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    1. Sun, GF; Tomita, H; Shakkottai, VG; Gargus, JJ
      Genomic organization and promoter analysis of human KCNN3 gene

      JOURNAL OF HUMAN GENETICS
    2. Ichikawa, Y; Goto, J; Hattori, M; Toyoda, A; Ishii, K; Jeong, SY; Hashida, H; Masuda, N; Ogata, K; Kasai, F; Hirai, M; Maciel, P; Rouleau, GA; Sakaki, Y; Kanazawa, I
      The genomic structure and expression of MJD, the Machado-Joseph disease gene

      JOURNAL OF HUMAN GENETICS
    3. Tallaksen, CME; Durr, A; Brice, A
      Recent advances in hereditary spastic paraplegia

      CURRENT OPINION IN NEUROLOGY
    4. Wallerand, H; Chabannes, E; Bittard, H
      Idiopathic male infertility and androgen receptors.

      PROGRES EN UROLOGIE
    5. Nance, MA; Myers, RH
      Juvenile onset Huntington's disease - Clinical and research perspectives

      MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS
    6. Buchanan, G; Greenberg, NM; Scher, HI; Harris, JM; Marshall, VR; Tilley, WD
      Collocation of androgen receptor gene mutations in prostate cancer

      CLINICAL CANCER RESEARCH
    7. Kovtun, IV; McMurray, CT
      Trinucleotide expansion in haploid germ cells by gap repair

      NATURE GENETICS
    8. Waerner, T; Gardellin, P; Pfizenmaier, K; Weith, A; Kraut, N
      Human RERE is localized to nuclear promyelocytic leukemia oncogenic domains and enhances apoptosis

      CELL GROWTH & DIFFERENTIATION
    9. Zeron, MM; Chen, NS; Moshaver, A; Lee, ATC; Wellington, CL; Hayden, MR; Raymond, LA
      Mutant huntingtin enhances excitotoxic cell death

      MOLECULAR AND CELLULAR NEUROSCIENCE
    10. Grattan-Smith, PJ; Healey, S; Grigg, JR; Christodoulou, J
      Spinocerebellar ataxia type 7: A distinctive form of autosomal dominant cerebellar ataxia with retinopathy and marked genetic anticipation

      JOURNAL OF PAEDIATRICS AND CHILD HEALTH
    11. Lund, A; Udd, B; Juvonen, V; Andersen, PM; Cederquist, K; Davis, M; Gellera, C; Kolmel, C; Ronnevi, LO; Sperfeld, AD; Sorensen, SA; Tranebjaerg, L; Van Maldergem, L; Watanabe, M; Weber, M; Yeung, L; Savontaus, ML
      Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Zuhlke, C; Hellenbroich, Y; Dalski, A; Kononowa, N; Hagenah, J; Vieregge, P; Riess, O; Klein, C; Schwinger, E
      Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

      EUROPEAN JOURNAL OF HUMAN GENETICS
    13. Schilling, G; Jinnah, HA; Gonzales, V; Coonfield, ML; Kim, Y; Wood, JD; Price, DL; Li, XJ; Jenkins, N; Copeland, N; Moran, T; Ross, CA; Borchelt, DR
      Distinct behavioral and neuropathological abnormalities in transgenic mouse models of HD and DRPLA

      NEUROBIOLOGY OF DISEASE
    14. Andreassen, OA; Dedeoglu, A; Ferrante, RJ; Jenkins, BG; Ferrante, KL; Thomas, M; Friedlich, A; Browne, SE; Schilling, G; Borchelt, DR; Hersch, SM; Ross, CA; Beal, MF
      Creatine increases survival and delays motor symptoms in a transgenic animal model of Huntington's disease

      NEUROBIOLOGY OF DISEASE
    15. Gomes-Pereira, M; Fortune, MT; Monckton, DG
      Mouse tissue culture models of unstable triplet repeats: in vitro selection for larger alleles, mutational expansion bias and tissue specificity, butno association with cell division rates

