Research Output 1986 2017

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2017

A placebo-controlled trial of simvastatin therapy in Smith-Lemli-Opitz syndrome

Wassif, C. A., Kratz, L., Sparks, S. E., Wheeler, C., Bianconi, S., Gropman, A., Calis, K. A., Kelley, R. I., Tierney, E. & Porter, F. D. Mar 1 2017 In : Genetics in Medicine. 19, 3, p. 297-305 9 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Simvastatin
Placebos
Therapeutics
Dehydrocholesterols

Randomized open-label trial of dextromethorphan in Rett syndrome

Smith-Hicks, C. L., Gupta, S., Ewen, J. B., Hong, M., Kratz, L., Kelley, R., Tierney, E., Vaurio, R., Bibat, G., Sanyal, A., Yenokyan, G., Brereton, N., Johnston, M. V. & Naidu, S. Oct 17 2017 In : Neurology. 89, 16, p. 1684-1690 7 p.

Research output: Research - peer-reviewArticle

Dextromethorphan
Rett Syndrome
Seizures
Checklist
Electroencephalography
2016

Abnormal lipid processing but normal long-term repopulation potential of myc-/- hepatocytes

Edmunds, L. R. , Otero, P. A. , Sharma, L. , D'Souza, S. , Dolezal, J. M. , David, S. , Lu, J. , Lamm, L. , Basantani, M. , Zhang, P. , Sipula, I. J. , Li, L. , Zeng, X. , Ding, Y. , Ding, F. , Beck, M. E. , Vockley, J. , Monga, S. P. S. , Kershaw, E. E. , O'Doherty, R. M. & 6 others Kratz, L. E., Yates, N. A., Goetzman, E. P., Scott, D., Duncan, A. W. & Prochownik, E. V. May 24 2016 In : Oncotarget. 7, 21, p. 30379-30395 17 p.

Research output: Research - peer-reviewArticle

Hepatocytes
Lipids
Liver
Cytochrome P-450 Enzyme System
Tyrosinemias

Altered cholesterol biosynthesis causes precocious neurogenesis in the developing mouse forebrain

Driver, A. M., Kratz, L. E., Kelley, R. I. & Stottmann, R. W. Jul 1 2016 In : Neurobiology of Disease. 91, p. 69-82 14 p.

Research output: Research - peer-reviewArticle

Neurogenesis
Prosencephalon
Cholesterol
Embryonic Structures
Neurons
2015

Adult presentation of X-linked Conradi-Hünermann-Happle syndrome

Posey, J. E., Burrage, L. C., Campeau, P. M., Lu, J. T., Eble, T. N., Kratz, L., Schlesinger, A. E., Gibbs, R. A., Lee, B. H. & Nagamani, S. C. S. Jun 1 2015 In : American Journal of Medical Genetics, Part A. 167, 6, p. 1309-1314 6 p.

Research output: Research - peer-reviewArticle

Chondrodysplasia Punctata
Cataract
Exome
Extremities
Mutation

Endogenous Sterol Metabolites Regulate Growth of EGFR/KRAS-Dependent Tumors via LXR

Gabitova, L., Restifo, D., Gorin, A., Manocha, K., Handorf, E., Yang, D. H., Cai, K. Q., Klein-Szanto, A. J., Cunningham, D., Kratz, L. E., Herman, G. E., Golemis, E. A. & Astsaturov, I. Sep 22 2015 In : Cell Reports. 12, 11, p. 1927-1938 12 p.

Research output: Research - peer-reviewArticle

Sterols
Metabolites
Epidermal Growth Factor Receptor
Liver
Tumors
2014

Decreased cerebral spinal fluid neurotransmitter levels in Smith-Lemli-Opitz syndrome

Sparks, S. E., Wassif, C. A., Goodwin, H., Conley, S. K., Lanham, D. C., Kratz, L. E., Hyland, K., Gropman, A., Tierney, E. & Porter, F. D. 2014 In : Journal of Inherited Metabolic Disease. 37, 3, p. 415-420 6 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Neurotransmitter Agents
Homovanillic Acid
Hydroxyindoleacetic Acid
Sterols

