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    1. Nadezhdin, EV; Lebedev, YB; Glazkova, DV; Bornholdt, D; Arman, IP; Grzeschik, KH; Hunsmann, G; Sverdlov, ED
      Identification of paralogous HERV-K LTRs on human chromosomes 3, 4, 7 and 11 in regions containing clusters of olfactory receptor genes

      MOLECULAR GENETICS AND GENOMICS
    2. Stern, MC; Umbach, DM; van Gils, CH; Lunn, RM; Taylor, JA
      DNA repair gene XRCC1 polymorphisms, smoking, and bladder cancer risk

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    3. Larkin, DM; Kuznetsov, SB; Astakhova, NM; Zhdanova, NS
      Using PCR markers for mapping pig chromosome 12

      RUSSIAN JOURNAL OF GENETICS
    4. Monnier, N; Romero, NB; Lerale, J; Landrieu, P; Nivoche, Y; Fardeau, M; Lunardi, J
      Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor

      HUMAN MOLECULAR GENETICS
    5. Poduslo, SE; Yin, X
      A new locus on chromosome 19 linked with late-onset Alzheimer's disease

      NEUROREPORT
    6. Venanzi, S; Malerba, G; Galavotti, R; Lauciello, MC; Trabetti, E; Zanoni, G; Pescollderungg, L; Martinati, LC; Boner, AL; Pignatti, PF
      Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma

      CLINICAL AND EXPERIMENTAL ALLERGY
    7. Santos, J; Herranz, M; Fernandez, M; Vaquero, C; Lopez, P; Fernandez-Piqueras, J
      Evidence of a possible epigenetic inactivation mechanism operating on a region of mouse chromosome 19 in gamma-radiation-induced thymic lymphomas

      ONCOGENE
    8. Kim, J; Gordon, L; Dehal, P; Badri, H; Christensen, M; Groza, M; Ha, C; Hammond, S; Vargas, M; Wehri, E; Wagner, M; Olsen, A; Stubbs, L
      Homology-driven assembly of a sequence-ready mouse BAC contig map spanningregions related to the 46-Mb gene-rich euchromatic segments of human chromosome 19

      GENOMICS
    9. Lagas, PA; Juvonen, V
      Schizophrenia in a patient with cerebral autosomally dominant arteriopathywith subcortical infarcts and leucoencephalopathy (CADASIL disease)

      NORDIC JOURNAL OF PSYCHIATRY
    10. Zhou, GQ; Zhang, Y; Hammarstrom, S
      The carcinoembryonic antigen (CEA) gene family in non-human primates

      GENE
    11. Yilmaz, F; Isbir, T; Agachan, B; Aydin, M
      Is epsilon 4 allele of apolipoprotein E associated with more severe end-organ damage in essential hypertension?

      CELL BIOCHEMISTRY AND FUNCTION
    12. Vinogradova, TV; Leppik, LP; Nikolaev, LG; Akopov, SB; Kleiman, AM; Senyuta, NB; Sverdlov, ED
      Solitary human endogenous retroviruses-K LTRs retain transcriptional activity in vivo, the mode of which is different in different cell types

      VIROLOGY
    13. Burger, PC; Pearl, DK; Aldape, K; Yates, AJ; Scheithauer, BW; Passe, SM; Jenkins, RB; James, CD
      Small cell architecture - A histological equivalent of EGFR amplification in glioblastoma multiforme?

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    14. Vargas, SO; French, CA; Faul, PN; Fletcher, JA; Davis, IJ; Dal Cin, P; Perez-Atayde, AR
      Upper respiratory tract carcinoma with chromosomal translocation 15;19 - Evidence for a distinct disease entity of young patients with a rapidly fatal course

      CANCER
    15. Takashima, H; Nishio, H; Wakao, H; Nishio, M; Koizumi, K; Oda, A; Koike, T; Sawada, K
      Molecular cloning and characterization of a KRAB-containing zinc finger protein, ZNF317, and its isoforms

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    16. Yousef, GM; Bharaj, BS; Yu, H; Poulopoulos, J; Diamandis, EP
      Sequence analysis of the human kallikrein gene locus identifies a unique polymorphic minisatellite element

