Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' SAHOTA A' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 45 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Deng, L; Yang, M; Frund, S; Wessel, T; De Abreu, RA; Tischfield, JA; Sahota, A
      2,8-dihydroxyadenine urolithiasis in a patient with considerable residual adenine phosphoribosyltransferase activity in cell extracts but with mutations in both copies of APRT

      MOLECULAR GENETICS AND METABOLISM
    2. Evan, AP; Bledsoe, SB; Connors, BA; Deng, L; Liang, L; Shao, CS; Fineberg, NS; Grynpas, MD; Stambrook, PJ; Youzhi, S; Sahota, A; Tischfield, JA
      Sequential analysis of kidney stone formation in the Aprt knockout mouse

      KIDNEY INTERNATIONAL
    3. Sahota, A; Gao, SJ; Hayes, J; Jindal, RM
      Microchimerism and rejection: a meta-analysis

      CLINICAL TRANSPLANTATION
    4. Scott, MA; Hopper, C; Sahota, A; Springett, R; McIlroy, BW; Bown, SG; MacRobert, AJ
      Fluorescence photodiagnostics and photobleaching studies of cancerous lesions using ratio imaging and spectroscopic techniques

      LASERS IN MEDICAL SCIENCE
    5. Wang, L; Raikwar, N; Deng, L; Yang, M; Liang, L; Shao, CS; Evan, AP; Stambrook, PJ; Sahota, A; Tischfield, JA
      Altered gene expression in kidneys of mice with 2,8-dihydroxyadenine nephrolithiasis

      KIDNEY INTERNATIONAL
    6. Evans, RM; Emsley, CL; Gao, S; Sahota, A; Hall, KS; Farlow, MR; Hendrie, H
      Serum cholesterol, APOE genotype, and the risk of Alzheimer's disease: A population-based study of African Americans

      NEUROLOGY
    7. Tay, E; Chinegwundoh, J; Sahota, A; Cerio, R
      Papulonecrotic tuberculide: a forgotten cutaneous manifestation of tuberculosis

      HOSPITAL MEDICINE
    8. Wang, L; Ou, X; Sebesta, I; Vondrak, K; Krijt, J; Elleder, M; Poupetova, H; Ledvinova, J; Zeman, J; Simmonds, HA; Tischfield, JA; Sahota, A
      Combined adenine phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate sulfatase deficiency

      MOLECULAR GENETICS AND METABOLISM
    9. McDaniel, HB; Yang, M; Sidner, RA; Jindal, RM; Sahota, A
      Prospective study of microchimerism in transplant recipients

      CLINICAL TRANSPLANTATION
    10. Bolante-Cervantes, R; Li, SN; Sahota, A; Tischfield, JA; Zwerdling, T; Stambrook, PJ
      Pattern of localization of primitive hematopoietic cells in vivo using a novel mouse model

      EXPERIMENTAL HEMATOLOGY
    11. Sahota, A; Yang, M; McDaniel, HB; Hall, M; Sidner, RA; Jindal, RM
      Microchimerism analysis using polymerase chain reaction assays that selectively amplify donor DNA

      TRANSPLANTATION PROCEEDINGS
    12. Shao, CS; Deng, L; Henegariu, O; Liang, L; Raikwar, N; Sahota, A; Stambrook, PJ; Tischfield, JA
      Mitotic recombination produces the majority of recessive fibroblast variants in heterozygous mice

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    13. MORGAN OS; ELDEMIRE DA; THESIGER CH; LUSEKO J; SAHOTA A; GAO SJ; HALL KS; HENDRIE HC
      APOE ALLELE FREQUENCIES IN DEMENTED AND NONDEMENTED ELDERLY JAMAICANS

      Annals of neurology
    14. STOCKELMAN MG; LORENZ JN; SMITH FN; BOIVIN GP; SAHOTA A; TISCHFIELD JA; STAMBROOK PJ
      CHRONIC-RENAL-FAILURE IN A MOUSE MODEL OF HUMAN ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY

      American journal of physiology. Renal, fluid and electrolyte physiology
    15. TYCKO B; FENG L; NGUYEN L; FRANCIS A; HAYS A; CHUNG WY; TANG MX; STERN Y; SAHOTA A; HENDRIE H; MAYEUX R
      POLYMORPHISMS IN THE HUMAN APOLIPOPROTEIN-J CLUSTERIN GENE - ETHNIC VARIATION AND DISTRIBUTION IN ALZHEIMERS-DISEASE (VOL 98, PG 430, 1996)/

      Human genetics
    16. Sahota, A; Yang, M; McDaniel, HB; Sidner, RA; Book, B; Barr, R; Brahmi, Z; Jindal, RM
      Evaluation of seven PCR-based assays for the analysis of microchimerism

      CLINICAL BIOCHEMISTRY
    17. CLASS CA; UNVERZAGT FW; GAO SJ; SAHOTA A; HALL KS; HENDRIE HC
      THE ASSOCIATION BETWEEN APO-E GENOTYPE AND DEPRESSIVE SYMPTOMS IN ELDERLY AFRICAN-AMERICAN SUBJECTS

