Published in Transplant Proc on December 01, 1972
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
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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
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
A survey of nasotracheal intubating skills among Advanced Trauma Life Support course graduates. Br J Anaesth (1994) 3.29
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nat Genet (1999) 3.25
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
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. Hum Genet (1987) 2.64
Adult Thymectomy: Effect on Recovery from Immunologic Depression in Mice. Science (1965) 2.41
Guidelines for the management of alopecia areata. Br J Dermatol (2003) 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
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 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene. Genomics (1988) 2.04
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
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
Spoiling of transverse magnetization in steady-state sequences. Magn Reson Med (1991) 1.83
Antiserum to lymphocytes: prolonged survival of canine renal allografts. Science (1966) 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
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
Elimination of transverse coherences in FLASH MRI. Magn Reson Med (1988) 1.67
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
Functional MRI of pain- and attention-related activations in the human cingulate cortex. J Neurophysiol (1997) 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
Willingness to follow breast cancer. Survey of family physicians. Can Fam Physician (1996) 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
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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
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Glycyrrhizic acid inhibits virus growth and inactivates virus particles. Nature (1979) 1.51
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
An episode of ventricular tachycardia during long-duration spaceflight. Am J Cardiol (1998) 1.48
Mutagenic and genotoxic effects of three vinyl chloride-induced DNA lesions: 1,N6-ethenoadenine, 3,N4-ethenocytosine, and 4-amino-5-(imidazol-2-yl)imidazole. Biochemistry (1993) 1.47
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
Who provides follow-up care for patients with early breast cancer? Can Fam Physician (1995) 1.41
Preemptive plasmapheresis and recurrence of FSGS in high-risk renal transplant recipients. Am J Transplant (2005) 1.38
Post transplantation donor-specific bone marrow transfusion in polyclonal antilymphocyte serum-treated recipients: the optimal cellular antigen for induction of unresponsiveness to organ allografts. Transplant Proc (1988) 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
Genetic advances in the study of speech and language disorders. Neuron (2010) 1.33
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High incidence of fungus infections in renal transplantation patients treated with antilymphocyte and conventional immunosuppression. Transplant Proc (1973) 1.31
MR image artifacts from periodic motion. Med Phys (1985) 1.29
Nucleic acid-based cross-linking assay for detection and quantification of hepatitis B virus DNA. J Clin Microbiol (1999) 1.29
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
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
Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins. Genomics (1997) 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
Studies on heterologous antilymphocyte serum in mice. VII. Optimal cellular antigen for induction of immunologic tolerance with antilymphocyte serum. Transplant Proc (1970) 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
Identification, clinical distribution, and susceptibility to methicillin and 18 additional antibiotics of clinical Staphylococcus isolates: nationwide investigation in Italy. J Clin Microbiol (1984) 1.21
Motion-insensitive, steady-state free precession imaging. Magn Reson Med (1990) 1.21
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
A Golgi localization signal identified in the Menkes recombinant protein. Hum Mol Genet (1998) 1.20
Enhanced survival of canine renal allografts of ALS- treated dogs given bone marrow. Transplant Proc (1973) 1.20