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    17. Yamawaki, K; Ito, M; Machida, H; Moriki, N; Okamoto, R; Isaka, N; Shimpo, H; Kohda, A; Okumura, K; Hartshorne, DJ; Nakano, T
      Identification of human CPI-17, an inhibitory phosphoprotein for myosin phosphatase

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    18. Scimeca, JC; Franchi, A; Trojani, C; Parrinello, H; Grosgeorge, J; Robert, C; Jaillon, O; Poirier, C; Gaudray, P; Carle, GF
      The gene encoding the mouse homologue of the human osteoclast-specific 116-kDa V-ATPase subunit bears a deletion in osteosclerotic (oc/oc) mutants

      BONE
    19. D'Alfonso, S; Nistico, L; Bocchio, D; Bomprezzi, R; Marrosu, MG; Murru, MR; Lai, M; Massacesi, L; Ballerini, C; Repice, A; Salvetti, M; Montesperelli, C; Ristori, G; Trojano, M; Liguori, M; Gambi, D; Quattrone, A; Tosi, R; Momigliano-Richiardi, P
      An attempt of identifying MS-associated loci as a follow-up of a genomic linkage study in the Italian population

      JOURNAL OF NEUROVIROLOGY
    20. Puttagunta, R; Gordon, LA; Meyer, GE; Kapfhamer, D; Lamerdin, JE; Kantheti, P; Portman, KM; Chung, WK; Jenne, DE; Olsen, AS; Burmeister, M
      Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints

      GENOME RESEARCH
    21. Kipnes, JR; Xu, L; Han, F; Rallapalli, R; Jimenez, S; Hall, DJ; Tuan, RS; Li, Y
      Molecular cloning and expression patterns of mouse cartilage oligomeric matrix protein gene

      OSTEOARTHRITIS AND CARTILAGE
    22. Sangiuolo, F; Bruscia, E; Capon, F; Servidei, S; Dallapiccola, B; Novelli, G
      Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3

      EUROPEAN JOURNAL OF HUMAN GENETICS
    23. Romagno, D; Chiarelli, B; Guarducci, S; Uziella, MLG; Sineo, L
      Chromosome mapping of GABRB3 and PML loci in Macaca and Cercopithecus indicates the mechanism of evolution of human chromosome 15

      CHROMOSOME RESEARCH
    24. Catalan, J; Auffray, JC; Pellestor, F; Britton-Davidian, J
      Spontaneous occurrence of a Robertsonian fusion involving chromosome 19 bysingle whole-arm reciprocal translocation (WART) in wild-derived house mice

      CHROMOSOME RESEARCH
    25. Eilertsen, KJ; Tran, T; Sundberg, JP; Stenn, KS; Parimoo, S
      High resolution genetic and physical mapping of the mouse asebia locus: A key gene locus for sebaceous gland differentiation

      JOURNAL OF EXPERIMENTAL ANIMAL SCIENCE
    26. Wada, H
      Analyses of serum concentrations of apolipoproteins in the demented elderly

      INTERNAL MEDICINE
    27. Lebedev, YB; Belonovitch, OS; Zybrova, NV; Khil, PP; Kurdyukov, SG; Vinogradova, TV; Hunsmann, G; Sverdlov, ED
      Differences in HERV-K LTR insertions in orthologous loci of humans and great apes

      GENE
    28. Scott, DA; Drury, S; Sundstrom, RA; Bishop, J; Swiderski, RE; Carmi, R; Ramesh, A; Elbedour, K; Srisailapathy, CRS; Keats, BJ; Sheffield, VC; Smith, RJH
      Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms ina novel gene, TMEM2

      GENE
    29. Kurkinen, KMA; Keinanen, RA; Karhu, R; Koistinaho, J
      Genomic structure and chromosomal localization of the rat protein kinase Cdelta-gene

      GENE
    30. Medica, I; Logar, N; Peterlin, B
      Characteristics of myotonic dystrophy in Istria: Molecular genetic approach. Part II: Analysis of genetic polymorphisms

      COLLEGIUM ANTROPOLOGICUM
    31. Nakauchi, J; Matsuo, H; Kim, DK; Goto, A; Chairoungdua, A; Cha, SH; Inatomi, J; Shiokawa, Y; Yamaguchi, K; Saito, I; Endou, H; Kanai, Y
      Cloning and characterization of a human brain Na+-independent transporter for small neutral amino acids that transports D-serine with high affinity

