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La ricerca find articoli where soggetti phrase all words 'LESCH-NYHAN SYNDROME' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 135 riferimenti
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    1. Albertini, RJ
      HPRT mutations in humans: biomarkers for mechanistic studies

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    2. Mizunuma, M; Fujimori, S; Ogino, H; Ueno, T; Inoue, H; Kamatani, N
      A recurrent large Alu-mediated deletion in the hypoxanthine phosphoribosyltransferase (HPRT1) gene associated with Lesch-Nyhan syndrome

      HUMAN MUTATION
    3. Mikhail, AG; King, BH
      Self-injurious behavior in mental retardation

      CURRENT OPINION IN PSYCHIATRY
    4. Moy, SS; Knapp, DJ; Breese, GR
      Effect of olanzapine on functional responses from sensitized D-1-dopamine receptors in rats with neonatal dopamine loss

      NEUROPSYCHOPHARMACOLOGY
    5. Connolly, GP
      Hypoxanthine-guanine phosphoribosyltransferase-deficiency produces aberrant neurite outgrowth of rodent neuroblastoma used to model the neurological disorder Lesch Nyhan syndrome

      NEUROSCIENCE LETTERS
    6. Boer, P; Brosh, S; Wasserman, L; Hammel, I; Zoref-Shani, E; Sperling, O
      Decelerated rate of dendrite outgrowth from dopaminergic neurons in primary cultures from brains of hypoxanthine phosphoribosyltransferase-deficient knockout mice

      NEUROSCIENCE LETTERS
    7. Connolly, GP
      Cell imaging and morphology - Application to studies of inherited purine metabolic disorders

      PHARMACOLOGY & THERAPEUTICS
    8. Rivero, MB; Olicio, R; Lima, CR; Bonvicino, CR; Moreira, MAM; Llerena, JC; Seuanez, HN
      Molecular analysis of HPRT1(+) somatic cell hybrids derived from a carrierof an HPRT1 mutation responsible for Lesch-Nyhan syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    9. Hamilton, BA; Frankel, WN
      Of mice and genome sequence

      CELL
    10. Puig, JG; Torres, RJ; Mateos, FA; Ramos, TH; Arcas, JM; Buno, AS; O'Neill, P
      The spectrum of hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency - Clinical experience based on 22 patients front 18 Spanish families

      MEDICINE
    11. Martinez, J; Dugaiczyk, LJ; Zielinski, R; Dugaiczyk, A
      Human genetic disorders, a phylogenetic perspective

      JOURNAL OF MOLECULAR BIOLOGY
    12. Connolly, GP; Duley, JA; Stacey, NC
      Abnormal development of hypoxanthine-guanine phosphoribosyltransferase-deficient CNS neuroblastoma

      BRAIN RESEARCH
    13. Smith, DW; Friedmann, T
      Characterization of the dopamine defect in primary cultures of dopaminergic neurons from hypoxanthine phosphoribosyltransferase knockout mice

      MOLECULAR THERAPY
    14. Kolter, T; Magin, TM; Sandhoff, K
      Biomolecule function: No reliable prediction from cell culture

      TRAFFIC
    15. Jinnah, HA; De Gregorio, L; Harris, JC; Nyhan, WL; O'Neill, JP
      The spectrum of inherited mutations causing HPRT deficiency: 75 new cases and a review of 196 previously reported cases

      MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
    16. Holding, C; Bolton, V; Monk, M
      Detection of human novel developmental genes in cDNA derived from replicate individual preimplantation embryos

      MOLECULAR HUMAN REPRODUCTION

    17. Genetics and stone

      PROGRES EN UROLOGIE
    18. Pesi, R; Micheli, V; Jacomelli, G; Peruzzi, L; Camici, M; Garcia-Gil, M; Allegrini, S; Tozzi, MG
      Cytosolic 5 '-nucleotidase hyperactivity in erythrocytes of Lesch-Nyhan syndrome patients

      NEUROREPORT
    19. Zoref-Shani, E; Feinstein, S; Frishberg, Y; Bromberg, Y; Sperling, O
      Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guaninephosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    20. Brosh, S; Boer, P; Sperling, O; Zoref-Shani, E
      Elevated UTP and CTP content in cultured neurons from HPRT-deficient transgenic mice

