Search Results - Ogata, T.

Dermatoscopic and clinical features of congenital or congenital-type nail matrix nevi: a multicenter prospective cohort study by the International Dermoscopy Society by Pham, Félix (Author) , Boespflug, Amélie (Author) , Duru, Gérard (Author) , Phan, Alice (Author) , Poulalhon, Nicolas (Author) , Weiler, Laura (Author) , Tanaka, Masaru (Author) , Lallas, Aimilios (Author) , Ogata, Dai (Author) , Davaine, Anne Céline (Author) , Bahadoran, Philippe (Author) , Balguerie, Xavier (Author) , Kamińska-Winciorek, Grażyna (Author) , Tromme, Isabelle (Author) , Correia, Osvaldo (Author) , Kim, Moon-Bum (Author) , Marghoob, Ashfaq A. (Author) , Martin, Linda (Author) , Pascale Guitera, Pascale (Author) , Meziane, Mariame (Author) , Miquel, Juliette (Author) , Mun, Je-Ho (Author) , Argenziano, Giuseppe (Author) , Bessis, Didier (Author) , Bourke, Johnny (Author) , Mijuskovic, Zeljko (Author) , Chiaverini, Christine (Author) , Corven-Benoit, Cloé (Author) , Droitcourt, Catherine (Author) , Skowron, François (Author) , Marque, Myriam (Author) , Zalaudek, Iris (Author) , Rosendahl, Cliff (Author) , Moreno-Ramirez, David (Author) , Vabres, Pierre (Author) , Hänßle, Holger (Author) , Malvehy, Josep (Author) , Puig, Susana (Author) , Robert, Caroline (Author) , Schopf, Thomas R. (Author) , Scope, Alon (Author) , Dalle, Stéphane (Author) , Thomas, Luc (Author) ,

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The bulge radial velocity assay for RR Lyrae stars (BRAVA-RR) DR2: a bimodal bulge? by Kunder, Andrea (Author) , Pérez-Villegas, Angeles (Author) , Rich, R. Michael (Author) , Ogata, Jonathan (Author) , Murari, Emma (Author) , Boren, Emilie (Author) , Johnson, Christian I. (Author) , Nataf, David (Author) , Walker, Alistair (Author) , Bono, Giuseppe (Author) , Koch-Hansen, Andreas (Author) , Propris, Roberto De (Author) , Storm, Jesper (Author) , Wojno, Jennifer (Author) ,

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• Verlag, lizenzpflichtig, Volltext

A track record on SHOX: from basic research to complex models and therapy by Marchini, Antonio (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) ,

• Verlag, Volltext
• Verlag, Volltext

Patterns and ecological drivers of ocean viral communities by Brum, Jennifer R. (Author) , Ignacio-Espinoza, J. Cesar (Author) , Roux, Simon (Author) , Doulcier, Guilhem (Author) , Acinas, Silvia G. (Author) , Alberti, Adriana (Author) , Chaffron, Samuel (Author) , Cruaud, Corinne (Author) , Vargas, Colomban de (Author) , Gasol, Josep M. (Author) , Gorsky, Gabriel (Author) , Gregory, Ann C. (Author) , Guidi, Lionel (Author) , Hingamp, Pascal (Author) , Iudicone, Daniele (Author) , Not, Fabrice (Author) , Ogata, Hiroyuki (Author) , Pesant, Stéphane (Author) , Poulos, Bonnie T. (Author) , Schwenck, Sarah M. (Author) , Speich, Sabrina (Author) , Dimier, Celine (Author) , Kandels-Lewis, Stefanie (Author) , Picheral, Marc (Author) , Searson, Sarah (Author) , Coordinators, Tara Oceans (Author) , Bork, Peer (Author) , Bowler, Chris (Author) , Sunagawa, Shinichi (Author) , Wincker, Patrick (Author) , Karsenti, Eric (Author) , Sullivan, Matthew B. (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Exploring nucleo-cytoplasmic large DNA viruses in Tara Oceans microbial metagenomes by Hingamp, Pascal (Author) , Grimsley, Nigel (Author) , Acinas, Silvia G. (Author) , Clerissi, Camille (Author) , Subirana, Lucie (Author) , Poulain, Julie (Author) , Ferrera, Isabel (Author) , Sarmento, Hugo (Author) , Villar, Emilie (Author) , Lima-Mendez, Gipsi (Author) , Faust, Karoline (Author) , Sunagawa, Shinichi (Author) , Claverie, Jean-Michel (Author) , Moreau, Hervé (Author) , Desdevises, Yves (Author) , Bork, Peer (Author) , Raes, Jeroen (Author) , de Vargas, Colomban (Author) , Karsenti, Eric (Author) , Kandels-Lewis, Stefanie (Author) , Jaillon, Olivier (Author) , Not, Fabrice (Author) , Pesant, Stéphane (Author) , Wincker, Patrick (Author) , Ogata, Hiroyuki (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population by Billingsley, Gail (Author) , Bin, Jenea (Author) , Fieggen, Karen J. (Author) , Duncan, Jacque L. (Author) , Gerth, Christina (Author) , Ogata, Koji (Author) , Wodak, Shoshana S. (Author) , Traboulsi, Elias I. (Author) , Fishman, Gerald A. (Author) , Paterson, Andrew (Author) , Chitayat, David (Author) , Knüppel, Tanja (Author) , Millán, José M. (Author) , Mitchell, Grant A. (Author) , Deveault, Catherine (Author) , Héon, Elise (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature by Rappold, Gudrun (Author) , Fukami, Maki (Author) , Niesler, Beate (Author) , Wöginger, Simone (Author) , Zumkeller, Walter (Author) , Bettendorf, Markus (Author) , Heinrich, Udo (Author) , Vlachopapadoupoulou, Elpis (Author) , Reinehr, Thomas (Author) , Onigata, Kazumichi (Author) , Ogata, Tsutomu (Author) ,

