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    1. Barth, TFE; Bentz, M; Dohner, H; Moller, P
      Molecular aspects of B-cell lymphomas of the gastrointestinal tract

      CLINICAL LYMPHOMA
    2. Rodeghiero, F; Castaman, G
      Congenital von Willebrand disease type I: definition, phenotypes, clinicaland laboratory assessment

      BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY
    3. Hiraoka, M; Rossi, F; Trese, MT; Shastry, BS
      X-linked juvenile retinoschisis: mutations at the retinoschisis and Norriedisease gene loci?

      JOURNAL OF HUMAN GENETICS
    4. Setlow, JK; Haines, D; Cabrera-Juarez, E
      Gyrase mutants affect mutation in a localized region of Haemophilus influenzae

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    5. Fenech, M; Ferguson, LR
      Vitamins/minerals and genomic stability in humans

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    6. Woodruff, NW; Durant, JL; Donhoffner, LL; Penman, BW; Crespi, CL
      Human cell mutagenicity of chlorinated and unchlorinated water and the disinfection byproduct 3-chloro-4-(dichloromethyl)-5-hydroxy-2(5H)-furanone (MX)

      MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS
    7. Knowles, MA
      What we could do now: molecular pathology of bladder cancer

      JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
    8. Komajda, M; Charron, P
      How will the human genome project change cardiovascular medicine?

      HEART
    9. Rhodes, RB; Lewis, K; Shultz, J; Huber, S; Voelkerding, KV; Leonard, DGB; Tsongalis, GJ; Kephart, DD
      Analysis of the factor V Leiden mutation using the READIT Assay

      MOLECULAR DIAGNOSIS
    10. Komajda, M; Charron, P
      The heart of genomics

      NATURE MEDICINE
    11. Sampram, ESK; Lindblad, B
      The impact of Factor V mutation on the risk for occlusion in patients undergoing peripheral vascular reconstructions

      EUROPEAN JOURNAL OF VASCULAR AND ENDOVASCULAR SURGERY
    12. Panasci, L; Paiement, JP; Christodouplopoulos, G; Belenkov, A; Malapetsa, A; Aloyz, R
      Chlorambucil drug resistance in chronic lymphocytic leukemia: The emergingrole of DNA repair

      CLINICAL CANCER RESEARCH
    13. Xiangming, C; Natsugoe, S; Takao, S; Hokita, S; Ishigami, S; Tanabe, G; Baba, M; Kuroshima, K; Aikou, T
      Preserved Smad4 expression in the transforming growth factor beta signaling pathway is a favorable prognostic factor in patients with advanced gastric cancer

      CLINICAL CANCER RESEARCH
    14. Parasole, R; Izzo, F; Perrone, F; Pignata, S; Galati, MG; Leonardi, E; Castiglione, F; Orlando, R; Castello, G; Esposito, G; Gallo, C; Daniele, B
      Prognostic value of serum biological markers in patients with hepatocellular carcinoma

      CLINICAL CANCER RESEARCH
    15. Girolami, A; Scarano, L; Tormene, D; Cella, G
      Homozygous patients with the 20210 G to A prothrombin polymorphism remain often asymptomatic in spite of the presence of associated risk factors

      CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS
    16. Jakobs, PM; Hanson, EL; Crispell, KA; Toy, W; Keegan, H; Schilling, K; Icenogle, TB; Litt, M; Hershberger, RE
      Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

      JOURNAL OF CARDIAC FAILURE
    17. Wuthrich, RP
      Factor V Leiden mutation: potential thrombogenic role in renal vein, dialysis graft and transplant vascular thrombosis

      CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
    18. Choi, D; Lee, E; Hwang, S; Jun, K; Kim, D; Yoon, BK; Shin, HS; Lee, JH
      The biological significance of phospholipase C beta 1 gene mutation in mouse sperm in the acrosome reaction, fertilization, and embryo development

      JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
    19. Gabriel, M; Henne-Bruns, D; Kalthoff, H
      ELISA-based Ki-ras gene mutation analyses in pancreatic and cholangiocarcinoma cells and tissues

      ONCOLOGY REPORTS
    20. Abe, Y; Masuda, H; Okubo, R
      Microsatellite instability of each tumor in sporadic synchronous multiple colorectal cancers