      NEUROSCIENCE LETTERS
    32. Bielec, P; Gallagher, D; Yang, YP; Womack, J; Davis, S; Taylor, J; Busbee, D
      Assignment of crystallin beta-polypeptide 1 (CRYBA1) to Atlantic bottlenose dolphin chromosome band 16p11 by in situ hybridization

      CYTOGENETICS AND CELL GENETICS
    33. LaPlante, JM; O'Rourke, F; Lu, XH; Fein, A; Olsen, A; Feinstein, MB
      Cloning of human Ca2+ homoeostasis endoplasmic reticulum protein (CHERP): regulated expression of antisense cDNA depletes CHERP, inhibits intracellular Ca2+ mobilization and decreases cell proliferation

      BIOCHEMICAL JOURNAL
    34. Bello, MJ; de Campos, JM; Vaquero, J; Ruiz-Barnes, P; Kusak, ME; Sarasa, JL; Rey, JA
      hRAD54 gene and 1p high-resolution deletion-mapping analyses in oligodendrogliomas

      CANCER GENETICS AND CYTOGENETICS
    35. Bhat, M; Morrison, PJ; Getty, A; McManus, D; Tubman, R; Nevin, NC
      First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH

      AMERICAN JOURNAL OF MEDICAL GENETICS
    36. Liu, WR; Kim, J; Nwankwo, C; Ashworth, LK; Arm, JP
      Genomic organization of the human leukocyte immunoglobulin-like receptors within the leukocyte receptor complex on Chromosome 19q13.4

      IMMUNOGENETICS
    37. Scacheri, PC; Hoffman, EP; Fratkin, JD; Semino-Mora, C; Senchak, A; Davis, MR; Laing, NG; Vedanarayanan, V; Subramony, SH
      A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy

      NEUROLOGY
    38. Nakamura, M; Yang, F; Fujisawa, H; Yonekawa, Y; Kleihues, P; Ohgaki, H
      Loss of heterozygosity on chromosome 19 in secondary glioblastomas

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    39. Brito, RM; Ribeiro, T; Viriato, L; Vieira-Silva, C; Espinheira, R; Pinto-Ribeiro, I; Geada, H
      Sequence variation of new alleles at the short tandem repeat D19S253 locus

      JOURNAL OF FORENSIC SCIENCES
    40. Berghs, S; Aggujaro, D; Dirkx, R; Maksimova, E; Stabach, P; Hermel, JM; Zhang, JP; Philbrick, W; Slepnev, V; Ort, T; Solimena, M
      beta IV spectrin, a new spectrin localized at axon initial segments and nodes of ranvier in the central and peripheral nervous system

      JOURNAL OF CELL BIOLOGY
    41. Domansky, AN; Kopantzev, EP; Snezhkov, EV; Lebedev, YB; Leib-Mosch, C; Sverdlov, ED
      Solitary HERV-K LTRs possess bi-directional promoter activity and contain a negative regulatory element in the U5 region

      FEBS LETTERS
    42. Mugneret, F; Chaffanet, M; Maynadie, M; Guasch, G; Favre, B; Casasnovas, O; Birnbaum, D; Pebusque, MJ
      The 8p12 myeloproliferative disorder. t(8;19)(p12;q13.3): a novel translocation involving the FGFR1 gene

      BRITISH JOURNAL OF HAEMATOLOGY
    43. Yousef, GM; Chang, A; Scorilas, A; Diamandis, EP
      Genomic organization of the human kallikrein gene family on chromosome 19q13.3-q13.4

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    44. Larkin, DM; Serov, OL; Zhdanova, NS
      Mapping of five genes from human chromosome 17 to chromosome hn of the common shrew Sorex araneus

      ACTA THERIOLOGICA
    45. Rippe, V; Belge, G; Meiboom, M; Kazmierczak, B; Fusco, A; Bullerdiek, J
      A KRAB zinc finger protein gene is the potential target of 19q13 translocation in benign thyroid tumors

