Smaller number of large myelinated fibers and focal myelin thickening in mutant quails deficient in neurofilaments.
Acta neuropathologica | 1993-01-01 | PMID 8213082
Zhao J X, Ohnishi A, Itakura C and 4 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 590 of 10600
The effect of prenatal diazepam exposure on TNF-alpha production by rat splenocytes.
Agents and actions | 1993-03-01 | PMID 8213353
Schreiber A A, Frei K, Lichtensteiger W and 1 more
Genes: TNF
Homozygous familial hypercholesterolemia: a paradigm for phenotypic variation.
The American journal of cardiology | 1993-09-30 | PMID 8213490
Hoeg J M
Familial hypercholesterolemia in French-Canadians: taking advantage of the presence of a "founder effect".
The American journal of cardiology | 1993-09-30 | PMID 8213499
Davignon J, Roy M
Characterization of nondeletion alpha-thalassemia mutations in the Greek population.
American journal of hematology | 1993-11-01 | PMID 8213764
Traeger-Synodinos J, Kanavakis E, Tzetis M and 2 more
Weak N activity of En(a-) human erythrocyte membranes.
American journal of hematology | 1993-11-01 | PMID 8213772
Shinozuka T, Miyata Y, Ohyama K and 4 more
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.
American journal of human genetics | 1993-10-01 | PMID 8213810
McConkie-Rosell A, Lachiewicz A M, Spiridigliozzi G A and 6 more
Overexpression of esterase D in kidney from trisomy 13 fetuses.
American journal of human genetics | 1993-10-01 | PMID 8213811
Loughna S, Bennett P, Gau G and 3 more
Mutations in acid beta-galactosidase cause GM1-gangliosidosis in American patients.
American journal of human genetics | 1993-10-01 | PMID 8213816
Boustany R M, Qian W H, Suzuki K
Hereditary overexpression of adenosine deaminase in erythrocytes: evidence for a cis-acting mutation.
American journal of human genetics | 1993-10-01 | PMID 8213817
Chen E H, Tartaglia A P, Mitchell B S
Genes: ADA
An autologistic model for the genetic analysis of familial binary data.
American journal of human genetics | 1993-10-01 | PMID 8213818
Abel L, Golmard J L, Mallet A
Pitfalls in the molecular genetic diagnosis of Leber hereditary optic neuropathy (LHON).
American journal of human genetics | 1993-10-01 | PMID 8213820
Johns D R, Neufeld M J
Prevalence of nine mutations among Jewish and non-Jewish Gaucher disease patients.
American journal of human genetics | 1993-10-01 | PMID 8213821
Horowitz M, Tzuri G, Eyal N and 6 more
Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes.
American journal of human genetics | 1993-10-01 | PMID 8213822
Williams R, Vesa J, Järvelä I and 7 more
Genes: CLN3
Confirmation of chromosome 9p linkage in familial melanoma.
American journal of human genetics | 1993-10-01 | PMID 8213823
Nancarrow D J, Mann G J, Holland E A and 7 more
Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).
American journal of human genetics | 1993-11-01 | PMID 8213829
Brunner H G, Brüggenwirth H T, Nillesen W and 7 more
Exclusion of the APC gene as the cause of a variant form of familial adenomatous polyposis (FAP)
American journal of human genetics | 1993-11-01 | PMID 8213830
Stella A, Resta N, Gentile M and 4 more
Genes: APC, FAP
A single-gene explanation for the probability of having idiopathic talipes equinovarus.
American journal of human genetics | 1993-11-01 | PMID 8213831
Rebbeck T R, Dietz F R, Murray J C and 1 more
Genotype-phenotype relationships in fragile X syndrome: a family study.
American journal of human genetics | 1993-11-01 | PMID 8213832
Loesch D Z, Huggins R, Hay D A and 3 more
Genes: FMR1
Normal phenotype with paternal uniparental isodisomy for chromosome 21.
American journal of human genetics | 1993-11-01 | PMID 8213833
Blouin J L, Avramopoulos D, Pangalos C and 1 more
Genotype relative risks: methods for design and analysis of candidate-gene association studies.
American journal of human genetics | 1993-11-01 | PMID 8213835
Schaid D J, Sommer S S
Molecular and statistical approaches to the detection and correction of errors in genotype databases.
