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    1. Frazer, KA; Sheehan, JB; Stokowski, RP; Chen, XY; Hosseini, R; Cheng, JF; Fodor, SPA; Cox, DR; Patil, N
      Evolutionarily conserved sequences on human chromosome 21

      GENOME RESEARCH
    2. Saccone, S; Pavlicek, A; Federico, C; Paces, J; Bernardi, G
      Genes, isochores and bands in human chromosomes 21 and 22

      CHROMOSOME RESEARCH
    3. Shinohara, T; Tomizuka, K; Miyabara, S; Takehara, S; Kazuki, Y; Inoue, J; Katoh, M; Nakane, H; Iino, A; Ohguma, A; Ikegami, S; Inokuchi, K; Ishida, I; Reeves, RH; Oshimura, M
      Mice containing a human chromosome 21 model behavioral impairment and cardiac anomalies of Down's syndrome

      HUMAN MOLECULAR GENETICS
    4. Tuggle, CK; Genet, C; Shi, XW; Chardon, P; Sanchez-Serrano, I; Cravens, G; Milan, D; Yerle, M
      Cytogenetic and radiation hybrid mapping reveals conserved synteny and gene order between human Chromosome 21 and pig Chromosome 13

      MAMMALIAN GENOME
    5. Chen, YW; Yu, P; Lu, D; Tagle, DA; Cai, T
      A novel isoform of beta-spectrin II localizes to cerebellar Purkinje-cell bodies and interacts with neurofibromatosis type 2 gene product schwannomin

      JOURNAL OF MOLECULAR NEUROSCIENCE
    6. Reymond, A; Friedli, M; Henrichsen, CN; Chapot, F; Deutsch, S; Ucla, C; Rossier, C; Lyle, R; Guipponi, M; Antonarakis, SE
      From PREDs and open reading frames to cDNA isolation: Revisiting the humanchromosome 21 transcription map

      GENOMICS
    7. Davisson, MT; Bechtel, LJ; Akeson, EC; Fortna, A; Slavov, D; Gardiner, K
      Evolutionary breakpoints on human chromosome 21

      GENOMICS
    8. Pletcher, MT; Wiltshire, T; Cabin, DE; Villanueva, M; Reeves, RH
      Use of comparative physical and sequence mapping to annotate mouse chromosome 16 and human chromosome 21

      GENOMICS
    9. Clay, O; Bernardi, G
      Compositional heterogeneity within and among isochores in mammalian genomes - II. Some general comments

      GENE
    10. Oliver, JL; Bernaola-Galvan, P; Carpena, P; Roman-Roldan, R
      Isochore chromosome maps of eukaryotic genomes

      GENE
    11. Tam, W
      Identification and characterization of human BIC, a gene on chromosome 21 that encodes a noncoding RNA

      GENE
    12. Kurdyukov, SG; Lebedev, YB; Artamonova, II; Gorodentseva, TN; Batrak, AV; Mamedov, IZ; Azhikina, TL; Legchilina, SP; Efimenko, IG; Gardiner, K; Sverdlov, ED
      Full-sized HERV-K (HML-2) human endogenous retroviral LTR sequences on human chromosome 21: map locations and evolutionary history

      GENE
    13. Akeson, EC; Lambert, JP; Narayanswami, S; Gardiner, K; Bechtel, LJ; Davisson, MT
      Ts65Dn - localization of the translocation breakpoint and trisomic gene content in a mouse model for Down syndrome

      CYTOGENETICS AND CELL GENETICS
    14. Fortna, A; Gardiner, K
      Genomic sequence analysis tools: a user's guide

      TRENDS IN GENETICS
    15. Reeves, RH; Baxter, LL; Richtsmeier, JT
      Too much of a good thing: mechanisms of gene action in Down syndrome

      TRENDS IN GENETICS
    16. Hyde, LA; Frisone, DF; Crnic, LS
      Ts65Dn mice, a model for Down syndrome, have deficits in context discrimination learning suggesting impaired hippocampal function

      BEHAVIOURAL BRAIN RESEARCH
    17. Antonarakis, SE; Lyle, R; Chrast, R; Scott, HS
      Differential gene expression studies to explore the molecular pathophysiology of Down syndrome