      GENES CHROMOSOMES & CANCER
    46. Smith, JS; Alderete, B; Minn, Y; Borell, TJ; Perry, A; Mohapatra, G; Hosek, SM; Kimmel, D; O'Fallon, J; Yates, A; Feuerstein, BG; Burger, PC; Scheithauer, BW; Jenkins, RB
      Localization of common deletion regions on 1p and 19q in human gliomas andtheir association with histological subtype

      ONCOGENE
    47. Ji, WZ; Herron, B; Jones, JM; Jenkins, NA; Gilbert, DJ; Copeland, NG; Swank, R; Flaherty, L; Meisler, MH
      Identification of genes within the Krd deletion on mouse chromosome 19

      MAMMALIAN GENOME
    48. Li, HZ; Wu, DK; Sullivan, SL
      Characterization and expression of sema4g, a novel member of the semaphorin gene family

      MECHANISMS OF DEVELOPMENT
    49. Sullivan, M; Olsen, AS; Houslay, MD
      Genomic organisation of the human cyclic AMP-specific phosphodiesterase PDE4C gene and its chromosomal localisation to 19p13.1, between RAB3A and JUND

      CELLULAR SIGNALLING
    50. Feliubadalo, L; Bisceglia, L; Font, M; Dello Strologo, L; Beccia, E; Arslan-Kirchner, M; Steinmann, B; Zelante, L; Estivill, X; Zorzano, A; Palacin, M; Gasparini, P; Nunes, V
      Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1

      GENOMICS
    51. Pras, E; Pras, E; Kreiss, Y; Frishberg, Y; Prosen, L; Aksentijevich, I; Kastner, DL
      Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1using historical recombinants in libyan Jewish cystinuria patients

      GENOMICS
    52. Higa, S; Yoshihama, M; Tanaka, T; Kenmochi, N
      Gene organization and sequence of the region containing the ribosomal protein genes RPL13A and RPS11 in the human genome and conserved features in the mouse genome

      GENE
    53. Frants, RR
      The use of isolates in migraine genetic research

      CEPHALALGIA
    54. Kim, HS; Wadekar, RV; Takenaka, O; Hyun, BH; Crow, TJ
      Phylogenetic analysis of HERV-K LTR-like elements in primates: presence insome New World monkeys and evidence of recent parallel evolution in these species and in Homo sapiens

      ARCHIVES OF VIROLOGY
    55. Iannuzzi, L; Gallagher, DS; Di Meo, GP; Yang, Y; Womack, JE; Davis, SK; Taylor, JF
      Comparative FISH-mapping of six expressed gene loci to river buffalo and sheep chromosomes

      CYTOGENETICS AND CELL GENETICS
    56. Gao, AC; Lou, W; Ichikawa, T; Denmeade, SR; Barrett, JC; Isaacs, JT
      Suppression of the tumorigenicity of prostatic cancer cells by gene(s) located on human chromosome 19p13.1-13.2

      PROSTATE
    57. Ludwig, A; Zong, XG; Stieber, J; Hullin, R; Hofmann, F; Biel, M
      Two pacemaker channels from human heart with profoundly different activation kinetics

      EMBO JOURNAL
    58. Rivera, MA; Perusse, L; Simoneau, JA; Gagnon, J; Dionne, FT; Leon, AS; Skinner, JS; Wilmore, JH; Province, M; Rao, DC; Bouchard, C
      Linkage between a muscle-specific CK gene marker and VO2max in the HERITAGE Family Study

      MEDICINE AND SCIENCE IN SPORTS AND EXERCISE
    59. Vaccari, T; Moroni, A; Rocchi, M; Gorza, L; Bianchi, ME; Beltrame, M; DiFrancesco, D
      The human gene coding for HCN2, a pacemaker channel of the heart

      BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION
    60. Magnani, I; Chiariello, E; Conti, AMF; Finocchiaro, G
      A recurrent 19q11-12 breakpoint suggested by cytogenetic and fluorescence in situ hybridization analysis of three glioblastoma cell lines

      CANCER GENETICS AND CYTOGENETICS
    61. Chernov, IP; Polyakov, AS; Akopov, SB; Nikolaev, LG; Azhikina, TL; Kostina, MB; Sverdlov, ED
      Identification and human chromosome 19 mapping of a chromosome-specific repeated element binding preferentially to nuclear matrix

