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1. Antonarakis, SE
   Chromosome 21: from sequence to applications
   CURRENT OPINION IN GENETICS & DEVELOPMENT
   
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2. Nugent, P; Barch, MJ; Weston, WM; Greene, RM; Pisano, MM
   Identification of trisomy 16 murine embryos by fluorescence in situ hybridization
   BIOTECHNIQUES
   
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3. Nizetic, D
   Functional genomics of the Down syndrome
   CROATIAN MEDICAL JOURNAL
   
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4. Nelson, PG; McCune, SK; Ades, AM; Nelson, KB
   Glial-neurotrophic mechanisms in Down syndrome
   JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
   
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5. Cairns, NJ
   Molecular neuropathology of transgenic mouse models of Down syndrome
   JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
   
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6. Quack, KC; Vassiliadou, N; Pudney, J; Anderson, DJ; Hill, JA
   Leukocyte activation in the decidua of chromosomally normal and abnormal fetuses from women with recurrent abortion
   HUMAN REPRODUCTION
   
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7. Orozco-Buenrostro, C; Godinez-Rodriguez, U; Winking, H; Arguello, LC; Torres, CM
   Altered action potential of myocardial cells from mouse fetuses with trisomy 16: A model of Down syndrome
   ARCHIVES OF MEDICAL RESEARCH
   
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8. Blasko, I; Ransmayr, G; Veerhuis, R; Eikelenboom, P; Grubeck-Loebenstein, B
   Does IFN gamma play a role in neurodegeneration?
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   I. Blasko et al., "Does IFN gamma play a role in neurodegeneration?", J NEUROIMM, 116(1), 2001, pp. 1-4
9. Antonarakis, SE; Lyle, R; Chrast, R; Scott, HS
   Differential gene expression studies to explore the molecular pathophysiology of Down syndrome
   BRAIN RESEARCH REVIEWS
   
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10. Galdzicki, Z; Siarey, R; Pearce, R; Stoll, J; Rapoport, SI
    On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models
    BRAIN RESEARCH REVIEWS
    
    Z. Galdzicki et al., "On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models", BRAIN RES R, 35(2), 2001, pp. 115-145
11. Klein, RC; Siarey, RJ; Caruso, A; Rapoport, SI; Castellino, FJ; Galdzicki, Z
    Increased expression of NR2A subunit does not alter NMDA-evoked responses in cultured fetal trisomy 16 mouse hippocampal neurons
    JOURNAL OF NEUROCHEMISTRY
    
    R.C. Klein et al., "Increased expression of NR2A subunit does not alter NMDA-evoked responses in cultured fetal trisomy 16 mouse hippocampal neurons", J NEUROCHEM, 76(6), 2001, pp. 1663-1669
12. Svensson, EC; Huggins, GS; Lin, H; Clendenin, C; Jiang, F; Tufts, R; Dardik, FB; Leiden, JM
    A syndrome of tricuspid atresia in mice with a targeted mutation of the gene encoding Fog-2
    NATURE GENETICS
    
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13. Huang, W; Galdzicki, Z; van Gelderen, P; Balbo, A; Chikhale, EG; Schapiro, MB; Rapoport, SI
    Brain myo-inositol level is elevated in Ts65Dn mouse and reduced after lithium treatment
    NEUROREPORT
    
    W. Huang et al., "Brain myo-inositol level is elevated in Ts65Dn mouse and reduced after lithium treatment", NEUROREPORT, 11(3), 2000, pp. 445-448
14. Schuchmann, S; Heinemann, U
    Increased mitochondrial superoxide generation in neurons from trisomy 16 mice: a model of Down's syndrome
    FREE RADICAL BIOLOGY AND MEDICINE
    
    S. Schuchmann e U. Heinemann, "Increased mitochondrial superoxide generation in neurons from trisomy 16 mice: a model of Down's syndrome", FREE RAD B, 28(2), 2000, pp. 235-250
15. Yao, FS; Caserta, MT; Wyrwicz, AM
    In vitro H-1 and P-31 NMR spectroscopic evidence of multiple aberrant biochemical pathways in murine trisomy 16 brain development
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE
    
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16. McVeigh, KE; Mallee, JJ; Lucente, A; Barnoski, BL; Wu, S; Berry, GT
    Murine chromosome 16 telomeric region, homologous with human chromosome 21q22, contains the osmoregulatory Na+/myo-inositol cotransporter (SLC5A3) gene
    CYTOGENETICS AND CELL GENETICS
    
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17. Haydar, TF; Nowakowski, RS; Yarowsky, PJ; Krueger, BK
    Role of founder cell deficit and delayed neuronogenesis in microencephaly of the trisomy 16 mouse
    JOURNAL OF NEUROSCIENCE
    
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18. Pettigrew, R; Kuo, HC; Scriven, P; Rowell, P; Pal, K; Handyside, A; Braude, P; Ogilvie, CM
    A pregnancy following PGD for X-linked autosomal dominant Incontinentia Pigmenti (Bloch-Sulzberger syndrome)
    HUMAN REPRODUCTION
    