      JOURNAL OF MOLECULAR NEUROSCIENCE
    21. Saito, Y; Takashima, S
      Neurotransmitter changes in the pathophysiology of Lesch-Nyhan syndrome

      BRAIN & DEVELOPMENT
    22. Stacey, NC; Ma, MHY; Duley, JA; Connolly, GP
      Abnormalities in cellular adhesion of neuroblastoma and fibroblast models of Lesch Nyhan syndrome

      NEUROSCIENCE
    23. Ernst, M
      Commentary: Considerations on the characterization and treatment of self-injurious behavior

      JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS
    24. Shishido, T; Watanabe, Y; Kato, K; Horikoshi, R; Niwa, SI
      Effects of dopamine, NMDA, opiate, and serotonin-related agents on acute methamphetamine-induced self-injurious behavior in mice

      PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
    25. White, T; Schultz, SK
      Naltrexone treatment for a 3-year-old boy with self-injurious behavior

      AMERICAN JOURNAL OF PSYCHIATRY
    26. Richards, SJ; Dunnett, SB
      Genetic models of Alzheimer's disease and their psychopathological validity

      ALZHEIMERS REPORTS
    27. Young, SN; Palmour, RM
      Research on genes: promises and limitations

      JOURNAL OF PSYCHIATRY & NEUROSCIENCE
    28. Ellis, CR; Singh, NN; Ruane, AL
      Nutritional, dietary, and hormonal treatments for individuals with mental retardation and developmental disabilities

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    29. Ordway, JM; Cearley, JA; Detloff, PJ
      CAG-polyglutamine-repeat mutations: independence from gene context

      PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
    30. Southgate, TD; Bain, D; Fairbanks, LD; Morelli, AE; Larregina, AT; Simmonds, HA; Castro, MG; Lowenstein, PR
      Adenoviruses encoding HPRT correct biochemical abnormalities of HPRT-deficient cells and allow their survival in negative selection medium

      METABOLIC BRAIN DISEASE
    31. Wojcik, BE; Jinnah, HA; Muller-Sieburg, CE; Friedmann, T
      Bone marrow transplantation does not ameliorate the neurologic symptoms inmice deficient in hypoxanthine guanine phosphoribosyl transferase (HPRT)

      METABOLIC BRAIN DISEASE
    32. Chang, SJ; Chang, JG; Chen, CJ; Wang, JC; Ou, TT; Chang, KL; Ko, YC
      Identification of a new single nucleotide substitution on the hypoxanthine-guanine phosphoribosyltransferase gene (HPRTTsou)from a Taiwanese aboriginal family with severe gout

      JOURNAL OF RHEUMATOLOGY
    33. Sponseller, PD; Ahn, NU; Choi, JC; Ahn, UM
      Orthopedic problems in Lesch-Nyhan syndrome

      JOURNAL OF PEDIATRIC ORTHOPAEDICS
    34. Ray, PF; Harper, JC; Ao, A; Taylor, DM; Winston, RML; Hughes, M; Handyside, AH
      Successful preimplantation genetic diagnosis for sex linked Lesch-Nyhan syndrome using specific diagnosis

      PRENATAL DIAGNOSIS
    35. Saito, Y; Ito, M; Hanaoka, S; Ohama, E; Akaboshi, S; Takashima, S
      Dopamine receptor upregulation in Lesch-Nyhan syndrome: A postmortem study

      NEUROPEDIATRICS
    36. Turner, C; Panksepp, J; Bekkedal, M; Borkowski, C; Burgdorf, J
      Paradoxical effects of serotonin and opioids in pemoline-induced self-injurious behavior

      PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
    37. Cromwell, HC; Levine, MS; King, BH
      Cortical damage enhances pemoline-induced self-injurious behavior in prepubertal rats

      PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
    38. Micheli, V; Sestini, S; Rocchigiani, M; Jacomelli, G; Manzoni, F; Peruzzi, L; Gathof, BS; Zammarchi, E; Pompucci, G
      Hypoxanthine-guanine phosphoribosyltransferase deficiency and erythrocyte synthesis of pyridine coenzymes

      LIFE SCIENCES
    39. Pelled, D; Sperling, O; Zoref-Shani, E
      Abnormal purine and pyrimidine nucleotide content in primary astroglia cultures from hypoxanthine-guanine phosphoribosyltransferase-deficient transgenic mice