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Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation by Ogata, Tsutomu (Author) , Wakui, Keiko (Author) , Kosho, Tomoki (Author) , Muroya, Koji (Author) , Yamanouchi, Yasuko (Author) , Takano, Takako (Author) , Fukushima, Yoshimitsu (Author) , Rappold, Gudrun (Author) , Suzuki, Yoshimi (Author) ,

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• Verlag, lizenzpflichtig, Volltext

FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY by Kirsch, Stefan (Author) , Weiß, Birgit (Author) , Rosa, M. De (Author) , Ogata, T. (Author) , Lombardi, G. (Author) , Rappold, Gudrun (Author) ,

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• Verlag, lizenzpflichtig, Volltext

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation by Fukami, Maki (Author) , Kirsch, Stefan (Author) , Wöginger, Simone (Author) , Richter, Alexandra (Author) , Benes, Vladimir (Author) , Franco, Brunella (Author) , Muroya, Koji (Author) , Rao, Ercole (Author) , Merker, Sabine (Author) , Niesler, Beate (Author) , Ballabio, Andrea (Author) , Ansorge, Wilhelm (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) ,

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Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome by Rao, Ercole (Author) , Weiß, Birgit (Author) , Fukami, Maki (Author) , Rump, Andreas (Author) , Niesler, Beate (Author) , Mertz, Annelyse (Author) , Muroya, Koji (Author) , Binder, Gerhard (Author) , Kirsch, Stefan (Author) , Winkelmann, Martina (Author) , Nordsiek, Gabriele (Author) , Heinrich, Udo (Author) , Breuning, Martijn H. (Author) , Ranke, Michael B. (Author) , Rosenthal, André (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) ,

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• Verlag, lizenzpflichtig, Volltext

FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes by Rao, Ercole (Author) , Weiß, Birgit (Author) , Fukami, Maki (Author) , Mertz, Andrea (Author) , Meder, J. (Author) , Ogata, Tsutomu (Author) , Heinrich, Udo (Author) , Garcia-Heras, J. (Author) , Schiebel, Katrin (Author) , Rappold, Gudrun (Author) ,

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Mental retardation in a boy with an interstitial deletion at Xp22.3 involving STS, KAL1, and OA1: Implication for the MRX locus by Muroya, Koji (Author) , Ogata, Tsutomu (Author) , Matsuo, Nobutake (Author) , Nagai, Toshiro (Author) , Franco, Brunella (Author) , Ballabio, Andrea (Author) , Rappold, Gudrun (Author) , Sakura, Nobiro (Author) , Fukushima, Yoshimitsu (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Turner phenotype and X-chromosome abnormalities: regarding short stature by Rappold, Gudrun (Author) , Rao, Ercole (Author) , Weiß, Birgit (Author) , Mertz, Andrea (Author) , Meder, J. (Author) , Schiebel, Katrin (Author) , Ogata, T. (Author) , Matsuo, N. (Author) ,

Short stature in a girl with partial monosomy of the pseudoautosomal region distal to DXYS15: further evidence for the assignment of the critical region for a pseudoautosomal growt... by Ogata, Tsutomu (Author) , Yoshizawa, Atsuko (Author) , Muroya, Koji (Author) , Matsuo, Nobutake (Author) , Fukushima, Yoshimitsu (Author) , Rappold, Gudrun (Author) , Yokoya, Susumu (Author) ,

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• Verlag, lizenzpflichtig, Volltext

Refinement of the locus for X-linked recessive chondrodysplasia punctata by Muroya, Koji (Author) , Ogata, Tsutomu (Author) , Rappold, Gudrun (Author) , Klink, Albrecht (Author) , Nakahori, Yutaka (Author) , Fukushima, Yoshimitsu (Author) , Aizu, Katsuya (Author) , Matsuo, Nobutake (Author) ,

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Chromosomal localisation of a pseudoautosomal growth gene(s). by Ogata, Tsutomu (Author) , Petit, Christine (Author) , Rappold, Gudrun (Author) , Matsuo, Nobutake (Author) , Matsumoto, Takahiko (Author) , Goodfellow, Peter (Author) ,

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• Verlag, lizenzpflichtig, Volltext