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19. Johnson, P; Duncan, K; Blunt, S; Bell, G; Ali, Z; Cox, P; Moore, GE
    Apparent confined placental mosaicism of trisomy 16 and multiple fetal anomalies: case report
    PRENATAL DIAGNOSIS
    
    P. Johnson et al., "Apparent confined placental mosaicism of trisomy 16 and multiple fetal anomalies: case report", PRENAT DIAG, 20(5), 2000, pp. 417-421
20. Farra, C; Giudicelli, B; Pellissier, MC; Philip, N; Piquet, C
    Fetoplacental chromosomal discrepancy
    PRENATAL DIAGNOSIS
    
    C. Farra et al., "Fetoplacental chromosomal discrepancy", PRENAT DIAG, 20(3), 2000, pp. 190-193
21. Hallam, DM; Capps, NL; Travelstead, AL; Brewer, GJ; Maroun, LE
    Evidence for an interferon-related inflammatory reaction in the trisomy 16mouse brain leading to caspase-1-mediated neuronal apoptosis
    JOURNAL OF NEUROIMMUNOLOGY
    
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22. Chan, Y; Silverman, N; Jackson, L; Wapner, R; Wallerstein, R
    Maternal uniparental disomy of chromosome 16 and body stalk anomaly
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
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23. Kohlhase, J; Janssen, P; Weidenauer, K; Harms, K; Bartels, I
    First confirmed case with paternal uniparental disomy of chromosome 16
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    J. Kohlhase et al., "First confirmed case with paternal uniparental disomy of chromosome 16", AM J MED G, 91(3), 2000, pp. 190-191
24. Schuchmann, S; Heinemann, U
    Diminished glutathione levels cause spontaneous and mitochondria-mediated cell death in neurons from trisomy 16 mice: A model of Down's syndrome
    JOURNAL OF NEUROCHEMISTRY
    
    S. Schuchmann e U. Heinemann, "Diminished glutathione levels cause spontaneous and mitochondria-mediated cell death in neurons from trisomy 16 mice: A model of Down's syndrome", J NEUROCHEM, 74(3), 2000, pp. 1205-1214
25. Granholm, ACE; Sanders, LA; Crnic, LS
    Loss of cholinergic phenotype in basal forebrain coincides with cognitive decline in a mouse model of Down's syndrome
    EXPERIMENTAL NEUROLOGY
    
    A.C.E. Granholm et al., "Loss of cholinergic phenotype in basal forebrain coincides with cognitive decline in a mouse model of Down's syndrome", EXP NEUROL, 161(2), 2000, pp. 647-663
26. Kirchhoff, S; Kim, JS; Hagendorff, A; Thonnissen, E; Kruger, O; Lamers, WH; Willecke, K
    Abnormal cardiac conduction and morphogenesis in connexin40 and connexin43double-deficient mice
    CIRCULATION RESEARCH
    
    S. Kirchhoff et al., "Abnormal cardiac conduction and morphogenesis in connexin40 and connexin43double-deficient mice", CIRCUL RES, 87(5), 2000, pp. 399-405
27. Waller, BR; McQuinn, T; Phelps, AL; Markwald, RR; Lo, CW; Thompson, RP; Wessels, A
    Conotruncal anomalies in the trisomy 16 mouse: an immunohistochemical analysis with emphasis on the involvement of the neural crest
    ANATOMICAL RECORD
    
    B.R. Waller et al., "Conotruncal anomalies in the trisomy 16 mouse: an immunohistochemical analysis with emphasis on the involvement of the neural crest", ANAT REC, 260(3), 2000, pp. 279-293
28. Gjertson, C; Sturm, KS; Berger, CN
    Hematopoietic deficiencies and core binding factor expression in murine Ts16, an animal model for Down syndrome
    CLINICAL IMMUNOLOGY
    
    C. Gjertson et al., "Hematopoietic deficiencies and core binding factor expression in murine Ts16, an animal model for Down syndrome", CLIN IMMUNO, 91(1), 1999, pp. 50-60
29. Cardenas, AM; Rodriguez, MP; Cortes, MP; Alvarez, RM; Wei, WZ; Rapoport, SI; Shimahara, T; Caviedes, R; Caviedes, P
    Calcium signals in cell lines derived from the cerebral cortex of normal and trisomy 16 mice
    NEUROREPORT
    
    A.M. Cardenas et al., "Calcium signals in cell lines derived from the cerebral cortex of normal and trisomy 16 mice", NEUROREPORT, 10(2), 1999, pp. 363-369
30. Leffler, A; Ludwig, M; Schmitt, O; Busch, LC
    Germ cell migration and early development of the gonads in the trisomy 16 mouse - an animal model for Down's syndrome
    ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER
    