      BIOORGANICHESKAYA KHIMIYA
    62. Berg, SF; Westgaard, IH; Fossum, S; Dissen, E
      A rat gene homologous to human granule membrane protein 17 is expressed bynatural killer cells, CD8(+) T cells, and a mast cell line

      IMMUNOGENETICS
    63. Kraimps, JL; Canzian, F; Jost, C; Menet, E; Amati, P; Levillian, P; Harach, R; Lesueur, F; Barbier, J; Romeo, G; Bonneau, D
      Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene

      SURGERY
    64. Murphy, C
      Loss of olfactory function in dementing disease

      PHYSIOLOGY & BEHAVIOR
    65. Rasko, JEJ; Battini, JL; Gottschalk, RJ; Mazo, I; Miller, AD
      The RD114 simian type D retrovirus receptor is a neutral amino acid transporter

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    66. Lapuk, AV; Khil, PP; Lavrentieva, IV; Lebedev, YB; Sverdlov, ED
      A human endogenous retrovirus-like (HERV) LTR formed more than 10 million years ago due to an insertion of HERV-H LTR into the 5 ' LTR of HERV-K is situated on human chromosomes 10, 19 and Y

      JOURNAL OF GENERAL VIROLOGY
    67. Jilani, A; Ramotar, D; Slack, C; Ong, C; Yang, XM; Scherer, SW; Lasko, DD
      Molecular cloning of the human gene, PNKP, encoding a polynucleotide kinase 3 '-phosphatase and evidence for its role in repair of DNA strand breaks caused by oxidative damage

      JOURNAL OF BIOLOGICAL CHEMISTRY
    68. Kozyrev, SV; Hansen, LL; Poltaraus, AB; Domninsky, DA; Kisselev, LL
      Structure of the human CpG-island-containing lung Kruppel-like factor (LKLF) gene and its location in chromosome 19p13.11-13 locus

      FEBS LETTERS
    69. Orho-Melander, M; Almgren, P; Kanninen, T; Forsblom, C; Groop, LC
      A paired-sibling analysis of the Xbal polymorphism in the muscle glycogen synthase gene

      DIABETOLOGIA
    70. Ramenghi, U; Garelli, E; Valtolina, S; Campagnoli, MF; Timeus, F; Crescenzio, N; Mair, M; Varotto, S; D'Avanzo, M; Nobili, B; Massolo, F; Mori, PG; Locatelli, F; Gustavsson, P; Dahl, N; Dianzani, I
      Diamond-Blackfan anaemia in the Italian population

      BRITISH JOURNAL OF HAEMATOLOGY
    71. Bigner, SH; Matthews, MR; Rasheed, BKA; Wiltshire, RN; Friedman, HS; Friedman, AH; Stenzel, TT; Dawes, DM; McLendon, RE; Bigner, DD
      Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization

      AMERICAN JOURNAL OF PATHOLOGY
    72. Slot, F; Olsen, AS; Rao, PN; Abraham, CR
      Localization of human endopeptidase EC 3.4.24.15 (THOP1) to chromosome 19p13.3

      ALZHEIMERS REPORTS
    73. LOUGHLIN J; IRVEN C; MUSTAFA Z; BRIGGS MD; CARR A; LYNCH SA; KNOWLTON RG; COHN DH; SYKES B
      IDENTIFICATION OF 5 NOVEL MUTATIONS IN CARTILAGE OLIGOMERIC MATRIX PROTEIN GENE IN PSEUDOACHRONDROPLASIA AND MULTIPLE EPIPHYSEAL DYSPLASIA

      Human mutation
    74. Ollendorff, V; Mattei, MG; Fournier, E; Adelaide, J; Lopez, M; Rosnet, O; Birnbaum, D
      A third human CBL gene is on chromosome 19

      INTERNATIONAL JOURNAL OF ONCOLOGY
    75. JOHNSON EW; DUBOVSKY J; RICH SS; ODONOVAN CA; ORR HT; ANDERSON VE; GILNAGEL A; AHMANN P; DOKKEN CG; SCHNEIDER DT; WEBER JL
      EVIDENCE FOR A NOVEL GENE FOR FAMILIAL FEBRILE CONVULSIONS, FEB2, LINKED TO CHROMOSOME 19P IN AN EXTENDED FAMILY FROM THE MIDWEST

