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    1. Komatsu, H; Fujisawa, T; Sogo, T; Isozaki, A; Inui, A; Sekine, I; Kobata, M; Ogawa, Y
      Acute self-limiting hepatitis B after immunoprophylaxis failure in an infant

      JOURNAL OF MEDICAL VIROLOGY
    2. Bailey, JA; Yavor, AM; Viggiano, L; Misceo, D; Horvath, JE; Archidiacono, N; Schwartz, S; Rocchi, M; Eichler, EE
      Human-specific duplication and mosaic transcripts: The recent paralogous structure of chromosome 22

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. Simsir, A; Palacios, D; Linehan, WM; Merino, MJ; Abati, A
      Detection of loss of heterozygosity at chromosome 3p25-26 in primary and metastatic ovarian clear-cell carcinoma: Utilization of microdissection and polymerase chain reaction in archival tissues

      DIAGNOSTIC CYTOPATHOLOGY
    4. Hernandez, OM; Housmans, PR; Potter, JD
      Plasticity in skeletal cardiac, and smooth muscle - Invited review: Pathophysiology of cardiac muscle contraction and relaxation as a result of alterations in thin filament regulation

      JOURNAL OF APPLIED PHYSIOLOGY
    5. Duby, F; Cardol, P; Matagne, RF; Remacle, C
      Structure of the telomeric ends of mt DNA, transcriptional analysis and complex I assembly in the dum24 mitochondrial mutant of Chlamydomonas reinhardtii

      MOLECULAR GENETICS AND GENOMICS
    6. Gellon, L; Barbey, R; van der Kemp, PA; Thomas, D; Boiteux, S
      Synergism between base excision repair, mediated by the DNA glycosylases Ntg1 and Ntg2, and nucleotide excision repair in the removal of oxidatively damaged DNA bases in Saccharomyces cerevisiae

      MOLECULAR GENETICS AND GENOMICS
    7. Woloszynska, M; Kieleczawa, J; Ornatowska, M; Wozniak, M; Janska, H
      The origin and maintenance of the small repeat in the bean mitochondrial genome

      MOLECULAR GENETICS AND GENOMICS
    8. Rehg, JE; Blackman, MA; Toth, LA
      Persistent transmission of mouse hepatitis virus by transgenic mice

      COMPARATIVE MEDICINE
    9. Macpherson, AJS; Lamarre, A; McCoy, K; Harriman, GR; Odermatt, B; Dougan, G; Hengartner, H; Zinkernagel, RM
      IgA production without mu or delta chain expression in developing B cells

      NATURE IMMUNOLOGY
    10. Albert, ML; Jegathesan, M; Darnell, RB
      Dendritic cell maturation is required for the cross-tolerization of CD8(+)T cells

      NATURE IMMUNOLOGY
    11. Nicholls, RD; Knepper, JL
      Genome organization, function and imprinting in Prader-Willi and Angelman syndromes

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    12. Cinato, E; Mirotsou, M; Sablitzky, F
      Cre-mediated transgene activation in the developing and adult mouse brain

      GENESIS
    13. Xu, XL; Li, CL; Garrett-Beal, L; Larson, D; Wynshaw-Boris, A; Deng, CX
      Direct removal in the mouse of a flexed neo gene from a three-loxP conditional knockout allele by two novel approaches

      GENESIS
    14. Constien, R; Forde, A; Liliensiek, B; Grone, HJ; Nawroth, P; Hammerling, G; Arnold, B
      Characterization of a novel EGFP reporter mouse to monitor Cre recombination as demonstrated by a Tie2 Cre mouse line

      GENESIS
    15. Kenneson, A; Warren, ST
      The female and the fragile X reviewed

      SEMINARS IN REPRODUCTIVE MEDICINE
    16. Marmor, M; Sheppard, HW; Donnell, D; Bozeman, S; Celum, C; Buchbinder, S; Koblin, B; Seage, GR
      Homozygous and heterozygous CCR5-Delta 32 genotypes are associated with resistance to HIV infection

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    17. Lockett, SF; Robertson, JR; Brettle, RP; Yap, PL; Middleton, D; Brown, AJL
      Mismatched human leukocyte antigen alleles protect against heterosexual HIV transmission

