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    1. Pandya, A; Wasfy, S; Hebert, D; Allen, UD
      Varicella-zoster infection in pediatric solid-organ transplant recipients:A hospital-based study in the prevaricella vaccine era

      PEDIATRIC TRANSPLANTATION
    2. Lee, MH; Gordon, D; Ott, J; Lu, KM; Ose, L; Miettinen, T; Gylling, H; Stalenhoef, AF; Pandya, A; Hidaka, H; Brewer, B; Kojima, H; Sakuma, N; Pegoraro, R; Salen, G; Patel, SB
      Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities

      EUROPEAN JOURNAL OF HUMAN GENETICS
    3. Radominska-Pandya, A; Chen, GP; Samokyszyn, VM; Little, JM; Gall, WE; Zawada, G; Terrier, N; Magdalou, J; Czernik, P
      Application of photoaffinity labeling with [H-3] all trans- and 9-cis-retinoic acids for characterization of cellular retinoic acid-binding proteins I and II

      PROTEIN SCIENCE
    4. Santin, AD; Hermonat, PL; Ravaggi, A; Bellone, S; Roman, JJ; Smith, CV; Pecorelli, S; Radominska-Pandya, A; Cannon, MJ; Parham, GP
      Phenotypic and functional analysis of tumor-infiltrating lymphocytes compared with tumor-associated lymphocytes from ascitic fluid and peripheral blood lymphocytes in patients with advanced ovarian cancer

      GYNECOLOGIC AND OBSTETRIC INVESTIGATION
    5. Tekin, M; Akar, N; Cin, S; Blanton, SH; Xia, XJ; Liu, XZ; Nance, WE; Pandya, A
      Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

      HUMAN GENETICS
    6. Fleck, BJ; Pandya, A; Vanner, L; Kerkering, K; Bodurtha, J
      Coffin-Siris syndrome: Review and presentation of new cases from a questionnaire study

      AMERICAN JOURNAL OF MEDICAL GENETICS
    7. Tekin, M; Jackson-Cook, C; Pandya, A
      De novo inverted tandem duplication of the short arm of chromosome 12 in apatient with microblepharon

      AMERICAN JOURNAL OF MEDICAL GENETICS
    8. Tekin, M; Arnos, KS; Pandya, A
      Advances in hereditary deafness

      LANCET
    9. Jude, AR; Little, JM; Bull, AW; Podgorski, I; Radominska-Pandya, A
      13-Hydroxy- and 13-oxooctadecadienoic acids: Novel substrates for human UDP-glucuronosyltransferases

      DRUG METABOLISM AND DISPOSITION
    10. Xie, W; Radominska-Pandya, A; Shi, YH; Simon, CM; Nelson, MC; Ong, ES; Waxman, DJ; Evans, RM
      An essential role for nuclear receptors SXR/PXR in detoxification of cholestatic bile acids

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    11. Ben-Yosef, T; Wattenhofer, M; Riazuddin, S; Ahmed, ZM; Scot, HS; Kudoh, J; Shibuya, K; Antonarakis, SE; Bonne-Tamir, B; Radhakrishna, U; Naz, S; Ahmed, Z; Riazuddin, S; Pandya, A; Nance, WE; Wilcox, ER; Friedman, TB; Morell, RJ
      Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness

      JOURNAL OF MEDICAL GENETICS
    12. Amann, ST; Gates, LK; Aston, CE; Pandya, A; Whitcomb, DC
      Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins

      GUT
    13. Tekin, M; Bodurtha, JN; Nance, WE; Pandya, A
      Waardenburg syndrome type 3 (Klein-Waardenburg syndrome) segregating with a heterozygous deletion in box domain of PAX3: a simple variant or a true syndrome

      CLINICAL GENETICS
    14. Liu, XZ; Blanton, SH; Bitner-Glindzicz, M; Pandya, A; Landa, B; MacArdle, B; Rajput, K; Bellman, S; Webb, BT; Ping, X; Smith, RJH; Nance, WE
      Haplotype analysis of the USH1D locus and genotype-phenotype correlations