    A. Leffler et al., "Germ cell migration and early development of the gonads in the trisomy 16 mouse - an animal model for Down's syndrome", ANN ANATOMY, 181(3), 1999, pp. 247-252
31. Leffler, A; Wedel, T; Busch, LC
    Congenital colonic hypoganglionosis in murine trisomy 16 - An animal modelfor Down's syndrome
    EUROPEAN JOURNAL OF PEDIATRIC SURGERY
    
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32. Sawa, A
    Neuronal cell death in Down's syndrome
    JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    
    A. Sawa, "Neuronal cell death in Down's syndrome", J NEUR TR-S, (57), 1999, pp. 87-97
33. Strovel, J; Stamberg, J; Yarowsky, PJ
    Interphase FISH for rapid identification of a Down syndrome animal model
    CYTOGENETICS AND CELL GENETICS
    
    J. Strovel et al., "Interphase FISH for rapid identification of a Down syndrome animal model", CYTOG C GEN, 86(3-4), 1999, pp. 285-287
34. Munne, S; Magli, C; Cohen, J; Morton, P; Sadowy, S; Gianaroli, L; Tucker, M; Marquez, C; Sable, D; Ferraretti, AP; Massey, JB; Scott, R
    Positive outcome after preimplantation diagnosis of aneuploidy in human embryos
    HUMAN REPRODUCTION
    
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35. Chen, CP; Chern, SR; Lee, CC; Town, DD; Chen, WL; Wang, WS
    Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3 : 1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)
    PRENATAL DIAGNOSIS
    
    C.P. Chen et al., "Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3 : 1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)", PRENAT DIAG, 19(8), 1999, pp. 783-786
36. Paladini, D; D'Agostino, A; Liguori, M; Teodoro, A; Tartaglione, A; Colombari, S; Martinelli, P
    Prenatal findings in trisomy 16q of paternal origin
    PRENATAL DIAGNOSIS
    
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37. Scortegagna, M; Galdzicki, Z; Rapoport, SI; Hanbauer, I
    Activator protein-1 DNA binding activation by hydrogen peroxide in neuronal and astrocytic primary cultures of trisomy-16 and diploid mice
    MOLECULAR BRAIN RESEARCH
    
    M. Scortegagna et al., "Activator protein-1 DNA binding activation by hydrogen peroxide in neuronal and astrocytic primary cultures of trisomy-16 and diploid mice", MOL BRAIN R, 73(1-2), 1999, pp. 144-150
38. Bacino, CA; Lee, B; Spikes, AS; Shaffer, LG
    Trisomy 16q in a female newborn with a de novo X;16 translocation and hypoplastic left heart
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
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39. Costa, ACS; Walsh, K; Davisson, MT
    Motor dysfunction in a mouse model for Down syndrome
    PHYSIOLOGY & BEHAVIOR
    
    A.C.S. Costa et al., "Motor dysfunction in a mouse model for Down syndrome", PHYSL BEHAV, 68(1-2), 1999, pp. 211-220
40. Berry, GT; Wang, ZYJ; Dreha, SF; Finucane, BM; Zimmerman, RA
    In vivo brain myo-inositol levels in children with Down syndrome
    JOURNAL OF PEDIATRICS
    
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41. Bambrick, LL; Krueger, BK
    Neuronal apoptosis in mouse trisomy 16: Mediation by caspases
    JOURNAL OF NEUROCHEMISTRY
    
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42. von Kaisenberg, CS; Nicolaides, KH; Jonat, W; Brand-Saberi, B
    Pathophysiology of increased nuchal translucency in chromosomally abnormalfetuses
    GYNAKOLOGE
    
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43. CARVER W
    ABNORMAL INTERACTIONS OF EMBRYONIC MOUSE TRISOMY-16 HEART FIBROBLASTSWITH EXTRACELLULAR-MATRIX COMPONENTS IN-VITRO
    Cell adhesion and communication (Softback)
    
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44. Anderson, RH; Webb, S; Brown, NA
    Morphologic analysis of animal models of congenital heart disease
    PROGRESS IN PEDIATRIC CARDIOLOGY
    
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45. ZANINI R; TARANTINI M; CERRI V; JACOBELLO C; BELLOTTI D; LANCETTI S; SCALCHI S; GROLI C; BIANCHI UA
    DUAL POSITIVITY FOR NEURAL-TUBE DEFECTS AND DOWN-SYNDROME AT MATERNALSERUM SCREENING - GESTATIONAL OUTCOME
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46. Hanbauer, I; Galdzicki, Z; Rapoport, SI; Scortegagna, M
    Evidence of increased oxidative stress in hippocampal primary cultures of trisomy 16 mouse. Studies on metallothionein-I/II
    RESTORATIVE NEUROLOGY AND NEUROSCIENCE
    
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47. CORSI P; FORLONI G; TROIA M; LETTINI T; COYLE JT
    SOMATOSTATIN EXPRESSION IN TS16 MOUSE-BRAIN CULTURES
    Journal of molecular neuroscience
    
