Kidney transplantation in diabetic patients using cyclosporine. Five-year follow-up.

PubWeight™: 0.75‹?›

🔗 View Article (PMID 7887795)

Published in Arch Surg on March 01, 1995

Authors

D Shaffer1, M A Simpson, P N Madras, A I Sahyoun, P A Conway, C P Davis, A P Monaco

Author Affiliations

1: Division of Organ Transplantation, New England Deaconess Hospital, Boston, Mass.

Articles by these authors

Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell (1987) 16.01

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. Cell (1988) 10.75

A forkhead-domain gene is mutated in a severe speech and language disorder. Nature (2001) 9.25

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene. Nature (1986) 6.45

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location. Nature (1986) 6.34

Studies on heterologous anti-lymphocyte serum in mice. I. In vitro and in vivo properties. J Immunol (1966) 5.59

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc Natl Acad Sci U S A (1985) 5.50

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment. Nature (1985) 4.62

Studies on heterologous anti-lymphocyte serum in mice. II. Effect on the immune response. J Immunol (1966) 4.49

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature (1986) 4.13

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. Nat Genet (1993) 3.63

Diagnostic strategies in CADASIL. Neurology (2002) 3.52

An improved method for isolation of mouse pancreatic islets. Transplantation (1985) 3.52

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry (2007) 3.49

Anaerobic bacteria on the mucosal epithelium of the murine large bowel. Infect Immun (1971) 3.37

Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nat Genet (1999) 3.25

Habitat, succession, attachment, and morphology of segmented, filamentous microbes indigenous to the murine gastrointestinal tract. Infect Immun (1974) 3.18

Evidence for pili-mediated adherence of Klebsiella pneumoniae to rat bladder epithelial cells in vitro. Infect Immun (1979) 2.97

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2. Nat Genet (2000) 2.96

The UTX gene escapes X inactivation in mice and humans. Hum Mol Genet (1998) 2.91

Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc Natl Acad Sci U S A (1991) 2.89

Microbial colonization of the intestinal epithelium in suckling mice. Infect Immun (1973) 2.68

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. Hum Genet (1987) 2.64

Location and description of spiral-shaped microorganisms in the normal rat cecum. Infect Immun (1972) 2.48

Adult Thymectomy: Effect on Recovery from Immunologic Depression in Mice. Science (1965) 2.41

A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet (1999) 2.38

Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science (1995) 2.38

Effect of piliation on Klebsiella pneumoniae infection in rat bladders. Infect Immun (1980) 2.35

Localisation of a gene implicated in a severe speech and language disorder. Nat Genet (1998) 2.33

Influence of rejection therapy on fungal and nocardial infections in renal-transplant recipients. Lancet (1973) 2.22

Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries. Proc Natl Acad Sci U S A (1991) 2.21

Reproducible high yield of rat islets by stationary in vitro digestion following pancreatic ductal or portal venous collagenase injection. Transplantation (1987) 2.14

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome. Cell (1986) 2.12

A randomized, placebo-controlled study to evaluate the role of salmeterol in the in-hospital management of asthma. Chest (2000) 2.06

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene. Genomics (1988) 2.04

Targeted disruption of the adipocyte lipid-binding protein (aP2 protein) gene impairs fat cell lipolysis and increases cellular fatty acid levels. J Lipid Res (1999) 1.99

Pulmonary nocardiosis. Therapy with minocycline and with erythromycin plus ampicillin. JAMA (1973) 1.94

Complete coverage of the Schizosaccharomyces pombe genome in yeast artificial chromosomes. Nat Genet (1992) 1.93

Mycoplasma pneumoniae and Mycoplasma genitalium mixture in synovial fluid isolate. J Clin Microbiol (1995) 1.90

Possible active enhancement of a human cadaver renal allograft with antilymphocyte serum (ALS) and donor bone marrow: case report of an initial attempt. Surgery (1976) 1.84

Antiserum to lymphocytes: prolonged survival of canine renal allografts. Science (1966) 1.81

A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23. Neurology (2008) 1.81

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16. Am J Hum Genet (1997) 1.79

Two hundred one consecutive living-donor nephrectomies. Arch Surg (1998) 1.75

Purification and chemical characterization of type 1 pili isolated from Klebsiella pneumoniae. J Biol Chem (1982) 1.74

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. J Med Genet (2005) 1.74

A conserved sorting-associated protein is mutant in chorea-acanthocytosis. Nat Genet (2001) 1.69

Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjects. Behav Genet (2010) 1.67

Conservation of the Duchenne muscular dystrophy gene in mice and humans. Science (1987) 1.66