      CLINICAL GENETICS
    15. Tekin, M; Arnos, KS; Xia, XJ; Oelrich, MK; Liu, XZ; Nance, WE; Pandya, A
      W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness

      CLINICAL GENETICS
    16. Jude, AR; Little, JM; Czernik, PJ; Tephly, TR; Grant, DF; Radominska-Pandya, A
      Glucuronidation of linoleic acid diols by human microsomal and recombinantUDP-glucuronosyltransferases: Identification of UGT2B7 as the major isoform involved

      ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
    17. Lu, KM; Lee, MH; Hazard, S; Brooks-Wilson, A; Hidaka, H; Kojima, H; Ose, L; Stalenhoef, AFH; Mietinnen, T; Bjorkhem, I; Bruckert, E; Pandya, A; Brewer, HB; Salen, G; Dean, M; Srivastava, A; Patel, SB
      Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectively

      AMERICAN JOURNAL OF HUMAN GENETICS
    18. Buller, A; Pandya, A; Jackson-Cook, C; Bodurtha, J; Tekin, M; Wilkinson, DS; Garrett, CT; Ferreira-Gonzalez, A
      Validation of a multiplex methylation-sensitive PCR assay for the diagnosis of Prader-Willi and Angelman's syndromes

      MOLECULAR DIAGNOSIS
    19. Santos, FR; Pandya, A; Kayser, M; Mitchell, RJ; Liu, AP; Singh, L; Destro-Bisol, G; Novelletto, A; Qamar, R; Mehdi, SQ; Adhikari, R; de Knijff, P; Tyler-Smith, C
      A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome

      HUMAN MOLECULAR GENETICS
    20. Liu, XZ; Xia, XJ; Xu, LR; Pandya, A; Liang, CY; Blanton, SH; Brown, SDM; Steel, KP; Nance, WE
      Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

      HUMAN MOLECULAR GENETICS
    21. Tessier, DC; Dignard, D; Zapun, A; Radominska-Pandya, A; Parodi, J; Bergeron, JJM; Thomas, DY
      Cloning and characterization of mammalian UDP-glucose glycoprotein: glucosyltransferase and the development of a specific substrate for this enzyme

      GLYCOBIOLOGY
    22. Bao, WD; Zhu, SL; Pandya, A; Zerjal, T; Xu, JJ; Shu, QF; Du, RF; Yang, HM; Tyler-Smith, C
      MSY2: a slowly evolving minisatellite on the human Y chromosome which provides a useful polymorphic marker in Chinese populations

      GENE
    23. Pandya, A; Vaijapurkar, SG; Bhatnagar, PK
      Radiation dosimetry by potassium feldspar

      BULLETIN OF MATERIALS SCIENCE
    24. Tekin, M; Jackson-Cook, C; Buller, A; Ferreira-Gonzalez, A; Pandya, A; Garrett, CT; Bodurtha, J
      Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Nance, WE; Liu, XZ; Pandya, A
      Relation between choice of partner and high frequency of cannexin-26 deafness

      LANCET
    26. Czernik, PJ; Little, JM; Barone, GW; Raufman, JP; Radominska-Pandya, A
      Glucuronidation of estrogens and retinoic acid and expression of UDP-glucuronosyltransferase 2B7 in human intestinal mucosa

      DRUG METABOLISM AND DISPOSITION
    27. Nye, JS; Hayes, EA; Amendola, M; Vaughn, D; Charrow, J; McLone, DG; Speer, MC; Nance, WE; Pandya, A
      Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies

      TERATOLOGY
    28. Hormbrey, E; Pandya, A; Humzah, D
      Drain fixation made foolproof

      ANNALS OF THE ROYAL COLLEGE OF SURGEONS OF ENGLAND
    29. Radominska-Pandya, A; Chen, GP; Czernik, PJ; Little, JM; Samokyszyn, VM; Carter, CA; Nowak, G
      Direct interaction of all-trans-retinoic acid with protein kinase C (PKC) - Implications for PKC signaling and cancer therapy