      ONCOLOGY REPORTS
    21. Kim, SK; Cho, BK; Paek, SH; Hong, SJ; Kim, HS; Hong, SY; Choe, G; Chi, JG; Nam, DH; Wang, KC
      The detection of p53 gene mutation using a microdissection technique in primary intracranial germ cell tumors

      INTERNATIONAL JOURNAL OF ONCOLOGY
    22. Kondo, N; Matsui, E; Kaneko, H; Fukao, T; Teramoto, T; Inoue, R; Watanabe, M; Kasahara, K; Morimoto, N
      Reduced interferon-gamma production and mutations of the interleukin-12 receptor beta(2) chain gene in atopic subjects

      INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
    23. Nishiyama, Y; Nejima, J; Watanabe, A; Kotani, E; Sakai, N; Hatamochi, A; Shinkai, H; Kiuchi, K; Tamura, K; Shimada, T; Takano, T; Katayama, Y
      Ehlers-Danlos syndrome type IV with a unique point mutation in COL3A1 and familial phenotype of myocardial infarction without organic coronary stenosis

      JOURNAL OF INTERNAL MEDICINE
    24. Poon, R; Smits, R; Li, C; Jagmohan-Changur, S; Kong, M; Cheon, S; Yu, CY; Fodde, R; Alman, BA
      Cyclooxygenase-two (COX-2) modulates proliferation in aggressive fibromatosis (desmoid tumor)

      ONCOGENE
    25. Maassen, JA; van Essen, E; van den Ouweland, JMW; Lemkes, HHJP
      Molecular and clinical aspects of mitochondrial diabetes mellitus

      EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES
    26. Ito, T; Kaneko, K; Makino, R; Ito, H; Konishi, K; Kurahashi, T; Kitahara, T; Mitamura, K
      Prognostic value of p53 mutations in patients with locally advanced esophageal carcinoma treated with definitive chemoradiotherapy

      JOURNAL OF GASTROENTEROLOGY
    27. Fukuzawa, Y; Takahashi, K; Furuta, K; Tagaya, T; Ishikawa, T; Wada, K; Omoto, Y; Koji, T; Kakumu, S
      Expression of Fas/Fas ligand (FasL) and its involvement in infiltrating lymphocytes in hepatocellular carcinoma (HCC)

      JOURNAL OF GASTROENTEROLOGY
    28. Shimada, H; Okazumi, S; Takeda, A; Nabeya, Y; Matsubara, H; Funami, Y; Hayashi, H; Gunji, Y; Suzuki, T; Ochiai, T
      Presence of serum p53 antibodies is associated with decreased in vitro chemosensitivity in patients with esophageal cancer

      SURGERY TODAY
    29. Barsotti, P; Muda, AO; Mazzucco, G; Massella, L; Basolo, B; De Marchi, M; Rizzoni, G; Monga, G; Faraggiana, T
      Distribution of alpha-chains of type IV collagen in glomerular basement membranes with ultrastructural alterations suggestive of Alport syndrome

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    30. Nagy, Z; Nagy, A; Karadi, O; Figler, M; Rumi, G; Suto, G; Vincze, A; Par, A; Mozsik, G
      Prevalence of the factor V Leiden mutation in human inflammatory bowel disease with different activity

      JOURNAL OF PHYSIOLOGY-PARIS
    31. Moriai, S; Daimon, M; Susa, S; Kurimura, M; Kawanami, T; Kurita, K; Kato, T
      Hypoceruloplasminemia in neurological diseases

      INTERNAL MEDICINE
    32. Leite, KRM; Franco, MF; Srougi, M; Nesrallah, LJ; Nesrallah, A; Bevilacqua, RG; Darini, E; Carvalho, CM; Meirelles, MI; Santana, I; Camara-Lopes, LH
      Abnormal expression of MDM2 in prostate carcinoma

      MODERN PATHOLOGY
    33. Galmarini, CM; Mackey, JR; Dumontet, C
      Nucleoside analogues: mechanisms of drug resistance and reversal strategies

      LEUKEMIA
    34. McDaniel, DO; Keats, B; Vedanarayanan, VV; Subramony, SH
      Sequence variation in GAA repeat expansions may cause differential penotype display in Friedreich's ataxia

