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    1. Maserati, E; Aprili, F; Vinante, F; Locatelli, F; Amendola, G; Zatterale, A; Milone, G; Minelli, A; Bernardi, F; Lo Curto, F; Pasquali, F
      Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20%of cases

      GENES CHROMOSOMES & CANCER
    2. Safadi, FF; Xu, J; Smock, SL; Rico, MC; Owen, TA; Popoff, SN
      Cloning and characterization of osteoactivin, a novel cDNA expressed in osteoblasts

      JOURNAL OF CELLULAR BIOCHEMISTRY
    3. Alarcon, M; Cantor, RM; Liu, JJ; Gilliam, TC; Geschwind, DH
      Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

      AMERICAN JOURNAL OF HUMAN GENETICS
    4. Spinella-Jaegle, S; Roman-Roman, S; Faucheu, C; Dunn, FW; Kawai, S; Gallea, S; Stiot, V; Blanchet, AM; Courtois, B; Baron, R; Rawadi, G
      Opposite effects of bone morphogenetic protein-2 and transforming growth factor-beta 1 on osteoblast differentiation

      BONE
    5. Koch, C; Cuppens, H; Rainisio, M; Madessani, U; Harms, HK; Hodson, ME; Mastella, G; Navarro, J; Strandvik, B; McKenzie, SG
      European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations

      PEDIATRIC PULMONOLOGY
    6. Kass, LJ; Bazzy, AR
      Chronic hypoxia modulates diaphragm function in the developing rat

      JOURNAL OF APPLIED PHYSIOLOGY
    7. Halayko, AJ; Solway, J
      Molecular mechanisms of phenotypic plasticity in smooth muscle cells

      JOURNAL OF APPLIED PHYSIOLOGY
    8. Kiyokawa, S; Kikuchi, Y; Kamada, H; Harada, H
      Transgenic Begonia

      BIOTECHNOLOGY IN AGRICULTURE AND FORESTRY 48
    9. Godo, T; Mii, M
      Transgenic Nierembergia scoparia (Tall cupflower)

      BIOTECHNOLOGY IN AGRICULTURE AND FORESTRY 48
    10. Daimon, H; Mii, M
      Transgenic Rudbeckia

      BIOTECHNOLOGY IN AGRICULTURE AND FORESTRY 48
    11. Silva, NF; Stone, SL; Christie, LN; Sulaman, W; Nazarian, KAP; Burnett, LA; Arnoldo, MA; Rothstein, SJ; Goring, DR
      Expression of the S receptor kinase in self-compatible Brassica napus cv. Westar leads to the allele-specific rejection of self-incompatible Brassicanapus pollen

      MOLECULAR GENETICS AND GENOMICS
    12. Di Paolo, MC; Paoluzi, OA; Pica, R; Iacopini, F; Crispino, P; Rivera, M; Spera, G; Paoluzi, P
      Sulphasalazine and 5-aminosalicylic acid in long-term treatment of ulcerative colitis: report on tolerance and side-effects

      DIGESTIVE AND LIVER DISEASE
    13. Tanaka, K; Sano, K; Tanaka, K; Kobayashi, M; Katsumura, K; Ikeda, T; Abe, M
      Demonstration of downregulation of alpha-smooth muscle actin in interferon-gamma-treated myofibroblast by a novel cell-capture enzyme immunoassay

      INTERNATIONAL IMMUNOPHARMACOLOGY
    14. Panteleyev, AA; Christiano, AM
      The Charles River "hairless" rat mutation is distinct from the hairless mouse alleles

      COMPARATIVE MEDICINE
    15. Campbell, DJ; Kim, CH; Butcher, EC
      Separable effector T cell populations specialized for B cell help or tissue inflammation

      NATURE IMMUNOLOGY
    16. Lynch, JW
      Commentary on "primary systemic anaplastic large-cell lymphoma (CD30(+)): Advances in biology and current therapeutic approaches"

      CLINICAL LYMPHOMA
    17. Lucia, MB; Rutella, S; Leone, G; Vella, S; Cauda, R
      HIV-protease inhibitors contribute to P-glycoprotein efflux function defect in peripheral blood lymphocytes from HIV-positive patients receiving HAART

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    18. Briones, C; Perez-Olmeda, M; Rodriguez, C; del Romero, J; Hertogs, K; Soriano, V
      Primary genotypic and phenotypic HIV-1 drug resistance in recent seroconverters in Madrid

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    19. Haubrich, R; Demeter, L
      Clinical utility of resistance testing: Retrospective and prospective datasupporting use and current recommendations

      JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
    20. Nakano, M; Aoki, K; Matsumoto, N; Ohnami, S; Hatanaka, K; Hibi, T; Terada, M; Yoshida, T
      Suppression of colorectal cancer growth using an adenovirus vector expressing an antisense K-ras RNA

      MOLECULAR THERAPY
    21. Kong, XT; Choi, SH; Bessho, F; Kobayashi, M; Hanada, R; Yamamoto, K; Hayashi, Y
      Codon 201(Gly) polymorphic type of the DCC gene is related to disseminatedneuroblastoma

      NEOPLASIA
    22. deMello, DE; Lin, ZW
      Pulmonary alveolar proteinosis: A review

      PEDIATRIC PATHOLOGY & MOLECULAR MEDICINE
    23. Hodgson, DJ; Vanbergen, AJ; Watt, AD; Hails, RS; Cory, JS
      Phenotypic variation between naturally co-existing genotypes of a Lepidopteran baculovirus

      EVOLUTIONARY ECOLOGY RESEARCH
    24. Jass, JR; Talbot, IC
      Molecular and cellular biology of pre-malignancy in the gastrointestinal tract

      BEST PRACTICE & RESEARCH IN CLINICAL GASTROENTEROLOGY
    25. Gloyn, AL; McCarthy, MI
      The genetics of type 2 diabetes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    26. Stewart, DM; Tian, L; Nelson, DL
      A case of X-linked agammaglobulinemia diagnosed in adulthood

      CLINICAL IMMUNOLOGY
    27. Wang, XL; Dao, MA; Kuo, I; Nolta, JA
      Phenotypic comparison of extrathymic human bone-marrow-derived T cells with thymic-selected T cells recovered from different tissues

      CLINICAL IMMUNOLOGY
    28. Robert, JS
      Interpreting the homeobox: metaphors of gene action and activation in development and evolution

      EVOLUTION & DEVELOPMENT
    29. Simpson, AJG; Caballero, OL; Pena, SDJ
      Microsatellite instability as a tool for the classification of gastric cancer

      TRENDS IN MOLECULAR MEDICINE
    30. Levite, M
      Nervous immunity: neurotransmitters, extracellular K+ and T-cell function

      TRENDS IN IMMUNOLOGY
    31. Lee, VM; Halligan, AWF; Ng, LL
      Leucocyte intracellular pH and Na+/H+ exchanger isoform-1 activity in postpartum women with pre-eclampsia

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    32. Ben-Chetrit, E; Ben-Chetrit, A
      Familial Mediterranean fever and menstruation

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    33. Reva, ON; Sorokulova, IB; Smirnov, VV
      Simplified technique for identification of the aerobic spore-forming bacteria by phenotype

      INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY
    34. Noone, PG; Knowles, MR
      'CFTR-opathies': disease phenotypes associated with cystic fibrosis transmembrane regulator gene mutations

      RESPIRATORY RESEARCH
    35. Lomas, DA; Silverman, EK
      The genetics of chronic obstructive pulmonary disease

      RESPIRATORY RESEARCH
    36. Sandell, LJ; Aigner, T
      Articular cartilage and changes in arthritis - An introduction: Cell biology of osteoarthritis

      ARTHRITIS RESEARCH
    37. Zimmermann, T; Kunisch, E; Pfeiffer, R; Hirth, A; Stahl, HD; Sack, U; Laube, A; Liesaus, E; Roth, A; Palombo-Kinne, E; Emmrich, F; Kinne, RW
      Isolation and characterization of rheumatoid arthritis synovial fibroblasts from primary culture - primary culture cells markedly differ from fourth-passage cells

      ARTHRITIS RESEARCH
    38. Ahman, AK; Jonsson, BA; Damber, JE; Bergh, A; Gronberg, H
      Low frequency of microsatellite instability in hereditary prostate cancer

      BJU INTERNATIONAL
    39. Niu, Y; Xu, Y; Zhang, J; Bai, J; Yang, H; Ma, T
      Proliferation and differentiation of prostatic stromal cells

      BJU INTERNATIONAL
    40. Kenny, B
      The enterohaemorrhagic Escherichia coli (serotype O157 : H7) Tir molecule is not functionally interchangeable for its enteropathogenic E-coli (serotype O127 : H6) homologue

      CELLULAR MICROBIOLOGY
    41. Ide, T; Laarmann, S; Greune, L; Schillers, H; Oberleithner, H; Schmidt, MA
      Characterization of translocation pores inserted into plasma membranes by type III-secreted Esp proteins of enteropathogenic Escherichia coli

      CELLULAR MICROBIOLOGY
    42. Ben-Chetrit, E; Sagi, M
      Genetic counselling in familial Mediterranean fever: has the time come?