American journal of human genetics | 1993-11-01 | PMID 8213837
Brzustowicz L M, Mérette C, Xie X and 3 more
Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes.
American journal of human genetics | 1993-11-01 | PMID 8213840
Scott H S, Litjens T, Nelson P V and 4 more
Genes: IDUA
Genetic heterogeneity among blue-cone monochromats.
American journal of human genetics | 1993-11-01 | PMID 8213841
Nathans J, Maumenee I H, Zrenner E and 7 more
Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: the usefulness of multiple study designs.
American journal of medical genetics | 1993-08-15 | PMID 8213911
Weissbecker K A, Wolf B, Eaves L J and 2 more
Hydrops-ectopic calcification-moth-eaten skeletal dysplasia (Greenberg dysplasia): prenatal diagnosis and further delineation of a rare genetic disorder.
American journal of medical genetics | 1993-08-15 | PMID 8213919
Chitayat D, Gruber H, Mullen B J and 4 more
Variable clinical expression of mosaic trisomy 16 in the newborn infant.
American journal of medical genetics | 1993-08-15 | PMID 8213923
Devi A S, Velinov M, Kamath M V and 5 more
Behçet's disease associated with one of the HLA-B51 subantigens, HLA-B* 5101.
American journal of ophthalmology | 1993-10-15 | PMID 8213969
Mizuki N, Inoko H, Ando H and 7 more
Epstein-Barr virus in pyothorax-associated pleural lymphoma.
The American journal of pathology | 1993-10-01 | PMID 8214001
Fukayama M, Ibuka T, Hayashi Y and 3 more
A tumorigenic murine Sertoli cell line that is temperature-sensitive for differentiation.
The American journal of pathology | 1993-10-01 | PMID 8214009
Boekelheide K, Lee J W, Hall S J and 2 more
A protein structural approach to the solution of biological problems: alpha 1-antitrypsin as a recent example.
The American journal of physiology | 1993-09-01 | PMID 8214081
Lomas D A, Carrell R W
Response of Plasmodium vivax variants to chloroquine as determined by microscopy and quantitative polymerase chain reaction.
The American journal of tropical medicine and hygiene | 1993-10-01 | PMID 8214278
Kain K C, Brown A E, Lanar D E and 2 more
Personality characteristics of sisters and spouses of male alcoholics.
Alcoholism, clinical and experimental research | 1993-08-01 | PMID 8214405
Hill S Y
Neural cell adhesion molecule and prognosis of surgically resected lung cancer.
The American review of respiratory disease | 1993-10-01 | PMID 8214927
Pujol J L, Simony J, Demoly P and 7 more
Expression of insulin-like growth factor-I in transgenic mice.
Annals of the New York Academy of Sciences | 1993-08-27 | PMID 8215019
D'Ercole A J
Identification of ring Y chromosome: cytogenetic analysis, Southern blot and fluorescent in situ hybridization.
Annales de genetique | 1993-01-01 | PMID 8215218
Pezzolo A, Perroni L, Gimelli G and 4 more
A specific phenotype associated with trisomy 15 mosaicism.
Annales de genetique | 1993-01-01 | PMID 8215220
Fryns J P, Kleczkowska A, Lagae L and 2 more
Genetic polymorphisms in the white population of Victoria, Australia.
Annals of human biology | 2000-01-01 | PMID 8215226
Mitchell R J, Hale C B, Kahwagi M
Genes: ABO, ESD, GLO1, KEL, PGM1
Phenotypic and genetic affinities among ethnic populations in Daghestan (Caucasus, Russia): a comparison of polymorphic, physical, neurophysiological and psychological traits.
Annals of human biology | 2000-01-01 | PMID 8215229
Bulayeva K B, Pavlova T A, Dubinin N P and 2 more
A gene conferring resistance to vancomycin but not teicoplanin in isolates of Enterococcus faecalis and Enterococcus faecium demonstrates homology with vanB, vanA, and vanC genes of enterococci.
Antimicrobial agents and chemotherapy | 1993-08-01 | PMID 8215270
Gold H S, Unal S, Cercenado E and 4 more
OXA-11, an extended-spectrum variant of OXA-10 (PSE-2) beta-lactamase from Pseudomonas aeruginosa.
