Convertible Securities: A Complete Guide to Investment and Corporate Financing Strategies von Maitland, Tracy V, Nelson, F. Barry, Partlow, Dan

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Mismatch in SIRPα, a regulatory protein in innate immunity, is associated with chronic GVHD in hematopoietic stem cell transplantation von Saliba, Rima M., Greenbaum, Uri, Ma, Qing, Srour, Samer A., Carmazzi, Yudith, Li, Liang, Oran, Betul, Moller, Michael, Wood, Janet, Ciurea, Stefan O., Kongtim, Piyanuch, Rondon, Gabriela, Partlow, David, Li, Dan, Rezvani, Katayoun, Shpall, Elizabeth J., Cao, Kai, Champlin, Richard E., Zou, Jun

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Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures von Zhang, Xiaochang, Ling, Jiqiang, Barcia, Giulia, Jing, Lili, Wu, Jiang, Barry, Brenda J., Mochida, Ganeshwaran H., Hill, R. Sean, Weimer, Jill M., Stein, Quinn, Poduri, Annapurna, Partlow, Jennifer N., Ville, Dorothée, Dulac, Olivier, Yu, Tim W., Lam, Anh-Thu N., Servattalab, Sarah, Rodriguez, Jacqueline, Boddaert, Nathalie, Munnich, Arnold, Colleaux, Laurence, Zon, Leonard I., Söll, Dieter, Walsh, Christopher A., Nabbout, Rima

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Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number von Hu, Wen F., Pomp, Oz, Ben-Omran, Tawfeg, Kodani, Andrew, Henke, Katrin, Mochida, Ganeshwaran H., Yu, Timothy W., Woodworth, Mollie B., Bonnard, Carine, Raj, Grace Selva, Tan, Thong Teck, Hamamy, Hanan, Masri, Amira, Shboul, Mohammad, Al Saffar, Muna, Partlow, Jennifer N., Al-Dosari, Mohammed, Alazami, Anas, Alowain, Mohammed, Alkuraya, Fowzan S., Reiter, Jeremy F., Harris, Matthew P., Reversade, Bruno, Walsh, Christopher A.

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Laws of the state of Illinois applicable to the city of Danville, and the ordinances of said city / compiled and arranged by O.M. Jones and A.A. Partlow ; published by the authority of the City Council of the city of Danville, Illinois von Illinois

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CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development von Mochida, Ganeshwaran H, Ganesh, Vijay S, de Michelena, Maria I, Dias, Hugo, Atabay, Kutay D, Kathrein, Katie L, Huang, Hsuan-Ting, Hill, R Sean, Felie, Jillian M, Rakiec, Daniel, Gleason, Danielle, Hill, Anthony D, Malik, Athar N, Barry, Brenda J, Partlow, Jennifer N, Tan, Wen-Hann, Glader, Laurie J, Barkovich, A James, Dobyns, William B, Zon, Leonard I, Walsh, Christopher A

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Somatic Mutations in Cerebral Cortical Malformations von Jamuar, Saumya S, Lam, Anh-Thu N, Kircher, Martin, D’Gama, Alissa M, Wang, Jian, Barry, Brenda J, Zhang, Xiaochang, Hill, Robert Sean, Partlow, Jennifer N, Rozzo, Aldo, Servattalab, Sarah, Mehta, Bhaven K, Topcu, Meral, Amrom, Dina, Andermann, Eva, Dan, Bernard, Parrini, Elena, Guerrini, Renzo, Scheffer, Ingrid E, Berkovic, Samuel F, Leventer, Richard J, Shen, Yiping, Wu, Bai Lin, Barkovich, A. James, Sahin, Mustafa, Chang, Bernard S, Bamshad, Michael, Nickerson, Deborah A, Shendure, Jay, Poduri, Annapurna, Yu, Timothy W, Walsh, Christopher A

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Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry von Morrow, Eric M, Yoo, Seung-Yun, Flavell, Steven W, Kim, Tae-Kyung, Lin, Yingxi, Hill, Robert Sean, Mukaddes, Nahit M, Balkhy, Soher, Gascon, Generoso, Hashmi, Asif, Al-Saad, Samira, Ware, Janice, Joseph, Robert M, Greenblatt, Rachel, Gleason, Danielle, Ertelt, Julia A, Apse, Kira A, Bodell, Adria, Partlow, Jennifer N, Barry, Brenda, Yao, Hui, Markianos, Kyriacos, Ferland, Russell J, Greenberg, Michael E, Walsh, Christopher A