Desmosterolosis: An illustration of diagnostic ambiguity of cholesterol synthesis disorders

Dias, C., Rupps, R., Millar, B., Choi, K., Marra, M., Demos, M., Kratz, L. E. & Boerkoel, C. F. Jun 25 2014 In : Orphanet Journal of Rare Diseases. 9, 1, 94

Research output: Research - peer-reviewArticle

Cholesterol
Desmosterolosis
Mutation
Agenesis of Corpus Callosum
Failure to Thrive
2013

A Liver-Specific Defect of Acyl-CoA Degradation Produces Hyperammonemia, Hypoglycemia and a Distinct Hepatic Acyl-CoA Pattern

Gauthier, N., Wu, J. W., Wang, S. P., Allard, P., Mamer, O. A., Sweetman, L., Moser, A. B., Kratz, L., Alvarez, F., Robitaille, Y., Lépine, F. & Mitchell, G. A. Jul 5 2013 In : PLoS One. 8, 7, e60581

Research output: Research - peer-reviewArticle

acyl coenzyme A
hypoglycemia
liver
degradation
mice

Targeting C4-demethylating genes in the cholesterol pathway sensitizes cancer cells to EGF receptor inhibitors via increased EGF receptor degradation

Sukhanova, A. , Gorin, A. , Serebriiskii, I. G. , Gabitova, L. , Zheng, H. , Restifo, D. , Egleston, B. L. , Cunningham, D. , Bagnyukova, T. , Liu, H. , Nikonova, A. , Adams, G. P. , Zhou, Y. , Yang, D. H. , Mehra, R. , Burtness, B. , Cai, K. Q. , Klein-Szanto, A. , Kratz, L. E. , Kelley, R. I. & 4 others Weiner, L. M., Herman, G. E., Golemis, E. A. & Astsaturov, I. Jan 2013 In : Cancer Discovery. 3, 1, p. 96-112 17 p.

Research output: Research - peer-reviewArticle

Epidermal Growth Factor Receptor
Cholesterol
Genes
Neoplasms
methylsterol monooxygenase
2012
Lysophosphatidylcholines
Carnitine
Choline
Screening
Blood

Disorders of sterol synthesis: Beyond Smith-Lemli-Opitz syndrome

Herman, G. E. & Kratz, L. Nov 15 2012 In : American Journal of Medical Genetics, Part A. 160 C, 4, p. 301-321 21 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Sterols
Cholesterol
Lanosterol
Enzymes

Hepatitis C virus selectively perturbs the distal cholesterol synthesis pathway in a genotype-specific manner

Clark, P. J., Thompson, A. J., Vock, D. M., Kratz, L. E., Tolun, A. A., Muir, A. J., Mchutchison, J. G., Subramanian, M., Millington, D. M., Kelley, R. I. & Patel, K. Jul 2012 In : Hepatology. 56, 1, p. 49-56 8 p.

Research output: Research - peer-reviewArticle

Hepacivirus
Cholesterol
Genotype
Lanosterol
Sterols
2011

Cholesterol metabolism is required for intracellular Hedgehog signal transduction in vivo

Stottmann, R. W., Turbe-Doan, A., Tran, P., Kratz, L. E., Moran, J. L., Kelley, R. I. & Beier, D. R. Sep 2011 In : PLoS Genetics. 7, 9, e1002224

Research output: Research - peer-reviewArticle

cholesterol metabolism
Erinaceidae
signal transduction
Hedgehogs
Signal Transduction

Desmosterolosis-phenotypic and molecular characterization of a third case and review of the literature

Schaaf, C. P., Koster, J., Katsonis, P., Kratz, L., Shchelochkov, O. A., Scaglia, F., Kelley, R. I., Lichtarge, O., Waterham, H. R. & Shinawi, M. Jul 2011 In : American Journal of Medical Genetics, Part A. 155, 7, p. 1597-1604 8 p.