      RHEUMATOLOGY
    43. Blount, JD; Moller, AP; Houston, DC
      Antioxidants, showy males and sperm quality

      ECOLOGY LETTERS
    44. Corrigan, KM; Zhu, H; Willcox, MDP
      Random amplified polymorphic DNA analysis of Acinetobacter species isolated from worn contact lenses

      CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    45. Wang, DQ; Wu, BQ; Li, Y; Heng, WJ; Zhong, HH; Mu, Y; Wang, JJ
      A Chinese homozygote of familial hypercholesterolemia: identification of anovel C263R mutation in the LDL receptor gene

      JOURNAL OF HUMAN GENETICS
    46. Itoh, T; Kikuchi, K; Odagawa, Y; Takata, S; Yano, K; Okada, S; Haneda, N; Ogawa, S; Nakano, O; Kawahara, Y; Kasai, H; Nakayama, T; Fukutomi, T; Sakurada, H; Shimizu, A; Yazaki, Y; Nagai, R; Nakamura, Y; Tanaka, T
      Correlation of genetic etiology with response to beta-adrenergic blockade among symptomatic patients with familial long-QT syndrome

      JOURNAL OF HUMAN GENETICS
    47. Takacs, M; Salamon, D; Myohanen, S; Li, H; Segesdi, J; Ujvari, D; Uhlig, J; Niller, HH; Wolf, H; Berencsi, G; Minarovits, J
      Epigenetics of latent Epstein-Barr virus genomes: High resolution methylation analysis of the bidirectional promoter region of latent membrane protein 1 and 2B genes

      BIOLOGICAL CHEMISTRY
    48. 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
    49. O'Shaughnessy, RFL; Christiano, AM
      Stem cells in the epidermis

      SKIN PHARMACOLOGY AND APPLIED SKIN PHYSIOLOGY
    50. Kotorii, S; Takahashi, K; Kamimura, K; Nishio, T; Arima, K; Yamada, H; Uyama, E; Uchino, M; Suenaga, A; Matsumoto, M; Kuchel, G; Rouleau, GA; Tabira, T
      Mutations of the Notch3 gene in non-caucasian patients with suspected CADASIL syndrome

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    51. Tao, T; Tartakoff, AM
      Nuclear relocation of normal huntingtin

      TRAFFIC
    52. Eksandh, L; Ekstrom, U; Abrahamson, M; Bauer, B; Andreasson, S
      Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1)

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    53. Anisimov, SV; Lakatta, EG; Boheler, KR
      Discovering altered genomic expression patterns in heart: transcriptome determination by serial analysis of gene expression

      EUROPEAN JOURNAL OF HEART FAILURE
    54. Vanhorebeek, I; Baes, M; Declercq, PE
      Isoprenoid biosynthesis is not compromised in a Zellweger syndrome mouse model

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS
    55. Baud-Camus, F; Marquet, P; Soursac, M; Davrinche, C; Farinotti, R
      Determination of N-acetylation phenotype using caffeine as a metabolic probe and high-performance liquid chromatography with either ultraviolet detection or electrospray mass spectrometry

      JOURNAL OF CHROMATOGRAPHY B
    56. Garcia-Lerma, JG; Heneine, W
      Resistance of human immunodeficiency virus type 1 to reverse transcriptaseand protease inhibitors: genotypic and phenotypic testing

      JOURNAL OF CLINICAL VIROLOGY
    57. Romney, CA; Paulauskis, JD; Little, JB
      X-ray induction of microsatellite instability at autosomal loci in human lymphoblastoid WTK1 cells

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    58. Wilson, VL; Wade, KR; Yin, XQ; Albertini, RJ
      Temporal delineation of sequential HPRT mutations arising in vivo in a T-cell clone with a mutator phenotype

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    59. Mullauer, L; Gruber, P; Sebinger, D; Buch, J; Wohlfart, S; Chott, A
      Mutations in apoptosis genes: a pathogenetic factor for human disease

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    60. Yokoyama, K; Kamata, N; Hayashi, E; Hoteiya, T; Ueda, N; Fujimoto, R; Nagayama, M
      Reverse correlation of E-cadherin and snail expression in oral squamous cell carcinoma cells in vitro

      ORAL ONCOLOGY
    61. Wheelwright, S; Baron-Cohen, S
      The link between autism and skills such as engineering, maths, physics andcomputing - A reply to Jarrold and Routh, Autism, 1998, 2 (3): 281-9