      HUMAN MOLECULAR GENETICS
    16. Fan, XP; Dion, P; Laganiere, J; Brais, B; Rouleau, GA
      Oligomerization of polyalanine expanded PABPN1 facilitates nuclear proteinaggregation that is associated with cell death

      HUMAN MOLECULAR GENETICS
    17. Richards, RI
      Dynamic mutations: a decade of unstable expanded repeats in human genetic disease

      HUMAN MOLECULAR GENETICS
    18. Orr, HT; Zoghbi, HY
      SCA1 molecular genetics: a history of a 13 year collaboration against glutamines

      HUMAN MOLECULAR GENETICS
    19. Nwosu, V; Carpten, J; Trent, JM; Sheridan, R
      Heterogeneity of genetic alterations in prostate cancer: evidence of the complex nature of the disease

      HUMAN MOLECULAR GENETICS
    20. Lin, CH; Tallaksen-Greene, S; Chien, WM; Cearley, JA; Jackson, WS; Crouse, AB; Ren, SR; Li, XJ; Albin, RL; Detloff, PJ
      Neurological abnormalities in a knock-in mouse model of Huntington's disease

      HUMAN MOLECULAR GENETICS
    21. Bontekoe, CJM; Bakker, CE; Nieuwenhuizen, IM; van der Linde, H; Lans, H; de Lange, D; Hirst, MC; Oostra, BA
      Instability of a (CGG)(98) repeat in the Fmr1 promoter

      HUMAN MOLECULAR GENETICS
    22. Yue, S; Serra, HG; Zoghbi, HY; Orr, HT
      The spinocerebellar ataxia type 1 protein, ataxin-1, has RNA-binding activity that is inversely affected by the length of its polyglutamine tract

      HUMAN MOLECULAR GENETICS
    23. Andreassen, OA; Ferrante, RJ; Dedeoglu, A; Beal, MF
      Lipoic acid improves survival in transgenic mouse models of Huntington's disease

      NEUROREPORT
    24. Ono, Y; De-Meyts, ER; Guellaen, G; Bulle, F
      Sporadic testicular germ cell cancers do not exhibit specific alteration in CAG/CTG repeats containing genes expressed in human testis

      ONCOGENE
    25. Kiehl, TR; Shibata, H; Vo, T; Huynh, DP; Pulst, SM
      Identification and expression of a mouse ortholog of A2BP1

      MAMMALIAN GENOME
    26. Karasawa, M; Tsukamoto, N; Yamane, A; Okamoto, K; Maehara, T; Yokohama, A; Nojima, Y; Omine, M
      Analysis of the distribution of CAG repeats and X-chromosome inactivation status of HUMARA gene in healthy female subjects using improved fluorescence-based assay

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    27. Grierson, AJ; Shaw, CE; Miller, CCJ
      Androgen induced cell death in SHSY5Y neuroblastoma cells expressing wild-type and spinal bulbar muscular atrophy mutant androgen receptors

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    28. Adachi, N; Arima, K; Asada, T; Kato, N; Minami, N; Goto, Y; Onuma, T; Ikeuchi, T; Tsuji, S; Hayashi, M; Fukutani, Y
      Dentatorubral-pallidoluysian atrophy (DRPLA) presenting with psychosis

      JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES
    29. Shen, HH; Huang, AM; Hoheisel, J; Tsai, SF
      Identification and characterization of a SET/NAP protein encoded by a brain-specific gene, MB20

      GENOMICS
    30. Kovtun, IV; Goellner, G; McMurray, CT
      Structural features of trinucleotide repeats associated with DNA expansion

      BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
    31. Zitzmann, M; Nieschlag, E
      Testosterone levels in healthy men and the relation to behavioural and physical characteristics: facts and constructs

      EUROPEAN JOURNAL OF ENDOCRINOLOGY
    32. Paulson, H; Ammache, Z
      Ataxia and hereditary disorders

