J. Chinsky

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Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food.

H. Bock, R. Steiner, P. Galvin-Parton, 2003, Molecular genetics and metabolism.

Molecular characterization of a unique patient with epimerase-deficiency galactosaemia

S. Almashanu, T. Cowan, M. Blitzer, 1998, Journal of Inherited Metabolic Disease.

Developmental expression of adenosine deaminase in the upper alimentary tract of mice.

T. Knudsen, F. Rudolph, W. Fanslow, 1990, Differentiation; research in biological diversity.

Comparison of endogenous murine leukemia virus proviral organization and RNA expression in 3-methylcholanthrene-induced and spontaneous thymic lymphomas in RF and AKR mice

L. Leinwand, G. Childs, M. Goodenow, 1985, Journal of virology.

Ontogeny of adenosine deaminase in the mouse decidua and placenta: immunolocalization and embryo transfer studies.

T. Knudsen, M. Blackburn, R. Kellems, 1991, Biology of reproduction.

Adenosine deaminase gene expression. Tissue-dependent regulation of transcriptional elongation.

M. Maa, R. Kellems, V. Ramamurthy, 1989, The Journal of biological chemistry.

Structural and functional analysis of the murine adenosine deaminase gene.

M. Al-Ubaidi, M. Maa, R. Kellems, 1990, Genomics.

Acidification and glucocorticoids independently regulate branched-chain alpha-ketoacid dehydrogenase subunit genes.

S. Price, P. Costeas, X. Wang, 2001, American journal of physiology. Cell physiology.

A Posthospitalization Home Visit Curriculum for Pediatric Patients

Megan M. Tschudy, J. Perin, J. Serwint, 2020, MedEdPORTAL : the journal of teaching and learning resources.

Molecular and biochemical basis of intermediate maple syrup urine disease. Occurrence of homozygous G245R and F364C mutations at the E1 alpha locus of Hispanic-Mexican patients.

D. Chuang, J. Davie, R. Wynn, 1995, The Journal of clinical investigation.

Noncoordinated responses of branched‐chain α‐ketoacid dehydrogenase subunit genes to dietary protein

P. Costeas, J. Chinsky, L. Bohlen, 1994, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Regulation of expression of branched-chain alpha-keto acid dehydrogenase subunits in permanent cell lines.

P. Costeas, J. Chinsky, 2000, Methods in enzymology.

Fv-1 host cell restriction of friend leukemia virus: microinjection of unintegrated viral DNA

J. Kopchick, R. Soeiro, J. Chinsky, 1984, Journal of virology.

Fv-1 host restriction of Friend leukemia virus: analysis of unintegrated proviral DNA

R. Soeiro, J. Chinsky, 1981, Journal of virology.

Dual bidirectional promoters at the mouse dhfr locus: cloning and characterization of two mRNA classes of the divergently transcribed Rep-1 gene

Z. Chen, R. Kellems, G. Crouse, 1989, Molecular and cellular biology.

Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations

S. Waisbren, M. Grompe, C. V. van Karnebeek, 2017, Genetics in Medicine.

Metabolic Strokes in Propionic Acidemia: Transient Hemiplegic Events Without Encephalopathy

S. Srivastava, J. Chinsky, Mohammed Almuqbil, 2019, Child neurology open.

Studies with aphidicolin on the Fv-1 host restriction of Friend murine leukemia virus

R. Soeiro, J. Chinsky, 1982, Journal of virology.

Comparison of chemically induced and spontaneous murine thymic lymphomas in RF and AKR mice: differential expression of c-myc and c-myb.

G. Childs, F. Lilly, J. Chinsky, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Molecular cloning of the murine branched chain alpha-ketoacid dehydrogenase E2 subunit: presence of 3' B1 repeat elements.

L. Tonelli, P. Costeas, J. Chinsky, 1996, Biochimica et biophysica acta.

Replication of proto-oncogenes early during the S phase in mammalian cell lines

M. A. Iqbal, J. Chinsky, V. Didamo, 1987, Nucleic Acids Res..

Late Development of Hepatocellular Carcinoma in Tyrosinemia Type 1 Despite Nitisinone (NTBC) Treatment.

J. Chinsky, J. Knoll, Mohammed Almuqbil, 2020, Journal of pediatric gastroenterology and nutrition.

Identification of transcription stop sites at the 5' and 3' ends of the murine adenosine deaminase gene.

M. Maa, R. Kellems, V. Ramamurthy, 1990, The Journal of biological chemistry.

Interstitial deletion of chromosome 2q32‐34 associated with multiple congenital anomalies and a urea cycle defect (CPS I deficiency)

A. Hamosh, M. Summar, G. Thomas, 2004, American journal of medical genetics. Part A.

Chapter 30 – INBORN ERRORS OF METABOLISM

R. Steiner, J. Chinsky, 2009 .

Isolation of the murine branched-chain α-ketoacid dehydrogenase E2 subunit promoter region 1 The sequence data reported in this paper have been submitted to the EMBL/GenBank Data Libraries under the accession number U95963. 1

P. Costeas, J. Chinsky, 1998 .

Molecular cloning and analysis of the expression of the E1β subunit of branched chain α-ketoacid dehydrogenase in mice

P. Costeas, J. Chinsky, 1993 .

Effects of insulin on the regulation of branched-chain α-keto acid dehydrogenase E 1 α subunit gene expression

P. Costeas, J. Chinsky, 1996 .

Developmental expression of adenosine deaminase in placental tissues of the early postimplantation mouse embryo and uterine stroma.

T. Knudsen, R. Kellems, H. Higley, 1988, Biology of reproduction.

Response to Neeleman et al.

C. Ficicioglu, J. Chinsky, C. Ronald Scott, 2019, Genetics in Medicine.

Hydranencephaly: Transillumination May Not Illuminate Diagnosis

J. Chinsky, 2012 .

A nonsense mutation (R242X) in the branched‐chain α‐keto acid dehydrogenase E1α subunit gene (BCKDHA) as a cause of maple syrup urine disease

S. Almashanu, R. Carmi, N. Ambulos, 1998 .

Six-Year-Old With Altered Mental Status: No “LACk” of Clues

J. Chinsky, E. Souganidis, Maria Grala, 2016, Pediatric emergency care.