      AUTISM
    62. Devouassoux-Shisheboran, M; Mauduit, C; Bouvier, R; Berger, F; Bouras, M; Droz, JP; Benahmed, M
      Expression of hMLH1 and hMSH2 and assessment of microsatellite instabilityin testicular and mediastinal germ cell tumours

      MOLECULAR HUMAN REPRODUCTION
    63. Martorelli, L; Virgos, C; Valero, J; Coll, G; Figuera, L; Joven, J; Pocovi, M; Labad, A; Vilella, E
      Schizophrenic women with the APOE epsilon 4 allele have a worse prognosis than those without it

      MOLECULAR PSYCHIATRY
    64. Morbidelli, L; Donnini, S; Ziche, M
      Nitric oxide modulates the angiogenic phenotype of middle-T transformed endothelial cells

      INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
    65. Kennedy, S; Bennett, S; Weeks, DE
      Genetics and infertility II - Affected sib-pair analysis in endometriosis

      HUMAN REPRODUCTION UPDATE
    66. Zhao, ZZ; Sugerman, PB; Zhou, XJ; Walsh, LJ; Savage, NW
      Mast cell degranulation and the role of T cell RANTES in oral lichen planus

      ORAL DISEASES
    67. Gabsi, S; Gouider-Khouja, N; Belal, S; Fki, M; Kefi, M; Turki, I; Ben Hamida, M; Kayden, H; Mebazaa, R; Hentati, F
      Effect of vitamin E supplementation in patients with ataxia with vitamin Edeficiency

      EUROPEAN JOURNAL OF NEUROLOGY
    68. Bellacosa, A
      Functional interactions and signaling properties of mammalian DNA mismatchrepair proteins

      CELL DEATH AND DIFFERENTIATION
    69. Pasqualetti, M; Rijli, FM
      Homeobox gene mutations and brain-stem developmental disorders: learning from knockout mice

      CURRENT OPINION IN NEUROLOGY
    70. Reynolds, PE; Ambur, OH; Casadewall, B; Courvalin, P
      The VanY(D) DD-carboxypeptidase of Enterococcus faecium BM4339 is a penicillin-binding protein

      MICROBIOLOGY-SGM
    71. Vickerman, MM; Minick, PE; Mather, NM
      Characterization of the Streptococcus gordonii chromosomal region immediately downstream of the glucosyltransferase gene

      MICROBIOLOGY-SGM
    72. Guo, RJ; Arai, H; Kitayama, Y; Igarashi, H; Hemmi, H; Arai, T; Hanai, H; Sugimura, H
      Microsatellite instability of papillary subtype of human gastric adenocarcinoma and hMLH1 promoter hypermethylation in the surrounding mucosa

      PATHOLOGY INTERNATIONAL
    73. Soares, AO; Coderre, D; Schanderl, H
      Fitness of two phenotypes of Harmonia axyridis (Coleoptera : Coccinellidae)

      EUROPEAN JOURNAL OF ENTOMOLOGY
    74. Pituch, H; van den Braak, N; van Leeuwen, W; van Belkum, A; Martirosian, G; Obuch-Woszczatynski, P; Luczak, M; Meisel-Mikolajczyk, F
      Clonal dissemination of a toxin-A-negative/toxin-B-positive Clostridium difficile strain from patients with antibiotic-associated diarrhea in Poland

      CLINICAL MICROBIOLOGY AND INFECTION
    75. Felmingham, D
      Microbiological profile of telithromycin, thee first ketolide antimicrobial

      CLINICAL MICROBIOLOGY AND INFECTION
    76. Boente, MD; Carrero-Valenzuela, RD; Frontini, MD; Asial, RA
      Costello syndrome: report of a new case with choanal atresia and fatal outcome

      EUROPEAN JOURNAL OF DERMATOLOGY
    77. Sundberg, JP; King, LE
      Morphology of hair in normal and mutant laboratory mice

      EUROPEAN JOURNAL OF DERMATOLOGY
    78. Resino, S; Sanchez-Ramon, S; Bellon, JM; Jimenez, JL; Munoz-Fernandez, MA
      Impaired interleukin-5 (IL-5) production by T cells as a prognostic markerof disease progression in human immunodeficiency virus type 1 (HIV-1)-infected children

      EUROPEAN CYTOKINE NETWORK
    79. Striz, I; Pokorna-Sochurkova, H; Zheng, L; Jaresova, M; Guzman, J; Costabel, U
      Calprotectin expression and mononuclear phagocyte subpopulations in peripheral blood and bronchoalveolar lavage