      BRAIN RESEARCH REVIEWS
    18. Nadal, M; Vigo, CG; Melaragno, MI; Andrade, JAD; Alonso, LG; Brunini, D; Pritchard, M; Estivill, X
      Clinical and cytogenetic characterisation of a patient with Down syndrome resulting from a 21q22.1 -> qter duplication

      JOURNAL OF MEDICAL GENETICS
    19. Rogers, MA; Langbein, L; Winter, H; Ehmann, C; Praetzel, S; Korn, B; Schweizer, J
      Characterization of a cluster of human high/ultrahigh sulfur keratin-associated protein genes embedded in the type I keratin gene domain on chromosome 17q12-21

      JOURNAL OF BIOLOGICAL CHEMISTRY
    20. Hyde, LA; Crnic, LS; Pollock, A; Bickford, PC
      Motor learning in Ts65Dn mice, a model for Down syndrome

      DEVELOPMENTAL PSYCHOBIOLOGY
    21. Lazzaro, SJ; Speevak, MD; Farrell, SA
      Recombinant Down syndrome: a case report and literature review

      CLINICAL GENETICS
    22. Groet, J; Ives, JH; Jones, TA; Danton, M; Flomen, RH; Sheer, D; Hrascan, R; Pavelic, K; Nizetic, D
      Narrowing of the region of allelic loss in 21q11-21 in squamous non-small cell lung carcinoma and cloning of a novel ubiquitin-specific protease genefrom the deleted segment

      GENES CHROMOSOMES & CANCER
    23. Prejean, C; Colamonici, OR
      Role of the cytoplasmic domains of the type I interferon receptor subunitsin signalling

      SEMINARS IN CANCER BIOLOGY
    24. Chrast, R; Scott, HS; Madani, R; Huber, L; Wolfer, DP; Prinz, M; Aguzzi, A; Lipp, HP; Antonarakis, SE
      Mice trisomic for a bacterial artificial chromosome with the single-minded2 gene (Sim2) show phenotypes similar to some of those present in the partial trisomy 16 mouse models of Down syndrome

      HUMAN MOLECULAR GENETICS
    25. Wynn, SL; Fisher, RA; Pagel, C; Price, M; Liu, QY; Khan, IM; Zammit, P; Dadrah, K; Mazrani, W; Kessling, A; Lee, JS; Buluwela, L
      Organization and conservation of the GART/SON/DONSON locus in mouse and human genomes

      GENOMICS
    26. Slavov, D; Hattori, M; Sakaki, Y; Rosenthal, A; Shimizu, N; Minoshima, S; Kudoh, J; Yaspo, ML; Ramser, J; Reinhardt, R; Reimer, C; Clancy, K; Rynditch, A; Gardiner, K
      Criteria for gene identification and features of genome organization: analysis of 6.5 Mb of DNA sequence from human chromosome 21

      GENE
    27. Baptista, MJ; Fairbrother, UL; Howard, CM; Farrer, MJ; Davies, GE; Trikka, D; Maratou, K; Redington, A; Greve, G; Njolstad, PR; Kessling, AM
      Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

      HUMAN GENETICS
    28. Tazi-Ahnini, R; di Giovine, FS; McDonagh, AJG; Messenger, AG; Amadou, C; Cox, A; Duff, GW; Cork, MJ
      Structure and polymorphism of the human gene for the interferon-induced p78 protein (MX1): evidence of association with alopecia areata in the Down syndrome region

      HUMAN GENETICS
    29. Maratou, K; Siddique, Y; Kessling, AM; Davies, GE
      Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction

      HUMAN GENETICS
    30. Hattori, M; Fujiyama, A; Taylor, TD; Watanabe, H; Yada, T; Park, HS; Toyoda, A; Ishii, K; Totoki, Y; Choi, DK; Soeda, E; Ohki, M; Takagi, T; Sakaki, Y; Taudien, S; Blechschmidt, K; Polley, A; Menzel, U; Delabar, J; Kumpf, K; Lehmann, R; Patterson, D; Reichwald, K; Rump, A; Schillhabel, M; Schudy, A; Zimmermann, W; Rosenthal, A; Kudoh, J; Shibuya, K; Kawasaki, K; Asakawa, S; Shintani, A; Sasaki, T; Nagamine, K; Mitsuyama, S; Antonarakis, SE; Minoshima, S; Shimizu, N; Nordsiek, G; Hornischer, K; Brandt, P; Scharfe, M; Schon, O; Desario, A; Reichelt, J; Kauer, G; Blocker, H; Ramser, J; Beck, A; Klages, S; Hennig, S; Riesselmann, L; Dagand, E; Haaf, T; Wehrmeyer, S; Borzym, K; Gardiner, K; Nizetic, D; Francis, F; Lehrach, H; Reinhardt, R; Yaspo, ML
      The DNA sequence of human chromosome 21