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    18. El-Rifai, W; Rutherford, S; Knuutila, S; Frierson, HF; Moskaluk, CA
      Novel DNA copy number losses in chromosome 12q12-q13 in adenoid cystic carcinoma

      NEOPLASIA
    19. Yang, HW; Chen, YZ; Piao, HY; Takita, J; Soeda, E; Hayashi, Y
      DNA Fragmentation Factor 45 (DFF45) gene at 1p36.2 is homozygously deletedand encodes variant transcripts in neuroblastoma cell line

      NEOPLASIA
    20. Rippin, JD; Patel, A; Bain, SC
      Genetics of diabetic nephropathy

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    21. Williams, O; Brady, HJM
      The role of molecules that mediate apoptosis in T-cell selection

      TRENDS IN IMMUNOLOGY
    22. Lindsay, EA
      Chromosomal microdeletions: Dissecting del22q11 syndrome

      NATURE REVIEWS GENETICS
    23. Yu, YJ; Bradley, A
      Engineering chromosomal rearrangements in mice

      NATURE REVIEWS GENETICS
    24. Wada, T; Louhelainen, J; Hemminki, K; Adolfsson, J; Wijkstrom, H; Norming, U; Borgstrom, E; Hansson, J; Steineck, G
      The prevalence of loss of heterozygosity in chromosome 3, including FHIT, in bladder cancer, using the fluorescent multiplex polymerase chain reaction

      BJU INTERNATIONAL
    25. Weis, U; Turner, B; Gibney, J; Watts, GF; Burke, V; Shaw, KM; Cummings, MH
      Long-term predictors of coronary artery disease and mortality in type 1 diabetes

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    26. Kim, DS; Choi, SI; Lee, HS; Park, JK; Yi, HK
      Determination of human angiotensin converting enzyme (ACE) gene polymorphisms in erectile dysfunction: Frequency differences of ACE gene polymorphisms according to the method of analysis

      CLINICAL CHEMISTRY AND LABORATORY MEDICINE
    27. Iida, A; Saito, S; Sekine, A; Kitamura, Y; Kondo, K; Mishima, C; Osawa, S; Harigae, S; Nakamura, Y
      High-density single-nucleotide polymorphism (SNP) map of the 150-kb regioncorresponding to the human ATP-binding cassette transporter A1 (ABCA1) gene

      JOURNAL OF HUMAN GENETICS
    28. Fujiwara, H; Emi, M; Nagai, H; Ohgaki, K; Imoto, I; Akimoto, M; Ogawa, O; Habuchi, T
      Definition of a 1-Mb homozygous deletion at 9q32-q33 in a human bladder-cancer cell line

      JOURNAL OF HUMAN GENETICS
    29. Kure, S; Kojima, K; Kudo, T; Kanno, K; Aoki, Y; Suzuki, Y; Shinka, T; Sakata, Y; Narisawa, K; Matsubara, Y
      Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia

      JOURNAL OF HUMAN GENETICS
    30. Ishikawa, Y; Tajima, T; Nakae, J; Nagashima, T; Satoh, K; Okuhara, K; Fujieda, K
      Two mutations of the Gs alpha gene in two Japanese patients with sporadic pseudohypoparathyroidism type Ia

      JOURNAL OF HUMAN GENETICS
    31. Tabara, Y; Kohara, K; Nakura, J; Miki, T
      Risk factor-gene interaction in carotid atherosclerosis: effect of gene polymorphisms of renin-angiotensin system

      JOURNAL OF HUMAN GENETICS
    32. Qian, YP; Chu, ZT; Dai, Q; Wei, CD; Chu, JY; Tajima, A; Horai, S
      Mitochondrial DNA polymorphisms in Yunnan nationalities in China

      JOURNAL OF HUMAN GENETICS
    33. Fucharoen, G; Fucharoen, S; Horai, S
      Mitochondrial DNA polymorphisms in Thailand

      JOURNAL OF HUMAN GENETICS
    34. Hiraoka, M; Rossi, F; Trese, MT; Shastry, BS
      X-linked juvenile retinoschisis: mutations at the retinoschisis and Norriedisease gene loci?