Antimicrobial agents and chemotherapy | 1993-08-01 | PMID 8215276
Hall L M, Livermore D M, Gur D and 2 more
Phenotypic characterization of copper-resistant mutants of Methylosinus trichosporium OB3b.
Applied and environmental microbiology | 1993-09-01 | PMID 8215352
Fitch M W, Graham D W, Arnold R G and 4 more
Variation in chlorobenzoate catabolism by Pseudomonas putida P111 as a consequence of genetic alterations.
Applied and environmental microbiology | 1993-09-01 | PMID 8215353
Brenner V, Hernandez B S, Focht D D
Application of multilocus enzyme electrophoresis in studies of the epidemiology of Listeria monocytogenes in Denmark.
Applied and environmental microbiology | 1993-09-01 | PMID 8215357
Nørrung B, Skovgaard N
Glucose toxicity in Prevotella ruminicola: methylglyoxal accumulation and its effect on membrane physiology.
Applied and environmental microbiology | 1993-09-01 | PMID 8215358
Russell J B
Recombinational inactivation of the gene encoding nitrate reductase in Aspergillus parasiticus.
Applied and environmental microbiology | 1993-09-01 | PMID 8215371
Wu T S, Linz J E
Role of sun exposure on nevus. First study in age-sex phenotype-controlled populations.
Archives of dermatology | 1993-10-01 | PMID 8215492
Richard M A, Grob J J, Gouvernet J and 4 more
Dermatosparaxis in children. A case report and review of the newly recognized phenotype.
Archives of dermatology | 1993-10-01 | PMID 8215497
Petty E M, Seashore M R, Braverman I M and 3 more
Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiency.
Archives of disease in childhood | 1993-09-01 | PMID 8215568
Wilcken B, Carpenter K H, Hammond J
Familial defective apolipoprotein B-100 is clinically indistinguishable from familial hypercholesterolemia.
Archives of internal medicine | 1993-10-25 | PMID 8215738
Defesche J C, Pricker K L, Hayden M R and 2 more
[Tools of molecular biology, what can be expected from them?].
Archives des maladies du coeur et des vaisseaux | 1993-01-01 | PMID 8215776
Delpech M
Strong inference, theory testing, and the neuroanatomy of schizophrenia.
Archives of general psychiatry | 1993-10-01 | PMID 8215806
Carpenter W T, Buchanan R W, Kirkpatrick B and 2 more
Continuity and discontinuity of affective disorders and schizophrenia. Results of a controlled family study.
Archives of general psychiatry | 1993-11-01 | PMID 8215813
Maier W, Lichtermann D, Minges J and 4 more
Machado-Joseph disease of Azorean ancestry in Brazil: the Catarina kindred. Neurological, neuroimaging, psychiatric and neuropsychological findings in the largest known family, the "Catarina" kindred.
Arquivos de neuro-psiquiatria | 1993-03-01 | PMID 8215926
Radvany J, Camargo C H, Costa Z M and 2 more
Molecular genetics of Huntington's disease.
Archives of neurology | 1993-11-01 | PMID 8215974
Gusella J F, MacDonald M E, Ambrose C M and 1 more
Molecular genetics of Alzheimer's disease.
Archives of neurology | 1993-11-01 | PMID 8215975
Clark R F, Goate A M
Genes: APP
The myotonic dystrophy gene.
Archives of neurology | 1993-11-01 | PMID 8215976
Pizzuti A, Friedman D L, Caskey C T
Charcot-Marie-Tooth syndrome.
Archives of neurology | 1993-11-01 | PMID 8215977
Chance P F, Pleasure D
Mitochondrial encephalomyopathies.
Archives of neurology | 1993-11-01 | PMID 8215979
DiMauro S, Moraes C T
The role of neurogenetics in Gaucher disease.
Archives of neurology | 1993-11-01 | PMID 8215980
Brady R O, Barton N W, Grabowski G A
Duchenne-Becker muscular dystrophy and the nondystrophic myotonias. Paradigms for loss of function and change of function of gene products.
Archives of neurology | 1993-11-01 | PMID 8215981
Hoffman E P, Wang J
Genotype-phenotype correlations in human skeletal muscle sodium channel diseases.
Archives of neurology | 1993-11-01 | PMID 8215982
Rüdel R, Ricker K, Lehmann-Horn F
Polyphenotypic small-cell orbitocranial tumor.