      NATURE
    31. Inoue, T; Shinohara, T; Takahara, S; Inoue, J; Kamino, H; Kugoh, H; Oshimura, M
      Specific impairment of cardiogenesis in mouse ES cells containing a human chromosome 21

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    32. Broman, KW; Weber, JL
      Characterization of human crossover interference

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. Hildmann, T; Kong, XG; O'Brien, J; Riesselman, L; Christensen, HM; Dagand, E; Lehrach, H; Yaspo, ML
      A contiguous 3-Mb sequence-ready map in the S3-MX region on 21q22.2 based on high-throughput nonisotopic library screenings

      GENOME RESEARCH
    34. Wang, SY; Cruts, M; Del-Favero, J; Zhang, Y; Tissir, F; Potier, MC; Patterson, D; Nizetic, D; Bosch, A; Chen, HM; Bennett, L; Estivill, X; Kessling, A; Antonarakis, SE; van Broeckhoven, C
      A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes

      GENOME RESEARCH
    35. Goldman, LA; Zafari, M; Cutrone, EC; Dang, AJ; Brickelmeier, M; Runkel, L; Benjamin, CD; Ling, LE; Langer, JA
      Characterization of antihuman IFNAR-1 monoclonal antibodies: Epitope localization and functional analysis

      JOURNAL OF INTERFERON AND CYTOKINE RESEARCH
    36. Pucharcos, C; Fuentes, JJ; Casas, C; de la Luna, S; Alcantara, S; Arbones, ML; Soriano, E; Estivill, X; Pritchard, M
      Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome

      EUROPEAN JOURNAL OF HUMAN GENETICS
    37. Laurent, AM; Puechberty, J; Roizes, G
      Hypothesis: for the worst and for the best, L1Hs retrotransposons activelyparticipate in the evolution of the human centromeric alphoid sequences

      CHROMOSOME RESEARCH
    38. Cole, SE; Wiltshire, T; Rue, EE; Morrow, D; Hieter, P; Brahe, C; Fisher, EM; Katsanis, N; Reeves, RH
      High-resolution comparative physical mapping of mouse Chromosome 10 in theregion of homology with human Chromosome 21

      MAMMALIAN GENOME
    39. Rothkamm, K; Lobrich, M
      Misrejoining of DNA double-strand breaks in primary and transformed human and rodent cells: a comparison between the HPRT region and other genomic locations

      MUTATION RESEARCH-DNA REPAIR
    40. Valero, R; Marfany, G; Gonzalez-Angulo, O; Gonzalez-Gonzalez, G; Puelles, L; Gonzalez-Duarte, R
      USP25, a novel gene encoding a deubiquitinating enzyme, is located in the gene-poor region 21q11.2

      GENOMICS
    41. Tassone, F; Villard, L; Clancy, K; Gardiner, K
      Structures, sequence characteristics, and synteny relationships of the transcription factor E4TF1, the splicing factor U2AF35 and the cystathionine beta synthetase genes from Fugu rubripes

      GENE
    42. Tassone, F; Lucas, R; Slavov, D; Kavsan, V; Crnic, L; Gardiner, K
      Gene expression relevant to Down Syndrome: problems and approaches

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    43. Schalkwyk, LC; Himmelbauer, H; Lehrach, H
      Toward the mammalian transcript map

      ARCHIV FUR TIERZUCHT-ARCHIVES OF ANIMAL BREEDING
    44. GROET J; IVES JH; SOUTH AP; BAPTISTA PR; JONES TA; YASPO ML; LEHRACH H; POTIER MC; VANBROECKHOVEN C; NIZETIC D
      BACTERIAL CONTIG MAP OF THE 21Q11 REGION ASSOCIATED WITH ALZHEIMERS-DISEASE AND ABNORMAL MYELOPOIESIS IN DOWN-SYNDROME