      SARCOIDOSIS VASCULITIS AND DIFFUSE LUNG DISEASES
    80. Yoshimatsu, T; Saitoh, A; Ryu, JNS; Shima, D; Handa, H; Hiramoto, M; Kawakami, Y; Aizawa, S
      Characterization of immortalized human chondrocytes originated from osteoarthritis cartilage

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    81. 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
    82. Ma, SK; Au, WY; Chan, AYY; Chan, LC
      Clinical phenotype of triplicated alpha-globin genes and heterozygosity for beta(0)-thalassemia in Chinese subjects

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    83. Chung, MY; Lu, JH; Chien, HP; Hwang, B
      Chromosome 22q11 microdeletion in conotruncal heart defects: Clinical presentation, parental origin and de novo mutations

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    84. Westphal, V; Peterson, S; Patterson, M; Tournay, A; Blumenthal, A; Treacy, EP; Freeze, HH
      Functional significance of PMM2 mutations in mildly affected patients withcongenital disorders of glycosylation Ia

      GENETICS IN MEDICINE
    85. Fan, YS; Zhang, Y; Speevak, M; Farrell, S; Jung, JH; Siu, VM
      Detection of submicroscopic aberrations in patients with unexplained mental retardation by fluorescence in situ hybridization using multiple subtelomeric probes

      GENETICS IN MEDICINE
    86. Keegan, CE; Mulliken, JB; Wu, BL; Korf, BR
      Townes-Brocks syndrome versus expanded spectrum hemifacial microsomia: Review of eight patients and further evidence of a "hot spot" for mutation in the SALL1 gene

      GENETICS IN MEDICINE
    87. Stickler, GB; Hughes, W; Houchin, P
      Clinical features of hereditary progressive arthroophthalmopathy (Sticklersyndrome): A survey

      GENETICS IN MEDICINE
    88. Barlow, GM; Chen, XN; Shi, ZY; Lyons, GE; Kurnit, DM; Celle, L; Spinner, NB; Zackai, E; Pettenati, MJ; Van Riper, AJ; Vekemans, MJ; Mjaatvedt, CH; Korenberg, JR
      Down syndrome congenital heart disease: A narrowed region and a candidate gene

      GENETICS IN MEDICINE
    89. Tuck-Muller, CM; Goodman, BK; Li, SB; Martinez, JE; Chen, XN; Wertelecki, W; Korenberg, JR; Stetten, G
      Partial trisomy 7p defined by analysis of a complex chromosome rearrangement using a BAC clone panel

      GENETICS IN MEDICINE
    90. 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
    91. 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
    92. 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
    93. Hokanson, JS; Pierpont, ME; Hirsch, B; Moller, JH
      22q11.2 microdeletions in adults with familial tetralogy of Fallot

      GENETICS IN MEDICINE
    94. 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
    95. Dipple, KM; Phelan, JK; McCabe, ERB
      Consequences of complexity within biological networks: Robustness and health, or vulnerability and disease

      MOLECULAR GENETICS AND METABOLISM
    96. Vladutiu, GD
      Heterozygosity: An expanding role in proteomics

      MOLECULAR GENETICS AND METABOLISM
    97. Hsu, BYL; Iacobazzi, V; Wang, ZL; Harvie, H; Chalmers, RA; Saudubray, JM; Palmieri, F; Ganguly, A; Stanley, CA
      Aberrant rnRNA splicing associated with coding region mutations in children with carnitine-acylcarnitine translocase deficiency

      MOLECULAR GENETICS AND METABOLISM
    98. Perkins, KJ; Muller, V; Weber, B; Hopwood, JJ
      Prediction of Sanfilippo phenotype severity from immunoquantification of heparan-N-sulfamidase in cultured fibroblasts from mucopolysaccharidosis type IIIA patients

      MOLECULAR GENETICS AND METABOLISM
    99. Tayebi, N; Callahan, M; Madike, V; Stubblefield, BK; Orvisky, E; Krasnewich, D; Fillano, JJ; Sidransky, E
      Gaucher disease and parkinsonism: A phenotypic and genotypic characterization

      MOLECULAR GENETICS AND METABOLISM
    100. Waters, PJ; Scriver, CR; Parniak, MA
      Homomeric and heteromeric interactions between wild-type and mutant phenylalanine hydroxylase subunits: Evaluation of two-hybrid approaches for functional analysis of mutations causing hyperphenylalaninemia

      MOLECULAR GENETICS AND METABOLISM


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Documento generato il 30/10/20 alle ore 00:22:26