Diagnosis of acute bone/bone marrow infarction of the mandible in sickle hemoglobinopathy : Report of a case von PODLESH, S. W, BOYDEN, D. K

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Location of incisive canal in relation to central incisor implants von Kraut, R A, Boyden, D K

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Protoplanetary Disk Properties in the Orion Nebula Cluster: Initial Results from Deep, High-resolution ALMA Observations von Eisner, J. A., Arce, H. G., Ballering, N. P., Bally, J., Andrews, S. M., Boyden, R. D., Francesco, J. Di, Fang, M., Johnstone, D., Kim, J. S., Mann, R. K., Matthews, B., Pascucci, I., Ricci, L., Sheehan, P. D., Williams, J. P.

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Gamma frequency sensory stimulation in mild probable Alzheimer's dementia patients: Results of feasibility and pilot studies von Chan, Diane, Suk, Ho-Jun, Jackson, Brennan L, Milman, Noah P, Stark, Danielle, Klerman, Elizabeth B, Kitchener, Erin, Fernandez Avalos, Vanesa S, de Weck, Gabrielle, Banerjee, Arit, Beach, Sara D, Blanchard, Joel, Stearns, Colton, Boes, Aaron D, Uitermarkt, Brandt, Gander, Phillip, Howard, 3rd, Matthew, Sternberg, Eliezer J, Nieto-Castanon, Alfonso, Anteraper, Sheeba, Whitfield-Gabrieli, Susan, Brown, Emery N, Boyden, Edward S, Dickerson, Bradford C, Tsai, Li-Huei

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An Ultra-Sensitive Step-Function Opsin for Minimally Invasive Optogenetic Stimulation in Mice and Macaques von Gong, Xin, Mendoza-Halliday, Diego, Ting, Jonathan T., Kaiser, Tobias, Sun, Xuyun, Bastos, André M., Wimmer, Ralf D., Guo, Baolin, Chen, Qian, Zhou, Yang, Pruner, Maxwell, Wu, Carolyn W.-H., Park, Demian, Deisseroth, Karl, Barak, Boaz, Boyden, Edward S., Miller, Earl K., Halassa, Michael M., Fu, Zhanyan, Bi, Guoqiang, Desimone, Robert, Feng, Guoping

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Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease von Lalaoui, Najoua, Boyden, Steven E., Oda, Hirotsugu, Wood, Geryl M., Stone, Deborah L., Chau, Diep, Liu, Lin, Stoffels, Monique, Kratina, Tobias, Lawlor, Kate E., Zaal, Kristien J. M., Hoffmann, Patrycja M., Etemadi, Nima, Shield-Artin, Kristy, Biben, Christine, Tsai, Wanxia Li, Blake, Mary D., Kuehn, Hye Sun, Yang, Dan, Anderton, Holly, Silke, Natasha, Wachsmuth, Laurens, Zheng, Lixin, Moura, Natalia Sampaio, Beck, David B., Gutierrez-Cruz, Gustavo, Ombrello, Amanda K., Pinto-Patarroyo, Gineth P., Kueh, Andrew J., Herold, Marco J., Hall, Cathrine, Wang, Hongying, Chae, Jae Jin, Dmitrieva, Natalia I., McKenzie, Mark, Light, Amanda, Barham, Beverly K., Jones, Anne, Romeo, Tina M., Zhou, Qing, Aksentijevich, Ivona, Mullikin, James C., Gross, Andrew J., Shum, Anthony K., Hawkins, Edwin D., Masters, Seth L., Lenardo, Michael J., Boehm, Manfred, Rosenzweig, Sergio D., Pasparakis, Manolis, Voss, Anne K., Gadina, Massimo, Kastner, Daniel L., Silke, John

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Expansion sequencing: Spatially precise in situ transcriptomics in intact biological systems von Alon, Shahar, Goodwin, Daniel R, Sinha, Anubhav, Wassie, Asmamaw T, Chen, Fei, Daugharthy, Evan R, Bando, Yosuke, Kajita, Atsushi, Xue, Andrew G, Marrett, Karl, Prior, Robert, Cui, Yi, Payne, Andrew C, Yao, Chun-Chen, Suk, Ho-Jun, Wang, Ru, Yu, Chih-Chieh Jay, Tillberg, Paul, Reginato, Paul, Pak, Nikita, Liu, Songlei, Punthambaker, Sukanya, Iyer, Eswar P R, Kohman, Richie E, Miller, Jeremy A, Lein, Ed S, Lako, Ana, Cullen, Nicole, Rodig, Scott, Helvie, Karla, Abravanel, Daniel L, Wagle, Nikhil, Johnson, Bruce E, Klughammer, Johanna, Slyper, Michal, Waldman, Julia, Jané-Valbuena, Judit, Rozenblatt-Rosen, Orit, Regev, Aviv, Church, George M, Marblestone, Adam H, Boyden, Edward S

