Electron tomography of fiber cell cytoplasm and dense cores of multilamellar bodies from human age-related nuclear cataracts von Costello, M. Joseph, Burette, Alain, Weber, Mariko, Metlapally, Sangeetha, Gilliland, Kurt O., Fowler, W. Craig, Mohamed, Ashik, Johnsen, Sönke

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Measurement of Fronto-limbic Activity Using an Emotional Oddball Task in Children with Familial High Risk for Schizophrenia von Hart, Sarah J., Shaffer, Joseph J., Bizzell, Joshua, Weber, Mariko, McMahon, Mary A., Gu, Hongbin, Perkins, Diana O., Belger, Aysenil

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Measurement of Fronto-limbic Activity Using an Emotional Oddball Task in Children with Familial High Risk for Schizophrenia von Hart, Sarah J, Shaffer, Joseph J, Bizzell, Joshua, Weber, Mariko, McMahon, Mary A, Gu, Hongbin, Perkins, Diana O, Belger, Aysenil

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Network analysis of epidermal growth factor signaling using integrated genomic, proteomic and phosphorylation data von Waters, Katrina M, Liu, Tao, Quesenberry, Ryan D, Willse, Alan R, Bandyopadhyay, Somnath, Kathmann, Loel E, Weber, Thomas J, Smith, Richard D, Wiley, H Steven, Thrall, Brian D

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Multiple endocrine neoplasia type 4: a new member of the MEN family von Singeisen, Hélène, Renzulli, Mariko Melanie, Pavlicek, Vojtech, Probst, Pascal, Hauswirth, Fabian, Muller, Markus K, Adamczyk, Magdalene, Weber, Achim, Kaderli, Reto Martin, Renzulli, Pietro

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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections von Mis, Emily K., Brodsky, Nina N., Ionita, Cristian, Darbinyan, Armine, Drummond-Borg, Margaret, McGee, Elisabeth, Nugent, Kimberly, Ortega, Lucy, Goodkin, Howard P., Sapp, Katie, McKee, Shane, Rea, Gillian, Cooper, Nicola, O’Driscoll, Mary, Scurr, Ingrid, Abbs, Steve, Armstrong, Ruth, Raymond, Lucy, Green, Andrew, Cleary, Elaine, Lampe, Anne, Castle, Bruce, Loughlin, Sam, Izatt, Louise, Roworth, Wendy, Yau, Shu, Jewell, Rosalyn, Sarkar, Ajoy, Canham, Natalie, Burkitt-Wright, Emma, Jones, Elizabeth, Smith, Audrey, Wright, Ronnie, Henderson, Alex, Allen, Zoe, Bernhard, Birgitta, Busby, Louise, Clowes, Virginia, Blair, Edward, Stewart, Alison, Kamath, Arveen, Halai, D., Holman, J.E., Jackson, R., Lopez, F.J., Rogers, T., Savage, K., Sieghart, A., Thomas, E.R.A., Thompson, S.R., Tucci, A., Alejandro, Mercedes E., Amendola, Laura, Andrews, Ashley, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bamshad, Michael, Bayrak-Toydemir, Pinar, Botto, Lorenzo, Coakley, Terra R., Coggins, Matthew, Cooper, Cynthia M., Cunningham, Michael, Dai, Hongzheng, Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Hahn, Sihoun, Hanchard, Neil A., Hayes, Nichole, High, Frances, Hisama, Fuki M., Holm, Ingrid A., Jamal, Fariha, Kennedy, Jennifer, LeBlanc, Kimberly, Macnamara, Ellen F., Maduro, Valerie V., Mak, Bryan, McCauley, Jacob, McGee, Elisabeth, Nickerson, Deborah, Nieves-Rodriguez, Shirley, Novacic, Donna, Pace, Laura, Potocki, Lorraine, Quinlan, Aaron, Raja, Archana N., Robertson, Amy K., Rodan, Lance H., Saporta, Mario, Schaechter, Judy, Signer, Rebecca, Solem, Emily, Solnica-Krezel, Lilianna, Sutton, Shirley, Velinder, Matt, Wheeler, Matthew T., Khokha, Mustafa K.

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Multiple endocrine neoplasia type 4: a new member of the MEN family von Singeisen, Hélène, Renzulli, Mariko Melanie, Pavlicek, Vojtech, Probst, Pascal, Hauswirth, Fabian, Muller, Markus K, Adamczyk, Magdalene, Weber, Achim, Kaderli, Reto Martin, Renzulli, Pietro

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Mouse p150Glued(Dynactin 1) cDNA Sequence and Evaluation as a Candidate for the Neuromuscular Disease Mutationmnd2 von Jang, Wonhee, Weber, John S., Tokito, Mariko K., Holzbaur, Erika L.F., Meisler, Miriam H.

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