      MOVEMENT DISORDERS
    35. Truninger, K; Kock, J; Wirth, HP; Muellhaupt, B; Arnold, C; von Weizsacker, F; Seifert, B; Ammann, RW; Blum, HE
      Trypsinogen gene mutations in patients with chronic or recurrent acute pancreatitis

      PANCREAS
    36. Buoni, S; Molinelli, M; Mariottini, A; Rango, C; Medaglini, S; Pieri, S; Strambi, M; Fois, A
      Homocystinuria with transverse sinus thrombosis

      JOURNAL OF CHILD NEUROLOGY
    37. Stefanutti, C; Di Giacomo, S; Vivenzio, A; Colloridi, V; Bosco, G; Berni, A; Rabbone, I; Cerutti, F; Bertolini, S
      Low-density lipoprotein apheresis in a patient aged 3.5 years

      ACTA PAEDIATRICA
    38. Topaloglu, R; Akierli, C; Bakkaloglu, A; Aydintug, O; Ozen, S; Besbas, N; Ozcelik, T
      Survey of factor V Leiden and prothrombin gene mutations in systemic lupuserythematosus

      CLINICAL RHEUMATOLOGY
    39. Sacchetti, A; Cappetti, V; Marra, P; Dell'Arciprete, R; El Sewedy, T; Crescenzi, C; Alberti, S
      Green fluorescent protein variants fold differentially in prokaryotic and eukaryotic cells

      JOURNAL OF CELLULAR BIOCHEMISTRY
    40. Warren, R
      Screening women at high risk of breast cancer on the basis of evidence

      EUROPEAN JOURNAL OF RADIOLOGY
    41. Guillen, M; Corella, D; Portoles, O; Gonzalez, JI; Mulet, F; Saiz, C
      Prevalence of the methylenetetrahydrofolate reductase 677C > T mutation inthe Mediterranean Spanish population. Association with cardiovascular riskfactors

      EUROPEAN JOURNAL OF EPIDEMIOLOGY
    42. Ma, ESK; Chan, AYY; Au, WY; Yeung, YM; Chan, LC
      Diagnosis of concurrent hemoglobin H disease and heterozygous beta-thalassemia

      HAEMATOLOGICA
    43. Sanz-Vaque, L; Colomer, D; Bosch, F; Lopez-Guillermo, A; Dreyling, MH; Ott, G; Montserrat, E; Campo, E
      Microsatellite instability analysis in typical and progressed mantle cell lymphoma and B-cell chronic lymphocytic leukemia

      HAEMATOLOGICA
    44. Harteveld, CL; Traeger-Synodinos, J; Ragusa, A; Fichera, M; Kanavakis, E; Kattamis, C; Giordano, P; Schiliro, G; Bernini, LF
      Different geographic origins of Hb constant spring [alpha(2) codon 142 TAA-> CAA]

      HAEMATOLOGICA
    45. Scheffer, IE; Wallace, R; Mulley, JC; Berkovic, SF
      Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)

      BRAIN & DEVELOPMENT
    46. Aoki, T; Tsuchida, A; Kasuya, K; Endo, M; Kitamura, K; Koyanagi, Y
      Is preventive resection of the extrahepatic bile duct necessary in cases of pancreaticobiliary maljunction without dilatation of the bile duct?

      JAPANESE JOURNAL OF CLINICAL ONCOLOGY
    47. Wu, JS; Gu, JM; Xu, J; Wang, J; Sun, ZM; Smirnov, MD; Morrissey, JH; Esmon, N
      Factor V Leiden mutation in one family of Chinese origin

      CHINESE MEDICAL JOURNAL
    48. Ren, XQ; He, YS; Du, CS; Jiang, WY; Chen, LM; Lin, QD
      A novel mis-sense mutation (G1381A) in the G6PD gene identified in a Chinese man

      CHINESE MEDICAL JOURNAL
    49. Ji, LN; Hou, XM; Han, XY
      Prevalence and clinical characteristics of mitochondrial tRNA leu ((UUR)) mt 3243 A -> G and ND -> 1 gene mt 3316 G -> A mutations in Chinese patients with type 2 diabetes

      CHINESE MEDICAL JOURNAL
    50. Carrera, P; Stenirri, S; Ferrari, M; Battistini, S
      Familial hemiplegic migraine: A ion channel disorder