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A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency von Jabara, Haifa H, Boyden, Steven E, Chou, Janet, Ramesh, Narayanaswamy, Massaad, Michel J, Benson, Halli, Bainter, Wayne, Fraulino, David, Rahimov, Fedik, Sieff, Colin, Liu, Zhi-Jian, Alshemmari, Salem H, Al-Ramadi, Basel K, Al-Dhekri, Hasan, Arnaout, Rand, Abu-Shukair, Mohammad, Vatsayan, Anant, Silver, Eli, Ahuja, Sanjay, Davies, E Graham, Sola-Visner, Martha, Ohsumi, Toshiro K, Andrews, Nancy C, Notarangelo, Luigi D, Fleming, Mark D, Al-Herz, Waleed, Kunkel, Louis M, Geha, Raif S

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High Bone Density Due to a Mutation in LDL-Receptor–Related Protein 5 von Boyden, Lynn M, Mao, Junhao, Belsky, Joseph, Mitzner, Lyle, Farhi, Anita, Mitnick, Mary A, Wu, Dianqing, Insogna, Karl, Lifton, Richard P

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HLA and autoantibodies define scleroderma subtypes and risk in African and European Americans and suggest a role for molecular mimicry von Gourh, Pravitt, Safran, Sarah A., Alexander, Theresa, Boyden, Steven E., Morgan, Nadia D., Shah, Ami A., Mayes, Maureen D., Doumatey, Ayo, Bentley, Amy R., Shriner, Daniel, Domsic, Robyn T., Medsger, Thomas A., Ramos, Paula S., Silver, Richard M., Steen, Virginia D., Varga, John, Hsu, Vivien, Saketkoo, Lesley Ann, Schiopu, Elena, Khanna, Dinesh, Gordon, Jessica K., Kron, Brynn, Criswell, Lindsey A., Gladue, Heather, Derk, Chris T., Bernstein, Elana J., Bridges, S. Louis, Shanmugam, Victoria K., Kolstad, Kathleen D., Chung, Lorinda, Kafaja, Suzanne, Jan, Reem, Trojanowski, Marcin, Goldberg, Avram, Korman, Benjamin D., Steinbacha, Peter J., Chandrasekharappab, Settara C., Mullikinc, James C., Adeyemo, Adebowale, Rotimi, Charles, Wigley, Fredrick M., Kastner, Daniel L., Boin, Francesco, Remmers, Elaine F.

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Integrated Neurophotonics: Toward Dense Volumetric Interrogation of Brain Circuit Activity—at Depth and in Real Time von Moreaux, Laurent C., Yatsenko, Dimitri, Sacher, Wesley D., Choi, Jaebin, Lee, Changhyuk, Kubat, Nicole J., Cotton, R. James, Boyden, Edward S., Lin, Michael Z., Tian, Lin, Tolias, Andreas S., Poon, Joyce K.S., Shepard, Kenneth L., Roukes, Michael L.

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High-speed mapping of synaptic connectivity using photostimulation in Channelrhodopsin-2 transgenic mice von Wang, H, Peca, J, Matsuzaki, M, Matsuzaki, K, Noguchi, J, Qiu, L, Wang, D, Zhang, F, Boyden, E, Deisseroth, K, Kasai, H, Hall, W.C, Feng, G, Augustine, G.J

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Vibratory Urticaria Associated with a Missense Variant in ADGRE2 von Boyden, Steven E, Desai, Avanti, Cruse, Glenn, Young, Michael L, Bolan, Hyejeong C, Scott, Linda M, Eisch, A. Robin, Long, R. Daniel, Lee, Chyi-Chia R, Satorius, Colleen L, Pakstis, Andrew J, Olivera, Ana, Mullikin, James C, Chouery, Eliane, Mégarbané, André, Medlej-Hashim, Myrna, Kidd, Kenneth K, Kastner, Daniel L, Metcalfe, Dean D, Komarow, Hirsh D

