Sustained diacylglycerol formation from inositol phospholipids in angiotensin II-stimulated vascular smooth muscle cells von Griendling, K K, Rittenhouse, S E, Brock, T A, Ekstein, L S, Gimbrone, M A, Alexander, R W

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Phorbol ester and 1-oleoyl-2-acetylglycerol inhibit angiotensin activation of phospholipase C in cultured vascular smooth muscle cells von Brock, T A, Rittenhouse, S E, Powers, C W, Ekstein, L S, Gimbrone, M A, Alexander, R W

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Angiotensin Increases Cytosolic Free Calcium in Cultured Vascular Smooth Muscle Cells von BROCK, TOMMY A, ALEXANDER, R WAYNE, EKSTEIN, LAURIE S, ATKINSON, WILLIAM J, GIMBRONE, MICHAEL A

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Characterization of the rabbit ventricular myocardial receptor for angiotensin II. Evidence for two sites of different affinities and specificities von G B Wright, R W Alexander, L S Ekstein, M A Gimbrone, Jr

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Sodium, Divalent Cations, and Guanine Nucleotides Regulate the Affinity of the Rat Mesenteric Artery Angiotensin II Receptor von Wright, Gregory B, Alexander, R Wayne, Ekstein, Laurie S, Gimbrone, Michael A

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Keloids: a review of therapeutic management von Ekstein, Samuel F., Wyles, Saranya P., Moran, Steven L., Meves, Alexander

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Timing of referral to evaluate for epilepsy surgery: Expert Consensus Recommendations from the Surgical Therapies Commission of the International League Against Epilepsy von Jehi, Lara, Jette, Nathalie, Kwon, Churl‐Su, Josephson, Colin B., Burneo, Jorge G., Cendes, Fernando, Sperling, Michael R., Baxendale, Sallie, Busch, Robyn M., Triki, Chahnez Charfi, Cross, J. Helen, Ekstein, Dana, Englot, Dario J., Luan, Guoming, Palmini, Andre, Rios, Loreto, Wang, Xiongfei, Roessler, Karl, Rydenhag, Bertil, Ramantani, Georgia, Schuele, Stephan, Wilmshurst, Jo M., Wilson, Sarah, Wiebe, Samuel

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Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1 von Suls, Arvid, Dedeken, Peter, Goffin, Karolien, Van Esch, Hilde, Dupont, Patrick, Cassiman, David, Kempfle, Judith, Wuttke, Thomas V., Weber, Yvonne, Lerche, Holger, Afawi, Zaid, Vandenberghe, Wim, Korczyn, Amos D., Berkovic, Samuel F., Ekstein, Dana, Kivity, Sara, Ryvlin, Philippe, Claes, Lieve R. F., Deprez, Liesbet, Maljevic, Snezana, Vargas, Alberto, Van Dyck, Tine, Goossens, Dirk, Del-Favero, Jurgen, Van Laere, Koen, De Jonghe, Peter, Van Paesschen, Wim

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A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing von Hirsch, Yoel, Tangshewinsirikul, Chayada, Booth, Kevin T, Azaiez, Hela, Yefet, Devorah, Quint, Adina, Weiden, Tzvi, Brownstein, Zippora, Macarov, Michal, Davidov, Bella, Pappas, John, Rabin, Rachel, Kenna, Margaret A, Oza, Andrea M, Lafferty, Katherine, Amr, Sami S, Rehm, Heidi L, Kolbe, Diana L, Frees, Kathy, Nishimura, Carla, Luo, Minjie, Farra, Chantal, Morton, Cynthia C, Scher, Sholem Y, Ekstein, Josef, Avraham, Karen B, Smith, Richard J H, Shen, Jun

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Burrowing Owl (Athene cunicularia) nest phenology influenced by drought on nonbreeding grounds von Porro, Catie M, Desmond, Martha J, Savidge, Julie A, Abadi, Fitsum, Cruz-McDonnell, Kirsten K, Davis, Jennifer L, Griebel, Randall L, Ekstein, Rebecca T, Rodríguez, Nancy Hernandez

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ARSA Variant Associated With Late Infantile Metachromatic Leukodystrophy and Carrier Rate in Individuals of Ashkenazi Jewish Ancestry von Rabin, Rachel, Hirsch, Yoel, Booth, Kevin T A, Hall, Patricia L, Yachelevich, Naomi, Mistry, Pramod K, Ekstein, Josef, Pappas, John

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Low-level constitutional mosaicism of a de novoBRCA1 gene mutation von Friedman, E, Efrat, N, Soussan-Gutman, L, Dvir, A, Kaplan, Y, Ekstein, T, Nykamp, K, Powers, M, Rabideau, M, Sorenson, J, Topper, S

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Utilizing Ethnic-Specific Differences in Minor Allele Frequency to Recategorize Reported Pathogenic Deafness Variants von Shearer, A. Eliot, Eppsteiner, Robert W., Booth, Kevin T., Ephraim, Sean S., Gurrola, José, Simpson, Allen, Black-Ziegelbein, E. Ann, Joshi, Swati, Ravi, Harini, Giuffre, Angelica C., Happe, Scott, Hildebrand, Michael S., Azaiez, Hela, Bayazit, Yildirim A., Erdal, Mehmet Emin, Lopez-Escamez, Jose A., Gazquez, Irene, Tamayo, Marta L., Gelvez, Nancy Y., Leal, Greizy Lopez, Jalas, Chaim, Ekstein, Josef, Yang, Tao, Usami, Shin-ichi, Kahrizi, Kimia, Bazazzadegan, Niloofar, Najmabadi, Hossein, Scheetz, Todd E., Braun, Terry A., Casavant, Thomas L., LeProust, Emily M., Smith, Richard J.H.