Research output: Research - peer-reviewArticle

Desmosterolosis
Desmosterol
Mutation
Enzymes
Megalencephaly

Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay

He, M., Kratz, L. E., Michel, J. J., Vallejo, A. N., Ferris, L., Kelley, R. I., Hoover, J. J., Jukic, D., Gibson, K. M., Wolfe, L. A., Ramachandran, D., Zwick, M. E. & Vockley, J. Mar 1 2011 In : Journal of Clinical Investigation. 121, 3, p. 976-984 9 p.

Research output: Research - peer-reviewArticle

Microcephaly
Meiosis
Dermatitis
Mutation
Genes
2010

A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3

Pei, W., Kratz, L. E., Bernardini, I., Sood, R., Yokogawa, T., Dorward, H., Ciccone, C., Kelley, R. I., Anikster, Y., Burgess, H. A., Huizing, M. & Feldman, B. Aug 1 2010 In : Development. 137, 15, p. 2587-2596 10 p.

Research output: Research - peer-reviewArticle

Acids
Costeff optic atrophy syndrome
Zebrafish
Movement Disorders
Ataxia

Clinical observations, molecular genetic analysis, and treatment of sitosterolemia in infants and children

Niu, D. M., Chong, K. W., Hsu, J. H., Wu, T. J. T., Yu, H. C., Huang, C. H., Lo, M. Y., Kwok, C. F., Kratz, L. E. & Ho, L. T. Aug 2010 In : Journal of Inherited Metabolic Disease. 33, 4, p. 437-443 7 p.

Research output: Research - peer-reviewArticle

Molecular Biology
Therapeutics
Sitosterolemia
Ezetimibe
Phytosterols

Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome

McLarren, K. W. , Severson, T. M. , Du Souich, C. , Stockton, D. W. , Kratz, L. E. , Cunningham, D. , Hendson, G. , Morin, R. D. , Wu, D. , Paul, J. E. , An, J. , Nelson, T. N. , Chou, A. , Debarber, A. E. , Merkens, L. S. , Michaud, J. L. , Waters, P. J. , Yin, J. , McGillivray, B. , Demos, M. & 20 others Rouleau, G. A., Grzeschik, K. H., Smith, R., Tarpey, P. S., Shears, D., Schwartz, C. E., Gecz, J., Stratton, M. R., Arbour, L., Hurlburt, J., Van Allen, M. I., Herman, G. E., Zhao, Y., Moore, R., Kelley, R. I., Jones, S. J. M., Steiner, R. D., Raymond, F. L., Marra, M. A. & Boerkoel, C. F. Dec 10 2010 In : American Journal of Human Genetics. 87, 6, p. 905-914 10 p.

Research output: Research - peer-reviewArticle

Alleles
Temperature
Cholesterol
Sterols
Intellectual Disability
2007

Dehydrosteroid measurements in maternal urine or serum for the prenatal diagnosis of Smith-Lemli-Opitz Syndrome (SLOS)

Shackleton, C. H. L., Marcos, J., Palomaki, G. E., Craig, W. Y., Kelley, R. I., Kratz, L. E. & Haddow, J. E. Sep 15 2007 In : American Journal of Medical Genetics, Part A. 143, 18, p. 2129-2136 8 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Prenatal Diagnosis
Mothers
Urine
Pregnancy
2006

Abnormalities of cholesterol metabolism in autism spectrum disorders

Tierney, E., Bukelis, I., Thompson, R. E., Ahmed, K., Aneja, A., Kratz, L. & Kelley, R. I. Sep 5 2006 In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 141, 6, p. 666-668 3 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Sterols
Cholesterol
Autism Spectrum Disorder
Incidence

Development and characterization of a hypomorphic Smith-Lemli-Opitz syndrome mouse model and efficacy of simvastatin therapy

Correa-Cerro, L. S., Wassif, C. A., Kratz, L., Miller, G. F., Munasinghe, J. P., Grinberg, A., Fliesler, S. J. & Porter, F. D. Mar 2006 In : Human Molecular Genetics. 15, 6, p. 839-851 13 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Simvastatin
Therapeutics
Central Nervous System
7-dehydrocholesterol

Identifying Smith-Lemli-Opitz syndrome in conjunction with prenatal screening for Down syndrome