Analysis of the human VPS13 gene family. Genomics (2004) 1.65

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Hum Mol Genet (1999) 1.65

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein. Cell (1994) 1.65

Melanoma chondroitin sulphate proteoglycan regulates cell spreading through Cdc42, Ack-1 and p130cas. Nat Cell Biol (1999) 1.65

FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet (2002) 1.63

Some effects of purified heterologous antihuman lymphocyte serum in man. Transplantation (1967) 1.62

Effect of adult thymectomy on the recovery from immunological depression induced by anti-lymphocyte serum. Surg Forum (1965) 1.60

The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. Am J Hum Genet (2000) 1.60

Clinical, hematologic, and immunologic cross-sectional evaluation of individuals exposed to human immunodeficiency virus type-2 (HIV-2). AIDS Res Hum Retroviruses (1988) 1.58

Severity of disease and risk of malignant change in hereditary multiple exostoses. A genotype-phenotype study. J Bone Joint Surg Br (2004) 1.57

Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis. Eur J Hum Genet (2002) 1.56

Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Mol Psychiatry (2006) 1.54

Studies in small bowel transplantation. Prevention of graft-versus-host disease with preservation of allograft function by donor pretreatment with antilymphocyte serum. Transplantation (1988) 1.52

Report of the committee on the genetic constitution of the X chromosome. Cytogenet Cell Genet (1990) 1.51

Immunologic and metabolic effects of caval versus portal venous drainage in small-bowel transplantation. Surgery (1988) 1.50

Preservation of gastrointestinal bacteria and their microenvironmental associations in rats by freezing. Appl Environ Microbiol (1976) 1.48

A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome. Nat Genet (1996) 1.47

Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene. Mol Psychiatry (2003) 1.47

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment. Genes Brain Behav (2007) 1.46

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility. Mol Psychiatry (2009) 1.45

McLeod neuroacanthocytosis: genotype and phenotype. Ann Neurol (2001) 1.45

Controversies in organ donation: the altruistic living donor. Nephrol Dial Transplant (2001) 1.45

Complexity of the healthcare crisis in rural America. J Am Osteopath Assoc (1994) 1.39

Preemptive plasmapheresis and recurrence of FSGS in high-risk renal transplant recipients. Am J Transplant (2005) 1.38

New approach to patency and flow assessment after left internal thoracic artery hypoperfusion syndrome with additional saphenous vein graft to the left anterior descending artery with phase-contrast magnetic resonance angiography. J Thorac Cardiovasc Surg (1997) 1.38

Autism: recent molecular genetic advances. Hum Mol Genet (2000) 1.34

Isolation of the human Xp21 glycerol kinase gene by positional cloning. Hum Mol Genet (1993) 1.34

Intracellular lipid-binding proteins and their genes. Annu Rev Nutr (1997) 1.34

Genetic advances in the study of speech and language disorders. Neuron (2010) 1.33

Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families. The International Molecular Genetic Study of Autism Consortium. Am J Med Genet (1999) 1.31

High incidence of fungus infections in renal transplantation patients treated with antilymphocyte and conventional immunosuppression. Transplant Proc (1973) 1.31

Evidence for a bladder cell glycolipid receptor for Escherichia coli and the effect of neuraminic acid and colominic acid on adherence. Infect Immun (1981) 1.27

DNA linkage analysis of X chromosome-linked chronic granulomatous disease. Proc Natl Acad Sci U S A (1986) 1.27

Characterization of the exon structure of the Menkes disease gene using vectorette PCR. Genomics (1995) 1.26

GATA zinc finger interactions modulate DNA binding and transactivation. J Biol Chem (2000) 1.26

Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region. Nat Genet (1992) 1.25

Heterologous antilymphocyte sera and some of their effects. Transplantation (1967) 1.25

Phytophotodermatitis: the other "lime" disease. J Emerg Med (1999) 1.24

Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins. Genomics (1997) 1.23

Electron microscopy of the coccoid form of Campylobacter jejuni. J Clin Microbiol (1983) 1.23

A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13. Hum Mol Genet (1993) 1.23

Construction and characterization of a 10-fold genome equivalent rat P1-derived artificial chromosome library. Genomics (1998) 1.22

Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination. Hum Mol Genet (1992) 1.22

Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK. J Med Genet (2004) 1.22

Studies on heterologous antilymphocyte serum in mice. VII. Optimal cellular antigen for induction of immunologic tolerance with antilymphocyte serum. Transplant Proc (1970) 1.22

Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. Hum Mol Genet (1997) 1.21

Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump. Hum Mol Genet (2000) 1.20