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Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities von Boyden, Lynn M., Choi, Murim, Choate, Keith A., Nelson-Williams, Carol J., Farhi, Anita, Toka, Hakan R., Tikhonova, Irina R., Bjornson, Robert, Mane, Shrikant M., Colussi, Giacomo, Lebel, Marcel, Gordon, Richard D., Semmekrot, Ben A., Poujol, Alain, Välimäki, Matti J., De Ferrari, Maria E., Sanjad, Sami A., Gutkin, Michael, Karet, Fiona E., Tucci, Joseph R., Stockigt, Jim R., Keppler-Noreuil, Kim M., Porter, Craig C., Anand, Sudhir K., Whiteford, Margo L., Davis, Ira D., Dewar, Stephanie B., Bettinelli, Alberto, Fadrowski, Jeffrey J., Belsha, Craig W., Hunley, Tracy E., Nelson, Raoul D., Trachtman, Howard, Cole, Trevor R. P., Pinsk, Maury, Bockenhauer, Detlef, Shenoy, Mohan, Vaidyanathan, Priya, Foreman, John W., Rasoulpour, Majid, Thameem, Farook, Al-Shahrouri, Hania Z., Radhakrishnan, Jai, Gharavi, Ali G., Goilav, Beatrice, Lifton, Richard P.

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Phenotypic spectrum of autosomal recessive congenital ichthyosis due to PNPLA1 mutation von Boyden, L.M., Craiglow, B.G., Hu, R.H., Zhou, J., Browning, J., Eichenfield, L., Lim, Y.L., Luu, M., Randolph, L.M., Ginarte, M., Fachal, L., Rodriguez‐Pazos, L., Vega, A., Kramer, D., Yosipovitch, G., Vahidnezhad, H., Youssefian, L., Uitto, J., Lifton, R.P., Paller, A.S., Milstone, L.M., Choate, K.A.

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Imaging mass cytometry and multiplatform genomics define the phenogenomic landscape of breast cancer von Ali, H Raza, Jackson, Hartland W, Zanotelli, Vito R T, Danenberg, Esther, Fischer, Jana R, Bardwell, Helen, Provenzano, Elena, Rueda, Oscar M, Chin, Suet-Feung, Aparicio, Samuel, Caldas, Carlos, Bodenmiller, Bernd

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Three-dimensional imaging mass cytometry for highly multiplexed molecular and cellular mapping of tissues and the tumor microenvironment von Kuett, Laura, Catena, Raúl, Özcan, Alaz, Plüss, Alex, Schraml, Peter, Moch, Holger, de Souza, Natalie, Bodenmiller, Bernd

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Wide-field three-photon excitation in biological samples von Rowlands, Christopher J, Park, Demian, Bruns, Oliver T, Piatkevich, Kiryl D, Fukumura, Dai, Jain, Rakesh K, Bawendi, Moungi G, Boyden, Edward S, So, Peter TC

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An Ultra-Sensitive Step-Function Opsin for Minimally Invasive Optogenetic Stimulation in Mice and Macaques von Gong, Xin, Mendoza-Halliday, Diego, Ting, Jonathan T., Kaiser, Tobias, Sun, Xuyun, Bastos, André M., Wimmer, Ralf D., Guo, Baolin, Chen, Qian, Zhou, Yang, Pruner, Maxwell, Wu, Carolyn W.-H., Park, Demian, Deisseroth, Karl, Barak, Boaz, Boyden, Edward S., Miller, Earl K., Halassa, Michael M., Fu, Zhanyan, Bi, Guoqiang, Desimone, Robert, Feng, Guoping

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Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210 von Smits, Patrick, Bolton, Andrew D, Funari, Vincent, Hong, Minh, Boyden, Eric D, Lu, Lei, Manning, Danielle K, Dwyer, Noelle D, Moran, Jennifer L, Prysak, Mary, Merriman, Barry, Nelson, Stanley F, Bonafé, Luisa, Superti-Furga, Andrea, Ikegawa, Shiro, Krakow, Deborah, Cohn, Daniel H, Kirchhausen, Tom, Warman, Matthew L, Beier, David R

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