      NEUROLOGIC CLINICS
    33. Abe, T; Abe, K; Tsuda, T; Itoyama, Y; Tamai, M
      Ophthalmological findings in patients with spinocerebellar ataxia type 1 are not correlated with neurological anticipation

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    34. Bellizzi, D; Losso, MA; Sgaramella, V
      A model for the involvement of Okazaki fragments maturation in the expansion of short tandem repeats

      GENE
    35. Seranski, P; Hoff, C; Radelof, U; Hennig, S; Reinhardt, R; Schwartz, CE; Heiss, NS; Poustka, A
      RAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients

      GENE
    36. Affaitati, A; de Cristofaro, T; Feliciello, A; Varrone, S
      Identification of alternative splicing of spinocerebellar ataxia type 2 gene

      GENE
    37. Srivastava, AK; Choudhry, S; Gopinath, MS; Roy, S; Tripathi, M; Brahmachari, SK; Jain, S
      Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12

      ANNALS OF NEUROLOGY
    38. Rasmussen, A; Matsuura, T; Ruano, L; Yescas, P; Ochoa, A; Ashizawa, T; Alonso, E
      Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10

      ANNALS OF NEUROLOGY
    39. Yamada, M; Wood, JD; Shimohata, T; Hayashi, S; Tsuji, S; Ross, CA; Takahashi, H
      Widespread occurrence of intranuclear atrophin-1 accumulation in the central nervous system neurons of patients with dentatorubral-pallidoluysian atrophy

      ANNALS OF NEUROLOGY
    40. Fujigasaki, H; Verma, IC; Camuzat, A; Margolis, RL; Zander, C; Lebre, AS; Jamot, L; Saxena, R; Anand, I; Holmes, SE; Ross, CA; Durr, A; Brice, A
      SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study ofan Indian family

      ANNALS OF NEUROLOGY
    41. Galvao, R; Mendes-Soares, L; Camara, J; Jaco, I; Carmo-Fonseca, M
      Triplet repeats, RNA secondary structure and toxic gain-of-function modelsfor pathogenesis

      BRAIN RESEARCH BULLETIN
    42. Merry, DE
      Molecular pathogenesis of spinal and bulbar muscular atrophy

      BRAIN RESEARCH BULLETIN
    43. Piccioni, F; Simeoni, S; Andriola, I; Armatura, E; Bassanini, S; Pozzi, P; Poletti, A
      Polyglutamine tract expansion of the androgen receptor in a motoneuronal model of spinal and bulbar muscular atrophy

      BRAIN RESEARCH BULLETIN
    44. Frontali, M
      Spinocerebellar ataxia type 6: Channelopathy or glutamine repeat disorder?

      BRAIN RESEARCH BULLETIN
    45. Squitieri, F; Cannella, M; Giallonardo, P; Maglione, V; Mariotti, C; Hayden, MR
      Onset and pre-onset studies to define the Huntington's disease natural history

      BRAIN RESEARCH BULLETIN
    46. Beauchemin, AMJ; Gottlieb, B; Beitel, LK; Elhaji, YA; Leonard, P; Trifiro, MA
      Cytochrome c oxidase subunit Vb interacts with human androgen receptor: A potential mechanism for neurotoxicity in spinobulbar muscular atrophy

      BRAIN RESEARCH BULLETIN
    47. Malaspina, A; Kaushik, N; de Belleroche, J
      A survey of trinucleotide/tandem repeat-containing transcripts (TNRTs) isolated from human spinal cord to identify genes containing unstable DNA regions as candidates for disorders of motor function

      BRAIN RESEARCH BULLETIN
    48. Calabresi, V; Guida, S; Servadio, A; Jodice, C
      Phenotypic effects of expanded ataxin-1 polyglutamines with interruptions in vitro

      BRAIN RESEARCH BULLETIN
    49. Holmes, SE; O'Hearn, E; Ross, CA; Margolis, RL
      SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia

