R. Erbe

发表

Food reinforcement, the dopamine D2 receptor genotype, and energy intake in obese and nonobese humans.

L. Epstein, J. Temple, J. Leddy, 2007, Behavioral neuroscience.

Two functional serotonin polymorphisms moderate the effect of food reinforcement on BMI.

L. Epstein, D. Allison, E. Stice, 2013, Behavioral neuroscience.

Neonatal Screening

R. Erbe, I. Sahai, 2022, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Newborn screening for Krabbe disease: the New York State model.

B. Kosofsky, T. Naidich, J. Provenzale, 2009, Pediatric neurology.

Newborn screening for Krabbe disease in New York State: the first eight years’ experience

Matthew J. Nichols, J. Kurtzberg, P. Galvin-Parton, 2016, Genetics in Medicine.

Chapter 27 – Neonatal Screening

R. Erbe, 2013 .

Decreased purine synthesis during amino acid starvation of human lymphoblasts.

G. Boss, R. Erbe, 1982, The Journal of biological chemistry.

Genetic screening programs: Principles and research

R. Erbe, 1977 .

Phenylketonuria in adulthood: A collaborative study

B. Burton, R. Koch, F. Guttler, 2002, Journal of Inherited Metabolic Disease.

Lysyl-protocollagen hydroxylase deficiency in fibroblasts from siblings with hydroxylysine-deficient collagen.

S. Krane, R. Erbe, S. Pinnell, 1972, Proceedings of the National Academy of Sciences of the United States of America.

Lack of genotype-phenotype correlations and outcome in MCAD deficiency diagnosed by newborn screening in New York State.

Matthew J. Nichols, P. Galvin-Parton, M. Caggana, 2010, Molecular genetics and metabolism.

Neonatal Screening

R. Erbe, I. Sahai, 2022, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Folate polyglutamate and monoglutamate accumulation in normal and SV40‐transformed human fibroblasts

R. Hoffman, R. Erbe, D. Coalson, 1981, Journal of cellular physiology.

Genetic aspects of folate metabolism.

R. Erbe, Richard W. Erbe, 1979, Advances in human genetics.

High in vivo rates of methionine biosynthesis in transformed human and malignant rat cells auxotrophic for methionine.

R. Hoffman, R. Erbe, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Does the dopamine transporter protein allele predict growth hormone testing results or response to growth hormone therapy?

T. Quattrin, Robbert J. Salis, R. Erbe, 2010, Endocrine.

Decreased methylation rates of DNA in SV40‐transformed human fibroblasts

G. Boss, R. Erbe, L. Levitt, 1986, Cancer.

Inborn errors of folate metabolism (second of two parts).

R. Erbe, 1975, The New England journal of medicine.

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 15-1989. A 52-year-old man with neurofibromatosis and jaundice.

C. Compton, R. Erbe, 1989, The New England journal of medicine.

Reversion to methionine independence in simian virus 40-transformed human and malignant rat fibroblasts is associated with altered ploidy and altered properties of transformation.

R. Hoffman, R. Erbe, S. Jacobsen, 1979, Proceedings of the National Academy of Sciences of the United States of America.

Reversion to methionine independence by malignant rat and SV40-transformed human fibroblasts.

R. Hoffman, R. Erbe, S. Jacobsen, 1978, Biochemical and biophysical research communications.

Attitudes toward the prenatal diagnosis of cystic fibrosis: factors in decision making among affected families.

R. Erbe, D. Wertz, S. R. Janes, 1992, American journal of human genetics.

Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 24-1987. A 56-year-old man with a substernal goiter, multiple cutaneous and mucosal lesions, and a positive stool test for occult blood.

C. Compton, R. Erbe, 1987, The New England journal of medicine.

Attitudes toward abortion among parents of children with cystic fibrosis.

R. Erbe, D. Wertz, S. R. Janes, 1991, American journal of public health.

Reciprocal changes in the levels of functionally related folate enzymes during the culture cycle in human fibroblasts.

D. Rosenblatt, R. Erbe, 1973, Biochemical and biophysical research communications.

Translation and translocation of defined RNA messengers.

P. Leder, M. Nau, R. Erbe, 1969, Journal of molecular biology.

Genetic prothrombotic mutations are common in neonates but are not associated with umbilical catheter-associated thrombosis

S. Lakshminrusimha, R. Ryan, R. Erbe, 2007, Journal of Perinatology.

Role of metals in the class II aldolases. Spectral studies of cobalt yeast aldolase.

W. Rutter, B. Vallee, R. Simpson, 1971, Biochemistry.

Methylenetetrahy drofolate Reductase in Cultured Human Cells. I. Growth and Metabolic Studies

D. Rosenblatt, R. Erbe, 1977, Pediatric Research.

Transfer of tumor cells between cell aggregates as a model for adhesive changes in metastasis.

R. Erbe, J. Umbreit, 1979, Cancer research.

The long-term outcomes of presymptomatic infants transplanted for Krabbe disease: Report of the workshop held on July 11 and 12, 2008, Holiday Valley, New York

V. Caviness, M. Patterson, C. Whitley, 2009, Genetics in Medicine.

Clinical outcomes of children with abnormal newborn screening results for Krabbe disease in New York State

T. Naidich, J. Provenzale, J. Kurtzberg, 2016, Genetics in Medicine.

Linkage of Methionine Dependence and Other Features of Malignancy.