      PCR methods and applications
    45. RICHARD F; DUTRILLAUX B
      ORIGIN OF HUMAN-CHROMOSOME-21 AND ITS CONSEQUENCES - A 50-MILLION-YEAR-OLD STORY

      Chromosome research
    46. GUIPPONI M; SCOTT HS; CHEN H; SCHEBESTA A; ROSSIER C; ANTONARAKIS SE
      2 ISOFORMS OF A HUMAN INTERSECTIN (ITSN) PROTEIN ARE PRODUCED BY BRAIN-SPECIFIC ALTERNATIVE SPLICING IN A STOP CODON

      Genomics (San Diego, Calif.)
    47. SAUPE S; ROIZES G; PETER M; BOYLE S; GARDINER K; DESARIO A
      MOLECULAR-CLONING OF A HUMAN CDNA IGSF3 ENCODING AN IMMUNOGLOBULIN-LIKE MEMBRANE-PROTEIN - EXPRESSION AND MAPPING TO CHROMOSOME BAND 1P13

      Genomics (San Diego, Calif.)
    48. POTIER MC; DUTRIAUX A; ORTI R; GROET J; GIBELIN N; KARADIMA G; LUTFALLA G; LYNN A; VANBROECKHOVEN C; CHAKRAVARTI A; PETERSEN M; NIZETIC D; DELABAR J; ROSSIER J
      2 SEQUENCE-READY CONTIGS SPANNING THE 2 COPIES OF A 200-KB DUPLICATION ON HUMAN 21Q - PARTIAL SEQUENCE AND POLYMORPHISMS

      Genomics (San Diego, Calif.)
    49. LAPENTA V; SOSSI V; GOSSET P; VAYSSETTES C; VITALI T; RABATEL N; TASSONE F; BLOUIN JL; SCOTT HS; ANTONARAKIS SE; CREAU N; BRAHE C
      CONSTRUCTION OF A 2.5-MB INTEGRATED PHYSICAL AND GENE MAP OF DISTAL 21Q22.3

      Genomics
    50. YASPO ML; AALTONEN J; HORELLIKUITUNEN N; PELTONEN L; LEHRACH H
      CLONING OF A NOVEL HUMAN PUTATIVE TYPE IA INTEGRAL MEMBRANE-PROTEIN MAPPING TO 21Q22.3

      Genomics
    51. DAHMANE N; GHEZALA GA; GOSSET P; CHAMOUN Z; DUFRESNEZACHARIA MC; LOPES C; RABATEL N; GASSANOVAMAUGENRE S; CHETTOUH Z; ABRAMOWSKI V; FAYET E; YASPO ML; KORN B; BLOUIN JL; LEHRACH H; POUTSKA A; ANTONARAKIS SE; SINET PM; CREAU N; DELABAR JM
      TRANSCRIPTIONAL MAP OF THE 2.5-MB CBR-ERG REGION OF CHROMOSOME-21 INVOLVED IN DOWN-SYNDROME

      Genomics
    52. OHIRA M; SEKI N; NAGASE T; ISHIKAWA K; NOMURA N; OHARA O
      CHARACTERIZATION OF A HUMAN HOMOLOG (BACH1) OF THE MOUSE BACH1 GENE ENCODING A BTB BASIC LEUCINE-ZIPPER TRANSCRIPTION FACTOR AND ITS MAPPING TO CHROMOSOME 21Q22.1

      Genomics
    53. SCOTT HS; KYRIAKOU DS; PETERSON P; HEINO M; TAHTINEN M; KROHN K; CHEN HM; ROSSIER C; LALIOTI MD; ANTONARAKIS SE
      CHARACTERIZATION OF A NOVEL GENE, C21ORF2, AN HUMAN-CHROMOSOME 21Q22.3 AND ITS EXCLUSION AS THE APECED GENE BY MUTATION ANALYSIS

      Genomics
    54. BLOUIN JL; SAIL GD; GUIPPONI M; ROSSIER C; PAPPASAVAS MP; ANTONARAKIS SE
      ISOLATION OF THE HUMAN BACH1 TRANSCRIPTION REGULATOR GENE, WHICH MAPSTO CHROMOSOME 21Q22.1

