About: Henry L. Nadler

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

physician

Attributes	Values
rdf:type	Item
description	лікар (uk) physician (en)
rdfs:label	Henry L. Nadler (en) Henry L. Nadler (nl)
skos:prefLabel	Henry L. Nadler (en) Henry L. Nadler (nl)
name	Henry L. Nadler (en) Henry L. Nadler (nl)
given name	wds:Q106570095-7DBFB32C-C1F6-402B-8E52-111B919724AC
given name	Henry
instance of	wds:Q106570095-BF77D4FE-9CFA-4BC0-AA55-4F81CD698D1B
instance of	Homo sapiens
occupation	wds:Q106570095-061ff537-45cd-20e2-4fa7-5128b4d2d2ef
sex or gender	wds:Q106570095-E43DAAC8-3E18-402C-9E82-EADFEA611113
ISNI	wds:Q106570095-c802797a-4baa-891c-d293-4307ed1bf68b
VIAF ID	wds:Q106570095-AFA511D3-F88D-41B1-966B-2E19D85371E7
Library of Congress authority ID	wds:Q106570095-3d436978-4b17-3a9f-2868-8d40cbfb1861
VIAF ID	http://viaf.org/viaf/23450728
Library of Congress authority ID	http://id.loc.gov/authorities/names/n80140742
occupation	physician
sex or gender	male
ISNI	0000000024509566
VIAF ID	23450728
Library of Congress authority ID	n80140742
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q106570095
is author of	Primary type I hyperlipoproteinemia with normal lipoprotein lipase activity Lactosyl ceramidosis: Deficient activity of neutral β-Galactsidase in liver and cultivated fibroblasts? Purification and properties of neutral β-galactosidases from human liver Intrauterine detection of GM1 gangliosidosis, type 2 Metabolic and biochemical studies in fructose 1,6-diphosphatase deficiency. Substrate-specificities of acid and alkaline ceramidases in fibroblasts from patients with Farber disease and controls Decreased sialic acid and altered binding to lectins of purified α2-macroglobulin from patients with cystic fibrosis Cultivated epithelial-like cells and fibroblasts from amniotic fluid: their relationship to enzymatic and cytologic analysis. Km defect in neuraminidase of dysmorphic type sialidosis with and without beta-galactosidase deficiency Plasma infusions in an infant with Hurler's syndrome. Diagnosis and carrier detection of Tay-Sachs disease: direct determination of hexosaminidase A using 4-methylumbelliferyl derivatives of beta-N-acetylglucosamine-6-sulfate and beta-N-acetylgalactosamine-6-sulfate. Enzymes in noncultured amniotic fluid cells Altered molecular size of N-acetylglucosamine 1-phosphotransferase in I-cell disease and pseudo-Hurler polydystrophy Correction of γ-Glutamyl Transpeptidase Deficiency in Amniotic Fluid of Some Cystic Fibrosis Fetuses by Mixing with Nondeficient Fluids Histidase activity in cultivated human amniotic fluid cells Unstable galactose-1-phosphate uridyl transferase: A new variant of galactosemia Deficiency of Kallikrein Activity in Plasma of Patients with Cystic Fibrosis Arginine Esterase in Cystic Fibrosis of the Pancreas Letter: Drs. Booth and Nadler's reply. Enzyme changes and polyribosome profiles in phytohemagglutinin stimulated lymphocytes Decreased formation of α2-macroglobulin-protease complexes in plasma of patients with cystic fibrosis Abnormal breakdown of α2-macroglobulin-trypsin complex in cystic fibrosis Genetic amniocentesis in twin gestations Reaction of 4-methylumbelliferylguanidinobenzoate with cultivated human skin fibroblasts derived from patients with cystic fibrosis Reaction of 4-methylumbelliferylguanidinobenzoate with proteases in plasma of patients with cystic fibrosis The Free Amino Acid Pool of Cultivated Human Skin Fibroblasts Amniocentesis in genetic counseling. Safety and reliability in early pregnancy Deficiency of Arginine Esterase in Cystic Fibrosis of the Pancreas: Demonstration of the Proteolytic Nature of the Activity Two immunologically distinct human acidic beta-galactosidase A isozymes Enhanced