      JOURNAL OF NEUROCHEMISTRY
    40. Rudolph, U; Mohler, H
      Genetically modified animals in pharmacological research: future trends

      EUROPEAN JOURNAL OF PHARMACOLOGY
    41. ONEIL JP; ROGAN PK; CARIELLO N; NICKLAS JA
      MUTATIONS THAT ALTER RNA SPLICING OF THE HUMAN HPRT GENE - A REVIEW OF THE SPECTRUM

      Mutation research. Reviews in mutation research
    42. DANIELS R; ADJAYE J; BOLTON V; MONK M
      DETECTION OF A NOVEL SPLICE VARIANT OF THE HYPOXANTHINE-GUANINE PHOSPHORIBOSYL TRANSFERASE GENE IN HUMAN OOCYTES AND PREIMPLANTATION EMBRYOS - IMPLICATIONS FOR A RT-PCR-BASED PREIMPLANTATION DIAGNOSIS OF LESCH-NYHAN-SYNDROME

      Molecular human reproduction (Print)
    43. LEWIS MH; BODFISH JW
      REPETITIVE BEHAVIOR DISORDERS IN AUTISM

      Mental retardation and developmental disabilities research reviews
    44. ZIMMERMAN AW; JINNAH HA; LOCKHART PJ
      BEHAVIORAL NEUROPHARMACOLOGY

      Mental retardation and developmental disabilities research reviews
    45. BOEHM T
      POSITIONAL CLONING AND GENE IDENTIFICATION

      Methods
    46. HANTRAYE P
      MODELING DOPAMINE SYSTEM DYSFUNCTION IN EXPERIMENTAL-ANIMALS

      Nuclear medicine and biology
    47. Kamatani, N
      Partial hypoxanthine phosphoribosyltransferase deficiency: Unrecognized until adult ages

      INTERNAL MEDICINE
    48. ONEILL JP; FINETTE BA
      TRANSITION MUTATIONS AT CPG DINUCLEOTIDES ARE THE MOST FREQUENT IN-VIVO SPONTANEOUS SINGLE-BASE SUBSTITUTION MUTATION IN THE HUMAN HPRT GENE

      Environmental and molecular mutagenesis
    49. Saito, Y; Hanaoka, S; Fukumizu, M; Morita, H; Ogawa, T; Takahashi, K; Ito, M; Hashimoto, T
      Polysomnographic studies of Lesch-Nyhan syndrome

      BRAIN & DEVELOPMENT
    50. KING BH; CROMWELL HC; LEE HT; BEHRSTOCK SP; SCHMANKE T; MAIDMENT NT
      DOPAMINERGIC AND GLUTAMATERGIC INTERACTIONS IN THE EXPRESSION OF SELF-INJURIOUS-BEHAVIOR

      Developmental neuroscience
    51. CURTO R; VOIT EO; CASCANTE M
      ANALYSIS OF ABNORMALITIES IN PURINE METABOLISM LEADING TO GOUT AND TONEUROLOGICAL DYSFUNCTIONS IN MAN

      Biochemical journal
    52. KHATTAK FH; MORRIS IM; HARRIS K
      KELLEY-SEEGMILLER-SYNDROME - A CASE-REPORT AND REVIEW OF THE LITERATURE

      British journal of rheumatology
    53. EDAMURA K; SASAI H
      NO SELF-INJURIOUS-BEHAVIOR WAS FOUND IN HPRT-DEFICIENT MICE TREATED WITH 9-ETHYLADENINE

      Pharmacology, biochemistry and behavior
    54. GROSSMAN R; VEROBYEV L
      THE NEUROBIOLOGY OF STEREOTYPIC BEHAVIORS AND STEREOTYPIC MOVEMENT-DISORDERS

      Psychiatric annals
    55. Puig, JG; Mateos, FA; Torres, RJ; Buno, AS
      Purine metabolism in female heterozygotes for hypoxanthine-guanine phosphoribosyltransferase deficiency

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    56. CLARKE DJ
      PSYCHOPHARMACOLOGY OF SEVERE SELF-INJURY ASSOCIATED WITH LEARNING-DISABILITIES