      JOURNAL OF BIOLOGICAL CHEMISTRY
    30. Samokyszyn, VM; Gall, WE; Zawada, G; Freyaldenhoven, MA; Chen, GP; Mackenzie, PI; Tephly, TR; Radominska-Pandya, A
      4-Hydroxyretinoic acid, a novel substrate for human liver microsomal UDP-glucuronosyltransferase(s) and recombinant UGT2B7

      JOURNAL OF BIOLOGICAL CHEMISTRY
    31. Chen, GP; Rabjohn, PA; York, JL; Wooldridge, C; Zhang, DQ; Falany, CN; Radominska-Pandya, A
      Carboxyl residues in the active site of human phenol sulfotransferase (SULT1A1)

      BIOCHEMISTRY
    32. Chen, GP; Radominska-Pandya, A
      Direct photoaffinity labeling of cellular retinoic acid-binding protein I (CRABP-I) with all-trans-retinoic acid: Identification of amino acids in the ligand binding site

      BIOCHEMISTRY
    33. Jude, AR; Little, JM; Freeman, JP; Evans, JE; Radominska-Pandya, A; Grant, DF
      Linoleic acid diols are novel substrates for human UDP-glucuronosyltransferases

      ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
    34. Baumgartner, FJ; Omari, BO; Robertson, JM; Nelson, RJ; Pandya, A; Pandya, A; Milliken, JC
      Annular abscesses in surgical endocarditis: Anatomic, clinical, and operative features

      ANNALS OF THORACIC SURGERY
    35. Rosser, ZH; Zerjal, T; Hurles, ME; Adojaan, M; Alavantic, D; Amorim, A; Amos, W; Armenteros, M; Arroyo, E; Barbujani, G; Beckman, G; Beckman, L; Bertranpetit, J; Bosch, E; Bradley, DG; Brede, G; Cooper, G; Corte-Real, HBSM; de Knijff, P; Decorte, R; Dubrova, YE; Evgrafov, O; Gilissen, A; Glisic, S; Golge, M; Hill, EW; Jeziorowska, A; Kalaydjieva, L; Kayser, M; Kivisild, T; Kravchenko, SA; Krumina, A; Kucinskas, V; Lavinha, J; Livshits, LA; Malaspina, P; Maria, S; McElreavey, K; Meitinger, TA; Mikelsaar, AV; Mitchell, RJ; Nafa, K; Nicholson, J; Norby, S; Pandya, A; Parik, J; Patsalis, PC; Pereira, L; Peterlin, B; Pielberg, G; Prata, ML; Previdere, C; Roewer, L; Rootsi, S; Rubinsztein, DC; Saillard, J; Santos, FR; Stefanescu, G; Sykes, BC; Tolun, A; Villems, R; Tyler-Smith, C; Jobling, MA
      Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language

      AMERICAN JOURNAL OF HUMAN GENETICS
    36. Pandya, A; Nance, WE
      Mutations in the mitochondrial tRNA Ser(UCN) and in the GJB2 (connexin 26)gene are not modifiers of the age at onset or severity of hearing loss in Spanish patients with the 12S rRNA A1555G mutation - Reply to Lopez-Bigas et al.

      AMERICAN JOURNAL OF HUMAN GENETICS
    37. Blanton, SH; Pandya, A; Landa, BL; Javaheri, R; Xia, XJ; Nance, WE; Pomponio, RJ; Norrgard, KJ; Swango, KL; Demirkol, M; Gulden, H; Coskun, T; Tokatli, A; Ozalp, I; Wolf, B
      Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations

      HUMAN HEREDITY
    38. Chen, GP; Battaglia, E; Senay, C; Falany, CN; Radominska-Pandya, A
      Photoaffinity labeling probe for the substrate binding site of human phenol sulfotransferase (SULT1A1): 7-azido-4-methylcoumarin