      The American journal of geriatric psychiatry
    18. SAHOTA A; YANG M; GAO SJ; HUI SL; BAIYEWU O; GUREJE O; OLUWOLE S; OGUNNIYI A; HALL KS; HENDRIE HC
      APOLIPOPROTEIN E-ASSOCIATED RISK FOR ALZHEIMERS-DISEASE IN THE AFRICAN-AMERICAN POPULATION IS GENOTYPE-DEPENDENT

      Annals of neurology
    19. GUPTA PK; SHAO C; ZHU Y; SAHOTA A; TISCHFIELD JA
      LOSS OF HETEROZYGOSITY ANALYSIS IN A HUMAN FIBROSARCOMA CELL-LINE

      Cytogenetics and cell genetics
    20. ALFONZO JD; SAHOTA A; TAYLOR HW
      PURIFICATION AND CHARACTERIZATION OF ADENINE PHOSPHORIBOSYLTRANSFERASE FROM SACCHAROMYCES-CEREVISIAE

      Biochimica et biophysica acta. Protein structure and molecular enzymology
    21. JINDAL RM; SAHOTA A
      THE ROLE OF CELL-MIGRATION AND MICROCHIMERISM IN THE INDUCTION OF TOLERANCE AFTER SOLID-ORGAN TRANSPLANTATION

      Postgraduate medical journal
    22. GUPTA PK; SAHOTA A; BOYADJIEV SA; BYE S; SHAO CS; ONEILL JP; HUNTER TC; ALBERTINI RJ; STAMBROOK PJ; TISCHFIELD JA
      HIGH-FREQUENCY IN-VIVO LOSS OF HETEROZYGOSITY IS PRIMARILY A CONSEQUENCE OF MITOTIC RECOMBINATION

      Cancer research
    23. LIANG L; DENG L; SHAO C; SAHOTA A; TISCHFIELD JA
      GENETIC AND BIOCHEMICAL-ANALYSIS OF A MOUSE MODEL FOR HUMAN DHA UROLITHIASIS

      American journal of human genetics
    24. CLASS CA; UNVERZAGT FW; SAHOTA A; HALL KS; HENDRIE HC
      DEPRESSIVE SYMPTOMS BY APOLIPOPROTEIN-E ALLELE STATUS IN ELDERLY AFRICAN-AMERICANS

      The American journal of geriatric psychiatry
    25. BOYADJIEV SA; SAHOTA A; TISCHFIELD JA
      IDENTIFICATION AND APPLICATION OF POLYMORPHISMS FLANKING THE HUMAN ADENINE PHOSPHORIBOSYLTRANSFERASE GENE

      Human mutation
    26. ENGLE SJ; WOMER DE; DAVIES PM; BOIVIN G; SAHOTA A; SIMMONDS HA; STAMBROOK PJ; TISCHFIELD JA
      HPRT-APRT-DEFICIENT MICE ARE NOT A MODEL FOR LESCH-NYHAN SYNDROME

      Human molecular genetics
    27. TYCKO B; FENG L; NGUYEN L; FRANCIS A; HAYS A; CHUNG WY; TANG MX; STERN Y; SAHOTA A; HENDRIE H; MAYEUX R
      POLYMORPHISMS IN THE HUMAN APOLIPOPROTEIN-J CLUSTERIN GENE - ETHNIC VARIATION AND DISTRIBUTION IN ALZHEIMERS-DISEASE/

      Human genetics
    28. SHAO C; GUPTA PK; SUN Y; SAHOTA A; TISCHFIELD JA
      COMPLEX CHROMOSOMAL MECHANISMS LEAD TO APRT LOSS OF HETEROZYGOSITY INHETEROPLOID CELLS

      Cytogenetics and cell genetics
    29. ENGLE SJ; STOCKELMAN MG; CHEN J; BOIVIN G; YUM MN; DAVIES PM; YING MY; SAHOTA A; SIMMONDS HA; STAMBROOK PJ; TISCHFIELD JA
      ADENINE PHOSPHORIBOSYLTRANSFERASE-DEFICIENT MICE DEVELOP 2,8-DIHYDROXYADENINE NEPHROLITHIASIS

      Proceedings of the National Academy of Sciences of the United Statesof America
    30. YANG M; HENDRIE HC; HALL KS; OLUWOLE OSA; HODES ME; SAHOTA A
      IMPROVED PROCEDURE FOR ELUTING DNA FROM DRIED BLOOD SPOTS

      Clinical chemistry
    31. ALFONZO JD; SAHOTA A; DEELEY MC; RANJEKAR P; TAYLOR MW
      CLONING AND CHARACTERIZATION OF THE ADENINE PHOSPHORIBOSYLTRANSFERASE-ENCODING GENE (APT1) FROM SACCHAROMYCES-CEREVISIAE