      Human genetics
    55. Guipponi, M; Scott, HS; Kudoh, J; Kawasaki, K; Shibuya, K; Shintani, A; Asakawa, S; Chen, HM; Lalioti, MD; Rossier, C; Minoshima, S; Shimizu, N; Antonarakis, SE
      Identification and characterization of a novel cyclic nucleotide phosphodiesterase gene (PDE9A) that maps to 21q22.3: alternative splicing of mRNA transcripts, genomic structure and sequence

      HUMAN GENETICS
    56. Orti, R; Potier, MC; Maunoury, C; Prieur, M; Creau, N; Delabar, JM
      Conservation of pericentromeric duplications of a 200-kb part of the human21q22.1 region in primates

      CYTOGENETICS AND CELL GENETICS
    57. HALLER O; FRESE M; KOCHS G
      MX PROTEINS - MEDIATORS OF INNATE RESISTANCE TO RNA VIRUSES

      Revue scientifique et technique - Office international des epizooties
    58. PLATANIAS LC; DOMANSKI P; NADEAU OW; YI TL; UDDIN S; FISH E; NEEL BG; COLAMONICI OR
      IDENTIFICATION OF A DOMAIN IN THE BETA-SUBUNIT OF THE TYPE-I INTERFERON (IFN) RECEPTOR THAT EXHIBITS A NEGATIVE REGULATORY EFFECT IN THE GROWTH-INHIBITORY ACTION OF TYPE-I IFNS

      The Journal of biological chemistry
    59. Mashkova, T; Oparina, N; Alexandrov, I; Zinovieva, O; Marusina, A; Yurov, Y; Lacroix, MH; Kisselev, L
      Unequal cross-over is involved in human alpha satellite DNA rearrangementson a border of the satellite domain

      FEBS LETTERS
    60. Rahmani, Z; Lopes, C; Rachidi, M; Delabar, JM
      Expression of the Mnb (dyrk) protein in adult and embryonic mouse tissues

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    61. LAFRENIERE RG; ROCHEFORT DL; CHRETIEN N; ROMMENS JM; COCHIUS JI; KALVIAINEN R; NOUSIAINEN U; PATRY G; FARRELL K; SODERFELDT B; FEDERICO A; HALE BR; COSSIO OH; SORENSEN T; POULIOT MA; KMIEC T; ULDALL P; JANSZKY J; PRANZATELLI MR; ANDERMANN F; ANDERMANN E; ROULEAU GA
      UNSTABLE INSERTION IN THE 5'-FLANKING REGION OF THE CYSTATIN-B GENE IS THE MOST COMMON MUTATION IN PROGRESSIVE MYOCLONUS EPILEPSY TYPE-1, EPM1

      Nature genetics
    62. AALTONEN J; HORELLIKUITUNEN N; FAN JB; BJORSES P; PERHEENTUPA J; MYERS R; PALOTIE A; PELTONEN L
      HIGH-RESOLUTION PHYSICAL AND TRANSCRIPTIONAL MAPPING OF THE AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY LOCUS ON CHROMOSOME 21Q22.3 FISH

      PCR methods and applications
    63. OHIRA M; SEKI N; NAGASE T; SUZUKI E; NOMURA N; OHARA O; HATTORI M; SAKAKI Y; EKI T; MURAKAMI Y; SAITO T; ICHIKAWA H; OHKI M
      GENE IDENTIFICATION IN 1.6-MB REGION OF THE DOWN-SYNDROME REGION ON CHROMOSOME-21

      PCR methods and applications
    64. SIMPSON S; WOODWORTH CD; DIPAOLO JA
      ALTERED EXPRESSION OF ERG AND ETS-2 TRANSCRIPTION FACTORS IS ASSOCIATED WITH GENETIC CHANGES AT 21Q22.2-22.3 IN IMMORTAL AND CERVICAL-CARCINOMA CELL-LINES

      Oncogene
    65. KATSANIS N; YASPO ML; FISHER EMC
      IDENTIFICATION AND MAPPING OF A NOVEL HUMAN GENE, HRMT1L1, HOMOLOGOUSTO THE RAT PROTEIN ARGININE N-METHYLTRANSFERASE-1 (PRMT1) GENE