      Human molecular genetics
    76. CARVER EA; ISSELTARVER L; RINE J; OLSEN AS; STUBBS L
      LOCATION OF MOUSE AND HUMAN GENES CORRESPONDING TO CONSERVED CANINE OLFACTORY RECEPTOR GENE SUBFAMILIES

      Mammalian genome
    77. VINAS AM; DRURY SS; DEANGELIS MM; DEN ZI; HUANG JM; BERLIN CI; HUNT JD; BATZER MA; DENINGER PL; KEATS BJB
      THE MOUSE DEAFNESS LOCUS (DN) IS ASSOCIATED WITH AN INVERSION ON CHROMOSOME-19

      Biochimica et biophysica acta. Molecular basis of disease
    78. MOHRENWEISER HW; TSUJIMOTO S; GORDON L; OLSEN AS
      REGIONS OF SEX-SPECIFIC HYPO-RECOMBINATION AND HYPER-RECOMBINATION IDENTIFIED THROUGH INTEGRATION OF 180 GENETIC-MARKERS INTO THE METRIC PHYSICAL MAP OF HUMAN-CHROMOSOME-19

      Genomics
    79. NIKOLAEV LG; AKOPOV SB; CHERNOV IP; GLOTOV BO; ASHWORTH LK; SVERDLOV ED
      POSITION OF 19 NUCLEAR MATRIX ASSOCIATED REGIONS (MARS) ON HUMAN-CHROMOSOME-19

      Doklady Akademii nauk. Rossijskaa akademia nauk
    80. KUGLER SL; JOHNSON WG
      GENETICS OF THE FEBRILE SEIZURE SUSCEPTIBILITY TRAIT

      Brain & development
    81. LENKKERI U; KESTILA M; LAMERDIN J; MCCREADY P; ADAMSON A; OLSEN A; TRYGGVASON K
      STRUCTURE OF THE HUMAN AMYLOID-PRECURSOR-LIKE PROTEIN GENE APLP1 AT 19Q13.1

      Human genetics
    82. Ikegawa, S; Ohashi, H; Nishimura, G; Kim, KC; Sannohe, A; Kimizuka, M; Fukushima, Y; Nagai, T; Nakamura, Y
      Novel and recurrent COMP (cartilage oligomeric matrix protein) mutations in pseudoachondroplasia and multiple epiphyseal dysplasia

      HUMAN GENETICS
    83. KLINOV DV; LAGUTINA IV; PROKHOROV VV; NERETINA T; KHIL PP; LEBEDEV YB; CHERNY DI; DEMIN VV; SVERDLOV ED
      HIGH-RESOLUTION MAPPING DNAS BY R-LOOP ATOMIC-FORCE MICROSCOPY

      Nucleic acids research
    84. SHINKAI T; OHMORI O; KOJIMA H; TERAO T; SUZUKI T; ABE K; NAKAMURA J
      APOLIPOPROTEIN-E REGULATORY REGION GENOTYPE IN SCHIZOPHRENIA

      Neuroscience letters
    85. VANMOURIK JBA; BUMA P; WILCOX WR
      ELECTRON-MICROSCOPIC STUDY IN MULTIPLE EPIPHYSEAL DYSPLASIA TYPE-II

      Ultrastructural pathology
    86. KUGLER SL; STENROOS ES; MANDELBAUM DE; LEHNER T; MCKOY VV; PROSSICK T; SASVARI J; SWANNICK K; KATZ J; JOHNSON WG
      HEREDITARY FEBRILE SEIZURES - PHENOTYPE AND EVIDENCE FOR A CHROMOSOME19P LOCUS

      American journal of medical genetics
    87. KULHARYA AS; MICHAELIS RC; NORRIS KS; TAYLOR HA; GARCIAHERAS J
      CONSTITUTIONAL DEL(19)(Q12Q13.1) IN A 3-YEAR-OLD GIRL WITH SEVERE PHENOTYPIC ABNORMALITIES AFFECTING MULTIPLE ORGAN SYSTEMS