      JOURNAL OF HUMAN GENETICS
    35. Iida, A; Saito, S; Sekine, A; Mishima, C; Kondo, K; Kitamura, Y; Harigae, S; Osawa, S; Nakamura, Y
      Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH : ubiquinone oxidoreductase flavoproteins

      JOURNAL OF HUMAN GENETICS
    36. Druck, T; Podolski, J; Byrski, T; Wyrwicz, L; Zajaczek, S; Kata, G; Borowka, A; Lubinski, J; Huebner, K
      The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation

      JOURNAL OF HUMAN GENETICS
    37. Iida, A; Saito, S; Sekine, A; Harigae, S; Osawa, S; Mishima, C; Kondo, K; Kitamura, Y; Nakamura, Y
      Catalog of 46 single-nucleotide polymorphisms (SNPs) in the microsomal glutathione S-transferase 1 (MGST1) gene

      JOURNAL OF HUMAN GENETICS
    38. Clerici, T; Schmid, C; Komminoth, P; Lange, F; Spinas, GA; Brandle, M
      10 Swiss kindreds with multiple endocrine neoplasia type 1: assessment of screening methods

      SWISS MEDICAL WEEKLY
    39. Krutmann, J
      New developments in photoprotection of human skin

      SKIN PHARMACOLOGY AND APPLIED SKIN PHYSIOLOGY
    40. Nicosia, F; Alberici, A; Benussi, L; Gasparini, L; Ghidoni, R; Mazzoli, F; Zanetti, O; Frisoni, GB; Geroldi, C; Binetti, G
      Analysis of alpha-2-macroglobulin-2 allele as a risk factor in Alzheimer'sdisease

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    41. Filler, G; Yang, F; Martin, A; Stolpe, J; Neumayer, HH; Hocher, B
      Renin angiotensin system gene polymorphisms in pediatric renal transplant recipients

      PEDIATRIC TRANSPLANTATION
    42. Riise, R; Storhaug, K; Brondum-Nielsen, K
      Rieger syndrome is associated with PAX6 deletion

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    43. Brooks, EM; Branda, RF; Nicklas, JA; O'Neill, JP
      Molecular description of three macro-deletions and an Alu-Alu recombination-mediated duplication in the HPRT gene in four patients with Lesch-Nyhan disease

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    44. Balestrieri, E; Zanier, R; Degrassi, F
      Molecular characterisation of camptothecin-induced mutations at the hprt locus in Chinese hamster cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    45. Mognato, M; Ferraro, P; Canova, S; Sordi, G; Russo, A; Cherubini, R; Celotti, L
      Analysis of mutational effects at the HPRT locus in human G(0) phase lymphocytes irradiated in vitro with gamma rays

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    46. Hartung, M; Slack, M; Kemper, B
      Analyses of spontaneous mutations of cloned gene 49 of phage T4

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    47. Albertini, RJ
      HPRT mutations in humans: biomarkers for mechanistic studies

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    48. Chao, JI; Yang, JL
      Alteration of cadmium-induced mutational spectrum by catalase depletion inChinese hamster ovary-K1 cells

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    49. Giver, CR; Wong, R; Moore, DH; Pallavicini, MG
      Persistence of aneuploid immature/primitive hemopoietic sub-populations inmice 8 months after benzene exposure in vivo

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    50. Viswanathan, M; Tsuchida, N; Shanmugam, G
      Selective deletion of p14(ARF) exon 1 beta of the INK4a locus in oral squamous cell carcinomas of Indians

      ORAL ONCOLOGY
    51. Uzawa, N; Akanuma, D; Negishi, A; Iwaki, H; Uzawa, Y; Amagasa, T; Yoshida, MA
      Homozygous deletions on the short arm of chromosome 3 in human oral squamous cell carcinomas

      ORAL ONCOLOGY
    52. Krishnamurthy, J; Kannan, K; Feng, J; Mohanprasad, BKC; Tsuchida, N; Shanmugam, G
      Mutational analysis of the candidate tumor suppressor gene ING1 in Indian oral squamous cell carcinoma