      British Journal of Psychiatry
    57. STODGELL CJ; LOUPE PS; SCHROEDER SR; TESSEL RE
      CROSS-SENSITIZATION BETWEEN FOOTSHOCK STRESS AND APOMORPHINE ON SELF-INJURIOUS-BEHAVIOR AND NEOSTRIATAL CATECHOLAMINES IN A RAT MODEL OF LESCH-NYHAN-SYNDROME

      Brain research
    58. VANKEUREN KR; STODGELL CJ; SCHROEDER SR; TESSEL RE
      FIXED-RATIO DISCRIMINATION-TRAINING AS REPLACEMENT THERAPY IN PARKINSONS-DISEASE - STUDIES IN A 6-HYDROXYDOPAMINE-TREATED RAT MODEL

      Brain research
    59. TEMPLETON NS; ROBERTS DD; SAFER B
      EFFICIENT GENE TARGETING IN MOUSE EMBRYONIC STEM-CELLS

      Gene therapy
    60. WILLIAMS KS; HANKERSON JG; ERNST M; ZAMETKIN A
      USE OF PROPOFOL ANESTHESIA DURING OUTPATIENT RADIOGRAPHIC IMAGING STUDIES IN PATIENTS WITH LESCH-NYHAN SYNDROME

      Journal of clinical anesthesia
    61. MOREADITH RW; RADFORD NB
      GENE TARGETING IN EMBRYONIC STEM-CELLS - THE NEW PHYSIOLOGY AND METABOLISM

      Journal of molecular medicine
    62. HIDALGOLAOS RI; KEDAR A; WILLIAMS CA; NEIBERGER RE
      A NEW POINT MUTATION IN A HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE-DEFICIENT PATIENT

      Pediatric nephrology
    63. ERHARD U; HERKENRATH P; BENZBOHM G; QUERFELD U
      LESCH-NYHAN SYNDROME - CLINICAL-DIAGNOSIS AND CONFIRMATION BY BIOCHEMICAL AND GENETIC METHODS

      Pediatric nephrology
    64. LI J; AYYADEVARA R; REIS RJS
      CARCINOGENS STIMULATE INTRACHROMOSOMAL HOMOLOGOUS RECOMBINATION AT ANENDOGENOUS LOCUS IN HUMAN-DIPLOID FIBROBLASTS

      Mutation research. DNA repair
    65. BURKHARTSCHULTZ KJ; JONES IM
      DELETION AND INSERTION IN-VIVO SOMATIC MUTATIONS IN THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) GENE OF HUMAN T-LYMPHOCYTES

      Environmental and molecular mutagenesis
    66. RENWICK PJ; BIRLEY AJ; HULTEN MA
      STUDY OF ALU SEQUENCES AT THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE (HPRT) ENCODING REGION OF MAN

      Gene
    67. MOY SS; CRISWELL HE; BREESE GR
      DIFFERENTIAL-EFFECTS OF BILATERAL DOPAMINE DEPLETION IN NEONATAL AND ADULT-RATS

      Neuroscience and biobehavioral reviews
    68. ORDWAY JM; TALLAKSENGREENE S; GUTEKUNST CA; BERNSTEIN EM; CEARLEY JA; WIENER HW; DURE LS; LINDSEY R; HERSCH SM; JOPE RS; ALBIN RL; DETLOFF PJ
      ECTOPICALLY EXPRESSED CAG REPEATS CAUSE INTRANUCLEAR INCLUSIONS AND APROGRESSIVE LATE-ONSET NEUROLOGICAL PHENOTYPE IN THE MOUSE

      Cell
    69. HARKNESS RA; SAUGSTAD OD
      THE IMPORTANCE OF THE MEASUREMENT OF ATP DEPLETION AND SUBSEQUENT CELL-DAMAGE WITH AN ESTIMATE OF SIZE AND NATURE OF THE MARKET FOR A PRACTICABLE METHOD - A REVIEW DESIGNED FOR TECHNOLOGY-TRANSFER

      Scandinavian journal of clinical & laboratory investigation
    70. JIMENEZ RT; ANTON FM; MATEOS JM; PUIG JG
      GENETIC DIAGNOSIS OF HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HGPRT) - A STUDY OF 12 CASES