      Gene
    32. OSUNTOKUN BO; SAHOTA A; OGUNNIYI AO; GUREJE O; BAIYEWU O; ADEYINKA A; OLUWOLE SO; KOMOLAFE O; HALL KS; UNVERZAGT FW; HUI SL; YANG M; HENDRIE HC
      LACK OF AN ASSOCIATION BETWEEN APOLIPOPROTEIN-E EPSILON-4 AND ALZHEIMERS-DISEASE IN ELDERLY NIGERIANS

      Annals of neurology
    33. HENDRIE HC; HALL KS; HUI S; UNVERZAGT FW; YU CE; LAHIRI DK; SAHOTA A; FARLOW M; MUSICK B; CLASS CA; BRASHEAR A; BURDINE VE; OSUNTOKUN BO; OGUNNIYI AO; GUREJE O; BAIYEWU O; SCHELLENBERG GD
      APOLIPOPROTEIN-E GENOTYPES AND ALZHEIMERS-DISEASE IN A COMMUNITY STUDY OF ELDERLY AFRICAN-AMERICANS

      Annals of neurology
    34. SHAO C; GUPTA PK; SUN Y; SAHOTA A; TISCHFIELD JA
      COMPLEX CHROMOSOME MECHANISMS LEADING TO THE LOSS OF WILD-TYPE ALLELEOF APRT GENE IN HETEROPLOID CELLS

      American journal of human genetics
    35. SAHOTA A; OSUNTOKUN BO; YANG M; HUI SL; UNVERZAGT FW; HALL KS; HENDRIE HC
      LACK OF AN ASSOCIATION BETWEEN THE E4 ALLELE OF APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE IN ELDERLY NIGERIANS

      American journal of human genetics
    36. YANG M; HENDRIE HC; HALL KS; OSUNTOKUN BO; SAHOTA A
      AN IMPROVED METHOD FOR ELUTING DNA FROM DRIED BLOOD SPOTS AND ITS APPLICATION TO APOLIPOPROTEIN-E GENOTYPING IN ALZHEIMER-DISEASE

      American journal of human genetics
    37. SAHOTA A; CHEN J; BYE S; JAING J; BERENYI M; FEKETE G; TISCHFIELD JA
      OCCURRENCE OF A MISSENSE MUTATION IN ONE ALLELE AND A 7-BASEPAIR DELETION IN THE OTHER ALLELE IN A PATIENT WITH ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY

      Human mutation
    38. SAHOTA A; CHEN J; BOYADJIEV SA; GAULT MH; TISCHFIELD JA
      MISSENSE MUTATION IN THE ADENINE PHOSPHORIBOSYLTRANSFERASE GENE CAUSING 2,8-DIHYDROXYADENINE UROLITHIASIS

      Human molecular genetics
    39. BYE S; MALLMANN R; DULEY J; SIMMONDS HA; CHEN J; TISCHFIELD JA; SAHOTA A
      IDENTIFICATION OF A 7-BASEPAIR DELETION IN THE ADENINE PHOSPHORIBOSYL-TRANSFERASE GENE AS A CAUSE OF 2,8-DIHYDROXYADENINE UROLITHIASIS

      The Clinical investigator
    40. CHEN J; SAHOTA A; MARTIN GF; HAKODA M; KAMATANI N; STAMBROOK PJ; TISCHFIELD JA
      ANALYSIS OF GERMLINE AND INVIVO SOMATIC MUTATIONS IN THE HUMAN ADENINE PHOSPHORIBOSYLTRANSFERASE GENE - MUTATIONAL HOT-SPOTS AT THE INTRON-4 SPLICE DONOR SITE AND AT CODON-87

      MUTATION RESEARCH
    41. GUPTA PK; SAHOTA A; ONEILL JP; HUNTER TC; ALBERTINI RJ; TISCHFIELD JA
      GENETIC-STRUCTURE ANALYSIS AND LOSS OF HETEROZYGOSITY (LOH) IN HUMAN-CELLS

      American journal of human genetics
    42. BOYADJIEV S; SAHOTA A; PRATT VM; DLOUHY SR; HODES ME
      DETECTION OF PLP GENE-MUTATIONS IN PATIENTS WITH PELIZAEUS-MERZBACHERDISEASE BY SINGLE-STRAND CONFORMATIONAL-ANALYSIS

      American journal of human genetics
    43. CHEN J; BYE S; SAHOTA A; TISCHFIELD JA
      EXON SKIPPING IN THE WILD-TYPE TRANSCRIPTS OF APRT AND ITS ENHANCEMENT BY A NONSENSE MUTATION

      American journal of human genetics
    44. TORRES W; SAHOTA A; BOYADJIEV S; VANCE GH; WEAVER DD
      FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS

      American journal of human genetics
    45. SAHOTA A; FUGMAN D; CRISP M; HODES ME
      MOLECULAR-GENETICS SERVICES AT INDIANA-UNIVERSITY

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 16/01/21 alle ore 04:47:44