      PROTEIN SCIENCE
    39. Gall, WE; Zawada, G; Mojarrabi, B; Tephly, TR; Green, MD; Coffman, BL; Mackenzie, PI; Radominska-Pandya, A
      Differential glucuronidation of bile acids, androgens and estrogens by human UGT1A3 and 2B7

      JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
    40. Radominska-Pandya, A; Czernik, PJ; Little, JM; Battaglia, E; Mackenzie, PI
      Structural and functional studies of UDP-glucuronosyltransferases

      DRUG METABOLISM REVIEWS
    41. Fisch, GS; Holden, JJK; Carpenter, NJ; Howard-Peebles, PN; Maddalena, A; Pandya, A; Nance, W
      Age-related language characteristics of children and adolescents with fragile X syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    42. Fisch, GS; Carpenter, NJ; Holden, JJA; Simensen, R; Howard-Peebles, PN; Maddalena, A; Pandya, A; Nance, W
      Longitudinal assessment of adaptive and maladaptive behaviors in fragile Xmales: Growth, development, and profiles

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Nowell, SA; Massengill, JS; Williams, S; Radominska-Pandya, A; Tephly, TR; Cheng, ZQ; Strassburg, CP; Tukey, RH; MacLeod, SL; Lang, NP; Kadlubar, FF
      Glucuronidation of 2-hydroxyamino-1-methyl-6-phenylimidazo[4,5-b]pyridine by human microsomal UDP-glucuronosyltransferases: identification of specific UGT1A family isoforms involved

      CARCINOGENESIS
    44. Cheng, ZQ; Radominska-Pandya, A; Tephly, TR
      Studies on the substrate specificity of human intestinal UDP-glucuronosyltransferases 1A8 and 1A10

      DRUG METABOLISM AND DISPOSITION
    45. Terrier, N; Benoit, E; Senay, C; Lapicque, F; Radominska-Pandya, A; Magdalou, J; Fournel-Gigleux, S
      Human and rat liver UDP-glucuronosyltransferases are targets of ketoprofenacylglucuronide

      MOLECULAR PHARMACOLOGY
    46. Senay, C; Battaglia, E; Chen, GP; Breton, R; Fournel-Gigleux, S; Magdalou, J; Radominska-Pandya, A
      Photoaffinity labeling of the aglycon binding site of the recombinant human liver UDP-glucuronosyltransferase UGT1A6 with 7-azido-4-methylcoumarin

      ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
    47. Marcus, DM; Papastergiou, GI; Patel, M; Pandya, A; Brooks, SE
      Discordant retinoblastoma in monozygotic twins

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    48. Pandya, A; Xia, XJ; Erdenetungalag, R; Amendola, M; Landa, B; Radnaabazar, J; Dangaasuren, B; Van Tuyle, G; Nance, WE
      Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia

      AMERICAN JOURNAL OF HUMAN GENETICS
    49. Hurles, ME; Veitia, R; Arroyo, E; Armenteros, M; Bertranpetit, J; Perez-Lezaun, A; Bosch, E; Shlumukova, M; Cambon-Thomsen, A; McElreavey, K; de Munain, AL; Rohl, A; Wilson, IJ; Singh, LJ; Pandya, A; Santos, FR; Tyler-Smith, C; Jobling, MA
      Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism

      AMERICAN JOURNAL OF HUMAN GENETICS
    50. Tyler-Smith, C; Gimelli, G; Giglio, S; Floridia, C; Pandya, A; Terzoli, G; Warburton, PE; Earnshaw, WC; Zuffardi, O
      Transmission of a fully functional human neocentromere through three generations

      AMERICAN JOURNAL OF HUMAN GENETICS
    51. Santos, FR; Pandya, A; Tyler-Smith, C; Pena, SDJ; Schanfield, M; Leonard, WR; Osipova, L; Crawford, MH; Mitchell, RJ
      The central Siberian origin for Native American Y chromosomes

