Consanguinity in a Midwestern United States Isolate

Por Hammond, David T., Jackson, Charles E.
Publicado em 1958

Revised 14.7-cM Locus for the Hyperparathyroidism–Jaw Tumor Syndrome Gene, HRPT2

Por Hobbs, Maurine R., Rosen, Irving B., Jackson, Charles E.
Publicado em 2002

X Chromosome Mapping of Genes for Red-Green Colorblindness and Xg

Por Jackson, Charles E., Symon, William E., Mann, Joseph D.
Publicado em 1964

Role of Nucleotide Binding in Septin-Septin Interactions and Septin Localization in Saccharomyces cerevisiae

Por Nagaraj, Satish, Rajendran, Ashok, Jackson, Charles E., Longtine, Mark S.
Publicado em 2008

Effects of Inhibiting VPS4 Support a General Role for ESCRTs in Extracellular Vesicle Biogenesis

Por Jackson, Charles E., Scruggs, Benjamin S., Schaffer, Jean E., Hanson, Phyllis I.
Publicado no Biophys J (2017)

Distinct Roles for CARMIL Isoforms in Cell Migration

Por Liang, Yun, Niederstrasser, Hanspeter, Edwards, Marc, Jackson, Charles E., Cooper, John A.
Publicado em 2009

Inheritance of Primary System Amyloidosis

Por Jackson, Charles E., Falls, Harold F., Block, Walter D., Rukavina, John K., Carey, Joshua H.
Publicado em 1960

Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish

Por McCauley, Jacob L, Hahs, Daniel W, Jiang, Lan, Scott, William K, Welsh-Bohmer, Kathleen A, Jackson, Charles E, Vance, Jeffery M, Pericak-Vance, Margaret A, Haines, Jonathan L
Publicado em 2006

Hereditary Hyperparathyroidism–Jaw Tumor Syndrome: The Endocrine Tumor Gene HRPT2 Maps to Chromosome 1q21-q31

Por Szabó, József, Heath, Brett, Hill, Virginia M., Jackson, Charles E., Zarbo, Richard J., Mallette, Lawrence E., Chew, Shern L., Besser, Gordon M., Thakker, Rajesh V., Huff, Vicki, Leppert, Mark F., Heath, Hunter
Publicado em 1995

Origin of Microsatellite Instability in Gastric Cancer

Por Halling, Kevin C., Harper, Jeffrey, Moskaluk, Christopher A., Thibodeau, Stephen N., Petroni, Gina R., Yustein, Aron S., Tosi, Piero, Minacci, Chiara, Roviello, Franco, Piva, Paolo, Hamilton, Stanley R., Jackson, Charles E., Powell, Steven M.
Publicado em 1999

Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish

Por EDWARDS, DIGNA R. VELEZ, GILBERT, JOHN R., JIANG, LAN, GALLINS, PAUL J., CAYWOOD, LAURA, CREASON, MARILYN, FUZZELL, DENISE, KNEBUSCH, CLARE, JACKSON, CHARLES E., PERICAK-VANCE, MARGARET A., HAINES, JONATHAN L., SCOTT, WILLIAM K.
Publicado em 2011

The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10

Por Wu, Jingshi, Carson, Nancy L., Myers, Shirley, Pakstis, Andrew J., Kidd, Judith R., Castiglione, Carmela M., Anderson, Linda, Hoyle, L. Suzanne, Genel, Myron, Verdy, Maurice, Jackson, Charles E., Simpson, Nancy E., Kidd, Kenneth K.
Publicado em 1990

Mitochondrial Haplogroup X is Associated with Successful Aging in the Amish

Por Courtenay, Monique D., Gilbert, John R., Jiang, Lan, Cummings, Anna C., Gallins, Paul J., Caywood, Laura, Reinhart-Mercer, Lori, Fuzzell, Denise, Knebusch, Claire, Laux, Renee, McCauley, Jacob L., Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L., Scott, William K.
Publicado no Hum Genet (2011)

A genome-wide linkage analysis of dementia in the Amish

Por Hahs, Daniel W., McCauley, Jacob L., Crunk, Amy E., McFarland, Lynne L., Gaskell, Perry C., Jiang, Lan, Slifer, Susan H., Vance, Jeffery M., Scott, William K., Welsh-Bohmer, Kathleen A., Johnson, Stephanie R., Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2006

Germline CDH1 deletions in hereditary diffuse gastric cancer families

Por Oliveira, Carla, Senz, Janine, Kaurah, Pardeep, Pinheiro, Hugo, Sanges, Remo, Haegert, Anne, Corso, Giovanni, Schouten, Jan, Fitzgerald, Rebecca, Vogelsang, Holger, Keller, Gisela, Dwerryhouse, Sarah, Grimmer, Donna, Chin, Suet-Feung, Yang, Han-Kwang, Jackson, Charles E., Seruca, Raquel, Roviello, Franco, Stupka, Elia, Caldas, Carlos, Huntsman, David
Publicado em 2009

Linkage and association of successful aging to the 6q25 region in large Amish kindreds

Por Edwards, Digna R. Velez, Gilbert, John R., Hicks, James E., Myers, Jamie L., Jiang, Lan, Cummings, Anna C., Guo, Shengru, Gallins, Paul J., Konidari, Ioanna, Caywood, Laura, Reinhart-Mercer, Lori, Fuzzell, Denise, Knebusch, Claire, Laux, Renee, Jackson, Charles E., Pericak-Vance, Margaret A., Haines, Jonathan L., Scott, William K.
Publicado em 2012

Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3

Por Senderek, Jan, Garvey, Sean M., Krieger, Michael, Guergueltcheva, Velina, Urtizberea, Andoni, Roos, Andreas, Elbracht, Miriam, Stendel, Claudia, Tournev, Ivailo, Mihailova, Violeta, Feit, Howard, Tramonte, Jeff, Hedera, Peter, Crooks, Kristy, Bergmann, Carsten, Rudnik-Schöneborn, Sabine, Zerres, Klaus, Lochmüller, Hanns, Seboun, Eric, Weis, Joachim, Beckmann, Jacques S., Hauser, Michael A., Jackson, Charles E.
Publicado em 2009

Identification of C7orf11 (TTDN1) Gene Mutations and Genetic Heterogeneity in Nonphotosensitive Trichothiodystrophy

Por Nakabayashi, Kazuhiko, Amann, Daniela, Ren, Yan, Saarialho-Kere, Ulpu, Avidan, Nili, Gentles, Simone, MacDonald, Jeffrey R., Puffenberger, Erik G., Christiano, Angela M., Martinez-Mir, Amalia, Salas-Alanis, Julio C., Rizzo, Renata, Vamos, Esther, Raams, Anja, Les, Clifford, Seboun, Eric, Jaspers, Nicolaas G. J., Beckmann, Jacques S., Jackson, Charles E., Scherer, Stephen W.
Publicado em 2005