R. Hoffman, R. Erbe, 2019, Methods in molecular biology.

Regulation of methionine adenosyltransferase in normal diploid and simian virus 40-transformed human fibroblasts.

R. Hoffman, R. Erbe, S. Jacobsen, 1980, Journal of the National Cancer Institute.

Newborn screening for X-linked adrenoleukodystrophy in New York State: diagnostic protocol, surveillance protocol and treatment guidelines.

G. Raymond, J. Orsini, M. Caggana, 2015, Molecular genetics and metabolism.

Altered Methionine Metabolism in Cancer Cells.

R. Hoffman, R. Erbe, D. Coalson, 2019, Methods in molecular biology.

Current concepts in genetics: principles of medical genetics (second of two parts).

R. Erbe, 1976, The New England journal of medicine.

A comparison of fragile X expression in lymphocyte and lymphoblastoid cultures.

P. Hunt, P. Jacobs, R. Erbe, 1986, American journal of human genetics.

Decreased rates of methionine synthesis by methylene tetrahydrofolate reductase-deficient fibroblasts and lymphoblasts.

G. Boss, R. Erbe, 1981, The Journal of clinical investigation.

Fragile sites and high-resolution chromosome studies in multiple endocrine neoplasia type 2A.

S. H. Gibson, R. Erbe, W. Noll, 1988, Cancer genetics and cytogenetics.

Expression of the marker (X) (q28) in lymphoblastoid cell lines.

P. Hunt, P. Jacobs, G. Boss, 1982, American journal of human genetics.

A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase Deficiency.

G. Enns, B. Burton, J. Kane, 2015, The New England journal of medicine.

Prevention of Fetal Damage Through Dietary Control of Maternal Hyperphenylalaninemia

H. Levy, R. Erbe, M. Ghavami, 1986, Clinical obstetrics and gynecology.

Severe methylenetetrahydrofolate reductase deficiency, methionine synthase, and nitrous oxide--a cautionary tale.

Robbert J. Salis, R. Erbe, 2003, The New England journal of medicine.

FTO polymorphisms moderate the association of food reinforcement with energy intake

L. Epstein, D. Allison, L. Sucheston, 2014, Physiology & Behavior.

Prenatal diagnosis of genetic disorders.

R. Erbe, W. Miller, Miller Wa, 1978, Southern medical journal.

Regulation of 5-methyltetrahydrofolate: homocysteine methyltransferase activity by methionine, vitamin B12, and folate in cultured baby hamster kidney cells.

J. Littlefield, R. Erbe, D. Kamely, 1973, Proceedings of the National Academy of Sciences of the United States of America.

Methylenetetrahydrofolate Reductase in Cultured Human Cells. II. Genetic and Biochemical Studies of Methylenetetrahydrofolate Reductase Deficiency

D. Rosenblatt, R. Erbe, 1977, Pediatric Research.

Inherited gastrointestinal-polyposis syndromes.

R. Erbe, 1976, The New England journal of medicine.

Folate metabolism in humans.

R. Erbe, J. C. Wang, 1984, American journal of medical genetics.

Folic acid therapy in the fragile X syndrome.

R. Erbe, 1984, American journal of medical genetics.

Acute Effects of Ghlorothiazide on Plasma Electrolytes and Acid-Base Pattern of Nephrectomized Rats and Dogs.∗

R. Erbe, J. Weller, 1962 .

Peritoneal dialysis during hemorrhagic shock.

R. Erbe, J. Greene, J. Weller, 1967, Journal of applied physiology.

L. Epstein, R. Paluch, W. Pelham, 2009, Journal of child and adolescent psychopharmacology.

Folate metabolism in cells from fragile X syndrome patients and carriers.

R. Erbe, J. C. Wang, 1984, American journal of medical genetics.

Initiation and protein synthesis: translation of di- and tri-codon messengers.

P. Leder, R. Erbe, 1968, Biochemical and biophysical research communications.

Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoin.

P. Jayakar, J. Vockley, G. Diaz, 2023, Molecular genetics and metabolism.

Folate Pathways in Cells from Fragile X Syndrome Patients and Carriers

R. Erbe, Jin-Chen C. Wang, 1983 .

Parent–child concordance of Taq1 A1 allele predicts similarity of parent–child weight loss in behavioral family-based treatment programs

Leonard H. Epstein, L. Epstein, K. K. Dearing, 2010, Appetite.

Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.

D. Watkins, D. Rosenblatt, R. Erbe, 1987, American journal of medical genetics.

Antifolate-induced misincorporation of deoxyuridine monophosphate into DNA by cells from patients with the fragile X syndrome.

G. P. Beardsley, R. Erbe, J. C. Wang, 1985, American journal of medical genetics.

Sodium transport in cystic fibrosis fibroblasts.

T. Boat, R. Stern, J. Breslow, 1981, New England Journal of Medicine.

Expression of the human argininosuccinate synthetase gene in hamster transferents.

L. Hudson, R. Erbe, L. Jacoby, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Current concepts in genetics: principles of medical genetics (second of two parts).

Francis S. Collins, F. Collins, T. Gelehrter, 1976 .

L. Epstein, R. Paluch, W. Pelham, 2009, Journal of child and adolescent psychopharmacology.