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48. SCHWARTZ PJ; COYLE JT
    EFFECTS OF OVEREXPRESSION OF THE CYTOPLASMIC COPPER-ZINC SUPEROXIDE-DISMUTASE ON THE SURVIVAL OF NEURONS IN-VITRO
    Synapse
    
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49. Stahl, T; Goldammer, A; Luschekina, E; Beck, M; Schliebs, R; Bigl, V
    Long-term basal forebrain cholinergic-rich grafts derived from trisomy 16 mice do not develop beta-amyloid pathology and neurodegeneration but demonstrate neuroinflammatory responses
    INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE
    
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50. VONKAISENBERG CS; KRENN V; LUDWIG M; NICOLAIDES KH; BRANDSABERI B
    MORPHOLOGICAL CLASSIFICATION OF NUCHAL SKIN IN HUMAN FETUSES WITH TRISOMY-21, TRISOMY-18, AND TRISOMY-13 AT 12-18 WEEKS AND IN A TRISOMY-16MOUSE
    Anatomy and embryology
    
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51. INSAUSTI AM; MEGIAS M; CRESPO D; CRUZORIVE LM; DIERSSEN M; VALLINA TF; INSAUSTI R; FLOREZ J
    HIPPOCAMPAL VOLUME AND NEURONAL NUMBER IN TS65DN MICE - A MURINE MODEL OF DOWN-SYNDROME
    Neuroscience letters
    
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52. HALLAM DM; MAROUN LE
    ANTI-GAMMA INTERFERON CAN PREVENT THE PREMATURE DEATH OF TRISOMY-16 MOUSE CORTICAL-NEURONS IN CULTURE
    Neuroscience letters
    
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53. SCHUCHMANN S; MULLER W; HEINEMANN U
    ALTERED CA2-NEURONS OF TRISOMY-16 MICE - A MODEL OF DOWNS-SYNDROME( SIGNALING AND MITOCHONDRIAL DEFICIENCIES IN HIPPOCAMPAL)
    The Journal of neuroscience
    
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54. DOMINGUEZ SA; BE C; AYARZA E; MONTENEGRO MA
    PLACENTAE OF FETUSES WITH CHROMOSOME-16 TRISOMY - A MORPHOMETRIC ANALYSIS OF THE INTERCHANGE CHORIONIC VILLI
    Medical science research
    
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55. VANOPSTAL D; VANDENBERG C; DEELEN WH; BRANDENBURG H; COHENOVERBEEK TE; HALLEY DJJ; VANDENOUWELAND AMW; TVELD PAI; LOS FJ
    PROSPECTIVE PRENATAL INVESTIGATIONS ON POTENTIAL UNIPARENTAL DISOMY IN CASES OF CONFINED PLACENTAL TRISOMY
    Prenatal diagnosis
    
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56. Astner, A; Schwinger, E; Caliebe, A; Jonat, W; Gembruch, U
    Sonographically detected fetal and placental abnormalities associated withtrisomy 16 confined to the placenta. A case report and review of the literature
    PRENATAL DIAGNOSIS
    
    A. Astner et al., "Sonographically detected fetal and placental abnormalities associated withtrisomy 16 confined to the placenta. A case report and review of the literature", PRENAT DIAG, 18(12), 1998, pp. 1308-1315
57. GALDZICKI Z; COAN EJ; RAPOPORT SI; STOLL J
    INCREASED EXPRESSION OF VOLTAGE-ACTIVATED CALCIUM CHANNELS IN CULTURED HIPPOCAMPAL-NEURONS FROM MOUSE TRISOMY-16, A MODEL FOR DOWN-SYNDROME
    Molecular brain research
    
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58. DEMAS GE; NELSON RJ; KRUEGER BK; YAROWSKY PJ
    IMPAIRED SPATIAL WORKING AND REFERENCE MEMORY IN SEGMENTAL TRISOMY (TS65DN) MICE
    Behavioural brain research
    
    G.E. Demas et al., "IMPAIRED SPATIAL WORKING AND REFERENCE MEMORY IN SEGMENTAL TRISOMY (TS65DN) MICE", Behavioural brain research, 90(2), 1998, pp. 199-201
59. BERSU ET; AHMAD FJ; SCHWEI MJ; BAAS PW
    CYTOPLASMIC ABNORMALITIES IN CULTURED CEREBELLAR NEURONS FROM THE TRISOMY-16 MOUSE
    Developmental brain research
    
