Novel syntaxin homologue, Pep12p, required for the sorting of lumenal hydrolases to the lysosome-like vacuole in yeast.
Molecular biology of the cell | 1996-04-01 | PMID 8730101
Becherer K A, Rieder S E, Emr S D and 1 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.
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Publications
Page 725 of 10600
Replacement of the glycoinositol phospholipid anchor of Drosophila acetylcholinesterase with a transmembrane domain does not alter sorting in neurons and epithelia but results in behavioral defects.
Molecular biology of the cell | 1996-04-01 | PMID 8730103
Incardona J P, Rosenberry T L
Genes: GPI
Scleroderma fibroblast phenotype is modulated by endothelial cell co-culture.
The Journal of rheumatology | 1996-04-01 | PMID 8730117
Denton C P, Xu S, Welsh K I and 2 more
Polymorphism in the LMP2 gene influences disease susceptibility and severity in HLA-B27 associated juvenile rheumatoid arthritis.
The Journal of rheumatology | 1996-04-01 | PMID 8730138
Pryhuber K G, Murray K J, Donnelly P and 5 more
Association of alcoholism with the N-glycosylation polymorphism of pseudodeficient human arylsulfatase A.
Alcoholism, clinical and experimental research | 1996-04-01 | PMID 8730212
Park D S, Poretz R D, Stein S and 2 more
Structural characterization of variant forms of arylsulfatase A that associate with alcoholism.
Alcoholism, clinical and experimental research | 1996-04-01 | PMID 8730213
Park D S, Manowitz P, Stein S and 1 more
Effect of diazepam on plasma gamma-aminobutyric acid in sons of alcoholic fathers.
Alcoholism, clinical and experimental research | 1996-04-01 | PMID 8730228
Cowley D S, Roy-Byrne P P, Greenblatt D J and 2 more
A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36.
Journal of medical genetics | 1996-04-01 | PMID 8730279
Tomlinson I P, Neale K, Talbot I C and 4 more
Genes: FAP, APC
Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene.
Journal of medical genetics | 1996-04-01 | PMID 8730280
Dobbie Z, Spycher M, Mary J L and 7 more
Genes: APC, FAP
Large scale deletions of the 5q13 region are specific to Werdnig-Hoffmann disease.
Journal of medical genetics | 1996-04-01 | PMID 8730281
Burlet P, Bürglen L, Clermont O and 4 more
Genes: NAIP
The dysmorphic human-mouse homology database (DHMHD): an interactive World-Wide Web resource for gene mapping.
Journal of medical genetics | 1996-04-01 | PMID 8730283
Evans C D, Searle A G, Schinzel A A and 1 more
Complementation analysis in patients with the clinical phenotype of a generalised peroxisomal disorder.
Journal of medical genetics | 1996-04-01 | PMID 8730284
Steinberg S J, Fensom A H
Genes: GPD1
Holt-Oram syndrome: a clinical genetic study.
Journal of medical genetics | 1996-04-01 | PMID 8730285
Newbury-Ecob R A, Leanage R, Raeburn J A and 1 more
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.
Journal of medical genetics | 1996-04-01 | PMID 8730286
Wallace R H, Berkovic S F, Howell R A and 2 more
Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
Journal of medical genetics | 1996-04-01 | PMID 8730290
Maher E R, Webster A R, Richards F M and 4 more
Genes: VHL
Clinical, enzymatic, and molecular characterisation of a Portuguese family with a chronic form of GM2-gangliosidosis B1 variant.
Journal of medical genetics | 1996-04-01 | PMID 8730294
Ribeiro M G, Sonin T, Pinto R A and 5 more
Genes: HEXA
Cerebrotendinous xanthomatosis: a family study of sterol 27-hydroxylase mutations and pharmacotherapy.
QJM : monthly journal of the Association of Physicians | 1996-01-01 | PMID 8730343
Watts G F, Mitchell W D, Bending J J and 2 more
Normal fibrinolytic responses to 1-desamino-8-D-arginine vasopressin in patients with nephrogenic diabetes insipidus caused by mutations in the aquaporin 2 gene.
Nephron | 1996-01-01 | PMID 8730418
van Lieburg A F, Knoers V V, Mallmann R and 3 more
Genes: AQP2
Biology and genetic heterogeneity of hepatitis C virus.
Clinical and experimental rheumatology | 2000-01-01 | PMID 8730468
Bukh J, Miller R H, Purcell R H
HCV and lymphoproliferative diseases.
Clinical and experimental rheumatology | 2000-01-01 | PMID 8730477
Santini G F, Giannini F, Crovatto M and 7 more
HCV genotypes and cryoglobulinemia.