      Medicina Clinica
    71. AUBRECHT J; GOAD MEP; SCHIESTL RH
      TISSUE-SPECIFIC TOXICITIES OF THE ANTICANCER DRUG 6-THIOGUANINE IS DEPENDENT ON THE HPRT STATUS IN TRANSGENIC MICE

      The Journal of pharmacology and experimental therapeutics
    72. YOKOYAMA C; OKAMURA H
      SELF-INJURIOUS-BEHAVIOR AND DOPAMINERGIC NEURON SYSTEM IN NEONATAL 6-HYDROXYDOPAMINE-LESIONED RAT .1. DOPAMINERGIC-NEURONS AND RECEPTORS

      The Journal of pharmacology and experimental therapeutics
    73. SAEMUNDSSON SR; ROBERTS MW
      ORAL SELF-INJURIOUS-BEHAVIOR IN THE DEVELOPMENTALLY DISABLED - REVIEWAND A CASE

      Journal of dentistry for children
    74. LARALEMUS A; PEREZDELAMORA M; MENDEZFRANCO J; PALOMERORIVERO M; DRUCKERCOLIN R
      EFFECTS OF REM-SLEEP DEPRIVATION ON THE D-AMPHETAMINE-INDUCED SELF-MUTILATING BEHAVIOR

      Brain research
    75. SAADE NE; ATWEH SF; BAHUTH NB; JABBUR SJ
      AUGMENTATION OF NOCICEPTIVE REFLEXES AND CHRONIC DEAFFERENTATION PAINBY CHEMICAL LESIONS OF EITHER DOPAMINERGIC TERMINALS OR MIDBRAIN DOPAMINERGIC-NEURONS

      Brain research
    76. DOWNS SM
      HYPOXANTHINE REGULATION OF OOCYTE MATURATION IN THE MOUSE - INSIGHTS USING HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE-DEFICIENT ANIMALS

      Biology of reproduction
    77. REDHEAD NJ; SELFRIDGE J; WU CL; MELTON DW
      MICE WITH ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY DEVELOP FATAL 2,8-DIHYDROXYADENINE LITHIASIS

      Human gene therapy
    78. YAMADA Y; GOTO H; SHIOMI M; YAMAMOTO T; HIGASHINO K; OGASAWARA N
      A NOVEL DE-NOVO MUTATION IN HPRT GENE RESPONSIBLE FOR LESCH-NYHAN SYNDROME (HPRT(OSAKA))

      Japanese journal of human genetics
    79. HUNTER TC; MELANCON SB; DALLAIRE L; TAFT S; SKOPEK TR; ALBERTINI RJ; ONEILL JP
      GERMINAL HPRT SPLICE DONOR SITE MUTATION RESULTS IN MULTIPLE RNA SPLICING PRODUCTS IN T-LYMPHOCYTE CULTURES

      Somatic cell and molecular genetics
    80. SHIMIZU N; KONOMI H; ARIMA M; AOKI T
      HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE GENE ANALYSIS FOR JAPANESE PATIENTS WITH LESCH-NYHAN SYNDROME

      Acta Paediatrica Japonica Overseas Edition
    81. SHEWELL PC; THOMPSON AG
      ATLANTOAXIAL INSTABILITY IN LESCH-NYHAN SYNDROME

      Spine (Philadelphia, Pa. 1976)
    82. MAILIS A
      COMPULSIVE TARGETED SELF-INJURIOUS-BEHAVIOR IN HUMANS WITH NEUROPATHIC PAIN - A COUNTERPART OF ANIMAL AUTOTOMY - 4 CASE-REPORTS AND LITERATURE-REVIEW

      Pain
    83. PLUMB TJ; BOSCH A; ROESSLER BJ; SHEWACH DS; DAVIDSON BL
      HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE (HPRT) EXPRESSION IN THE CENTRAL-NERVOUS-SYSTEM OF HPRT-DEFICIENT MICE FOLLOWING ADENOVIRAL-MEDIATED GENE-TRANSFER

      Neuroscience letters
    84. ALLEN SM; RICE SN
      RISPERIDONE ANTAGONISM OF SELF-MUTILATION IN A LESCH-NYHAN PATIENT

      Progress in neuro-psychopharmacology & biological psychiatry
    85. GRAHAM GW; AITKEN DA; CONNOR JM
      PRENATAL-DIAGNOSIS BY ENZYME ANALYSIS IN 15 PREGNANCIES AT RISK FOR THE LESCH-NYHAN SYNDROME

