in regulation of islet function in man by Prokopenko, I, Poon, W, Mägi, R, Prasad B, R, Salehi, SA, Almgren, P, Osmark, P, Bouatia-Naji, N, Wierup, N, Fall, T, Stančáková, A, Barker, A, Lagou, V, Osmond, C, Xie, W, Lahti, J, Jackson, A, Cheng, Y, Liu, J, O'Connell, JR, Blomstedt, P, Fadista, J, Alkayyali, S, Dayeh, T, Ahlqvist, E, Taneera, J, Lecoeur, C, Kumar, A, Hansson, O, Hansson, K, Voight, B, Kang, H, Levy-Marchal, C, Vatin, V, Palotie, A, Syvänen, A, Mari, A, Weedon, M, Loos, R, Ong, K, Nilsson, P, Isomaa, B, Tuomi, T, Wareham, N, Stumvoll, M, Widen, E, Lakka, T, Langenberg, C, Tönjes, A, Rauramaa, R, Kuusisto, J, Frayling, T, Froguel, P, Walker, M, Eriksson, J, Ling, C, Kovacs, P, Ingelsson, E, McCarthy, M, Shuldiner, A, Silver, K, Laakso, M, Groop, L, Lyssenko, V