Clinical and experimental rheumatology | 2000-01-01 | PMID 8730482
Crovatto M, Ceselli S, Mazzaro C and 7 more
Significance of hepatitis C virus genotypes and viral load in patients with "essential" mixed cryoglobulinemia.
Clinical and experimental rheumatology | 2000-01-01 | PMID 8730483
Sinico R A, Ribero M L, Fornasieri A and 7 more
HCV genotypes in bone marrow and peripheral blood mononuclear cells of patients with mixed cryoglobulinemia.
Clinical and experimental rheumatology | 2000-01-01 | PMID 8730484
Zehender G, de Maddalena C, Monti G and 6 more
Alpha interferon treatment in chronic hepatitis C.
Clinical and experimental rheumatology | 2000-01-01 | PMID 8730501
Idéo G, Bellobuono A, Mondazzi L and 4 more
Multidrug resistance in acute myeloid leukaemia.
Bailliere's clinical haematology | 1996-03-01 | PMID 8730557
Sonneveld P
Immunocytochemical evidence for the presence of vasopressin in intermediate sized neurosecretory granules of solitary neurohypophyseal terminals in the homozygous Brattleboro rat.
Neuroscience | 1996-05-01 | PMID 8730719
Sonnemans M S, Evans D A, Burbach J P and 1 more
Role of neurotrophins and trk receptors in the development and maintenance of sensory neurons: an overview.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 1996-03-29 | PMID 8730773
Lindsay R M
Genes: NGF, BDNF
Dorsal root ganglion neurons require functional neurotrophin receptors for survival during development.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 1996-03-29 | PMID 8730777
Snider W D, Silos-Santiago I
Neurotrophins and the specification of neuronal phenotype.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 1996-03-29 | PMID 8730778
Lewin G R
Phenotypic modification of primary sensory neurons: the role of nerve growth factor in the production of persistent pain.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 1996-03-29 | PMID 8730783
Woolf C J
Genes: NGF
The systematics of North American Daphnia (Crustacea: Anomopoda): a molecular phylogenetic approach.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences | 1996-03-29 | PMID 8730787
Colbourne J K, Hebert P D
Altered dopamine transporter densities in alcohol-preferring vervet monkeys.
Neuroreport | 1996-01-31 | PMID 8730805
Mash D C, Staley J K, Doepel F M and 3 more
Genes: CIT
Neuronal defects in genotyped dominant megacolon (Dom) mouse embryos, a model for Hirschsprung disease.
Neuroreport | 1996-01-31 | PMID 8730812
Puliti A, Poirier V, Goossens M and 1 more
Polymorphism in AACT gene may lower age of onset of Alzheimer's disease.
Neuroreport | 1996-01-31 | PMID 8730823
Talbot C, Houlden H, Craddock N and 7 more
Alteration of haem-attachment and signal-cleavage sites for Paracoccus denitrificans cytochrome C550 probes pathway of c-type cytochrome biogenesis in Escherichia coli.
Molecular microbiology | 1996-03-01 | PMID 8730862
Sambongi Y, Stoll R, Ferguson S J
Generation of Campylobacter fetus S-layer protein diversity utilizes a single promoter on an invertible DNA segment.
Molecular microbiology | 1996-03-01 | PMID 8730866
Dworkin J, Blaser M J
Saccharomyces cerevisiae TEC1 is required for pseudohyphal growth.
Molecular microbiology | 1996-03-01 | PMID 8730867
Gavrias V, Andrianopoulos A, Gimeno C J and 1 more
Genes: TEF
Isolation of periplasmic nitrate reductase genes from Rhodobacter sphaeroides DSM 158: structural and functional differences among prokaryotic nitrate reductases.
Molecular microbiology | 1996-03-01 | PMID 8730872
Reyes F, Roldán M D, Klipp W and 2 more
Genes: NAPA, NAPB
Tetrapac (tpc), a novel genotype of Neisseria gonorrhoeae affecting epithelial cell invasion, natural transformation competence and cell separation.
Molecular microbiology | 1996-03-01 | PMID 8730876
Fussenegger M, Kahrs A F, Facius D and 1 more
Mutational analysis of the Escherichia coli spoT gene identifies distinct but overlapping regions involved in ppGpp synthesis and degradation.
Molecular microbiology | 1996-03-01 | PMID 8730877
Gentry D R, Cashel M
The influence of the sparteine/debrisoquine genetic polymorphism on the disposition of dexfenfluramine.
