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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
Sequential analysis of kidney stone formation in the Aprt knockout mouse
KIDNEY INTERNATIONAL
Microchimerism and rejection: a meta-analysis
CLINICAL TRANSPLANTATION
Fluorescence photodiagnostics and photobleaching studies of cancerous lesions using ratio imaging and spectroscopic techniques
LASERS IN MEDICAL SCIENCE
Altered gene expression in kidneys of mice with 2,8-dihydroxyadenine nephrolithiasis
KIDNEY INTERNATIONAL
Serum cholesterol, APOE genotype, and the risk of Alzheimer's disease: A population-based study of African Americans
NEUROLOGY
Papulonecrotic tuberculide: a forgotten cutaneous manifestation of tuberculosis
HOSPITAL MEDICINE
Combined adenine phosphoribosyltransferase and N-acetylgalactosamine-6-sulfate sulfatase deficiency
MOLECULAR GENETICS AND METABOLISM
Prospective study of microchimerism in transplant recipients
CLINICAL TRANSPLANTATION
Pattern of localization of primitive hematopoietic cells in vivo using a novel mouse model
EXPERIMENTAL HEMATOLOGY
Microchimerism analysis using polymerase chain reaction assays that selectively amplify donor DNA
TRANSPLANTATION PROCEEDINGS
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
APOE ALLELE FREQUENCIES IN DEMENTED AND NONDEMENTED ELDERLY JAMAICANS
Annals of neurology
CHRONIC-RENAL-FAILURE IN A MOUSE MODEL OF HUMAN ADENINE PHOSPHORIBOSYLTRANSFERASE DEFICIENCY
American journal of physiology. Renal, fluid and electrolyte physiology
POLYMORPHISMS IN THE HUMAN APOLIPOPROTEIN-J CLUSTERIN GENE - ETHNIC VARIATION AND DISTRIBUTION IN ALZHEIMERS-DISEASE (VOL 98, PG 430, 1996)/
Human genetics
Evaluation of seven PCR-based assays for the analysis of microchimerism
CLINICAL BIOCHEMISTRY
THE ASSOCIATION BETWEEN APO-E GENOTYPE AND DEPRESSIVE SYMPTOMS IN ELDERLY AFRICAN-AMERICAN SUBJECTS
The American journal of geriatric psychiatry
APOLIPOPROTEIN E-ASSOCIATED RISK FOR ALZHEIMERS-DISEASE IN THE AFRICAN-AMERICAN POPULATION IS GENOTYPE-DEPENDENT
Annals of neurology
LOSS OF HETEROZYGOSITY ANALYSIS IN A HUMAN FIBROSARCOMA CELL-LINE
Cytogenetics and cell genetics
PURIFICATION AND CHARACTERIZATION OF ADENINE PHOSPHORIBOSYLTRANSFERASE FROM SACCHAROMYCES-CEREVISIAE
Biochimica et biophysica acta. Protein structure and molecular enzymology
THE ROLE OF CELL-MIGRATION AND MICROCHIMERISM IN THE INDUCTION OF TOLERANCE AFTER SOLID-ORGAN TRANSPLANTATION
Postgraduate medical journal
HIGH-FREQUENCY IN-VIVO LOSS OF HETEROZYGOSITY IS PRIMARILY A CONSEQUENCE OF MITOTIC RECOMBINATION
Cancer research
GENETIC AND BIOCHEMICAL-ANALYSIS OF A MOUSE MODEL FOR HUMAN DHA UROLITHIASIS
American journal of human genetics
DEPRESSIVE SYMPTOMS BY APOLIPOPROTEIN-E ALLELE STATUS IN ELDERLY AFRICAN-AMERICANS
The American journal of geriatric psychiatry
IDENTIFICATION AND APPLICATION OF POLYMORPHISMS FLANKING THE HUMAN ADENINE PHOSPHORIBOSYLTRANSFERASE GENE
Human mutation
HPRT-APRT-DEFICIENT MICE ARE NOT A MODEL FOR LESCH-NYHAN SYNDROME
Human molecular genetics
POLYMORPHISMS IN THE HUMAN APOLIPOPROTEIN-J CLUSTERIN GENE - ETHNIC VARIATION AND DISTRIBUTION IN ALZHEIMERS-DISEASE/
Human genetics
COMPLEX CHROMOSOMAL MECHANISMS LEAD TO APRT LOSS OF HETEROZYGOSITY INHETEROPLOID CELLS
Cytogenetics and cell genetics
ADENINE PHOSPHORIBOSYLTRANSFERASE-DEFICIENT MICE DEVELOP 2,8-DIHYDROXYADENINE NEPHROLITHIASIS
Proceedings of the National Academy of Sciences of the United Statesof America
IMPROVED PROCEDURE FOR ELUTING DNA FROM DRIED BLOOD SPOTS
Clinical chemistry
CLONING AND CHARACTERIZATION OF THE ADENINE PHOSPHORIBOSYLTRANSFERASE-ENCODING GENE (APT1) FROM SACCHAROMYCES-CEREVISIAE
Gene
LACK OF AN ASSOCIATION BETWEEN APOLIPOPROTEIN-E EPSILON-4 AND ALZHEIMERS-DISEASE IN ELDERLY NIGERIANS
Annals of neurology
APOLIPOPROTEIN-E GENOTYPES AND ALZHEIMERS-DISEASE IN A COMMUNITY STUDY OF ELDERLY AFRICAN-AMERICANS
Annals of neurology
COMPLEX CHROMOSOME MECHANISMS LEADING TO THE LOSS OF WILD-TYPE ALLELEOF APRT GENE IN HETEROPLOID CELLS
American journal of human genetics
LACK OF AN ASSOCIATION BETWEEN THE E4 ALLELE OF APOLIPOPROTEIN-E AND ALZHEIMER-DISEASE IN ELDERLY NIGERIANS
American journal of human genetics
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
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
MISSENSE MUTATION IN THE ADENINE PHOSPHORIBOSYLTRANSFERASE GENE CAUSING 2,8-DIHYDROXYADENINE UROLITHIASIS
Human molecular genetics
IDENTIFICATION OF A 7-BASEPAIR DELETION IN THE ADENINE PHOSPHORIBOSYL-TRANSFERASE GENE AS A CAUSE OF 2,8-DIHYDROXYADENINE UROLITHIASIS
The Clinical investigator
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
GENETIC-STRUCTURE ANALYSIS AND LOSS OF HETEROZYGOSITY (LOH) IN HUMAN-CELLS
American journal of human genetics
DETECTION OF PLP GENE-MUTATIONS IN PATIENTS WITH PELIZAEUS-MERZBACHERDISEASE BY SINGLE-STRAND CONFORMATIONAL-ANALYSIS
American journal of human genetics
EXON SKIPPING IN THE WILD-TYPE TRANSCRIPTS OF APRT AND ITS ENHANCEMENT BY A NONSENSE MUTATION
American journal of human genetics
FRAGILE-X FULL MUTATION IN 2 CLINICALLY UNAFFECTED BROTHERS
American journal of human genetics
MOLECULAR-GENETICS SERVICES AT INDIANA-UNIVERSITY
American journal of human genetics