      American journal of medical genetics
    88. Deere, M; Sanford, T; Ferguson, HL; Daniels, K; Hecht, JT
      Identification of twelve mutations in cartilage oligomeric matrix protein (COMP) in patients with pseudoachondroplasia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    89. KHIL PP; LEBEDEV YB; SVERDLOV ED
      THE HUMAN ENDOGENOUS VIRUS HERV-K LONG TE RMINAL REPEAT IN AN INTRON OF THE ZNF91 GENE

      Bioorganiceskaa himia
    90. KHIL PP; LEBEDEV YB; SVERDLOV ED
      A NEW PUTATIVE GENE PREFERENTIALLY EXPRES SED IN THE HUMAN BRAIN LOCATED ON CHROMOSOME 19Q12 NEAR THE HUMAN ENDOGENOUS VIRUS HERV-K LTR

      Bioorganiceskaa himia
    91. SUTO Y; ISHIKAWA Y; KASAHARA M; KASAI F; YABE T; AKAZA T; JUJI T
      GENE ARRANGEMENT OF THE KILLER-CELL INHIBITORY RECEPTOR FAMILY ON HUMAN-CHROMOSOME 19Q13.4 DETECTED BY FIBER FISH

      Immunogenetics (New York)
    92. GHAFFARI SR; BOYD E; CONNOR JM; JONES AM; TOLMIE JL
      MOSAIC SUPERNUMERARY RING CHROMOSOME-19 IDENTIFIED BY COMPARATIVE GENOMIC HYBRIDIZATION

      Journal of Medical Genetics
    93. AKOPOV SB; NIKOLAEV LG; KHIL PP; LEBEDEV YB; SVERDLOV ED
      LONG TERMINAL REPEATS OF HUMAN ENDOGENOUS RETROVIRUS-K FAMILY (HERV-K) SPECIFICALLY BIND HOST-CELL NUCLEAR PROTEINS

      FEBS letters
    94. GUSTAVSSON P; GARELLI E; DRAPTCHINSKAIA N; BALL S; WILLIG TN; TENTLER D; DIANZANI I; PUNNETT HH; SHAFER FE; CARIO H; RAMENGHI U; GLOMSTEIN A; PFEIFFER RA; GORINGE A; OLIVIERI NF; SMIBERT E; TCHERNIA G; ELINDER G; DAHL N
      IDENTIFICATION OF MICRODELETIONS SPANNING THE DIAMOND-BLACKFAN ANEMIALOCUS ON 19Q13 AND EVIDENCE FOR GENETIC-HETEROGENEITY

      American journal of human genetics
    95. BRIGGS MD; MORTIER GR; COLE WG; KING LM; GOLIK SS; BONAVENTURE J; NUYTINCK L; DEPAEPE A; LEROY JG; BIESECKER L; LIPSON M; WILCOX WR; LACHMAN RS; RIMOIN DL; KNOWLTON RG; COHN DH
      DIVERSE MUTATIONS IN THE GENE FOR CARTILAGE OLIGOMERIC MATRIX PROTEININ THE PSEUDOACHONDROPLASIA MULTIPLE EPIPHYSEAL DYSPLASIA DISEASE SPECTRUM

      American journal of human genetics
    96. Canzian, F; Amati, P; Harach, HR; Kraimps, JL; Lesueur, F; Barbier, J; Levillain, P; Romeo, G; Bonneau, D
      A gene predisposing to familial thyroid tumors with cell oxyphilia maps tochromosome 19p13.2

      AMERICAN JOURNAL OF HUMAN GENETICS
    97. PALLAGI E; MOLNAR M; MOLNAR P; DIOSZEGHY P
      CENTRAL CORE AND NEMALINE RODS IN THE SAME PATIENT

      Acta Neuropathologica
    98. BELGE G; GARCIA E; RIPPE V; FUSCO A; BARTNITZKE S; BULLERDIEK J
      BREAKPOINTS OF 19Q13 TRANSLOCATIONS OF BENIGN THYROID-TUMORS MAP WITHIN A 400 KILOBASE REGION

      Genes, chromosomes & cancer
    99. SULLIVAN AA; TEH BT; JEAVONS S; SCHALLING M; SILBURN P; LARSSON C; BOYLE R
      CEREBRAL AUTOSOMAL-DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY

      Journal of clinical neuroscience
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      Human molecular genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/10/20 alle ore 13:37:34