      ORAL ONCOLOGY
    53. Martinez, A; Walker, RA; Shaw, JA; Dearing, SJ; Maher, ER; Latif, F
      Chromosome 3p allele loss in early invasive breast cancer: detailed mapping and association with clinicopathological features

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    54. Knowles, MA
      What we could do now: molecular pathology of bladder cancer

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    55. O'Connor, DP; Kay, EW; Leader, M; Murphy, GM; Atkins, GJ; Mabruk, MJEMF
      A high degree of chromosomal instability at 13q14 in cutaneous squamous cell carcinomas: indication for a role of a tumour suppressor gene other thanRb

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    56. Van Landuyt, L; Lissens, W; Stouffs, K; Tournaye, H; Van Steirteghem, A; Liebaers, I
      The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis

      MOLECULAR HUMAN REPRODUCTION
    57. Mehmet, D; Ahmed, F; Cummins, JM; Martin, R; Whelan, J
      Quantification of the common deletion in human testicular mitochondrial DNA by competitive PCR assay using a chimaeric competitor

      MOLECULAR HUMAN REPRODUCTION
    58. Burton, EA; Glorioso, JC
      Multi-modal combination gene therapy for malignant glioma using replication-defective HSV vectors

      DRUG DISCOVERY TODAY
    59. Julve, R; Chaves, FJ; Rovira, E; Pascual, JM; Miralles, A; Armengod, ME; Redon, J
      Polymorphism insertion/deletion of the ACE gene and ambulatory blood pressure circadian variability in essential hypertension

      BLOOD PRESSURE MONITORING
    60. Black, JL; Krahn, LE; Jalal, SM
      Voltage-gated calcium channel gamma 2 subunit gene is not deleted in velo-cardio-facial syndrome

      MOLECULAR PSYCHIATRY
    61. Baghai, TC; Schule, C; Zwanzger, P; Minov, C; Schwarz, MJ; de Jonge, S; Rupprecht, R; Bondy, B
      Possible influence of the insertion/deletion polymorphism in the angiotensin I-converting enzyme gene on therapeutic outcome in affective disorders

      MOLECULAR PSYCHIATRY
    62. Feng, J; Zheng, J; Gelernter, J; Kranzler, H; Cook, E; Goldman, D; Jones, IR; Craddock, N; Heston, LL; Delisi, L; Peltonen, L; Bennett, WP; Sommer, SS
      An in-frame deletion in the alpha(2C) adrenergic receptor is common in African-Americans

      MOLECULAR PSYCHIATRY
    63. Kaiser, R; Tremblay, PB; Schmider, J; Henneken, M; Dettling, M; Muller-Oerlinghausen, B; Uebelhack, R; Roots, I; Brockmoller, J
      Serotonin transporter polymorphisms: no association with response to antipsychotic treatment, but associations with the schizoparanoid and residual subtypes of schizophrenia

      MOLECULAR PSYCHIATRY
    64. Yamashita, N; Shimazaki, N; Ibe, S; Kaneko, R; Tanabe, A; Toyomoto, T; Fujita, K; Hasegawa, T; Toji, S; Tamai, K; Yamamoto, H; Koiwai, O
      Terminal deoxynucleotidyltransferase directly interacts with a novel nuclear protein that is homologous to p65

      GENES TO CELLS
    65. Gelperin, D; Horton, L; Beckman, J; Hensold, J; Lemmon, SK
      Bms1p, a novel GTP-binding protein, and the related Tsr1p are required fordistinct steps of 40S ribosome biogenesis in yeast

      RNA-A PUBLICATION OF THE RNA SOCIETY
    66. Del Campo, M; Kaya, Y; Ofengand, J
      Identification and site of action of the remaining four putative pseudouridine synthases in Escherichia coli

      RNA-A PUBLICATION OF THE RNA SOCIETY
    67. Francis, SE; Camp, NJ; Burton, AJ; Dewberry, RM; Gunn, J; Stephens-Lloyd, A; Cumberland, DC; Gershlick, A; Crossman, DC
      Interleukin 1 receptor antagonist gene polymorphism and restenosis after coronary angioplasty