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60. Hsu, WT; Shchepin, DA; Mao, R; Berry-Kravis, E; Garber, AP; Fischel-Ghodsian, N; Falk, RE; Carlson, DE; Roeder, ER; Leeth, EA; Hajianpour, MJ; Wang, JCC; Rosenblum-Vos, LS; Bhatt, SD; Karson, EM; Hux, CH; Trunca, C; Bialer, MG; Linn, SK; Schreck, RR
    Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    W.T. Hsu et al., "Mosaic trisomy 16 ascertained through amniocentesis: Evaluation of 11 new cases", AM J MED G, 80(5), 1998, pp. 473-480
61. ANDERSON RH; WEBB S; BROWN NA
    THE MOUSE WITH TRISOMY-16 AS A MODEL OF HUMAN HEARTS WITH COMMON ATRIOVENTRICULAR JUNCTION
    Cardiovascular Research
    
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62. SCORTEGAGNA M; GALDZICKI Z; RAPOPORT SI; HANBAUER I
    IN CORTICAL CULTURES OF TRISOMY-16 MOUSE-BRAIN THE UP-REGULATED METALLOTHIONEIN-I II FAILS TO RESPOND TO H2O2 EXPOSURE OR GLUTAMATE-RECEPTOR STIMULATION/
    Brain research
    
    M. Scortegagna et al., "IN CORTICAL CULTURES OF TRISOMY-16 MOUSE-BRAIN THE UP-REGULATED METALLOTHIONEIN-I II FAILS TO RESPOND TO H2O2 EXPOSURE OR GLUTAMATE-RECEPTOR STIMULATION/", Brain research, 787(2), 1998, pp. 292-298
63. LUDWIG M; BUSCH LC; WINKING H
    THE EMBRYONIC-DEVELOPMENT OF SENSORY ORGANS AND THE SKULL IN THE TRISOMY-16 MOUSE, AN ANIMAL-MODEL FOR DOWNS-SYNDROME
    ANNALS OF ANATOMY-ANATOMISCHER ANZEIGER
    
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64. SIAREY RJ; COAN EJ; RAPOPORT SI; GALDZICKI Z
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    Neuroscience letters
    
    R.J. Siarey et al., "RESPONSES TO NMDA IN CULTURED HIPPOCAMPAL-NEURONS FROM TRISOMY-16 EMBRYONIC MICE", Neuroscience letters, 232(3), 1997, pp. 131-134
65. MULLER W; HEINEMANN U; SCHUCHMANN S
    IMPAIRED CA-SIGNALING IN ASTROCYTES FROM THE TS16 MOUSE MODEL OF DOWN-SYNDROME
    Neuroscience letters
    
    W. Muller et al., "IMPAIRED CA-SIGNALING IN ASTROCYTES FROM THE TS16 MOUSE MODEL OF DOWN-SYNDROME", Neuroscience letters, 223(2), 1997, pp. 81-84
66. SANCHEZ JM; DEDIAZ SL; PANAL MJ; MOYA G; KENNY A; IGLESIAS D; WOLSTENHOLME J
    SEVERE FETAL MALFORMATIONS ASSOCIATED WITH TRISOMY-16 CONFINED TO THEPLACENTA
    Prenatal diagnosis
    
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67. BENN PA
    DOWN-SYNDROME AND OPEN NEURAL-TUBE DEFECT SCREEN-POSITIVE PREGNANCIES- PREMATURE DELIVERY AND PREMATURE PLACENTAL KARYOTYPING
    Prenatal diagnosis
    
    P.A. Benn, "DOWN-SYNDROME AND OPEN NEURAL-TUBE DEFECT SCREEN-POSITIVE PREGNANCIES- PREMATURE DELIVERY AND PREMATURE PLACENTAL KARYOTYPING", Prenatal diagnosis, 17(3), 1997, pp. 282-284
68. XU J; CHERNOS J; ROLAND B
    TRISOMY 16PTER TO 16Q12.1 AND MONOSOMY 22PTER TO 22Q11.2 RESULTING FROM ADJACENT-2 SEGREGATION OF A MATERNAL COMPLEX CHROMOSOME REARRANGEMENT
    American journal of medical genetics
    
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69. WOO V; BRIDGE PJ; BAMFORTH JS
    MATERNAL UNIPARENTAL HETERODISOMY FOR CHROMOSOME-16 - CASE-REPORT
    American journal of medical genetics
    
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70. SIAREY RJ; STOLL J; RAPOPORT SI; GALDZICKI Z
    ALTERED LONG-TERM POTENTIATION IN THE YOUNG AND OLD TS65DN MOUSE, A MODEL FOR DOWN-SYNDROME
    Neuropharmacology
    
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71. DEAN J; COHEN G; KEMP J; ROBSON L; TEMBE V; HASSELAAR J; WEBSTER B; LAMMI A; SMITH A
    KARYOTYPE 69,XXX 47,XX,+15 IN A 2 1/2 YEAR-OLD CHILD/
    Journal of Medical Genetics
    
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72. STABELBUROW J; KLEU A; SCHUCHMANN S; HEINEMANN U
    GLUTATHIONE LEVELS AND NERVE-CELL LOSS IN HIPPOCAMPAL CULTURES FROM TRISOMY-16 MOUSE - A MODEL OF DOWN-SYNDROME
    Brain research
    
