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Results: 1-25 | 26-27
Results: 1-25/27
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain
Authors: Nothwang, HG Kim, HG Aoki, J Geisterfer, M Kubart, S Wegner, RD van Moers, A Ashworth, LK Haaf, T Bell, J Arai, H Tommerup, N Ropers, HH Wirth, J
Citation: Hg. Nothwang et al., Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain, HUM MOL GEN, 10(8), 2001, pp. 797-806
A translocation breakpoint cluster disrupts the newly defined 3 ' end of the SNURF-SNRPN transcription unit on chromosome 15
Authors: Wirth, J Back, E Huttenhofer, A Nothwang, HG Lich, C Gross, S Menzel, C Schinzel, A Kioschis, P Tommerup, N Ropers, HH Horsthemke, B Buiting, K
Citation: J. Wirth et al., A translocation breakpoint cluster disrupts the newly defined 3 ' end of the SNURF-SNRPN transcription unit on chromosome 15, HUM MOL GEN, 10(3), 2001, pp. 201-210
Microgeographic variation, habitat effects and individual signature cues in calls of chiffchaffs Phylloscopus collybita canarensis
Authors: Naguib, M Hammerschmidt, K Wirth, J
Citation: M. Naguib et al., Microgeographic variation, habitat effects and individual signature cues in calls of chiffchaffs Phylloscopus collybita canarensis, ETHOLOGY, 107(4), 2001, pp. 341-355
Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2)
Authors: Zhu, G Gillessen-Kaesbach, G Wirth, J Passarge, E Bartsch, O
Citation: G. Zhu et al., Girl with phenotypic abnormalities and a de novo, apparently balanced translocation 46,XX,t(5;10)(q35.2q11.2), AM J MED G, 98(4), 2001, pp. 317-319
Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18
Authors: Stankiewicz, P Brozek, I Helias-Rodzewicz, Z Wierzba, J Pilch, J Bocian, E Balcerska, A Wozniak, A Kardas, I Wirth, J Mazurczak, T Limon, J
Citation: P. Stankiewicz et al., Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18, AM J MED G, 101(3), 2001, pp. 226-239
Problem solving as transdisciplinary competence - Conception and first results of a study on school achievement
Authors: Klieme, E Funke, J Leutner, D Reimann, P Wirth, J
Citation: E. Klieme et al., Problem solving as transdisciplinary competence - Conception and first results of a study on school achievement, Z PADAGOG, 47(2), 2001, pp. 179-200
Elliptic flow in Au plus Au collisions at root s(NN)=130 GeV
Authors: Ackermann, KH Adams, N Adler, C Ahammed, Z Ahmad, S Allgower, C Amsbaugh, J Anderson, M Anderssen, E Arnesen, H Arnold, L Averichev, GS Baldwin, A Balewski, J Barannikova, O Barnby, LS Baudot, J Beddo, M Bekele, S Belaga, VV Bellwied, R Bennett, S Bercovitz, J Berger, J Betts, W Bichsel, H Bieser, F Bland, LC Bloomer, M Blyth, CO Boehm, J Bonner, BE Bonnet, D Bossingham, R Botlo, M Boucham, A Bouillo, N Bouvier, S Bradley, K Brady, FP Braithwaite, ES Braithwaite, W Brandin, A Brown, RL Brugalette, G Byrd, C Caines, H Sanchez, MCD Cardenas, A Carr, L Carroll, J Castillo, J Caylor, B Cebra, D Chatopadhyay, S Chen, ML Chen, W Chen, Y Chernenko, SP Cherney, M Chikanian, A Choi, B Chrin, J Christie, W Coffin, JP Conin, L Consiglio, C Cormier, TM Cramer, JG Crawford, HJ Danilov, VI Dayton, D DeMello, M Deng, WS Derevschikov, AA Dialinas, M Diaz, H DeYoung, PA Didenko, L Dimassimo, D Dioguardi, J Dominik, W Drancourt, C Draper, JE Dunin, VB Dunlop, JC Eckardt, V Edwards, WR Efimov, LG Eggert, T Emelianov, V Engelage, J Eppley, G Erazmus, B Etkin, A