Search Results - "Hart, Thomas C"

Emergence of corpse cremation during the Pre-Pottery Neolithic of the Southern Levant: A multidisciplinary study of a pyre-pit burial by Bocquentin, Fanny, Anton, Marie, Berna, Francesco, Rosen, Arlene, Khalaily, Hamoudi, Greenberg, Harris, Hart, Thomas C, Lernau, Omri, Horwitz, Liora Kolska

“…Renewed excavations at the Neolithic site of Beisamoun (Upper Jordan Valley, Israel) has resulted in the discovery of the earliest occurrence of an intentional…”
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Phenotype and Course of Hutchinson–Gilford Progeria Syndrome by Merideth, Melissa A, Gordon, Leslie B, Clauss, Sarah, Sachdev, Vandana, Smith, Ann C.M, Perry, Monique B, Brewer, Carmen C, Zalewski, Christopher, Kim, H. Jeffrey, Solomon, Beth, Brooks, Brian P, Gerber, Lynn H, Turner, Maria L, Domingo, Demetrio L, Hart, Thomas C, Graf, Jennifer, Reynolds, James C, Gropman, Andrea, Yanovski, Jack A, Gerhard-Herman, Marie, Collins, M.D. Francis S, Nabel, Elizabeth G, Cannon, Richard O, Gahl, William A, Introne, Wendy J

“…This article describes the detailed phenotype of 15 children, 1 to 17 years of age, with Hutchinson–Gilford progeria syndrome, a rare, sporadic autosomal…”
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Variable clinical presentation of an MUC1 mutation causing medullary cystic kidney disease type 1 by Bleyer, Anthony J, Kmoch, Stanislav, Antignac, Corinne, Robins, Vicki, Kidd, Kendrah, Kelsoe, John R, Hladik, Gerald, Klemmer, Philip, Knohl, Stephen J, Scheinman, Steven J, Vo, Nam, Santi, Ann, Harris, Alese, Canaday, Omar, Weller, Nelson, Hulick, Peter J, Vogel, Kristen, Rahbari-Oskoui, Frederick F, Tuazon, Jennifer, Deltas, Constantinos, Somers, Douglas, Megarbane, Andre, Kimmel, Paul L, Sperati, C John, Orr-Urtreger, Avi, Ben-Shachar, Shay, Waugh, David A, McGinn, Stella, Bleyer, Jr, Anthony J, Hodanová, Katerina, Vylet'al, Petr, Živná, Martina, Hart, Thomas C, Hart, P Suzanne

“…The genetic cause of medullary cystic kidney disease type 1 was recently identified as a cytosine insertion in the variable number of tandem repeat region of…”
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Interleukin 1 genetic tests provide no support for reduction of preventive dental care by Diehl, Scott R., PhD, Kuo, Fengshen, MS, PhD, Hart, Thomas C., DDS, PhD

“…Abstract Background It has been proposed that the PST and PerioPredict genetic tests that are based on polymorphisms in interleukin 1 (IL-1) genes identify a…”
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Disorders of human dentin by Hart, P Suzanne, Hart, Thomas C

“…Dentin, the most abundant tissue in teeth, is produced by odontoblasts, which differentiate from mesenchymal cells of the dental papilla. Dentinogenesis is a…”
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A characterization of the oral microbiome in allogeneic stem cell transplant patients by Ames, Nancy J, Sulima, Pawel, Ngo, Thoi, Barb, Jennifer, Munson, Peter J, Paster, Bruce J, Hart, Thomas C

“…The mouth is a complex biological structure inhabited by diverse bacterial communities. The purpose of this study is to describe the effects of allogeneic stem…”
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Mutant DLX 3 disrupts odontoblast polarization and dentin formation by Choi, S.J., Song, I.S., Feng, J.Q., Gao, T., Haruyama, N., Gautam, P., Robey, P.G., Hart, Thomas C.

“…Tricho-dento-osseous (TDO) syndrome is an autosomal dominant disorder characterized by abnormalities in the thickness and density of bones and teeth. A 4-bp…”
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Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4 by Wright, J Timothy, Hart, Thomas C, Hart, P Suzanne, Simmons, Darrin, Suggs, Cynthia, Daley, Bill, Simmer, Jim, Hu, Jan, Bartlett, John D, Li, Yong, Yuan, Zhi-An, Seow, W Kim, Gibson, Carolyn W

“…Amelogenesis imperfecta (AI) is caused by AMEL, ENAM, MMP20 and KLK4 gene mutations. Mice lacking expression of the AmelX, Enam and Mmp20 genes have been…”
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A Mutation in the SOS1 Gene Causes Hereditary Gingival Fibromatosis Type 1 by Hart, Thomas C., Zhang, Yingze, Gorry, Michael C., Hart, P. Suzanne, Cooper, Margaret, Marazita, Mary L., Marks, Jared M., Cortelli, Jose R., Pallos, Debora

“…Hereditary gingival fibromatosis (HGF) is a rare, autosomal dominant form of gingival overgrowth. Affected individuals have a benign, slowly progressive,…”
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Evaluating the usefulness of phytoliths and starch grains found on survey artifacts by Hart, Thomas C.