Craig, W. Y., Haddow, J. E., Palomaki, G. E., Kelley, R. I., Kratz, L. E., Shackleton, C. H. L., Marcos, J., Stephen Tint, G., MacRae, A. R., Nowaczyk, M. J., Kloza, E. M., Irons, M. B. & Roberson, M. Sep 2006 In : Prenatal Diagnosis. 26, 9, p. 842-849 8 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Down Syndrome
Prenatal Diagnosis
Pregnancy
Mothers

Noninvasive Assessment of Brain Injury in a Canine Model of Hypothermic Circulatory Arrest Using Magnetic Resonance Spectroscopy

Barreiro, C. J., Williams, J. A., Fitton, T. P., Lange, M. S., Blue, M. E., Kratz, L., Barker, P. B., Degaonkar, M., Gott, V. L., Troncoso, J. C., Johnston, M. V. & Baumgartner, W. A. May 2006 In : Annals of Thoracic Surgery. 81, 5, p. 1593-1598 6 p.

Research output: Research - peer-reviewArticle

Diazoxide
Choline
Brain Injuries
Canidae
Magnetic Resonance Spectroscopy

Valproic Acid Prevents Brain Injury in a Canine Model of Hypothermic Circulatory Arrest: A Promising New Approach to Neuroprotection During Cardiac Surgery

Williams, J. A., Barreiro, C. J., Nwakanma, L. U., Lange, M. S., Kratz, L. E., Blue, M. E., Berrong, J., Patel, N. D., Gott, V. L., Troncoso, J. C., Johnston, M. V. & Baumgartner, W. A. Jun 2006 In : Annals of Thoracic Surgery. 81, 6, p. 2235-2242 8 p.

Research output: Research - peer-reviewArticle

Valproic Acid
Brain Injuries
Thoracic Surgery
Canidae
Neuroprotection
2003

Clinical variability in Rett syndrome

Naidu, S., Bibat, G., Kratz, L., Kelley, R. I., Pevsner, J., Hoffman, E., Cuffari, C., Rohde, C., Blue, M. E. & Johnston, M. V. Oct 2003 In : Journal of Child Neurology. 18, 10, p. 662-668 7 p.

Research output: Research - peer-reviewArticle

Rett Syndrome
Mutation
Neurons
X Chromosome Inactivation
Missense Mutation

Lathosterolosis: An inborn error of human and murine cholesterol synthesis due to lathosterol 5-desaturase deficiency

Krakowiak, P. A., Wassif, C. A., Kratz, L., Cozma, D., Kovářová, M., Harris, G., Grinberg, A., Yang, Y., Hunter, A. G. W., Tsokos, M., Kelley, R. I. & Porter, F. D. Jul 1 2003 In : Human Molecular Genetics. 12, 13, p. 1631-1641 11 p.

Research output: Research - peer-reviewArticle

Cholesterol
lathosterol delta-5-dehydrogenase
Lathosterolosis
lathosterol
Micrognathism

Response of obligate heterozygotes for phytosterolemia to a low-fat diet and to a plant sterol ester dietary challenge

Kwiterovich, P. O., Chen, S. C., Virgil, D. G., Schweitzer, A., Arnold, D. R. & Kratz, L. E. Jun 2003 In : Journal of Lipid Research. 44, 6, p. 1143-1155 13 p.

Research output: Research - peer-reviewArticle

Phytosterols
Fat-Restricted Diet
Heterozygote
Esters
Sitosterolemia
2002

Abnormal sterol metabolism in a patient with Antley-Bixler syndrome and ambiguous genitalia

Kelley, R. I., Kratz, L. E., Glaser, R. L., Netzloff, M. L., Wolf, L. M. & Jabs, E. W. Jun 15 2002 In : American Journal of Medical Genetics. 110, 2, p. 95-102 8 p.

Research output: Research - peer-reviewArticle

Antley-Bixler Syndrome Phenotype
Disorders of Sex Development
Sterols
Mutation
Cholesterol

Desmosterolosis presenting with multiple congenital anomalies and profound developmental delay

Andersson, H. C., Kratz, L. & Kelley, R. Dec 15 2002 In : American Journal of Medical Genetics. 113, 4, p. 315-319 5 p.

