R. Mulivor

发表

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia.

H. Harris, M. Weiss, K. Ray, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Juvenile onset diabetes.

R. Mulivor, D. Buck, A. Greene, 1980, Cytogenetics and cell genetics.

Origin of cell-culture lines.

R. Mulivor, A. Greene, L. Coriell, 1983, The New England journal of medicine.

INTRAUTERINE CYTOMEGALOVIRUS INFECTION PRESENTING AS FETAL MECONIUM PERITONITIS

B. Pletcher, R. Mulivor, Marjorie K. Williams, 1991, Obstetrics and gynecology.

Infantile hypophosphatasia: localization within chromosome region 1p36.1-34 and prenatal diagnosis using linked DNA markers.

C. Greenberg, J. Evans, R. Mulivor, 1990, American journal of human genetics.

Differential inhibition of the products of the human alkaline phosphatase loci

R. Mulivor, H. Harris, LARRY I. Plotkin, 1978, Annals of human genetics.

Analysis of fetal intestinal enzymes in amniotic fluid for the prenatal diagnosis of cystic fibrosis.

E. Pergament, F. Muller, D. Cook, 1987, American journal of human genetics.

Prenatal diagnostic options in cystic fibrosis.

K. Tsao, C. Denning, R. Mulivor, 1988, American journal of obstetrics and gynecology.

An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

R. Greenstein, R. Mulivor, A. Greene, 1980, Cytogenetics and cell genetics.

In vivo replication of hepatic deoxyribonucleic acid of rats treated with dimethylnitrosamine: presence of dimethylnitrosamine-induced O6-methylguanine, N7-methylguanine, and N3-methyladenine in the replicated hybrid deoxyribonucleic acid.

A. Columbano, S. Rajalakshmi, D. Sarma, 1980, Biochemistry.

Xeroderma pigmentosum variants.

J. Cleaver, R. Mulivor, A. Greene, 1981, Cytogenetics and cell genetics.

Validation of routine mycoplasma testing by PCR

J. Sarama, R. Mulivor, L. Toji, 1998, In Vitro Cellular & Developmental Biology - Animal.

Alkaline lysis of mammalian cells for sedimentation analysis of nuclear DNA. Conformation of released DNA as monitored by physical, electron microscopic and enzymological techniques.

S. Parodi, C. Nicolini, D. Sarma, 1975, Biochimica et biophysica acta.

Analysis of the binding of phenylalanine to phenylalanyl-tRNA synthetase.

R. Mulivor, H. Rappaport, 1973, Journal of Molecular Biology.

Developmental change in human intestinal alkaline phosphatase.

H. Harris, R. Mulivor, V. Hannig, 1978, Proceedings of the National Academy of Sciences of the United States of America.

Analysis of liver/bone/kidney alkaline phosphatase mRNA, DNA, and enzymatic activity in cultured skin fibroblasts from 14 unrelated patients with severe hypophosphatasia.

H. Harris, M. Weiss, K. Ray, 1989, American journal of human genetics.

A (Y;17) translocation in a fibroblast culture from a female with 46 chromosomes. Repository identification No. GM-2598.

R. Mulivor, J. Rary, A. Greene, 1979, Cytogenetics and cell genetics.

Regional mapping panels for chromosomes 3, 4, 5, 11, 15, 17, 18, and X.

P. Bender, J. Beck, R. Mulivor, 1997, Genomics.

Prenatal diagnosis of hypophosphatasia; genetic, biochemical, and clinical studies.

E. Zackai, H. Harris, R. Mulivor, 1978, American journal of human genetics.

Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carriers of hypophosphatasia corrects during pregnancy.

P. Henthorn, S. Coburn, M. Whyte, 1995, The Journal of clinical investigation.

Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study

Stephanie A. Santorico, Trina M. Norden-Krichmar, E. Boerwinkle, 2021, Diabetology & Metabolic Syndrome.

Quantitative analysis of alkaline phosphatases in serum and amniotic fluid: comparison of biochemical and immunologic assays.

H. Harris, R. Mulivor, D. Boccelli, 1985, The Journal of laboratory and clinical medicine.

Benign familial hyperphosphatasemia.

J. Mulvihill, R. W. Miller, R. Mulivor, 1989, JAMA.

First identification of a gene defect for hypophosphatasia: evidence that alkaline phosphatase acts in skeletal mineralization.

H. Harris, M. Weiss, K. Ray, 1989, Connective tissue research.

Origin of the alkaline phosphatases in amniotic fluid.

H. Harris, R. Mulivor, M. Mennuti, 1979, American journal of obstetrics and gynecology.

Benign hyperphosphatasemia.

P. Wilding, L. Kricka, W. Long, 1990, Clinical chemistry.

Prenatal Diagnosis of Hypophosphatasia

B. Kousseff, R. Mulivor, 1981, Obstetrics and gynecology.

NIGMS human/rodent somatic cell hybrid mapping panels 1 and 2.

R. Mulivor, H. Drwinga, L. Toji, 1993, Genomics.

Raised urinary excretion of inorganic pyrophosphate in asymptomatic members of a hypophosphatasia kindred.

J. Macfarlane, A. Caswell, R. Mulivor, 1991, Clinica chimica acta; international journal of clinical chemistry.

Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.

G. Donnell, R. Mulivor, W. Ng, 1984, Cytogenetics and Cell Genetics.