D. Hoar

发表

Altered expression of genes for amyloid and cytoskeletal proteins in alzheimer cortex

A. Clark, J. Julien, I. Parhad, 1989, Annals of neurology.

Severe combined immune deficiency presenting with cyclic hematopoiesis

M. Poon, A. Junker, P. Rogers, 1991, Journal of Clinical Immunology.

Exaggerated triglyceride accretion in human preadipocyte-murine renal line hybrids composed of cells from massively obese subjects.

D. Roncari, D. Hoar, P. Le Blanc, 1988, The Journal of clinical investigation.

Hepatitis B virus DNA is enriched in polymorphonuclear leukocytes.

M. Poon, D. Hoar, T. Bowen, 1985, Blood.

Mental retardation, distinct facial changes, short stature, obesity, and hypogonadism: a new X-linked mental retardation syndrome.

A. Chudley, R. Lowry, D. Hoar, 1988, American journal of medical genetics.

Primer-mediated enzymatic amplification of cytomegalovirus (CMV) DNA. Application to the early diagnosis of CMV infection in marrow transplant recipients.

Richard, James, M. Naylor, 1989, Journal of Clinical Investigation.

The use of DNA probes to establish parental origin in Down syndrome

C. Greentree, D. Hoar, N. Rudd, 1988, Human Genetics.

A new HLA-DRB1 allele formed by an intraexonic interallelic crossover.

P. Goodfellow, P. Keown, A. Junker, 1993, Tissue antigens.

Altered expression of neuronal messenger RNA in Alzheimer cortex.

A. Clark, J. Julien, I. Parhad, 1989, Progress in clinical and biological research.

Molecular Diagnosis: New Horizons in Medicine

D. Hoar, 2008 .

Neurofilament gene expression following β,β′-iminodipropionitrile (IDPN) intoxication

A. Clark, I. Parhad, C. A. Krekoski, 1988 .

Efficacy of commercial condoms in the prevention of hepatitis B virus infection.

M. Gill, G. Minuk, S. Cassol, 1987, Gastroenterology.

A novel DRβ1∗03 allele identified by polymerase chain reaction—Restriction fragment length polymorphism

P. Keown, D. Hoar, B. Fenske, 1996 .

Fertility Regulation in F-Like Resistance Transfer Factors

D. Hoar, 1970, Journal of bacteriology.

Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria.

D. Chitayat, O. Mamer, C. Scriver, 1992, The Journal of pediatrics.

Hemopoietic origin of factor XIII A subunits in platelets, monocytes, and plasma. Evidence from bone marrow transplantation studies.

M. Poon, J. Russell, A. Jones, 1989, The Journal of clinical investigation.

Hemophilia B (Christmas disease) variants and carrier detection analyzed by DNA probes.

M. Poon, D. Chui, M. Patterson, 1987, The Journal of clinical investigation.

A frequent restriction fragment length polymorphism in the human metallothionein-II processed gene region is evolutionarily conserved.

U. Varshney, L. Gedamu, D. Hoar, 1984, Molecular biology & medicine.

Ground squirrel hepatitis virus (GSHV) infection and hepatocellular carcinoma in the Canadian Richardson ground squirrel (Spermophilus richardsonii).

G. Minuk, E. Shaffer, D. Hoar, 2008, Liver.

Studies on the mechanism of activation of human natural killer function by interferon and inhibitors of thymidylate synthesis.

D. Hoar, S. Friedman, D. Matheson, 1988, Cellular immunology.

DNA repair in Cockayne syndrome.

D. Hoar, C. Waghorne, 1978, American journal of human genetics.

Policy statement concerning DNA banking and molecular genetic diagnosis. Canadian College of Medical Geneticists.

J. Hamerton, R. Korneluk, D. Rosenblatt, 1991, Clinical and investigative medicine. Medecine clinique et experimentale.

Hemophilia A carrier detection by restriction fragment length polymorphism analysis and discriminant analysis based on ELISA of factor VIII and vWf.

M. Poon, D. Hoar, G. Sinclair, 1992, The Journal of laboratory and clinical medicine.

PRENATAL DIAGNOSIS OF HYPOPHOSPHATASIA

D. Hoar, N. Rudd, K. Blau, 1976, The Lancet.

Kinetochore analysis of micronuclei allows insights into the actions of colcemid and mitomycin C.

S. Williams, D. Hoar, M. Evans, 1991, Mutation research.

Induction of mitochondrial mutations in human cells by methotrexate.

D. Hoar, L. Dimnik, 1985, Basic life sciences.

Host-cell reactivation of UV-irradiated adenovirus in Cockayne syndrome.

F. Davis, D. Hoar, 1979, Mutation research.

Chemical mutagen hypersensitivity in ataxia telangiectasia

D. Hoar, P. Sargent, 1976, Nature.

Improved direct molecular diagnosis and rapid fetal sexing

D. Haslam, D. Hoar, D. Starozik, 1984, Prenatal diagnosis.

Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe

C. Disteche, D. Luthy, D. Haslam, 2004, Human Genetics.

DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA.