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Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder von Dias, Caroline M., Punetha, Jaya, Zheng, Céline, Mazaheri, Neda, Rad, Abolfazl, Efthymiou, Stephanie, Petersen, Andrea, Dehghani, Mohammadreza, Pehlivan, Davut, Partlow, Jennifer N., Posey, Jennifer E., Salpietro, Vincenzo, Gezdirici, Alper, Malamiri, Reza Azizi, Al Menabawy, Nihal M., Selim, Laila A., Vahidi Mehrjardi, Mohammad Yahya, Banu, Selina, Polla, Daniel L., Yang, Edward, Rezazadeh Varaghchi, Jamileh, Mitani, Tadahiro, van Beusekom, Ellen, Najafi, Maryam, Sedaghat, Alireza, Keller-Ramey, Jennifer, Durham, Leslie, Coban-Akdemir, Zeynep, Karaca, Ender, Orlova, Valeria, Schaeken, Lieke L.M., Sherafat, Amir, Jhangiani, Shalini N., Stanley, Valentina, Shariati, Gholamreza, Galehdari, Hamid, Gleeson, Joseph G., Walsh, Christopher A., Lupski, James R., Seiradake, Elena, Houlden, Henry, van Bokhoven, Hans, Maroofian, Reza

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Silk Fibroin Degradation Related to Rheological and Mechanical Properties von Partlow, Benjamin P., Tabatabai, A. Pasha, Leisk, Gary G., Cebe, Peggy, Blair, Daniel L., Kaplan, David L.

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Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy von Osborn, Daniel P.S., Pond, Heather L., Mazaheri, Neda, Dejardin, Jeremy, Munn, Christopher J., Mushref, Khaloob, Cauley, Edmund S., Moroni, Isabella, Pasanisi, Maria Barbara, Sellars, Elizabeth A., Hill, R. Sean, Partlow, Jennifer N., Willaert, Rebecca K., Bharj, Jaipreet, Malamiri, Reza Azizi, Galehdari, Hamid, Shariati, Gholamreza, Maroofian, Reza, Mora, Marina, Swan, Laura E., Voit, Thomas, Conti, Francesco J., Jamshidi, Yalda, Manzini, M. Chiara

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Silk Molecular Weight Influences the Kinetics of Enzymatically Cross-linked Silk Hydrogel Formation von Tabatabai, A. Pasha, Partlow, Benjamin P, Raia, Nicole R, Kaplan, David L, Blair, Daniel L

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A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts von Mochida, Ganeshwaran H., Ganesh, Vijay S., Felie, Jillian M., Gleason, Danielle, Hill, R. Sean, Clapham, Katie Rose, Rakiec, Daniel, Tan, Wen-Hann, Akawi, Nadia, Al-Saffar, Muna, Partlow, Jennifer N., Tinschert, Sigrid, Barkovich, A. James, Ali, Bassam, Al-Gazali, Lihadh, Walsh, Christopher A.

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Convertible Securities von Maitland, Tracy V, Nelson, F. Barry, Partlow, Daniel

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Convertible Securities: A Complete Guide to Investment And: A Complete Guide to Investment and Corporate Financing Strategies von Maitland, Tracy V, Nelson, F. Barry, Partlow, Daniel

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Levodopa and the Progression of Parkinson's Disease von Fahn, Stanley, Oakes, David, Shoulson, Ira, Kieburtz, Karl, Rudolph, Alice, Lang, Anthony, Olanow, C Warren, Tanner, Caroline, Marek, Kenneth

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Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome von Evrony, Gilad D, Cordero, Dwight R, Shen, Jun, Partlow, Jennifer N, Yu, Timothy W, Rodin, Rachel E, Hill, R Sean, Coulter, Michael E, Lam, Anh-Thu N, Jayaraman, Divya, Gerrelli, Dianne, Diaz, Diana G, Santos, Chloe, Morrison, Victoria, Galli, Antonella, Tschulena, Ulrich, Wiemann, Stefan, Martel, M Jocelyne, Spooner, Betty, Ryu, Steven C, Elhosary, Princess C, Richardson, Jillian M, Tierney, Danielle, Robinson, Christopher A, Chibbar, Rajni, Diudea, Dana, Folkerth, Rebecca, Wiebe, Sheldon, Barkovich, A James, Mochida, Ganeshwaran H, Irvine, James, Lemire, Edmond G, Blakley, Patricia, Walsh, Christopher A

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Multi-targeted 1H/19F MRI unmasks specific danger patterns for emerging cardiovascular disorders von Flögel, Ulrich, Temme, Sebastian, Jacoby, Christoph, Oerther, Thomas, Keul, Petra, Flocke, Vera, Wang, Xiaowei, Bönner, Florian, Nienhaus, Fabian, Peter, Karlheinz, Schrader, Jürgen, Grandoch, Maria, Kelm, Malte, Levkau, Bodo

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Developmental and degenerative features in a complicated spastic paraplegia von Manzini, M. Chiara, Rajab, Anna, Maynard, Thomas M., Mochida, Ganeshwaran H., Tan, Wen-Hann, Nasir, Ramzi, Hill, R. Sean, Gleason, Danielle, Al Saffar, Muna, Partlow, Jennifer N., Barry, Brenda J., Vernon, Mike, LaMantia, Anthony-Samuel, Walsh, Christopher A.

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Water quality impacts of small-scale hydromodification in an urban stream in Connecticut, USA von Zhu, Bin, Smith, Daniel S., Benaquista, Anthony P., Rossi, Dylan M., Kadapuram, Betsy M., Yu, Man Lok, Partlow, Andrew S., Burtch, Nathan R.

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