      BRAIN RESEARCH BULLETIN
    51. Tribius, S; Pidel, A; Casper, D
      ATM protein expression correlates with radioresistance in primary glioblastoma cells in culture

      INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
    52. Kashiwabara, K; Sano, T; Oyama, T; Najahima, T; Makita, F; Hashimoto, N; Iwanami, K; Kawashima, O; Matsumoto, T; Matsuzaki, Y
      A case of esophageal sarcomatoid carcinoma with molecular evidence of a monoclonal origin

      PATHOLOGY RESEARCH AND PRACTICE
    53. Glueck, CJ; Fontaine, RN; Wang, P
      Interaction of heritable and estrogen-induced thrombophilia: Possible etiologies for ischemic optic neuropathy and ischemic stroke

      THROMBOSIS AND HAEMOSTASIS
    54. Handra-Luca, A; Terris, B; Couvelard, A; Molas, G; Degott, C; Flejou, JF
      Spindle cell squamous carcinoma of the oesophagus: an analysis of 17 cases, with new immunohistochemical evidence for a clonal origin

      HISTOPATHOLOGY
    55. Tanakamaru, Z; Mori, I; Nishikawa, A; Furukawa, F; Takahashi, M; Mori, H
      Essential similarities between spontaneous and MeIQx-promoted aberrant crypt foci in the F344 rat colon

      CANCER LETTERS
    56. Tolnay, M; Probst, A
      Frontotemporal lobar degeneration - An update on clinical, pathological and genetic findings

      GERONTOLOGY
    57. Heckmann, JG; Tomandl, B; Erbguth, F; Neidhardt, B; Zingsem, H; Neundorfer, B
      Cerebral vein thrombosis and prothrombin gene (G20210A) mutation

      CLINICAL NEUROLOGY AND NEUROSURGERY
    58. Kotani, T; Umeki, K; Yamamoto, I; Ohtaki, S; Adachi, M; Tachibana, K
      Iodide organification defects resulting from cosegregation of mutated and null thyroid peroxidase alleles

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    59. Achermann, JC; Weiss, J; Lee, EJ; Jameson, JL
      Inherited disorders of the gonadotropin hormones

      MOLECULAR AND CELLULAR ENDOCRINOLOGY
    60. Byrd, JC; Shinn, C; Willis, CR; Flinn, IW; Lehman, T; Suasville, E; Lucas, D; Gerver, MR
      UCN-01 induces cytotoxicity toward human CLL cells through a p53-independent mechanism

      EXPERIMENTAL HEMATOLOGY
    61. Berdon, WE
      Hepatoblastoma

      PEDIATRIC RADIOLOGY
    62. Ko, HM; Chung, JH; Lee, JH; Jung, IS; Choi, IS; Juhng, SW; Choi, C
      Androgen receptor gene mutation associated with complete androgen insensitivity syndrome and Sertoli cell adenoma

      INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
    63. Johnson, TM; El-Defrawy, S; Hodge, WG; Leonard, BC; Kertes, PJ; Taylor, SAM; Lillicrap, DP
      Prevalence of factor V Leiden and activated protein C resistance in central retinal vein occlusion

      RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
    64. Fischereder, M; Schneeberger, H; Lohse, P; Kramer, BK; Schlondorff, D; Land, W
      Increased rate of renal transplant failure in patients with the G20210A mutation of the prothrombin gene

      AMERICAN JOURNAL OF KIDNEY DISEASES
    65. Ebert, M; Schandl, L; Schmid, RM
      Differentiation of chronic pancreatitis from pancreatic cancer: Recent advances in molecular diagnosis

      DIGESTIVE DISEASES
    66. Zborovsky, SS; Misyurin, AV; Scherbinina, SP
      The first experience with genetic tests for inherited hemochromatosis in Russia

      GEMATOLOGIYA I TRANSFUZIOLOGIYA
    67. Chen, CP; Chern, SR; Shih, JC; Wang, WS; Yeh, LF; Chang, TY; Tzen, CY
      Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia

      PRENATAL DIAGNOSIS
    68. Kluijtmans, LAJ; Whitehead, AS
      Methylenetetrahydrofolate reductase genotypes and predisposition to atherothrombotic disease - Evidence that all three MTHFR C677T genotypes confer different levels of risk