Research output: Research - peer-reviewArticle

Desmosterol
Desmosterolosis
Cholesterol
Sterols
Oxidoreductases
2001

Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith-Lemli-Opitz syndrome

Wassif, C. A., Zhu, P., Kratz, L., Krakowiak, P. A., Battaile, K. P., Weight, F. F., Grinberg, A., Steiner, R. D., Nwokoro, N. A., Kelley, R. I., Stewart, R. R. & Porter, F. D. Mar 15 2001 In : Human Molecular Genetics. 10, 6, p. 555-564 10 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Genetic Models
Intellectual Disability
Oxidoreductases
Cholesterol

Dehydro-oestriol and dehydropregnanetriol are candidate analytes for prenatal diagnosis of Smith-Lemli-Opitz syndrome

Shackleton, C. H. L., Roitman, E., Kratz, L. & Kelley, R. 2001 In : Prenatal Diagnosis. 21, 3, p. 207-212 6 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Prenatal Diagnosis
dehydropregnanetriol
dehydroestriol
Urine

Lethal form of chondrodysplasia punctata with normal plasmalogen and cholesterol biosynthesis

Kumada, S., Hayashi, M., Kenmochi, J., Kurosawa, S., Shimozawa, N., Kratz, L. E., Kelley, R. I., Taki, K. & Okaniwa, M. Jan 22 2001 In : American Journal of Medical Genetics. 98, 3, p. 250-255 6 p.

Research output: Research - peer-reviewArticle

Rhizomelic Chondrodysplasia Punctata
Chondrodysplasia Punctata
Plasmalogens
Fibroblasts
Cholesterol
2000

CHILD syndrome caused by deficiency of 3β-hydroxysteroid-Δ8, Δ7- isomerase

Grange, D. K., Kratz, L. E., Braverman, N. E. & Kelley, R. I. 2000 In : American Journal of Medical Genetics. 90, 4, p. 328-335 8 p.

Research output: Research - peer-reviewArticle

Hydroxysteroids
Isomerases
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects
Extremities
Skin

Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome

Nowaczyk, M. J. M., Heshka, T., Kratz, L. E. & Kelley, R. E. Dec 11 2000 In : American Journal of Medical Genetics. 95, 4, p. 396-398 3 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Prenatal Diagnosis
Fetus
Pregnancy
7-dehydrocholesterol
1999

Abnormal sterol metabolism in patients with Conradi-Hunermann-Happle syndrome and sporadic lethal chondrodysplasia punctata

Kelley, R. I., Wilcox, W. G., Smith, M., Kratz, L. E., Moser, A. & Rimoin, D. S. Mar 19 1999 In : American Journal of Medical Genetics. 83, 3, p. 213-219 7 p.

Research output: Research - peer-reviewArticle

Chondrodysplasia Punctata
Sterols
Cholesterol
Hydroxysteroids
Isomerases

Equine type estrogens produced by a pregnant woman carrying a Smith- Lemli-Opitz syndrome fetus

Shackleton, C. H. L., Roitman, E., Kratz, L. E. & Kelley, R. I. 1999 In : Journal of Clinical Endocrinology and Metabolism. 84, 3, p. 1157-1159 3 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Horses
Pregnant Women
Estrogens
Fetus

Midgestational maternal urine steroid markers of fetal Smith-Lemli- Opitz (SLO) syndrome (7-dehydrocholesterol 7-reductase deficiency)

Shackleton, C. H. L., Roitman, E., Kratz, L. E. & Kelley, R. I. Jul 1999 In : Steroids. 64, 7, p. 446-452 7 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Steroids
Mothers
Urine
Oxidoreductases

Mutations in the gene encoding 3β-hydroxysteroid-Δ8,Δ7-isomerase cause X-linked dominant Conradi-Hunermann syndrome

Braverman, N., Lin, P., Moebius, F. F., Obie, C., Moser, A., Glossmann, H., Wilcox, W. R., Rimoin, D. L., Smith, M., Kratz, L., Kelley, R. I. & Valle, D. Jul 1999 In : Nature Genetics. 22, 3, p. 291-294 4 p.