      Prenatal diagnosis
    86. JIRALERSPONG S; PATEL PI
      REGULATION OF THE HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE GENE - IN-VITRO AND IN-VIVO APPROACHES

      Proceedings of the Society for Experimental Biology and Medicine
    87. JASIN M; MOYNAHAN ME; RICHARDSON C
      TARGETED TRANSGENESIS

      Proceedings of the National Academy of Sciences of the United Statesof America
    88. DEUBEL W; BASSUKAS ID; SCHLERETH W; LORENZ R; HEMPEL K
      AGE-DEPENDENT SELECTION AGAINST HPRT DEFICIENT T-LYMPHOCYTES IN THE HPRT+ - HETEROZYGOUS MOUSE/

      Mutation research
    89. SIVAM SP
      DOPAMINE, SEROTONIN AND TACHYKININ IN SELF-INJURIOUS-BEHAVIOR

      Life sciences
    90. FLINT J
      ANNOTATION - BEHAVIORAL PHENOTYPES - A WINDOW ONTO THE BIOLOGY OF BEHAVIOR

      Journal of child psychology and psychiatry and allied disciplines
    91. YAMADA Y; SUZUMORI K; TANEMURA M; GOTO H; OGASAWARA N
      MOLECULAR ANALYSIS OF A JAPANESE FAMILY WITH LESCH-NYHAN SYNDROME - IDENTIFICATION OF MUTATION AND PRENATAL-DIAGNOSIS

      Clinical genetics
    92. BURGEMEISTER R; ROTZER E; GUTENSOHN W; GEHRKE M; SCHIEL W
      IDENTIFICATION OF A NEW MISSENSE MUTATION IN EXON-2 OF THE HUMAN HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE GENE (HPRTI(ISAR)) - A FURTHER EXAMPLE OF CLINICAL HETEROGENEITY IN HPRT DEFICIENCIES

      Human mutation
    93. XU ZD; YU YJ; SCHWARTZ JL; MELTZ ML; HSIE AW
      MOLECULAR NATURE OF SPONTANEOUS MUTATIONS AT THE HYPOXANTHINE-GUANINEPHOSPHORIBOSYLTRANSFERASE (HPRT) LOCUS IN CHINESE-HAMSTER OVARY CELLS

      Environmental and molecular mutagenesis
    94. RAINVILLE IR; ALBERTINI RJ; NICKLAS JA
      BREAKPOINTS AND JUNCTIONAL REGIONS OF INTRAGENIC DELETIONS IN THE HPRT GENE IN HUMAN T-CELLS

      Somatic cell and molecular genetics
    95. ZOREFSHANI E; BROMBERG Y; LILLING G; GOZES I; BROSH S; SIDI Y; SPERLING O
      DEVELOPMENTAL-CHANGES IN PURINE NUCLEOTIDE-METABOLISM IN CULTURED RATASTROGLIA

      International journal of developmental neuroscience
    96. KING BH; AU D; POLAND RE
      PRETREATMENT WITH MK-801 INHIBITS PEMOLINE-INDUCED SELF-BITING BEHAVIOR IN PREPUBERTAL RATS

      Developmental neuroscience
    97. WOLF U
      THE GENETIC CONTRIBUTION TO THE PHENOTYPE

      Human genetics
    98. PIES RW; POPLI AP
      SELF-INJURIOUS-BEHAVIOR - PATHOPHYSIOLOGY AND IMPLICATIONS FOR TREATMENT

      The Journal of clinical psychiatry
    99. SHIMAHARA H; KATO T; HIRAI Y; AKIYAMA M
      SPECTRUM OF IN-VIVO HPRT MUTATIONS IN T-LYMPHOCYTES FROM ATOMIC-BOMB SURVIVORS .1. SEQUENCE ALTERATIONS IN CDNA

      Carcinogenesis
    100. OLIVER C
      ANNOTATION - SELF-INJURIOUS-BEHAVIOR IN CHILDREN WITH LEARNING-DISABILITIES - RECENT ADVANCES IN ASSESSMENT AND INTERVENTION

      Journal of child psychology and psychiatry and allied disciplines


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/01/21 alle ore 03:31:44