UDP-galactose:glycoprotein galactosyl transferase activity in cultivated skin fibroblasts from patients with cystic fibrosis and its possible relationship to the pathogenesis of the disease Antenatal diagnosis of genetic disease Apparently normal extracellular acidic alpha-mannosidase in fibroblast cultures from patients with mannosidosis Quantitation of the enzymically deficient cross reacting material in GM1 gangliosidoses The nature of mutation in Krabbe disease Mannosidosis: Clinical and biochemical studies in a family of affected adolescents and adults Demonstration of the heterozygous state in Hunter's syndrome Molecular size of N-acetylglucosaminylphosphotransferase and alpha-N-acetylglucosaminyl phosphodiesterase as determined in situ in Golgi membranes by radiation inactivation Thermal activation of hexosaminidase A in a genetic compound with Tay‐Sachs disease Radiometric assays of N-acetylglucosaminylphosphotransferase and α-N-acetylglucosaminyl phosphodiesterase with substrates labeled in the glucosamine moiety Demonstration of altered acidic hydrolases in fibroblasts from patients with mucolipidosis II by lectin titration Present status of intrauterine diagnosis of genetic defects Binding of human liver hydrolases by immobilized lectins First trimester prenatal evaluation for I-cell disease by N-acetyl-glucosamine 1-phosphotransferase assay Detection of Krabbe disease using tritiated galactosylceramides with medium-chain fatty acids. Detection of fructose-1,6-diphosphatase deficiency with use of white blood cells In vitro selection for the Hunter gene The interrelations between high- and low-molecular weight forms of normal and mutant (Krabbe-disease) galactocerebrosidase Cleft palate and multiple anomalies in one of two siblings with partial 13 trisomy Characterization of the mutant N-acetylglucosaminylphosphotransferase in I-cell disease and pseudo-Hurler polydystrophy: complementation analysis and kinetic studies Catalytically defective ganglioside neuraminidase in mucolipidosis IV Lymphocyte and granulocyte enzyme activity in patients with Down's syndrome. Enzymes in cultivated human fibroblasts derived from patients with autosomal trisomy syndromes Normal two-dimensional gel electrophoresis of alpha-2-macroglobulin in cystic fibrosis Prenatal monitoring and genetic counseling in a 47, XXX female with the oro-facial digital syndrome-type 1. Cerebroside sulfatase activity in cultivated human skin fibroblasts and amniotic fluid cells Deficient phosphorylation of mannose residues of mannan in fibroblasts of patients with mucolipidoses II and III. Lysosomal enzyme activities in fresh and frozen chorionic villi and in cultured trophoblasts Comparison between purified alpha2-macroglobulin preparations from normal controls and patients with cystic fibrosis. Kinetic and structural properties of the complex with bovine trypsin Aldolase in cultivated human fibroblasts. Glucose-6-phosphate Dehydrogenase in the Developing Human Liver Prenatal detection of cystic fibrosis Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotype
is author of	wds:Q54509534-2C978E8E-8867-4332-AFE8-5C214ABE7192 wds:Q67563651-A001E4F4-6586-452E-85B3-B9D8211F09AA wds:Q53966058-B25A37B2-E9A6-4B9E-BB40-E282D13C85E6 wds:Q67012517-E45D7A65-4973-4B46-8DAB-947B504D6341 wds:Q93644186-2BBDFEBC-3F0F-43F8-A165-0E7CBC5739DD wds:Q28367380-3FBECF6D-C260-49A8-9EFD-1EBC72FFB090 wds:Q35201901-EA2EA0F8-A9FA-4EE4-99EA-C1A8347F37D9 wds:Q35202587-6DDB3E58-47F2-47EF-95FC-7815E6592BEA wds:Q35203381-2AA28FFB-BFDA-4DAE-B551-EFC59C3FEF6D wds:Q42561519-0006D476-05A3-4E9C-965C-D9C7B3E543D4 wds:Q51678469-924D1624-B91D-4563-94A3-FB9594336777 wds:Q67371308-4E92303F-BC2E-494E-9887-0FFBF85BD4E1

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