      HEART
    68. van Geel, PP; Pinto, YM; Zwinderman, AH; Henning, RH; van Boven, A; Jukema, JW; Bruschke, AVG; Kastelein, JJP; van Gilst, WH
      Increased risk for ischaemic events is related to combined RAS polymorphism

      HEART
    69. Kleivdal, H; Puntervoll, P; Jensen, HB
      Topological investigations of the FomA porin from Fusobacterium nucleatum and identification of the constriction loop L6

      MICROBIOLOGY-UK
    70. Tang, S; Lai, KN
      Gene polymorphism in IgA nephropathy

      NEPHROLOGY
    71. Papiernik, M; Banz, A
      Natural regulatory CD4 T cells expressing CD25

      MICROBES AND INFECTION
    72. Katsanos, KH; Nastos, D; Noussias, V; Christodoulou, D; Kappas, A; Tsianos, EV
      Manometric study in Kearns-Sayre syndrome

      DISEASES OF THE ESOPHAGUS
    73. Strippoli, P; Sarchielli, S; Santucci, R; Bagnara, GP; Brandi, G; Biasco, G
      Cold single-strand conformation polymorphism analysis: Optimization for detection of APC gene mutations in patients with familial adenomatous polyposis

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    74. Yuan, QP; Lindblad-Toh, K; Zander, C; Burgess, C; Durr, A; Schalling, M
      A cloning strategy for identification of genes containing trinucleotide repeat expansions

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    75. Toth, T; Kupka, S; Esmer, H; Zeissler, U; Sziklai, I; Zenner, HP; Blin, N; Pfister, M
      Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    76. Tonini, GP; McConville, C; Cusano, R; Rees, SA; Dagnino, M; Longo, L; De Bernardi, B; Conte, M; Garaventa, A; Romeo, G; Devoto, M; Seri, M
      Exclusion of candidate genes and chromosomal regions in familial neuroblastoma

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    77. Wong, LJC
      Recognition of mitochondrial DNA deletion syndrome with non-neuromuscular multisystemic manifestation

      GENETICS IN MEDICINE
    78. Gripp, KW; Kasparcova, V; McDonald-McGinn, DM; Bhatt, S; Bartlett, SP; Storm, AL; Drumheller, TC; Emanuel, BS; Zackai, EH; Stolle, CA
      A diagnostic approach to identifying submicroscopic 7p21 deletions in Saethre-Chotzen syndrome: Fluorescence in situ hybridization and dosage-sensitive Southern blot analysis

      GENETICS IN MEDICINE
    79. De Decker, HP; Lawrenson, JB
      The 22q11.2 deletion: From diversity to a single gene theory

      GENETICS IN MEDICINE
    80. Shaikh, TH; Kurahashi, H; Emanuel, BS
      Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review

      GENETICS IN MEDICINE
    81. Driscoll, DA
      Prenatal diagnosis of the 22q11.2 deletion syndrome

      GENETICS IN MEDICINE
    82. Weinzimer, SA
      Endocrine aspects of the 22q11.2 deletion syndrome

      GENETICS IN MEDICINE
    83. Digilio, MC; Marino, B; Cappa, M; Cambiaso, P; Giannotti, A; Dallapiccola, B
      Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome(deletion 22q11.2 syndrome)

      GENETICS IN MEDICINE
    84. Woodin, M; Wang, PP; Aleman, D; McDonald-McGinn, D; Zackai, E; Moss, E
      Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion

      GENETICS IN MEDICINE
    85. Marino, B; Digilio, MC; Toscano, A; Anaclerio, S; Giannotti, A; Feltri, C; de Ioris, MA; Angioni, A; Dallapiccola, B
      Anatomic patterns of conotruncal defects associated with deletion 22q11

      GENETICS IN MEDICINE
    86. Eliez, S; Blasey, CM; Menon, V; White, CD; Schmitt, JE; Reiss, AL
      Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2)

      GENETICS IN MEDICINE
    87. Momma, K; Takao, A; Matsuoka, R; Imai, Y; Muto, A; Osawa, M; Takayama, M
      Tetralogy of Fallot associated with chromosome 22q11.2 deletion in adolescents and young adults