      AMERICAN JOURNAL OF HUMAN GENETICS
    52. Little, JM; Lester, R; Kuipers, F; Vonk, R; Mackenzie, PI; Drake, RR; Frame, L; Radominska-Pandya, A
      Variability of human hepatic UDP-glucuronosyltransferase activity

      ACTA BIOCHIMICA POLONICA
    53. SANTOS FR; PANDYA A; TYLERSMITH C
      RELIABILITY OF DNA-BASED SEX TESTS

      Nature genetics
    54. Jobling, MA; Williams, G; Schiebel, K; Pandya, A; McElreavey, K; Salas, L; Rappold, GA; Affara, NA; Tyler-Smith, C
      A selective difference between human Y-chromosomal DNA haplotypes

      CURRENT BIOLOGY
    55. BAUMGARTNER FJ; PANDYA A; OMARI BO; PANDYA A; TURNER C; MILLIKEN JC; ROBERTSON JM
      ULTRASONIC DEBRIDEMENT OF MITRAL CALCIFICATION

      Journal of cardiac surgery
    56. DESTEFANO AL; CUPPLES LA; ARNOS KS; ASHER JH; BALDWIN CT; BLANTON S; CAREY ML; DASILVA EO; FRIEDMAN TB; GREENBERG J; LALWANI AK; MILUNSKY A; NANCE WE; PANDYA A; RAMESAR RS; READ AP; TASSABEJHI M; WILCOX ER; FARRER LA
      CORRELATION BETWEEN WAARDENBURG-SYNDROME PHENOTYPE AND GENOTYPE IN A POPULATION OF INDIVIDUALS WITH IDENTIFIED PAX3 MUTATIONS

      Human genetics
    57. POMPONIO RJ; HYMERS J; PANDYA A; LANDA B; MELONE P; JAVAHERI R; MARDACH R; MORTON SW; MEYERS GA; REYNOLDS T; BUCK G; NANCE WE; WOLF B
      PRENATAL-DIAGNOSIS OF HETEROZYGOSITY FOR BIOTINIDASE DEFICIENCY BY ENZYMATIC AND MOLECULAR ANALYSES

      Prenatal diagnosis
    58. ZIEGLSCHMIDADAMS ME; PANDYA A; COHEN SB; SONTHEIMER RD
      THE VALUE OF METHOTREXATE IN DERMATOMYOSITIS

      Journal of the American Academy of Dermatology
    59. TYLERSMITH C; PANDYA A; SANTOS FR
      A BRIGHT FUTURE FOR THE HUMAN PAST

      Trends in genetics
    60. PANDYA A; BAUMGARTNER FJ; NGUYEN D; OMARI BO
      THORACIC CASTLEMANS-DISEASE - IMPLICATIONS FOR RESECTION

      The Annals of thoracic surgery
    61. JOBLING MA; PANDYA A; TYLERSMITH C
      THE Y-CHROMOSOME IN FORENSIC ANALYSIS AND PATERNITY TESTING

      International journal of legal medicine
    62. KAYSER M; CAGLIA A; CORACH D; FRETWELL N; GEHRIG C; GRAZIOSI G; HEIDORN F; HERRMANN S; HERZOG B; HIDDING M; HONDA K; JOBLING M; KRAWCZAK M; LEIM K; MEUSER S; MEYER E; OESTERREICH W; PANDYA A; PARSON W; PENACINO G; PEREZLEZAUN A; PICCININI A; PRINZ M; SCHMITT C; SCHNEIDER PM; SZIBOR R; TEIFELGREDING J; WEICHOLD G; DEKNIJFF P; ROEWER L
      EVALUATION OF Y-CHROMOSOMAL STRS - A MULTICENTER STUDY