Fachini, P Feliciano, C Ferenc, D Ferguson, MI Fessler, H Finch, E Fine, V Fisyak, Y Flierl, D Flores, I Foley, KJ Fritz, D Gagunashvili, N Gans, J Gazdzicki, M Germain, M Geurts, F Ghazikhanian, V Gojak, C Grabski, J Grachov, O Grau, M Greiner, D Greiner, L Grigoriev, V Grosnick, D Gross, J Guilloux, G Gushin, E Hall, J Hallman, TJ Hardtke, D Harper, G Harris, JW He, P Heffner, M Heppelmann, S Herston, T Hill, D Hippolyte, B Hirsch, A Hjort, E Hoffmann, GW Horsley, M Howe, M Huang, HZ Humanic, TJ Hummler, H Hunt, W Hunter, J Igo, GJ Ishihara, A Ivanshin, YI Jacobs, P Jacobs, WW Jacobson, S Jared, R Jensen, P Johnson, I Jones, PG Judd, E Kaneta, M Kaplan, M Keane, D Kenney, VP Khodinov, A Klay, J Klein, SR Klyachko, A Koehler, G Konstantinov, AS Kormilitsyne, V Kotchenda, L Kotov, I Kovalenko, AD Kramer, M Kravtsov, P Krueger, K Krupien, T Kuczewski, P Kuhn, C Kunde, GJ Kunz, CL Kutuev, RK Kuznetsov, AA Lakehal-Ayat, L Lamas-Valverde, J Lamont, MAC Landgraf, JM Lange, S Lansdell, CP Lasiuk, B Laue, F Lebedev, A LeCompte, T Leonhardt, WJ Leontiev, VM Leszczynski, P LeVine, MJ Li, Q Li, Q Li, Z Liaw, CJ Lin, J Lindenbaum, SJ Lindenstruth, V Lindstrom, PJ Lisa, MA Liu, H Ljubicic, T Llope, WJ LoCurto, G Long, H Longacre, RS Lopez-Noriega, M Lopiano, D Love, WA Lutz, JR Lynn, D Madansky, L Maier, R Majka, R Maliszewski, A Margetis, S Marks, K Marstaller, R Martin, L Marx, J Matis, HS Matulenko, YA Matyushevski, EA McParland, C McShane, TS Meier, J Melnick, Y Meschanin, A Middlekamp, P Mikhalin, N Miller, B Milosevich, Z Minaev, NG Minor, B Mitchell, J Mogavero, E Moiseenko, VA Moltz, D Moore, CF Morozov, V Morse, R de Moura, MM Munhoz, MG Mutchler, GS Nelson, JM Nevski, P Ngo, T Nguyen, M Nguyen, T Nikitin, VA Nogach, LV Noggle, T Norman, B Nurushev, SB Nussbaum, T Nystrand, J Odyniec, G Ogawa, A Ogilvie, CA Olchanski, K Oldenburg, M Olson, D Ososkov, GA Ott, G Padrazo, D Paic, G Pandey, SU Panebratsev, Y Panitkin, SY Pavlinov, AI Pawlak, T Pentia, M Perevotchikov, V Peryt, W Petrov, VA Pinganaud, W Pirogov, S Platner, E Pluta, J Polk, I Porile, N Porter, J Poskanzer, AM Potrebenikova, E Prindle, D Pruneau, C Puskar-Pasewicz, J Rai, G Rasson, J Ravel, O Ray, RL Razin, SV Reichhold, D Reid, J Renfordt, RE Retiere, F Ridiger, A Riso, J Ritter, HG Roberts, JB Roehrich, D Rogachevski, OV Romero, JL Roy, C Russ, D Rykov, V Sakrejda, I Sanchez, R Sandler, Z Sandweiss, J Sappenfield, P Saulys, AC Savin, I Schambach, J Scharenberg, RP Scheblien, J Scheetz, R Schlueter, R Schmitz, N Schroeder, LS Schulz, M Schuttauf, A Sedlmeir, J Seger, J Seliverstov, D Seyboth, J Seyboth, P Seymour, R Shakaliev, EI Shestermanov, KE Shi, Y Shimanskii, SS Shuman, D Shvetcov, VS Skoro, G Smirnov, N Smykov, LP Snellings, R Solberg, K Sowinski, J Spinka, HM Srivastava, B Stephenson, EJ Stock, R Stolpovsky, A Stone, N Stone, R Strikhanov, M Stringfellow, B Stroebele, H Struck, C Suaide, AAP Sugarbaker, E Suire, C Symons, TJM Takahashi, J Tang, AH Tarchini, A Tarzian, J Thomas, JH Tikhomirov, V de Toledo, AS Tonse, S Trainor, T Trentalange, S Tokarev, M Tonjes, MB Trofimov, V Tsai, O Turner, K Ullrich, T Underwood, DG Vakula, I Van Buren, G VanderMolen, AM Vanyashin, A Vasilevski, IM Vasiliev, AN Vigdor, SE Visser, G Voloshin, SA Vu, C Wang, F Ward, H Weerasundara, D Weidenbach, R Wells, R Wells, R Wenaus, T Westfall, GD Whitfield, JP Whitten, C Wieman, H Willson, R Wilson, K Wirth, J Wisdom, J Wissink, SW Witt, R Wolf, J Wood, L Xu, N Xu, Z Yakutin, AE Yamamoto, E Yang, J Yepes, P Yokosawa, A Yurevich, VI Zanevski, YV Zhang, J Zhang, WM Zhu, J Zimmerman, D Zoulkarneev, R Zubarev, AN