      GENETICS IN MEDICINE
    88. Hokanson, JS; Pierpont, ME; Hirsch, B; Moller, JH
      22q11.2 microdeletions in adults with familial tetralogy of Fallot

      GENETICS IN MEDICINE
    89. Manji, S; Roberson, JR; Wiktor, A; Vats, S; Rush, P; Diment, S; Van Dyke, DL
      Prenatal diagnosis of 22q11.2 deletion when ultrasound examination revealsa heart defect

      GENETICS IN MEDICINE
    90. Solot, CB; Gerdes, M; Kirschner, RE; McDonald-McGinn, DM; Moss, E; Woodin, M; Aleman, D; Zackai, EH; Wang, P
      Communication issues in 22q11.2 deletion syndrome: Children at risk

      GENETICS IN MEDICINE
    91. Niklasson, L; Rasmussen, P; Oskarsdottir, S; Gillberg, C
      Neuropsychiatric disorders in the 22q11 deletion syndrome

      GENETICS IN MEDICINE
    92. Harnpicharnchai, P; Jakovljevic, J; Horsey, E; Miles, T; Roman, J; Rout, M; Meagher, D; Imai, B; Guo, YR; Brame, CJ; Shabanowitz, J; Hunt, DF; Woolford, JL
      Composition and functional characterization of yeast 66S ribosome assemblyintermediates

      MOLECULAR CELL
    93. Luzi, P; Rafi, MA; Zaka, M; Curtis, M; Vanier, MT; Wenger, DA
      Generation of a mouse with low galactocerebrosidase activity by gene targeting: A new model of globoid cell leukodystrophy (Krabbe disease)

      MOLECULAR GENETICS AND METABOLISM
    94. Toone, JR; Applegarth, DA; Coulter-Mackie, MB; James, ER
      Recurrent mutations in P- and T-proteins of the glycine cleavage complex and a novel T-protein mutation (N1451): A strategy for the molecular investigation of patients with nonketotic hyperglycinemia (NKH)

      MOLECULAR GENETICS AND METABOLISM
    95. Gomez-Zaera, M; Strom, TM; Rodriguez, B; Estivill, X; Meitinger, T; Nunes, V
      Presence of a major WFS1 mutation in Spanish wolfram syndrome pedigrees

      MOLECULAR GENETICS AND METABOLISM
    96. Wyatt-Ashmead, J; Kleinschmidt-DeMasters, B; Mierau, GW; Malkin, D; Orsini, E; McGavran, L; Foreman, NK
      Choroid plexus carcinomas and rhabdoid tumors: Phenotypic and genotypic overlap

      PEDIATRIC AND DEVELOPMENTAL PATHOLOGY
    97. Ruibal-Ares, B; Belmonte, L; Bare, P; Scolnik, M; Palacios, MF; Bayo-Hanza, C; Galmarini, CM; Mendez, G; de Bracco, MME
      Immortalized Epstein-Barr virus-positive B-cell lines obtained by prolonged culture of peripheral blood mononuclear cells from human immunodeficiencyvirus type 1-positive patients

      JOURNAL OF HUMAN VIROLOGY
    98. Semprini, S; Tacconelli, A; Capon, F; Brancati, F; Dallapiccola, B; Novelli, G
      A single strand conformation polymorphism-based carrier test for spinal muscular atrophy

      GENETIC TESTING
    99. Alvarez, R; Gonzalez, P; Batalla, A; Reguero, JR; Iglesias-Cubero, G; Hevia, S; Cortina, A; Merino, E; Gonzalez, I; Alvarez, V; Coto, E
      Association between the NOS3 (-786 T/C) and the ACE (I/D) DNA genotypes and early coronary artery disease

      NITRIC OXIDE-BIOLOGY AND CHEMISTRY
    100. Stankiewicz, P; Park, SS; Inoue, K; Lupski, JR
      The evolutionary chromosome translocation 4;19 in Gorilla gorilla is associated with microduplication of the chromosome fragment syntenic to sequences surrounding the human proximal CMT1A-REP

      GENOME RESEARCH


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Documento generato il 26/05/20 alle ore 12:59:46