Research output: Research - peer-reviewArticle

Chondrodysplasia Punctata
Hydroxysteroids
Isomerases
Sterols
Mutation

Prenatal diagnosis of the RSH/Smith-Lemli-Opitz syndrome

Kratz, L. E. & Kelley, R. I. Feb 19 1999 In : American Journal of Medical Genetics. 82, 5, p. 376-381 6 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Prenatal Diagnosis
Mothers
Serum
Pregnancy
1997

Clinical and biochemical spectrum of patients with RSH/Smith-Lemli- Opitz syndrome and abnormal cholesterol metabolism

Cunniff, C., Kratz, L. E., Moser, A., Natowicz, M. R. & Kelley, R. I. 1997 In : American Journal of Medical Genetics. 68, 3, p. 263-269 7 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
Cholesterol
7-dehydrocholesterol
Syndactyly
Toes
1995

3-methylglutaconic acidemia in smith-lemli-opitz syndrome

Kelley, R. I. & Kratz, L. 1995 In : Pediatric Research. 37, 5, p. 671-674 4 p.

Research output: Research - peer-reviewArticle

Smith-Lemli-Opitz Syndrome
3-Methylglutaconic Aciduria
Terpenes
Sterols
3-methylglutaconic acid

Cloning of glutaryl-coa dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli

I.goodman, S., Kratz, L. E., Digiulio, K. A., Biery, B. J., Goodman, K. E., Isaya, G. & Frerman, F. E. Sep 1995 In : Human Molecular Genetics. 4, 9, p. 1493-1498 6 p.

Research output: Research - peer-reviewArticle

CDNA
Mutant
Escherichia Coli
Enzymes
Human
1993

Short-term response to dietary therapy in molybdenum cofactor deficiency

Boles, R. G., Ment, L. R., Meyn, M. S., Horwich, A. L., Kratz, L. E. & Rinaldo, P. Nov 1993 In : Annals of Neurology. 34, 5, p. 742-744 3 p.

Research output: Research - peer-reviewArticle

Sulfites
Therapeutics
Molybdenum cofactor deficiency
Microcephaly
Lactic Acidosis
1992

Pork and human cDNAs encoding glutaryl-CoA dehydrogenase.

Goodman, S. I., Kratz, L. E. & Frerman, F. E. 1992 In : Progress in Clinical and Biological Research. 375, p. 169-173 5 p.

Research output: Research - peer-reviewArticle

1991

1,3-Dialkyltriazenes: Reactive intermediates and DNA alkylation

Kroeger-Koepke, M. B., Smith, R. H., Goodnow, E. A., Brashears, J., Kratz, L., Andrews, A. W., Alvord, W. G. & Michejda, C. J. 1991 In : Chemical Research in Toxicology. 4, 3, p. 334-340 7 p.

Research output: Research - peer-reviewArticle

Alkylation
Ionic strength
DNA
Osmolar Concentration
Ions
1990

Association of scleroderma with a T cell antigen receptor γ gene restriction fragment length polymorphism

Kratz, L. E., Boughman, J. A., Pincus, T., Cohen, D. I. & Needleman, B. W. Apr 1990 In : Arthritis and Rheumatism. 33, 4, p. 569-573 5 p.

Research output: Research - peer-reviewArticle

T-Cell Receptor gamma Genes
T-Cell Antigen Receptor
Restriction Fragment Length Polymorphisms
T-Cell Receptor alpha Genes
T-Cell Receptor beta Genes
1989

Lack of an association between diffuse systemic sclerosis and HLA-DR1 or HLA-DR5

Kratz, L. E., Boughman, J. A. & Needleman, B. W. 1989 In : Disease Markers. 7, 4, p. 209-213 5 p.

Research output: Research - peer-reviewArticle

HLA-DR5 Antigen
HLA-DR1 Antigen
Diffuse Scleroderma
HLA-DR Antigens
Systemic Scleroderma