Citation: Kh. Ackermann et al., Elliptic flow in Au plus Au collisions at root s(NN)=130 GeV, PHYS REV L, 86(3), 2001, pp. 402-407
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome
Authors: Borck, G Wirth, J Hardt, T Tonnies, H Brondum-Nielsen, K Bugge, M Tommerup, N Nothwang, HG Ropers, HH Haaf, T
Citation: G. Borck et al., Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome, J MED GENET, 38(2), 2001, pp. 117-120
Volatile compounds released by enzymatic hydrolysis of glycoconjugates of leaves and grape berries from Vitis vinifera Muscat of Alexandria and Shiraz cultivars
Authors: Wirth, J Guo, WF Baumes, R Gunata, Z
Citation: J. Wirth et al., Volatile compounds released by enzymatic hydrolysis of glycoconjugates of leaves and grape berries from Vitis vinifera Muscat of Alexandria and Shiraz cultivars, J AGR FOOD, 49(6), 2001, pp. 2917-2923
Influence of gender on rates of hospitalization, hospital course, and hypercapnea in high-risk patients admitted for asthma - A 10-year retrospectivestudy at Yale-New Haven Hospital
Authors: Trawick, DR Holm, C Wirth, J
Citation: Dr. Trawick et al., Influence of gender on rates of hospitalization, hospital course, and hypercapnea in high-risk patients admitted for asthma - A 10-year retrospectivestudy at Yale-New Haven Hospital, CHEST, 119(1), 2001, pp. 115-119
High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes
Authors: Kirchhoff, M Rose, H Maahr, J Gerdes, T Bugge, M Tommerup, N Tumer, Z Lespinasse, J Jensen, PKA Wirth, J Lundsteen, C
Citation: M. Kirchhoff et al., High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes, EUR J HUM G, 8(9), 2000, pp. 661-668
Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes
Authors: Vollmer, M Kremer, M Ruf, R Miot, S Nothwang, HG Wirth, J Otto, E Krapf, R Hildebrandt, F
Citation: M. Vollmer et al., Molecular cloning of the critical region for glomerulopathy with fibronectin deposits (GFND) and evaluation of candidate genes, GENOMICS, 68(2), 2000, pp. 127-135
DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner
Authors: Scheer, MP van der Maarel, S Kubart, S Schulz, A Wirth, J Schweiger, S Ropers, HH Nothwang, HG
Citation: Mp. Scheer et al., DXS6673E encodes a predominantly nuclear protein, and its mouse ortholog DXHXS6673E is alternatively spliced in a developmental- and tissue-specific manner, GENOMICS, 63(1), 2000, pp. 123-132
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations
Authors: Nothwang, HG Schroer, A van der Maarel, S Kubart, S Schneider, S Riesselmann, L Menzel, C Hinzmann, B Vogt, D Rosenthal, A Fryns, JP Tommerup, N Haaf, T Ropers, HH Wirth, J
Citation: Hg. Nothwang et al., Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations, CYTOG C GEN, 90(1-2), 2000, pp. 126-133
Improved accuracy in the diagnosis of intrahepatic bile duct ectasia in Caroli's disease by combination of ultrasound and endoscopic retrograde cholangiography
Authors: Rickes, S Neye, H Wirth, J Ortner, M Lochs, H Wermke, W
Citation: S. Rickes et al., Improved accuracy in the diagnosis of intrahepatic bile duct ectasia in Caroli's disease by combination of ultrasound and endoscopic retrograde cholangiography, ULTRASC MED, 21(5), 2000, pp. 223-225