      BRAIN RESEARCH BULLETIN
    50. Ishiguro, H; Yamada, K; Sawada, H; Nishii, K; Ichino, N; Sawada, M; Kurosawa, Y; Matsushita, N; Kobayashi, K; Goto, J; Hashida, H; Masuda, N; Kanazawa, I; Nagatsu, T
      Age-dependent and tissue-specific CAG repeat instability occurs in mouse knock-in for a mutant Huntington's disease gene

      JOURNAL OF NEUROSCIENCE RESEARCH
    51. Deckel, AW
      Nitric oxide and nitric oxide synthase in Huntington's disease

      JOURNAL OF NEUROSCIENCE RESEARCH
    52. Georgiou, I; Sermon, K; Lissens, W; De Vos, A; Platteau, P; Lolis, D; Van Steirteghem, A; Liebaers, I
      Preimplantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA)

      HUMAN GENETICS
    53. Julien, J; Denier, C; Ferrer, X; Ducros, A; Saintarailles, J; Lagueny, A; Tournier-Lasserve, E; Vital, C
      Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

      JOURNAL OF NEUROLOGY
    54. Ishihara, H; Kanda, F; Nishio, H; Sumino, K; Chihara, K
      Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy

      JOURNAL OF NEUROLOGY
    55. Jardim, LB; Silveira, I; Pereira, ML; Ferro, A; Alonso, I; Moreira, MDC; Mendonca, P; Ferreirinha, F; Sequeiros, J; Giugliani, R
      A survey of spinocerebellar ataxia in South Brazil - 66 new cases with Machado-Joseph disease, SCA7, SCA8, or unidentified disease - Causing mutations

      JOURNAL OF NEUROLOGY
    56. De Fonzo, V; Bersani, E; Aluffi-Pentini, F; Parisi, V
      DNA quadruplexes and dynamical genetics

      MEDICAL HYPOTHESES
    57. Kubota, S
      The extinction program for Homo sapiens and cloning humans: trinucleotide expansion as a one-way track to extinction

      MEDICAL HYPOTHESES
    58. Sieradzan, KA; Mann, DMA
      The selective vulnerability of nerve cells in Huntington's disease

      NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
    59. Eder, IE; Culig, Z; Putz, T; Nessler-Menardi, C; Bartsch, G; Klocker, H
      Molecular biology of the androgen receptor: From molecular understanding to the clinic

      EUROPEAN UROLOGY
    60. Vaswani, M; Kapur, S
      Genetic basis of schizophrenia: Trinucleotide repeats - An update

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    61. Ohara, K
      Anticipation, imprinting, trinucleotide repeat expansions and psychoses

      PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
    62. Reiner, A; Del Mar, N; Meade, CA; Yang, HT; Dragatsis, I; Zeitlin, S; Goldowitz, D
      Neurons lacking huntingtin differentially colonize brain and survive in chimeric mice

      JOURNAL OF NEUROSCIENCE
    63. Miller, EA; Stanford, JL; Hsu, L; Noonan, E; Ostrander, EA
      Polymorphic repeats in the androgen receptor gene in high-risk sibships

      PROSTATE
    64. Suzuki, Y; Sasagawa, I; Tateno, T; Ashida, J; Nakada, T; Muroya, K; Ogata, T
      Mutation screening and CAG repeat length analysis of the androgen receptorgene in Klinefelter's syndrome patients with and without spermatogenesis

      HUMAN REPRODUCTION
    65. Mori, M; Adachi, Y; Kusumi, M; Nakashima, K
      A genetic epidemiological study of spinocerebellar ataxias in Tottori Prefecture, Japan

      NEUROEPIDEMIOLOGY
    66. Patrizio, P; Leonard, DGB; Chen, KL; Hernandez-Ayup, S; Trounson, AO
      Larger trinucleotide repeat size in the androgen receptor gene of infertile men with extremely severe oligozoospermia

      JOURNAL OF ANDROLOGY
    67. Makridakis, NM; Reichardt, JKV
      Molecular epidemiology of hormone-metabolic loci in prostate cancer

      EPIDEMIOLOGIC REVIEWS
    68. Hayes, RB
      Gene-environment interrelations in prostate cancer