      International journal of legal medicine
    63. DEKNIJFF P; KAYSER M; CAGLIA A; CORACH D; FRETWELL N; GEHRIG C; GRAZIOSI G; HEIDORN F; HERRMANN S; HERZOG B; HIDDING M; HONDA K; JOBLING M; KRAWCZAK M; LEIM K; MEUSER S; MEYER E; OESTERREICH W; PANDYA A; PARSON W; PENACINO G; PEREZLEZAUN A; PICCININI A; PRINZ M; SCHMITT C; SCHNEIDER PM; SZIBOR R; TEIFELGREDING J; WEICHHOLD G; ROEWER L
      CHROMOSOME-Y MICROSATELLITES - POPULATION GENETIC AND EVOLUTIONARY ASPECTS

      International journal of legal medicine
    64. KAYSER M; DEKNIJFF P; DIELTJES P; KRAWCZAK M; NAGY M; ZERJAL T; PANDYA A; TYLERSMITH C; ROEWER L
      APPLICATIONS OF MICROSATELLITE-BASED Y-CHROMOSOME HAPLOTYPING

      Electrophoresis
    65. PANDYA A; XIA X; RADNAABAZAR J; BATSUURI J; DANGAANSUREN B; FISCHELGHODSIAN N; NANCE WE
      MUTATION IN THE MITOCHONDRIAL 12S RIBOSOMAL-RNA GENE IN 2 FAMILIES FROM MONGOLIA WITH MATRILINEAL AMINOGLYCOSIDE OTOTOXICITY

      Journal of Medical Genetics
    66. BAUMGARTNER FJ; OMARI BO; PANDYA A; PANDYA A; BETHENCOURT DM
      LOCAL TRANSVERSE ARCH REPAIR FOR TYPE-A AORTIC DISSECTION

      The Annals of thoracic surgery
    67. WINTERS J; PANDYA A; JACKSONCOOK C
      4 CASES OF MULTIPLE ANEUPLOIDY - DETERMINATION OF THE ORIGIN OF NONDISJUNCTION AND PARENTAL GAMETIC STUDIES

      American journal of human genetics
    68. PANDYA A; XIAJUAN X; BLANTON SH; LANDA B; MARKELLO T; NANCE WE
      DIAGNOSTIC-VALUE OF DIRECT MUTATION ANALYSIS IN FAMILIES WITH HEREDITARY PANCREATITIS

      American journal of human genetics
    69. ZERJAL T; DASHNYAM B; PANDYA A; KAYSER M; ROEWER L; SANTOS FR; SCHIEFENHOVEL W; FRETWELL N; JOBLING MA; HARIHARA S; SHIMIZU K; SEMJIDMAA D; SAJANTILA A; SALO P; CRAWFORD MH; GINTER EK; EVGRAFOV OV; TYLERSMITH C
      GENETIC-RELATIONSHIPS OF ASIANS AND NORTHERN EUROPEANS, REVEALED BY Y-CHROMOSOMAL DNA ANALYSIS

      American journal of human genetics
    70. PANDYA A; XIA XJ; LANDA BL; ARNOS KS; ISRAEL J; LLOYD J; JAMES AL; DIEHL SR; BLANTON SH; NANCE WE
      PHENOTYPIC VARIATION IN WAARDENBURG SYNDROME - MUTATIONAL HETEROGENEITY, MODIFIER GENES OR POLYGENIC BACKGROUND

      Human molecular genetics
    71. JOBLING MA; SAMARA V; PANDYA A; FRETWELL N; BERNASCONI B; MITCHELL RJ; GERELSAIKHAN T; DASHNYAM B; SAJANTILA A; SALO PJ; NAKAHORI Y; DISTECHE CM; THANGARAJ K; SINGH L; CRAWFORD MH; TYLERSMITH C
      RECURRENT DUPLICATION AND DELETION POLYMORPHISMS ON THE LONG ARM OF THE Y-CHROMOSOME IN NORMAL MALES

      Human molecular genetics
    72. PANDYA A; BLANTON SH; LANDA B; JAVAHERI R; MELVIN E; NANCE WE; MARKELLO T
      LINKAGE STUDIES IN A LARGE KINDRED WITH HEREDITARY PANCREATITIS CONFIRMS MAPPING OF THE GENE TO A 16-CM REGION ON 7Q