Attenuation of atherosclerosis in apolipoprotein E-deficient mice by ramipril is dissociated from its antihypertensive effect and from potentiation of bradykinin
Authors: Keidar, S Attias, J Coleman, R Wirth, J Scholkens, B Hayek, T
Citation: S. Keidar et al., Attenuation of atherosclerosis in apolipoprotein E-deficient mice by ramipril is dissociated from its antihypertensive effect and from potentiation of bradykinin, J CARDIO PH, 35(1), 2000, pp. 64-72
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review
Authors: Heller, A Seidel, J Hubler, A Starke, H Beensen, V Senger, G Rocchi, M Wirth, J Chudoba, I Claussen, U Liehr, T
Citation: A. Heller et al., Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review, J MED GENET, 37(7), 2000, pp. 529-532
Taking positions. On the erotic in Renaissance culture
Authors: Wirth, J
Citation: J. Wirth, Taking positions. On the erotic in Renaissance culture, BIBL HUM R, 62(2), 2000, pp. 443-445
Tilman Riemenschneider, master sculptor of the Late Middle Ages (Catalogueof the exhibit at the National Gallery in Washington, D.C., October 3, 1999 to January 9, 2000 and New York, Metropolitan Museum, February 7 to May 14, 2000)
Authors: Wirth, J
Citation: J. Wirth, Tilman Riemenschneider, master sculptor of the Late Middle Ages (Catalogueof the exhibit at the National Gallery in Washington, D.C., October 3, 1999 to January 9, 2000 and New York, Metropolitan Museum, February 7 to May 14, 2000), BIBL HUM R, 62(2), 2000, pp. 446-448
Mouse dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud
Authors: Caubit, X Thangarajah, R Theil, T Wirth, J Nothwang, HG Ruther, U Krauss, S
Citation: X. Caubit et al., Mouse dac, a novel nuclear factor with homology to Drosophila dachshund shows a dynamic expression in the neural crest, the eye, the neocortex, and the limb bud, DEV DYNAM, 214(1), 1999, pp. 66-80
Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome
Authors: Silahtaroglu, A Hol, FA Jensen, PKA Erdel, M Duba, HC Geurds, MPA Knoers, NVAM Mariman, ECM Tumer, Z Utermann, G Wirth, J Bugge, M Tommerup, N
Citation: A. Silahtaroglu et al., Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome, EUR J HUM G, 7(1), 1999, pp. 68-76
Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma
Authors: Stumm, M Koch, A Wieacker, PF Phillip, C Steinbach, F Allhoff, EP Buhtz, P Walter, H Tonnies, H Wirth, J
Citation: M. Stumm et al., Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenoma, CANC GENET, 115(1), 1999, pp. 82-85
The anemia in continuous ambulatory peritoneal dialysis patients is related to Kt/V index
Authors: Opatrny, K Opatrna, S Sefrna, F Wirth, J
Citation: K. Opatrny et al., The anemia in continuous ambulatory peritoneal dialysis patients is related to Kt/V index, ARTIF ORGAN, 23(1), 1999, pp. 65-69
The Oxford hypothesis - Origins of perspective
Authors: Wirth, J
Citation: J. Wirth, The Oxford hypothesis - Origins of perspective, REV FR SOC, 40(3), 1999, pp. 619-622
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes
Authors: Wirth, J Nothwang, HG van der Maarel, S Menzel, C Borck, G Lopez-Pajares, I Brondum-Nielsen, K Tommerup, N Bugge, M Ropers, HH Haaf, T
Citation: J. Wirth et al., Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes, J MED GENET, 36(4), 1999, pp. 271-278
Risultati: 1-25 | 26-27