      Mammalian genome
    66. ONODERA K; PATTERSON D
      STRUCTURE OF HUMAN-CHROMOSOME-21 - FOR AN UNDERSTANDING OF GENETIC-DISEASES INCLUDING DOWNS-SYNDROME

      Bioscience, biotechnology, and biochemistry
    67. GUIMERA J; PUCHARCOS C; DOMENECH A; CASAS C; SOLANS A; GALLARDO T; ASHLEY J; LOVETT M; ESTIVILL X; PRITCHARD M
      COSMID CONTIG AND TRANSCRIPTIONAL MAP OF 3 REGIONS OF HUMAN-CHROMOSOME 21Q22 - IDENTIFICATION OF 37 NOVEL TRANSCRIPTS BY DIRECT SELECTION

      Genomics
    68. PAOLONIGIACOBINO A; CHEN HM; PEITSCH MC; ROSSIER C; ANTONARAKIS SE
      CLONING OF THE TMPRSS2 GENE, WHICH ENCODES A NOVEL SERINE-PROTEASE WITH TRANSMEMBRANE, LDLRA, AND SRCR DOMAINS AND MAPS TO 21Q22.3

      Genomics
    69. ORTI R; MEGARBANE A; MAUNOURY C; VANBROECKHOVEN C; SINET PM; DELABAR JM
      HIGH-RESOLUTION PHYSICAL MAPPING OF A 6.7-MB YAC CONTIG SPANNING A REGION CRITICAL FOR THE MONOSOMY-21 PHENOTYPE IN 21Q21.3-Q22.1

      Genomics
    70. PAOLONIGIACOBINO A; CHEN HM; ANTONARAKIS SE
      CLONING OF A NOVEL HUMAN NEURAL CELL-ADHESION MOLECULE GENE (NCAM2) THAT MAPS TO CHROMOSOME REGION 21Q21 AND IS POTENTIALLY INVOLVED IN DOWN-SYNDROME

      Genomics
    71. NOTHWANG HG; STRAHM B; DENICH D; KUBLER M; SCHWABE J; GINGRICH JC; JAUCH A; COX A; NICKLIN MJH; KURNIT DM; HILDEBRANDT F
      MOLECULAR-CLONING OF THE INTERLEUKIN-1 GENE-CLUSTER - CONSTRUCTION OFAN INTEGRATED YAC PAC CONTIG AND A PARTIAL TRANSCRIPTIONAL MAP IN THEREGION OF CHROMOSOME 2Q13/

      Genomics
    72. CHEN HM; ROSSIER C; NAKAMURA Y; LYNN A; CHAKRAVARTI A; ANTONARAKIS SE
      CLONING OF A NOVEL HOMEOBOX-CONTAINING GENE, PKNOX1, AND MAPPING TO HUMAN-CHROMOSOME 21Q22.3

      Genomics
    73. MITTAZ L; SCOTT HS; ROSSIER C; SEEBURG PH; HIGUCHI M; ANTONARAKIS SE
      CLONING OF A HUMAN RNA EDITING DEAMINASE (ADARB1) OF GLUTAMATE RECEPTORS THAT MAPS TO CHROMOSOME 21Q22.3

      Genomics
    74. LAPENTA V; CHIURAZZI P; VANDERSPEK P; PIZZUTI A; HANAOKA F; BRAHE C
      SMT3A, A HUMAN HOMOLOG OF THE S-CEREVISIAE-SMT3 GENE, MAPS TO CHROMOSOME-21QTER AND DEFINES A NOVEL GENE FAMILY

      Genomics
    75. VILLARD L; TASSONE F; HAYMOWICZ M; WELBORN R; GARDINER K
      MAP LOCATION, GENOMIC ORGANIZATION AND EXPRESSION PATTERNS OF THE HUMAN RED1 RNA EDITASE

      Somatic cell and molecular genetics
    76. GARDINER K
      CLONABILITY AND GENE DISTRIBUTION ON HUMAN-CHROMOSOME-21 - REFLECTIONS OF JUNK DNA CONTENT

      Gene
    77. LAFRENIERE RG; KIBAR Z; ROCHEFORT DL; HAN FY; FON EA; DUBE MP; KANG XL; BAIRD S; KORNELUK RG; ROMMENS JM; ROULEAU GA
      GENOMIC STRUCTURE OF THE HUMAN GT334 (EHOC-1) GENE-MAPPING TO 21Q22.3