      EUROPEAN HEART JOURNAL
    69. Bremer, M; Steinmann, D; Dork, T; Borger, J; Rades, D; Karstens, JH
      Bilateral breast cancer and local relapse: A hospital-based study of the prevalence of BRCA 1 and BRCA 2 gene mutations

      STRAHLENTHERAPIE UND ONKOLOGIE
    70. Rodriguez-Salas, N; Palacios, J; Moreno, G; de Castro, J; Gonzalez-Baron, M; Gamallo, C
      Correlation of p53 oncoprotein expression with chemotherapy response in small cell lung carcinomas

      LUNG CANCER
    71. Izumoto, S; Ohnishi, T; Kanemura, H; Arita, N; Maruno, M; Moriuchi, S; Suzuki, T; Yoshimine, T
      PTEN mutations in malignant gliomas and their relation with meningeal gliomatosis

      JOURNAL OF NEURO-ONCOLOGY
    72. Fujino, N; Shimizu, M; Ino, H; Okeie, K; Yamaguchi, M; Yasuda, T; Kokado, H; Mabuchi, H
      Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy

      CLINICAL CARDIOLOGY
    73. Camera, G; Baldi, M; Strisciuglio, G; Concolino, D; Mastroiacovo, P; Baffico, M
      Occurrence of thanatophoric dysplasia type I (R248C) and hypochondroplasia(N540K) mutations in two patients with achondroplasia phenotype

      AMERICAN JOURNAL OF MEDICAL GENETICS
    74. Johnston, C; Eliez, S; Dyer-Friedman, J; Hessl, D; Glaser, B; Blasey, C; Taylor, A; Reiss, A
      Neurobehavioral phenotype in carriers of the fragile X premutation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    75. Chamyan, G; Debich-Spicer, D; Opitz, JM; Gilbert-Barness, E
      Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18

      AMERICAN JOURNAL OF MEDICAL GENETICS
    76. Harada, S; Agarwal, DP; Nomura, F; Higuchi, S
      Metabolic and ethnic determinants of alcohol drinking habits and vulnerability to alcohol-related disorder

      ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
    77. Rehman, HU
      Diabetes mellitus in the young

      JOURNAL OF THE ROYAL SOCIETY OF MEDICINE
    78. Wrone, EM; Zehnder, JL; Hornberger, JM; McCann, LM; Coplon, NS; Fortmann, SP
      An MTHFR variant, homocysteine, and cardiovascular comorbidity in renal disease

      KIDNEY INTERNATIONAL
    79. Buzza, M; Wang, YY; Dagher, H; Babon, JJ; Cotton, RG; Powell, H; Dowling, J; Savige, J
      COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome

      KIDNEY INTERNATIONAL
    80. Jadoul, M; Dode, C; Cosyns, JP; Abramowicz, D; Georges, B; Delpech, M; Pirson, Y
      Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid communication

      KIDNEY INTERNATIONAL
    81. Hiraoka, M; Taniguchi, T; Nakai, H; Kino, M; Okada, Y; Tanizawa, A; Tsukahara, H; Ohshima, Y; Muramatsu, I; Mayumi, M
      No evidence for AT2R gene derangement in human urinary tract anomalies

      KIDNEY INTERNATIONAL
    82. Bisceglia, L; Purroy, J; Jimenez-Vidal, M; d'Adamo, AP; Rousaud, F; Beccia, E; Penza, R; Rizzoni, G; Gallucci, M; Palacin, M; Gasparini, P; Nunes, V; Zelante, L
      Cystinuria type I: Identification of eight new mutations in SLC3A1

      KIDNEY INTERNATIONAL
    83. Vianello, F; Lombardi, AM; Boldrin, C; Luni, S; Girolami, A
      A new Factor X defect (Factor X Padua 3) - A compound heterozygous betweentrue deficiency (Gly(380)-> Arg) and an abnormality (Ser(334)-> Pro)

      THROMBOSIS RESEARCH
    84. Knoll, B; Hach-Wunderle, V; Rieger, S; Haring, D; Mannhalter, C
      Combined occurrence of a heterozygous missense mutation in the protein C gene and allelic exclusion of one protein S allele leading to severe venous thrombosis