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73. DIERSSEN M; VALLINA IF; BAAMONDE C; GARCIACALATAYUD S; LUMBRERAS MA; FLOREZ J
    ALTERATIONS OF CENTRAL NORADRENERGIC TRANSMISSION IN TS65DN MOUSE, A MODEL FOR DOWN-SYNDROME
    Brain research
    
    M. Dierssen et al., "ALTERATIONS OF CENTRAL NORADRENERGIC TRANSMISSION IN TS65DN MOUSE, A MODEL FOR DOWN-SYNDROME", Brain research, 749(2), 1997, pp. 238-244
74. LANE NJ; BALBO A; RAPOPORT SI
    A FINE-STRUCTURAL STUDY OF THE HIPPOCAMPUS AND DORSAL-ROOT GANGLION IN MOUSE TRISOMY-16, A MODEL OF DOWNS-SYNDROME
    Cell biology international
    
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75. WEBB S; ANDERSON RH; BROWN NA
    ENDOCARDIAL CUSHION DEVELOPMENT AND HEART LOOP ARCHITECTURE IN THE TRISOMY-16 MOUSE
    Developmental dynamics
    
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76. HAYDAR TF; BLUE ME; MOLLIVER ME; KRUEGER BK; YAROWSKY PJ
    CONSEQUENCES OF TRISOMY-16 FOR MOUSE-BRAIN DEVELOPMENT - CORTICOGENESIS IN A MODEL OF DOWN-SYNDROME
    The Journal of neuroscience
    
    T.F. Haydar et al., "CONSEQUENCES OF TRISOMY-16 FOR MOUSE-BRAIN DEVELOPMENT - CORTICOGENESIS IN A MODEL OF DOWN-SYNDROME", The Journal of neuroscience, 16(19), 1996, pp. 6175-6182
77. GROLI C; CERRI V; TARANTINI M; BELLOTTI D; JACOBELLO C; GIANELLO R; ZANINI R; LANCETTI S; ZAGLIO S
    MATERNAL SERUM SCREENING AND TRISOMY-16 CONFINED TO THE PLACENTA
    Prenatal diagnosis
    
    C. Groli et al., "MATERNAL SERUM SCREENING AND TRISOMY-16 CONFINED TO THE PLACENTA", Prenatal diagnosis, 16(8), 1996, pp. 685-689
78. SUNDBERG K; LUNDSTEEN C; PHILIP J
    EARLY FILTRATION AMNIOCENTESIS FOR FURTHER INVESTIGATION OF MOSAICISMDIAGNOSED BY CHORIONIC VILLUS SAMPLING
    Prenatal diagnosis
    
    K. Sundberg et al., "EARLY FILTRATION AMNIOCENTESIS FOR FURTHER INVESTIGATION OF MOSAICISMDIAGNOSED BY CHORIONIC VILLUS SAMPLING", Prenatal diagnosis, 16(12), 1996, pp. 1121-1127
79. PAULYSON KJ; SHERER DM; CHRISTIAN SL; LEWIS KM; LEDBETTER DH; SALAFIA CM; MECK JM
    PRENATAL-DIAGNOSIS OF AN INFANT WITH MOSAIC TRISOMY-16 OF PATERNAL ORIGIN
    Prenatal diagnosis
    
    K.J. Paulyson et al., "PRENATAL-DIAGNOSIS OF AN INFANT WITH MOSAIC TRISOMY-16 OF PATERNAL ORIGIN", Prenatal diagnosis, 16(11), 1996, pp. 1021-1026
80. DIERSSEN M; VALLINA IF; BAAMONDE C; LUMBRERAS MA; MARTINEZCUE C; CALATAYUD SG; FLOREZ J
    IMPAIRED CYCLIC-AMP PRODUCTION IN THE HIPPOCAMPUS OF A DOWN-SYNDROME MURINE MODEL
    Developmental brain research
    
    M. Dierssen et al., "IMPAIRED CYCLIC-AMP PRODUCTION IN THE HIPPOCAMPUS OF A DOWN-SYNDROME MURINE MODEL", Developmental brain research, 95(1), 1996, pp. 122-124
81. SCHNEIDER AS; BISCHOFF FZ; MCCASKILL C; COADY ML; STOPFER JE; SHAFFER LG
    COMPREHENSIVE 4-YEAR FOLLOW-UP ON A CASE OF MATERNAL HETERODISOMY FORCHROMOSOME-16
    American journal of medical genetics
    
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82. BRANDENBURG H; LOS FJ; INTVELD P
    CLINICAL-SIGNIFICANCE OF PLACENTA-CONFINED NONMOSAIC TRISOMY-16
    American journal of obstetrics and gynecology
    