      EPIDEMIOLOGIC REVIEWS
    69. Luesse, HG; Schiefer, J; Spruenken, A; Puls, C; Block, F; Kosinski, CM
      Evaluation of R6/2 HD transgenic mice for therapeutic studies in Huntington's disease: behavioral testing and impact of diabetes mellitus

      BEHAVIOURAL BRAIN RESEARCH
    70. Cattaneo, E; Rigamonti, D; Goffredo, D; Zuccato, C; Squitieri, F; Sipione, S
      Loss of normal huntingtin function: new developments in Huntington's disease research

      TRENDS IN NEUROSCIENCES
    71. McMurray, CT
      Huntington's disease: new hope for therapeutics

      TRENDS IN NEUROSCIENCES
    72. Maat-Kievit, A; Helderman-van den Enden, P; Losekoot, M; de Knijff, P; Belfroid, R; Vegter-van der Vlis, M; Roos, R; Breuning, M
      Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    73. Rosenblatt, A; Brinkman, RR; Liang, KY; Almqvist, EW; Margolis, RL; Huang, CY; Sherr, M; Franz, ML; Abbott, MH; Hayden, MR; Ross, CA
      Familial influence on age of onset among siblings with Huntington disease

      AMERICAN JOURNAL OF MEDICAL GENETICS
    74. Sasagawa, I; Nakada, T
      Epidemiology of prostatic cancer in East Asia

      ARCHIVES OF ANDROLOGY
    75. Schatzl, G; Gsur, A; Bernhofer, G; Haidinger, G; Hinteregger, S; Vutuc, C; Haitel, A; Micksche, M; Marberger, M; Madersbacher, S
      Association of vitamin D receptor and 17 hydroxylase gene polymorphisms with benign prostatic hyperplasia and benign prostatic enlargement

      UROLOGY
    76. Ho, LW; Carmichael, J; Swartz, J; Wyttenbach, A; Rankin, J; Rubinsztein, DC
      The molecular biology of Huntington's disease

      PSYCHOLOGICAL MEDICINE
    77. Terstappen, GC; Pula, G; Carignani, C; Chen, MX; Roncarati, R
      Pharmacological characterisation of the human small conductance calcium-activated potassium channel hSK3 reveals sensitivity to tricyclic antidepressants and antipsychotic phenothiazines

      NEUROPHARMACOLOGY
    78. Mariotti, C; Gellera, C; Grisoli, M; Mineri, R; Castucci, A; Di Donato, S
      Pathogenic effect of an intermediate-size SCA-6 allele (CAG)(19) in a homozygous patient

      NEUROLOGY
    79. Rantamaki, M; Krahe, R; Paetau, A; Cormand, B; Mononen, I; Udd, B
      Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family

      NEUROLOGY
    80. Gambardella, A; Muglia, M; Labate, A; Magariello, A; Gabriele, AL; Mazzei, R; Pirritano, D; Conforti, FL; Patitucci, A; Valentino, P; Zappia, M; Quattrone, A
      Juvenile Huntington's disease presenting as progressive myoclonic epilepsy

      NEUROLOGY
    81. Miyoshi, Y; Yamada, T; Tanimura, M; Taniwaki, T; Arakawa, K; Ohyagi, Y; Furuya, H; Yamamoto, K; Sakai, K; Sasazuki, T; Kira, J
      A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1

      NEUROLOGY
    82. Devos, D; Schraen-Maschke, S; Vuillaume, I; Dujardin, K; Naze, P; Willoteaux, C; Destee, A; Sablonniere, B
      Clinical features and genetic analysis of a new form of spinocerebellar ataxia

      NEUROLOGY
    83. Holbert, S; Denghien, I; Kiechle, T; Rosenblatt, A; Wellington, C; Hayden, MR; Margolis, RL; Ross, CA; Dausset, J; Ferrante, RJ; Neri, C
      The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: Neuropathologic and genetic evidence for a role in Huntington's diseasepathogenesis