Archives of ophthalmology (Chicago, Ill. : 1960) | 1993-10-01 | PMID 8216022
Lyon D B, Dortzbach R K, Gilbert-Barness E
Use of site-directed mutagenesis of allele-specific PCR primers to identify the GSTM1 A, GSTM1 B, GSTM1 A,B and GSTM1 null polymorphisms at the glutathione S-transferase, GSTM1 locus.
The Biochemical journal | 1993-10-01 | PMID 8216235
Fryer A A, Zhao L, Alldersea J and 2 more
Genes: GSTM1
Use of hybridization for distance measurement by fluorescence energy transfer in oligomeric proteins: distance between two functional sites in aspartase.
Biochemical and biophysical research communications | 1993-09-30 | PMID 8216244
Murase S, Kawata Y, Yumoto N
Fluorescence properties of the three tyrosine residues in the ribose-binding protein.
Biochemical and biophysical research communications | 1993-09-30 | PMID 8216255
Kim D, Park C
P-cadherin and E-cadherin are co-expressed in MDCK cells.
Biochemical and biophysical research communications | 1993-09-30 | PMID 8216265
Wu J C, Gregory C W, DePhilip R M
Polymorphisms of the D4 dopamine receptor alleles in chronic alcoholism.
Biochemical and biophysical research communications | 1993-10-15 | PMID 8216280
George S R, Cheng R, Nguyen T and 2 more
Threonine on amino acid position 868 in the human androgen receptor is essential for androgen binding specificity and functional activity.
Biochemical and biophysical research communications | 1993-10-15 | PMID 8216289
Ris-Stalpers C, Verleun-Mooijman M C, Trapman J and 1 more
The stimulation of pp42mapkinase by insulin does not correlate with its metabolic actions in cells overexpressing mutant insulin receptors.
Biochemical and biophysical research communications | 1993-10-15 | PMID 8216304
Pang L, Lazar D F, Moller D E and 2 more
BQ-123 identifies heterogeneity and allosteric interactions at the rat heart endothelin receptor.
Biochemical and biophysical research communications | 1993-10-15 | PMID 8216306
Sokolovsky M
Exon structure at the human ACP1 locus supports alternative splicing model for f and s isozyme generation.
Biochemical and biophysical research communications | 1993-10-15 | PMID 8216326
Lazaruk K D, Dissing J, Sensabaugh G F
Genes: ACP1
HLA-linked susceptibility to rheumatoid arthritis. A study of forty-one multicase families from northern India.
Arthritis and rheumatism | 1993-10-01 | PMID 8216398
Taneja V, Mehra N K, Anand C and 1 more
Biased T cell receptor V gene usage in rheumatoid arthritis. Oligoclonal expansion of T cells expressing V alpha 2 genes in synovial fluid but not in peripheral blood.
Arthritis and rheumatism | 1993-09-01 | PMID 8216417
Bröker B M, Korthäuer U, Heppt P and 4 more
Apolipoprotein E phenotype is related to macro- and microangiopathy in patients with non-insulin-dependent diabetes mellitus.
Atherosclerosis | 1993-06-01 | PMID 8216506
Ukkola O, Kervinen K, Salmela P I and 3 more
Loss of heterozygosity: the most frequent cause of recessive phenotype expression at the heterozygous human adenine phosphoribosyltransferase locus.
Molecular carcinogenesis | 1993-01-01 | PMID 8216732
Zhu Y, Stambrook P J, Tischfield J A
Genes: APRT
Genetic analysis of carcinogen enhancement of type 5 adenovirus transformation of cloned Fischer rat embryo fibroblast cells.
Molecular carcinogenesis | 1993-01-01 | PMID 8216734
Su Z Z, Shen R, Young C S and 1 more
Comparison of pulmonary O6-methylguanine DNA adduct levels and Ki-ras activation in lung tumors from resistant and susceptible mouse strains.
Molecular carcinogenesis | 1993-01-01 | PMID 8216736
Devereux T R, Belinsky S A, Maronpot R R and 6 more
Ki-ras oncogene mutations in tumors and DNA adducts formed by benz[j]aceanthrylene and benzo[a]pyrene in the lungs of strain A/J mice.