    H. Brandenburg et al., "CLINICAL-SIGNIFICANCE OF PLACENTA-CONFINED NONMOSAIC TRISOMY-16", American journal of obstetrics and gynecology, 174(5), 1996, pp. 1663-1664
83. MUNNE S; DAILEY T; SULTAN KM; GRIFO J; COHEN J
    THE USE OF FIRST POLAR BODIES FOR PREIMPLANTATION DIAGNOSIS OF ANEUPLOIDY
    Human reproduction
    
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84. PELEDKAMAR M; LOTEM J; OKON E; SACHS L; GRONER Y
    THYMIC ABNORMALITIES AND ENHANCED APOPTOSIS OF THYMOCYTES AND BONE-MARROW CELLS IN TRANSGENIC MICE OVEREXPRESSING CU ZN-SUPEROXIDE DISMUTASE - IMPLICATIONS FOR DOWN-SYNDROME/
    EMBO journal
    
    M. Peledkamar et al., "THYMIC ABNORMALITIES AND ENHANCED APOPTOSIS OF THYMOCYTES AND BONE-MARROW CELLS IN TRANSGENIC MICE OVEREXPRESSING CU ZN-SUPEROXIDE DISMUTASE - IMPLICATIONS FOR DOWN-SYNDROME/", EMBO journal, 14(20), 1995, pp. 4985-4993
85. WHITEFORD ML; COUTTS J; ALROOMI L; MATHER A; LOWTHER G; COOKE A; VAUGHAN JI; MOORE GE; TOLMIE JL
    UNIPARENTAL ISODISOMY FOR CHROMOSOME-16 IN A GROWTH-RETARDED INFANT WITH CONGENITAL HEART-DISEASE
    Prenatal diagnosis
    
    M.L. Whiteford et al., "UNIPARENTAL ISODISOMY FOR CHROMOSOME-16 IN A GROWTH-RETARDED INFANT WITH CONGENITAL HEART-DISEASE", Prenatal diagnosis, 15(6), 1995, pp. 579-584
86. WOLSTENHOLME J
    AN AUDIT OF TRISOMY-16 IN MAN
    Prenatal diagnosis
    
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87. ZIMMERMANN R; LAUPER U; STREICHER A; HUCH R; HUCH A
    ELEVATED ALPHA-FETOPROTEIN AND HUMAN CHORIONIC-GONADOTROPIN AS A MARKER FOR PLACENTAL TRISOMY 16 IN THE 2ND TRIMESTER
    Prenatal diagnosis
    
    R. Zimmermann et al., "ELEVATED ALPHA-FETOPROTEIN AND HUMAN CHORIONIC-GONADOTROPIN AS A MARKER FOR PLACENTAL TRISOMY 16 IN THE 2ND TRIMESTER", Prenatal diagnosis, 15(12), 1995, pp. 1121-1124
88. ARTAN S; BASARAN N; HASSA H; OZALP S; SENER T; SAYLI BS; CENGIZ C; OZDEMIR M; DURAK T; DOLEN I; OZGUNEN T; TUNA M
    CONFINED PLACENTAL MOSAICISM IN TERM PLACENTAE - ANALYSIS OF 125 CASES
    Prenatal diagnosis
    
    S. Artan et al., "CONFINED PLACENTAL MOSAICISM IN TERM PLACENTAE - ANALYSIS OF 125 CASES", Prenatal diagnosis, 15(12), 1995, pp. 1135-1142
89. CUSICK W; BORK M; FABRI B; BENN P; RODIS JF; BUTTINO L
    TRISOMY-16 FETUS SURVIVING INTO THE 2ND-TRIMESTER
    Prenatal diagnosis
    
    W. Cusick et al., "TRISOMY-16 FETUS SURVIVING INTO THE 2ND-TRIMESTER", Prenatal diagnosis, 15(11), 1995, pp. 1078-1081
90. KORNGUTH S; BERSU E; MACK K
    MHC CLASS-I GENE-EXPRESSION
    Science
    
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91. LANGLOIS S; YONG SL; WILSON RD; KWONG LC; KALOUSEK DK
    PRENATAL AND POSTNATAL-GROWTH FAILURE ASSOCIATED WITH MATERNAL HETERODISOMY FOR CHROMOSOME-7
    Journal of Medical Genetics
    
    S. Langlois et al., "PRENATAL AND POSTNATAL-GROWTH FAILURE ASSOCIATED WITH MATERNAL HETERODISOMY FOR CHROMOSOME-7", Journal of Medical Genetics, 32(11), 1995, pp. 871-875
92. ACEVEDO LD; GALDZICKI Z; MCINTOSH AR; RAPOPORT SI
    INCREASED INWARD CURRENT IN SEPTAL NEURONS FROM THE TRISOMY-16, MOUSE, A MODEL FOR DOWNS-SYNDROME
    Brain research
    
