Search Results - "Yamaguti, Paulo M"

Rehabilitation of an adolescent with autosomal dominant amelogenesis imperfecta: case report by Yamaguti, Paulo M, Acevedo, Ana C, de Paula, Lilian M

“…Amelogenesis imperfecta is a hereditary condition that affects tooth enamel without systemic involvement. In the most severely affected patients, teeth can…”
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Changes in amelogenesis in the rat incisor following short-term hypocalcaemia by Yamaguti, Paulo M., Arana-Chavez, Victor E., Acevedo, Ana Carolina

“…There is a relationship between hypocalcaemia and the enamel hypoplasia. Earlier studies in rats have reported a severe hypocalcaemia and enamel hypoplasia a…”
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Claudin‐16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation by Bardet, Claire, Courson, Frédéric, Wu, Yong, Khaddam, Mayssam, Salmon, Benjamin, Ribes, Sandy, Thumfart, Julia, Yamaguti, Paulo M, Rochefort, Gael Y, Figueres, Marie‐Lucile, Breiderhoff, Tilman, Garcia‐Castaño, Alejandro, Vallée, Benoit, Le Denmat, Dominique, Baroukh, Brigitte, Guilbert, Thomas, Schmitt, Alain, Massé, Jean‐Marc, Bazin, Dominique, Lorenz, Georg, Morawietz, Maria, Hou, Jianghui, Carvalho‐Lobato, Patricia, Manzanares, Maria Cristina, Fricain, Jean‐Christophe, Talmud, Deborah, Demontis, Renato, Neves, Francisco, Zenaty, Delphine, Berdal, Ariane, Kiesow, Andreas, Petzold, Matthias, Menashi, Suzanne, Linglart, Agnes, Acevedo, Ana Carolina, Vargas‐Poussou, Rosa, Müller, Dominik, Houillier, Pascal, Chaussain, Catherine

“…ABSTRACT Claudin‐16 protein (CLDN16) is a component of tight junctions (TJ) with a restrictive distribution so far demonstrated mainly in the kidney. Here, we…”
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Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations by Acevedo, Ana Carolina, Poulter, James A, Alves, Priscila Gomes, de Lima, Caroline Lourenço, Castro, Luiz Claudio, Yamaguti, Paulo Marcio, Paula, Lilian M, Parry, David A, Logan, Clare V, Smith, Claire E L, Johnson, Colin A, Inglehearn, Chris F, Mighell, Alan J

“…Raine syndrome (RS) is a rare autosomal recessive bone dysplasia typified by osteosclerosis and dysmorphic facies due to FAM20C mutations. Initially reported…”
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Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations by Jaureguiberry, Graciana, De la Dure-Molla, Muriel, Parry, David, Quentric, Mickael, Himmerkus, Nina, Koike, Toshiyasu, Poulter, James, Klootwijk, Enriko, Robinette, Steven L, Howie, Alexander J, Patel, Vaksha, Figueres, Marie-Lucile, Stanescu, Horia C, Issler, Naomi, Nicholson, Jeremy K, Bockenhauer, Detlef, Laing, Christopher, Walsh, Stephen B, McCredie, David A, Povey, Sue, Asselin, Audrey, Picard, Arnaud, Coulomb, Aurore, Medlar, Alan J, Bailleul-Forestier, Isabelle, Verloes, Alain, Le Caignec, Cedric, Roussey, Gwenaelle, Guiol, Julien, Isidor, Bertrand, Logan, Clare, Shore, Roger, Johnson, Colin, Inglehearn, Christopher, Al-Bahlani, Suhaila, Schmittbuhl, Matthieu, Clauss, François, Huckert, Mathilde, Laugel, Virginie, Ginglinger, Emmanuelle, Pajarola, Sandra, Spartà, Giuseppina, Bartholdi, Deborah, Rauch, Anita, Addor, Marie-Claude, Yamaguti, Paulo M, Safatle, Heloisa P, Acevedo, Ana Carolina, Martelli-Júnior, Hercílio, dos Santos Netos, Pedro E, Coletta, Ricardo D, Gruessel, Sandra, Sandmann, Carolin, Ruehmann, Denise, Langman, Craig B, Scheinman, Steven J, Ozdemir-Ozenen, Didem, Hart, Thomas C, Hart, P Suzanne, Neugebauer, Ute, Schlatter, Eberhard, Houillier, Pascal, Gahl, William A, Vikkula, Miikka, Bloch-Zupan, Agnès, Bleich, Markus, Kitagawa, Hiroshi, Unwin, Robert J, Mighell, Alan, Berdal, Ariane, Kleta, Robert

“…Calcium homeostasis requires regulated cellular and interstitial systems interacting to modulate the activity and movement of this ion. Disruption of these…”
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