Molecular carcinogenesis | 1993-01-01 | PMID 8216737
Mass M J, Jeffers A J, Ross J A and 4 more
ras mutations in 2-amino-3-methylimidazo-[4,5-f]quinoline-induced tumors in the CDF1 mouse.
Molecular carcinogenesis | 1993-01-01 | PMID 8216739
Herzog C R, Schut H A, Maronpot R R and 1 more
Effect of recipient doe genotype on survival rate at birth of frozen rabbit embryos.
Reproduction, nutrition, development | 1993-01-01 | PMID 8216751
Vicente J S, Garciá-Ximénez F
Genomic instability and metastatic progression.
Pathobiology : journal of immunopathology, molecular and cellular biology | 1993-01-01 | PMID 8216826
Usmani B A
Diversity of the V3 region of HIV in Paris, France.
AIDS (London, England) | 1993-09-01 | PMID 8216976
Chaix M L, Chappey C, Couillin I and 3 more
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuroma.
Archives of otolaryngology--head & neck surgery | 1993-11-01 | PMID 8217082
Irving R M, Moffat D A, Hardy D G and 3 more
Genes: VHL
Inner ear morphology in CBA/Ca and C57BL/6J mice in relationship to noise, age and phenotype.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery | 1993-01-01 | PMID 8217126
Hultcrantz M, Li H S
An association of the RB gene with osteosarcoma: molecular genetic evaluation of a case of hereditary retinoblastoma.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery | 1993-01-01 | PMID 8217129
Issing W J, Wustrow T P, Oeckler R and 2 more
Automation of large-scale HLA oligotyping using a robotic workstation.
BioTechniques | 1993-09-01 | PMID 8217169
Caillat-Zucman S, Garchon H J, Costantino F and 2 more
Molecular genetics of oculocutaneous albinism.
Seminars in dermatology | 1993-09-01 | PMID 8217557
Spritz R A
Dystrophic forms of epidermolysis bullosa.
Seminars in dermatology | 1993-09-01 | PMID 8217558
Uitto J, Christiano A M
The Ehlers-Danlos syndromes.
Seminars in dermatology | 1993-09-01 | PMID 8217561
Yeowell H N, Pinnell S R
Molecular biology of the neurofibromatoses.
Seminars in dermatology | 1993-09-01 | PMID 8217563
Riccardi V M
Mechanisms of oncogenesis in patients with familial retinoblastoma.
British journal of cancer | 1993-11-01 | PMID 8217609
Onadim Z, Hogg A, Cowell J K
Difference in clinical features and HLA antigens between familial and non-familial vitiligo of non-segmental type.
The British journal of dermatology | 1993-10-01 | PMID 8217754
Ando I, Chi H I, Nakagawa H and 1 more
Extramedullary plasmacytoma: cytological and genotypic studies.
The British journal of dermatology | 1993-10-01 | PMID 8217765
Tamamori T, Nakayama F, Sugimoto H and 3 more
Identification of nine novel mutations in type I antithrombin deficiency by heteroduplex screening.
British journal of haematology | 1993-08-01 | PMID 8217824
Chowdhury V, Olds R J, Lane D A and 7 more
Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresis.
British journal of haematology | 1993-08-01 | PMID 8217825
Tartary M, Vidaud D, Piao Y and 7 more
The retinal ganglion cell distribution and the representation of the visual field in area 17 of the owl monkey, Aotus trivirgatus.
Visual neuroscience | 2000-01-01 | PMID 8217938
Silveira L C, Perry V H, Yamada E S
The relation of lipoprotein[a] concentrations and apolipoprotein[a] phenotypes with asymptomatic atherosclerosis in subjects of the Atherosclerosis Risk in Communities (ARIC) Study.
Arteriosclerosis and thrombosis : a journal of vascular biology | 1993-11-01 | PMID 8218095
Brown S A, Morrisett J D, Boerwinkle E and 2 more
Age-dependent changes of baroreflex efficiency in Dahl rats: effects of high salt intake.
Physiological research | 1993-01-01 | PMID 8218156
Nedvídek J, Zicha J
Molecular recognition in cytochrome P-450: mechanism for the control of uncoupling reactions.
Biochemistry | 1993-11-02 | PMID 8218220
Loida P J, Sligar S G