    L.D. Acevedo et al., "INCREASED INWARD CURRENT IN SEPTAL NEURONS FROM THE TRISOMY-16, MOUSE, A MODEL FOR DOWNS-SYNDROME", Brain research, 701(1-2), 1995, pp. 89-98
93. PEARCE R; GALDZICKI Z; RAPOPORT SI
    DECREASED SENSITIVITY TO NERVE GROWTH-FACTOR OF DORSAL-ROOT GANGLION NEURONS CULTURED FROM MOUSE TRISOMY-16, A MODEL OF DOWNS-SYNDROME
    Brain research
    
    R. Pearce et al., "DECREASED SENSITIVITY TO NERVE GROWTH-FACTOR OF DORSAL-ROOT GANGLION NEURONS CULTURED FROM MOUSE TRISOMY-16, A MODEL OF DOWNS-SYNDROME", Brain research, 680(1-2), 1995, pp. 108-116
94. KIM JH; HAMMOND DN
    SEPTAL CELL-LINES DERIVED FROM THE TRISOMY-16 MOUSE - GENERATION, CHARACTERIZATION, AND RESPONSE TO NGF
    Brain research
    
    J.H. Kim e D.N. Hammond, "SEPTAL CELL-LINES DERIVED FROM THE TRISOMY-16 MOUSE - GENERATION, CHARACTERIZATION, AND RESPONSE TO NGF", Brain research, 671(2), 1995, pp. 299-304
95. CASERTA MT
    NEUROPEPTIDE-Y IMMUNOREACTIVE NEURONS IN MURINE TRISOMY-16 CORTICAL CULTURES PLASTICITY OF EXPRESSION AND DIFFERENTIATION
    Molecular and chemical neuropathology
    
    M.T. Caserta, "NEUROPEPTIDE-Y IMMUNOREACTIVE NEURONS IN MURINE TRISOMY-16 CORTICAL CULTURES PLASTICITY OF EXPRESSION AND DIFFERENTIATION", Molecular and chemical neuropathology, 22(3), 1994, pp. 197-210
96. LORKE DE; ALBRECHT H
    ALTERED POSTNATAL-DEVELOPMENT OF THE VISUAL-CORTEX IN TRISOMY-19 MICE
    Brain research bulletin
    
    D.E. Lorke e H. Albrecht, "ALTERED POSTNATAL-DEVELOPMENT OF THE VISUAL-CORTEX IN TRISOMY-19 MICE", Brain research bulletin, 34(6), 1994, pp. 563-570
97. COUSINEAU AJ; LAUER RM; PIERPONT ME; BURNS TL; ARDINGER RH; PATIL SR; SHEFFIELD VC
    LINKAGE ANALYSIS OF AUTOSOMAL-DOMINANT ATRIOVENTRICULAR-CANAL DEFECTS- EXCLUSION OF CHROMOSOME-21
    Human genetics
    
    A.J. Cousineau et al., "LINKAGE ANALYSIS OF AUTOSOMAL-DOMINANT ATRIOVENTRICULAR-CANAL DEFECTS- EXCLUSION OF CHROMOSOME-21", Human genetics, 93(2), 1994, pp. 103-108
98. SEIPP S; BUSELMAIER W
    ISOLATION OF GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE (GAPDH) CDNA FROM THE DISTAL HALF OF MOUSE CHROMOSOME-16 - FURTHER INDICATION OF A LINK BETWEEN ALZHEIMERS-DISEASE AND GLYCOLYSIS
    Neuroscience letters
    
    S. Seipp e W. Buselmaier, "ISOLATION OF GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE (GAPDH) CDNA FROM THE DISTAL HALF OF MOUSE CHROMOSOME-16 - FURTHER INDICATION OF A LINK BETWEEN ALZHEIMERS-DISEASE AND GLYCOLYSIS", Neuroscience letters, 182(1), 1994, pp. 91-94
99. GARBER A; CARLSON D; SCHRECK R; FISCHELGHODSIAN N; HSU WT; OEZTAS S; PEPKOWITZ S; GRAHAM JM
    PRENATAL-DIAGNOSIS AND DYSMORPHIC FINDINGS IN MOSAIC TRISOMY-16
    Prenatal diagnosis
    
    A. Garber et al., "PRENATAL-DIAGNOSIS AND DYSMORPHIC FINDINGS IN MOSAIC TRISOMY-16", Prenatal diagnosis, 14(4), 1994, pp. 257-266
100. PLETCHER BA; SANZ MM; SCHLESSEL JS; KUNAPORN S; MCKENNA C; BIALER MG; ALONSO ML; ZASLAV AL; BROWN WT; RAY JH
     POSTNATAL CONFIRMATION OF PRENATALLY DIAGNOSED TRISOMY-16 MOSAICISM IN 2 PHENOTYPICALLY ABNORMAL LIVEBORNS
     Prenatal diagnosis
     
     B.A. Pletcher et al., "POSTNATAL CONFIRMATION OF PRENATALLY DIAGNOSED TRISOMY-16 MOSAICISM IN 2 PHENOTYPICALLY ABNORMAL LIVEBORNS", Prenatal diagnosis, 14(10), 1994, pp. 933-940