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Carrier screening of RTEL1 mutations in the Ashkenazi Jewish population von Fedick, A.M., Shi, L., Jalas, C., Treff, N.R., Ekstein, J., Kornreich, R., Edelmann, L., Mehta, L., Savage, S.A.

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Epilepsy surgery in infants up to 3 months of age: Safety, feasibility, and outcomes: A multicenter, multinational study von Roth, Jonathan, Constantini, Shlomi, Ekstein, Margaret, Weiner, Howard L., Tripathi, Manjari, Chandra, Poodipedi Sarat, Cossu, Massimo, Rizzi, Michele, Bollo, Robert J., Machado, Hélio Rubens, Santos, Marcelo Volpon, Keating, Robert F., Oluigbo, Chima O., Rutka, James T., Drake, James M., Jallo, George I., Shimony, Nir, Treiber, Jeffrey M., Consales, Alessandro, Mangano, Francesco T., Wisoff, Jeffrey H., Teresa Hidalgo, Eveline, Bingaman, William E., Gupta, Ajay, Erdemir, Gozde, Sundar, Swetha J., Benifla, Mony, Shapira, Vladimir, Lam, Sandi K., Fallah, Aria, Maniquis, Cassia A. B., Tisdall, Martin, Chari, Aswin, Cinalli, Giuseppe, Blount, Jeffrey P., Dorfmüller, Georg, Christine Bulteau, Uliel‐Sibony, Shimrit

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Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss von Richard, Elodie M., Bakhtiari, Somayeh, Marsh, Ashley P.L., Kaiyrzhanov, Rauan, Wagner, Matias, Shetty, Sheetal, Pagnozzi, Alex, Nordlie, Sandra M., Cornejo, Patricia, Magee, Helen, Liu, James, Norton, Bethany Y., Webster, Richard I., Hakonarson, Hakon, Li, Jiankang, Guo, Yiran, Jain, Mahim, Blesson, Alyssa, Rodan, Lance H., Abbott, Mary-Alice, Comi, Anne, Cohen, Julie S., Alhaddad, Bader, Meitinger, Thomas, Lenz, Dominic, Ziegler, Andreas, Kotzaeridou, Urania, Brunet, Theresa, Chassevent, Anna, Smith-Hicks, Constance, Ekstein, Joseph, Weiden, Tzvi, Hahn, Andreas, Zharkinbekova, Nazira, Turnpenny, Peter, Tucci, Arianna, Yelton, Melissa, Horvath, Rita, Gungor, Serdal, Hiz, Semra, Oktay, Yavuz, Lochmuller, Hanns, Zollino, Marcella, Morleo, Manuela, Marangi, Giuseppe, Nigro, Vincenzo, Torella, Annalaura, Pinelli, Michele, Amenta, Simona, Husain, Ralf A., Grossmann, Benita, Rapp, Marion, Steen, Claudia, Marquardt, Iris, Grimmel, Mona, Grasshoff, Ute, Korenke, G. Christoph, Owczarek-Lipska, Marta, Neidhardt, John, Radio, Francesca Clementina, Mancini, Cecilia, Claps Sepulveda, Dianela Judith, McWalter, Kirsty, Begtrup, Amber, Crunk, Amy, Guillen Sacoto, Maria J., Schnur, Rhonda E., Mancardi, Maria Margherita, Kreuder, Florian, Striano, Pasquale, Zara, Federico, Chung, Wendy K., Marks, Warren A., van Eyk, Clare L., Webber, Dani L., Corbett, Mark A., Harper, Kelly, Berry, Jesia G., MacLennan, Alastair H., Gecz, Jozef, Tartaglia, Marco, Salpietro, Vincenzo, Christodoulou, John, Kaslin, Jan, Padilla-Lopez, Sergio, Bilguvar, Kaya, Munchau, Alexander, Ahmed, Zubair M., Hufnagel, Robert B., Fahey, Michael C., Maroofian, Reza, Houlden, Henry, Mane, Shrikant M., Rad, Aboulfazl, Jin, Sheng Chih, Haack, Tobias B., Makowski, Christine, Hirsch, Yoel, Riazuddin, Saima, Kruer, Michael C.

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Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation von Edvardson, Simon, Shaag, Avraham, Zenvirt, Shamir, Erlich, Yaniv, Hannon, Gregory J., Shanske, Alan L., Gomori, John Moshe, Ekstein, Joseph, Elpeleg, Orly

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Familial Dysautonomia Is Caused by Mutations of the IKAP Gene von Anderson, Sylvia L., Coli, Rocco, Daly, Ira W., Kichula, Elizabeth A., Rork, Matthew J., Volpi, Sabrina A., Ekstein, Josef, Rubin, Berish Y.

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A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews von Hirsch, Yoel, Zeevi, David A., Lam, Byron L., Scher, Sholem Y., Bringer, Rachel, Cherki, Bitya, Cohen, Cadina C., Muallem, Hagit, Chiang, John (Pei-Wen), Pantrangi, Madhulatha, Ekstein, Josef, Johansson, Martin M.

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Tracking inflammation in the epileptic rat brain by bi-functional fluorescent and magnetic nanoparticles von Portnoy, Emma, Polyak, Boris, Inbar, Dorrit, Kenan, Gilad, Rai, Ahmad, Wehrli, Suzanne L, Roberts, Timothy P.L, Bishara, Ameer, Mann, Aniv, Shmuel, Miriam, Rozovsky, Katya, Itzhak, Gal, Hur, Tamir Ben, Magdassi, Shlomo, Ekstein, Dana, Eyal, Sara

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