L. Madisen, M. Hodes, M. E. Hodes, 1987, American journal of medical genetics.

Humoral immune response in patients with hemophilia.

M. Fritzler, M. Poon, D. Hoar, 1987, Clinical immunology and immunopathology.

Prenatal diagnosis of hypophosphatasia.

D. Hoar, N. Rudd, M. Miskin, 1976, The New England journal of medicine.

A familial interstitial deletion of the long arm of chromosome 21

D. Hoar, A. Robertson, S. B. Fowlow, 1990, Clinical genetics.

Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter study.

D. Bentley, A. Covone, C. Junien, 1992, JAMA.

Primate evolution of a human chromosome 1 hypervariable repetitive element

D. Hoar, K. Tynan, 1989, Journal of Molecular Evolution.

Natural killer cell activity from hemophiliacs exhibits differential responses to various forms of interferon.

M. Fritzler, M. Poon, D. Hoar, 1986, Blood.

T Lymphocytes from Hemophiliacs Proliferate after Exposure to Factor VIII Product

M. Fritzler, M. Poon, D. Hoar, 1986, Vox sanguinis.

Kinetochore immunofluorescence in micronuclei: a rapid method for the in situ detection of aneuploidy and chromosome breakage in human fibroblasts.

D I Hoar, N L Rudd, U G Hennig, 1988, Mutation research.

Familial mutagen sensitivities: are these the hallmarks of meiotic or mutator mutants in humans?

D. Hoar, 1979, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

Tentative assignment of gene for oto-palato-digital syndrome to distal Xq (Xq26-q28).

L. Field, G. Hoganson, D. Hoar, 1992, American journal of medical genetics.

Identification of four novel dinucleotide repeat polymorphisms in the TNF-α and TNF-β genes

D. Horsman, P. Keown, A. Khani-Hanjani, 2000 .

Molecular detection of a translocation (Y;15) in a 45,X male

L. Brown, D. Page, C. Disteche, 1986, Human Genetics.

An Evaluation of the Use of DNA Probe hMF1 in Cases of Disputed Paternity by Comparison with a Range of Well Established Blood Group Polymorphisms

C. Phillips, J. Thomson, P. Lincoln, 1988 .

Association between dinucleotide repeat in non-coding region of interferon-gamma gene and susceptibility to, and severity of, rheumatoid arthritis

D. Lacaille, P. Keown, D. Horsman, 2000, The Lancet.

Factors distinguishing couples at risk for nondisjunction.

D. Hoar, N. Rudd, R. Martin, 1984, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

The influence of methotrexate and thymidine on the human natural killer cell function in vitro.

D. Hoar, D. Matheson, B. Green, 1983, Journal of immunology.

Genotype and the cryopreservation process affect the levels of aneuploidy and chromosome breakage in cultured human fibroblasts.

S. Williams, D. Hoar, N. Rudd, 1989, Genome.

KILLER ACTIVITY IN VITRO

D. Hoar, S. Friedman, D. Matheson, 1985 .

Agents which decrease intracellular thymidine pools cause an augmentation in human natural killer activity in vitro.

D. Hoar, S. Friedman, D. Matheson, 1985, Basic life sciences.

Successful paternity of twins following bone marrow transplantation with busulfan, melphalan and cyclophosphamide conditioning.

P. Keown, J. Shepherd, D. Hoar, 1996, Bone marrow transplantation.

Micronucleus assay in human fibroblasts: a measure of spontaneous chromosomal instability and mutagen hypersensitivity.

C. Greentree, D. Hoar, N. Rudd, 1988, Environmental and molecular mutagenesis.

Assessment of the sephadex technique for selection of X-bearing human sperm by analysis of sperm chromosomes, deoxyribonucleic acid and Y-bodies.

D. Hoar, R. Martin, T. A. Beckett, 1989, Fertility and sterility.

Immune Response Gene Polymorphisms in Renal Transplant Recipients

R. Balshaw, P. Keown, D. Hoar, 2005, Transplantation.

Adenosine 3',5'-cyclic monophosphate regulation of chloramphenicol acetyltransferase synthesis in vitro from P1CM DNA.

R. Dottin, D. Hoar, L. Shiner, 1973, Virology.

Genetic Evidence for Subunits in the Fertility Repressor Produced by F-Like R Factors

D. Hoar, 1971, Journal of bacteriology.

Pallister-Killian syndrome: additional manifestations of cleft palate and sacral appendage.

D. Hoar, D. R. Mcleod, L. Wesselman, 1991, Journal of medical genetics.

PRENATAL DIAGNOSIS OF HYPOPHOSPHATASIA

D. Hoar, N. Rudd, 1976, The Lancet.

Identification of factor IX mutations in haemophilia B: application of polymerase chain reaction and single strand conformation analysis

M. Poon, D. Hoar, B. M. Fraser, 1992, Human Genetics.

Condoms and the prevention of AIDS.

G. Minuk, S. Cassol, D. Hoar, 1986, JAMA.

An evaluation of the use of DNA probes hMF1 and YNH24 in parentage testing.

J A Thomson, D I Hoar, P J Lincoln, 1989, Acta medicinae legalis et socialis.