      THROMBOSIS RESEARCH
    85. Girolami, A; Tormene, D; Simioni, P; Zanon, E
      Long-term use of oral contraceptive therapy in women with the prothrombin 20210 G-A polymorphism without thrombotic complications: A study of 13 women (12 heterozygotes and 1 homozygote)

      THROMBOSIS RESEARCH
    86. Astermark, J; Tengborn, L; Hedner, U; Berntorp, E
      Anti- and procoagulant activities in factor VII-deficient subjects

      THROMBOSIS RESEARCH
    87. Filipitsch, T; Wolf, B; Karner-Hanusch, J
      Results of molecular diagnosis in 30 Austrian families with familial adenomatous polyposis

      WIENER KLINISCHE WOCHENSCHRIFT
    88. Ducros, A; Denier, C; Joutel, A; Cecillon, M; Lescoat, C; Vahedi, K; Darcel, F; Vicaut, E; Bousser, M; Tournier-Lasserve, E
      The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

      NEW ENGLAND JOURNAL OF MEDICINE
    89. Yu, WG; Horowitz, SH
      Familial hemiplegic migraine and its abortive therapy with intravenous verapamil

      NEUROLOGY
    90. Real, JT; Chaves, FJ; Civera, M; Garcia-Garcia, AB; Ascaso, JF; Armengod, ME; Carmena, R
      Influence of FH Valencia 1 and 2 mutations of the LDL receptor gene on theresponse to simvastatin in subjects with molecularly defined heterozygous familial hypercholesterolemia in Spain

      MEDICINA CLINICA
    91. Lipovetsky, BM; Churakov, GA
      Clinical assessment of elevated and low plasma levels of high density lipoproteins

      KARDIOLOGIYA
    92. Miyajima, H; Ouchi, Y; Sakamoto, M; Takahashi, Y; Kono, S; Suzuki, H
      Increased anaerobic glycolysis in mitochondrial trifunctional protein-deficient brain

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    93. Ikeda, Y; Takagi, A; Nakata, Y; Sera, Y; Hyoudou, S; Hamamoto, K; Nishi, Y; Yamamoto, A
      Novel compound heterozygous mutations for lipoprotein lipase deficiency: aG-to-T transversion at the first position of exon 5 causing G154V missensemutation and a 5 ' splice site mutation of intron 8

      JOURNAL OF LIPID RESEARCH
    94. Chan, LC; Ma, SK; Chan, AYY; Ha, SY; Waye, JS; Lau, YL; Chui, DHK
      Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia?

      JOURNAL OF CLINICAL PATHOLOGY
    95. Isermann, B; Hendrickson, SB; Zogg, M; Wing, M; Cummiskey, M; Kisanuki, YY; Yanagisawa, M; Weiler, H
      Endothelium-specific loss of murine thrombomodulin disrupts the protein C anticoagulant pathway and causes juvenile-onset thrombosis

      JOURNAL OF CLINICAL INVESTIGATION
    96. Kasid, A; Rhyne, J; Zeller, K; Pritchard, H; Miller, M
      A novel TC deletion resulting in Pro(260)-> Stop in the human LCAT gene isassociated with a dominant effect on HDL-cholesterol

      ATHEROSCLEROSIS
    97. Deguchi, R; Takagi, A; Kawata, H; Inoko, H; Miwa, T
      Association between CagA(+) Helicobacter pylori infection and p53, BAX andtransforming growth factor-B-RII gene mutations in gastric cancer patients

      INTERNATIONAL JOURNAL OF CANCER
    98. Miller, A; Ruzicka, T
      Differential diagnosis of chronic leg ulcers

      HAUTARZT
    99. Hammond, JA; Preston, RR
      Isolation and characterization of magbane, a magnesium-lethal mutant of Paramecium

      GENETICS
    100. Maltzman, T; Knoll, K; Martinez, ME; Byers, T; Stevens, BR; Marshall, JR; Reid, ME; Einspahr, J; Hart, N; Bhattacharyya, AK; Kramer, CB; Sampliner, R; Alberts, DS; Ahnen, DJ
      Ki-ras proto-oncogene mutations in sporadic colorectal adenomas: Relationship to histologic and clinical characteristics

      GASTROENTEROLOGY


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Documento generato il 30/05/20 alle ore 18:27:50