      Gene
    78. GIBBS VC; PENNICA D
      CRF2-4 - ISOLATION OF CDNA CLONES ENCODING THE HUMAN AND MOUSE PROTEINS

      Gene
    79. SCOTT HS; CHEN HM; ROSSIER C; LALIOTI MD; ANTONARAKIS SE
      ISOLATION OF A HUMAN GENE (HES1) WITH HOMOLOGY TO AN ESCHERICHIA-COLIAND A ZEBRAFISH PROTEIN THAT MAPS TO CHROMOSOME 21Q122.3

      Human genetics
    80. SCARTEZZINI P; EGEO A; COLELLA S; FUMAGALLI P; ARRIGO P; NIZETIC D; TARAMELLI R; RASOREQUARTINO A
      CLONING A NEW HUMAN GENE FROM CHROMOSOME 21Q22.3 ENCODING A GLUTAMIC ACID-RICH PROTEIN EXPRESSED IN HEART AND SKELETAL-MUSCLE

      Human genetics
    81. CHEN HM; ANTONARAKIS SE
      LOCALIZATION OF A HUMAN HOMOLOG OF THE DROSOPHILA MNB AND RAT DYRK GENES TO CHROMOSOME 21Q22.2

      Human genetics
    82. KATSANIS N; BECK JA; FISHER EMC
      MAPPING OF A NOVEL SH3 DOMAIN PROTEIN AND 2 PROTEINS OF UNKNOWN FUNCTION TO HUMAN-CHROMOSOME-21

      Human genetics
    83. OSOEGAWA K; SUSUKIDA R; OKANO S; KUDO J; MINOSIMA S; SHIMIZU N; DEJONG P; GROET J; IVES; LEHRACH H; NIZETIC D; SOEDA E
      A SEQUENCE READY MAP WITH COSMID PAC CONTIGS FROM A 4-MB DOWN-SYNDROME CHROMOSOMAL REGION/

      Cytogenetics and cell genetics
    84. CHEN H; ANTONARAKIS SE
      THE SH3D1A GENE MAPS TO HUMAN-CHROMOSOME 21Q22.1-]Q22.2

      Cytogenetics and cell genetics
    85. PFEFFER LM
      BIOLOGIC ACTIVITIES OF NATURAL AND SYNTHETIC TYPE-I INTERFERONS

      Seminars in oncology
    86. YU JW; TONG SH; SHEN YP; KAO FT
      GENE IDENTIFICATION AND DNA-SEQUENCE ANALYSIS IN THE GC-POOR 20 MEGABASE REGION OF HUMAN-CHROMOSOME-21

      Proceedings of the National Academy of Sciences of the United Statesof America
    87. FLOMEN RH; GORMAN PA; VATCHEVA R; GROET J; BARISIC I; LIGUTIC I; SHEER D; NIZETIC D
      RIEGER SYNDROME LOCUS - A NEW RECIPROCAL TRANSLOCATION T(4-12)(Q25-Q15) AND A DELETION DEL(4)(Q25Q27) BOTH BREAK BETWEEN MARKERS D4S2945 AND D4S193

      Journal of Medical Genetics
    88. NADAL M; MORENO S; PRITCHARD M; PRECIADO MA; ESTIVILL X; RAMOSARROYO MA
      DOWN-SYNDROME - CHARACTERIZATION OF A CASE WITH PARTIAL TRISOMY OF CHROMOSOME-21 OWING TO A PATERNAL BALANCED TRANSLOCATION (15-21)(Q26-Q22.1) BY FISH

      Journal of Medical Genetics
    89. CARSON SD; CHAPMAN NN; TRACY SM
      PURIFICATION OF THE PUTATIVE COXSACKIEVIRUS B-RECEPTOR FROM HELA-CELLS

      Biochemical and biophysical research communications
    90. SONG WJ; CHUNG SH; KURNIT DM
      THE MURINE DYRK PROTEIN MAPS TO CHROMOSOME-16, LOCALIZES TO THE NUCLEUS, AND CAN FORM MULTIMERS

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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/05/20 alle ore 04:03:41