      Genomics
    73. BOON C; MARKELLO T; JACKSONCOOK C; PANDYA A
      PARTIAL TRISOMY-10 MOSAICISM WITH CUTANEOUS MANIFESTATIONS - REPORT OF A CASE AND REVIEW OF THE LITERATURE

      Clinical genetics
    74. PANDYA A; ELLESTAD MH; CRUMP R
      TIME-COURSE OF CHANGES IN P-WAVE DURATION DURING EXERCISE

      Cardiology
    75. JACKSONCOOK C; PANDYA A
      STRATEGIES AND LOGISTICAL REQUIREMENTS FOR EFFICIENT TESTING IN GENETIC-DISEASE

      Clinics in laboratory medicine
    76. PANDYA A; BRAVERMAN N; PYERITZ RE; YING KL; KLINE AD; FALK RE
      INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME-6 ASSOCIATED WITHUNUSUAL LIMB ANOMALIES - REPORT OF 2 NEW PATIENTS AND REVIEW OF THE LITERATURE

      American journal of medical genetics
    77. MARKELLO T; PANDYA A; NANCE W; BLANTON SH
      THE PANCREATIC STONE PROTEIN (LITHOSTANTINE) IS EXCLUDED AS THE CAUSEOF HEREDITARY PANCREATITIS IN A LARGE KINDRED

      American journal of human genetics
    78. LLEWELLYN BE; KALOW W; TANG BK; PANDYA A; SCHIEKEN RM; MEYER JM; NANCE WE
      EFFECT OF PASSIVE SMOKING ON CYP1A2 ACTIVITY IN TWINS

      American journal of human genetics
    79. VAIJAPURKAR SG; PATURKAR RT; RAMAN R; BHATNAGAR PK; PANDYA A; ROY SC
      A NEUTRON SENSOR-BASED ON SUPERHEATED DROPLETS

      Radiation measurements
    80. LEBMAN DA; PARK MJ; HANSENBUNDY S; PANDYA A
      MECHANISM FOR TRANSFORMING GROWTH-FACTOR-BETA REGULATION OF ALPHA-MESSENGER-RNA IN LIPOPOLYSACCHARIDE-STIMULATED B-CELLS

      International immunology
    81. SAVIN R; ATTON AV; BERGSTRESSER PR; ELEWSKI B; JONES HE; LEVINE N; LEYDEN J; MONROE A; PANDYA A; SHUPACK J; STILLER M; TSCHEN E; WEINSTEIN G; ZAIAS N; BIRNBAUM JE
      EFFICACY OF TERBINAFINE 1-PERCENT CREAM IN THE TREATMENT OF MOCCASIN-TYPE TINEA-PEDIS - RESULTS OF PLACEBO-CONTROLLED MULTICENTER TRIALS

      Journal of the American Academy of Dermatology
    82. PANDYA A; YANG JL; GIBSON HW
      A NEW POLYKETONE SYNTHESIS INVOLVING NUCLEOPHILIC-SUBSTITUTION VIA CARBANIONS DERIVED FROM BIS(ALPHA-AMINONITRILE)S .1. SEMICRYSTALLINE POLY(ARYLENE KETONE SULFONE)S

      Macromolecules
    83. BHATNAGAR PK; PANDYA A; REDDY AR; THAKUR DK
      FAST-NEUTRON IRRADIATION FOR FABRICATION OF NARROW FORWARD VOLTAGE P-I-N-DIODES

      Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment
    84. PANDYA A; GIBSON HW
      SYNTHESIS AND STEREOCHEMISTRY OF REISSERT COMPOUNDS FROM BENZOTHIAZOLE

      Journal of organic chemistry
    85. PANDYA A; MARKELLO T
      AN UNUSUAL UTERINE ANOMALY IN A PATIENT WITH MOSAIC TURNER SYNDROME

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/01/21 alle ore 14:10:30