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    84. Stanbrough, M; Leav, I; Kwan, PWL; Bubley, GJ; Balk, SP
      Prostatic intraepithelial neoplasia in mice expressing an androgen receptor transgene in prostate epithelium

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    85. Shibata, A; Stamey, TA; McNeal, JE; Cheng, I; Peehl, DM
      Genetic polymorphisms in the androgen receptor and type II 5 alpha-reductase genes in prostate enlargement

      JOURNAL OF UROLOGY
    86. Hashida, H; Goto, J; Suzuki, T; Jeong, SY; Masuda, N; Ooie, T; Tachiiri, Y; Tsuchiya, H; Kanazawa, I
      Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA)

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    87. Mori, M; Adachi, Y; Kusumi, M; Nakashima, K
      Spinocerebellar ataxia type 6: founder effect in western Japan

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    88. Montgomery, JS; Price, DK; Figg, WD
      The androgen receptor gene and its influence on the development and progression of prostate cancer

      JOURNAL OF PATHOLOGY
    89. Yabe, I; Sasaki, H; Yamashita, I; Tashiro, K; Takei, A; Suzuki, Y; Kida, H; Takiyama, Y; Nishizawa, M; Hokezu, Y; Nagamatsu, K; Oda, T; Ohnishi, A; Inoue, I; Hata, A
      Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese

      JOURNAL OF MEDICAL GENETICS
    90. Kusakabe, M; Mangiarini, L; Laywell, ED; Bates, GP; Yoshiki, A; Hiraiwa, N; Inoue, J; Steindler, DA
      Loss of cortical and thalamic neuronal tenascin-C expression in a transgenic mouse expressing exon 1 of the human Huntington disease gene

      JOURNAL OF COMPARATIVE NEUROLOGY
    91. Yu, B; Handelsman, DJ
      Pharmacogenetic polymorphisms of the AR and metabolism and susceptibility to hormone-induced azoospermia

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    92. Taplin, ME; Ho, SM
      The endocrinology of prostate cancer

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    93. Lim, HN; Nixon, RM; Chen, H; Hughes, IA; Hawkins, JR
      Evidence that longer androgen receptor polyglutamine repeats are a causal factor for genital abnormalities

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    94. Khorram, O; Patrizio, P; Wang, C; Swerdloff, R
      Reproductive technologies for male infertility

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    95. Westberg, L; Baghaei, F; Rosmond, R; Hellstrand, M; Landen, M; Jansson, M; Holm, G; Bjorntorp, P; Erikson, E
      Polymorphisms of the androgen receptor gene and the estrogen receptor betagene are associated with androgen levels in women

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    96. Lima, M; Smith, MT; Silva, C; Abade, A; Mayer, FM; Coutinho, P
      Natural selection at the MJD locus: Phenotypic diversity, survival and fertility among Machado-Joseph Disease patients from the Azores

      JOURNAL OF BIOSOCIAL SCIENCE
    97. Miller, MJ; Rauer, H; Tomita, H; Rauer, H; Gargus, JJ; Gutman, GA; Cahalan, MD; Chandy, KG
      Nuclear localization and dominant-negative suppression by a mutant SKCa3N-terminal channel fragment identified in a patient with schizophrenia

      JOURNAL OF BIOLOGICAL CHEMISTRY
    98. Wallerand, H; Remy-Martin, A; Chabannes, E; Bermont, L; Adessi, GL; Bittard, H
      Relationship between expansion of the CAG repeat in exon 1 of the androgenreceptor gene and idiopathic male infertility

      FERTILITY AND STERILITY
    99. Almqvist, EW; Elterman, DS; MacLeod, PM; Hayden, MR
      High incidence rate and absent family histories in one quarter of patientsnewly diagnosed with Huntington disease in British Columbia

      CLINICAL GENETICS
    100. Levine, DA; Boyd, J
      The androgen receptor and genetic susceptibility to ovarian cancer: Results from a case series

      CANCER RESEARCH


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Documento generato il 09/08/20 alle ore 19:51:42