“…Archaeologists use survey artifacts to study any number of interesting topics. The focus of this study is to test the usefulness of starch grains and…”
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Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein by Bleyer, Anthony J., Hart, Thomas C., Shihabi, Zak, Robins, Vicki, Hoyer, John R.

“…Mutations in the uromodulin gene decrease urinary excretion of Tamm-Horsfall protein. Mutations in the uromodulin (UMOD) gene that encodes Tamm-Horsfall…”
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Heritability of Oral Microbial Species in Caries-Active and Caries-Free Twins by Corby, Patricia M., Bretz, Walter A., Hart, Thomas C., Schork, Nicholas J., Wessel, J, Lyons-Weiler, James, Paster, Bruce J.

“…Oral microbes that colonize in the mouths of humans contribute to disease susceptibility, but it is unclear if host genetic factors mediate colonization. We…”
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Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome by Hart, Thomas C, Hart, P Suzanne, Bowden, Donald W, Michalec, Michael D, Callison, Scott A, Walker, Steve J, Zhang, Yingze, Firatli, Erhan

“…Papillon-Lefèvre syndrome (PLS) is an autosomal recessive disorder characterised by palmoplantar hyperkeratosis and severe early onset periodontitis that…”
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A Critical Assessment of Interleukin‐1 (IL‐1) Genotyping When Used in a Genetic Susceptibility Test for Severe Chronic Periodontitis by Greenstein, Gary, Hart, Thomas C

“…Background: This review addresses the ability of commercially available genetic susceptibility test to determine the risk of developing severe chronic…”
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Mutant Tamm-Horsfall glycoprotein accumulation in endoplasmic reticulum induces apoptosis reversed by colchicine and sodium 4-phenylbutyrate by SUNG WON CHOI, OK HEE RYU, SUN JIN CHOI, IN SUN SONG, BLEYER, Anthony J, HART, Thomas C

“…As a consequence of uromodulin gene mutations, individuals develop precocious hyperuricemia, gout, and progressive renal failure. In vitro studies suggest that…”
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Germ Line Gain of Function with SOS1 Mutation in Hereditary Gingival Fibromatosis by Jang, Shyh-Ing, Lee, Eun-Jin, Hart, P. Suzanne, Ramaswami, Mukundhan, Pallos, Debora, Hart, Thomas C.

“…Mutation of human SOS1 is responsible for hereditary gingival fibromatosis type 1, a benign overgrowth condition of the gingiva. Here, we investigated…”
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Changes in salivary proteome following allogeneic hematopoietic stem cell transplantation by Imanguli, Matin M, Atkinson, Jane C, Harvey, Kristen E, Hoehn, Gerard T, Ryu, Ok Hee, Wu, Tianxia, Kingman, Albert, Barrett, A. John, Bishop, Michael R, Childs, Richard W, Fowler, Daniel H, Pavletic, Steven Z, Hart, Thomas C

“…Objective Allogeneic hematopoietic stem cell transplantation (allo-HCT) is frequently complicated by severe infections and graft-vs-host disease (GVHD). Saliva…”
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The burning issue of dung in archaeobotanical samples: a case-study integrating macro-botanical remains, dung spherulites, and phytoliths to assess sample origin and fuel use at Tell Zeidan, Syria by Smith, Alexia, Proctor, Lucas, Hart, Thomas C., Stein, Gil J.

“…Since Naomi Miller’s first discussion of dung fuel within macro-botanical samples from Malyan, Iran, considerations of dung fuel across Southwest Asia have…”
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The American Dental Association Caries Classification System for clinical practice: a report of the American Dental Association Council on Scientific Affairs by Young, Douglas A, Nový, Brian B, Zeller, Gregory G, Hale, Robert, Hart, Thomas C, Truelove, Edmond L

“…The caries lesion, the most commonly observed sign of dental caries disease, is the cumulative result of an imbalance in the dynamic demineralization and…”
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The American Dental Association Caries Classification System for Clinical Practice by Young, Douglas A., DDS, EdD, MBA, MS, Nový, Brian B., DDS, Zeller, Gregory G., DDS, MS, Hale, Robert, DDS, Hart, Thomas C., DDS, PhD, Truelove, Edmond L., DDS, MSD

“…Abstract Background The caries lesion, the most commonly observed sign of dental caries disease, is the cumulative result of an imbalance in the dynamic…”
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