British journal of clinical pharmacology | 1996-04-01 | PMID 8730977
Gross A S, Phillips A C, Rieutord A and 1 more
Lack of effect of chloroquine on the debrisoquine (CYP2D6 and S-mephenytoin (CYP2C19) hydroxylation phenotypes.
British journal of clinical pharmacology | 1996-04-01 | PMID 8730982
Masimirembwa C M, Gustafsson L L, Dahl M L and 2 more
Mouse Meckel's cartilage chondrocytes evoke bone-like matrix and further transform into osteocyte-like cells in culture.
The Anatomical record | 1996-05-01 | PMID 8731036
Ishizeki K, Takigawa M, Nawa T and 1 more
Expression of a nonmuscle myosin heavy chain in glomerular cells differentiates various types of glomerular disease in rats.
Kidney international | 1996-05-01 | PMID 8731086
Hiroi J, Kimura K, Aikawa M and 6 more
Differentiation of smooth muscle phenotypes in mouse mesangial cells.
Kidney international | 1996-05-01 | PMID 8731098
Iehara N, Takeoka H, Tsuji H and 6 more
Continuous ambulatory peritoneal dialysis impairs T lymphocyte selection in the peritoneum.
Kidney international | 1996-05-01 | PMID 8731104
Fricke H, Hartmann J, Sitter T and 3 more
Molecular genetics of cystinuria in French Canadians: identification of four novel mutations in type I patients.
Kidney international | 1996-05-01 | PMID 8731106
Horsford J, Saadi I, Raelson J and 2 more
Debrisoquine hydroxylase gene polymorphism frequencies in patients with amyotrophic lateral sclerosis.
Neuroscience letters | 1996-04-12 | PMID 8731176
Siddons M A, Pickering-Brown S M, Mann D M and 2 more
The underlying cellular mechanism of fibrosis.
Kidney international. Supplement | 1996-05-01 | PMID 8731191
Rodemann H P, Binder A, Burger A and 3 more
A mutation affecting gluconate catabolism in Escherichia coli: the locus for the main high affinity transport.
Acta cientifica venezolana | 1994-01-01 | PMID 8731292
De Rekarte U D, Istúriz T
Molecular analysis of CYP21 and C4 genes in Brazilian families with the classical form of steroid 21-hydroxylase deficiency.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas | 1996-01-01 | PMID 8731325
de-Araujo M, Sanches M R, Suzuki L A and 3 more
Poliovirus type 1 isolated from a vaccine-associated case of paralytic poliomyelitis in Brazil.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas | 1996-01-01 | PMID 8731326
Friedrich F, Filippis A M, Ferreira F C and 3 more
V3 peptide binding pattern and HIV-1 transmission route in Rio de Janeiro.
Memorias do Instituto Oswaldo Cruz | 2000-01-01 | PMID 8731364
Pinto M E, Schechter M
Apolipoprotein E genotype and Alzheimer's disease in an elderly Norwegian cohort.
Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration | 1996-03-01 | PMID 8731381
Benjamin R, Leake A, McArthur F K and 6 more
Blood superoxide dismutase, catalase and glutathione peroxidase activities in familial and sporadic amyotrophic lateral sclerosis.
Neurodegeneration : a journal for neurodegenerative disorders, neuroprotection, and neuroregeneration | 1996-03-01 | PMID 8731383
Przedborski S, Donaldson D M, Murphy P L and 5 more
Maladaptive behaviour in Prader-Willi syndrome in adult life.
Journal of intellectual disability research : JIDR | 1996-04-01 | PMID 8731473
Clarke D J, Boer H, Chung M C and 2 more
A new, fast, and simple DNA extraction method for HLA and VNTR genotyping by PCR amplification.
Journal of clinical laboratory analysis | 1996-01-01 | PMID 8731498
Planelles D, Llopis F, Puig N and 1 more
Association of HLA types A1-B8-DR3 and B27 with rapid and slow progression of HIV disease.
QJM : monthly journal of the Association of Physicians | 1996-03-01 | PMID 8731561
McNeil A J, Yap P L, Gore S M and 7 more
[Evaluation of multidrug resistance phenotype on medullary specimens from patients with acute leukemia by determination of nuclear efflux of tetrahydropyranyl-doxorubicin. Approach by confocal laser microspectrofluorometry].
Annales de biologie clinique | 1996-01-01 | PMID 8731789
Morjani H, Pignon B, Vilque J P and 6 more
[Predictive value of intracellular accumulation of daunorubicin and P-glycoprotein expression simultaneously determined by flow cytometry in adult acute myeloid leukemias].
Annales de biologie clinique | 1996-01-01 | PMID 8731790
Guerci A, Merlin J L, Missoum N and 3 more
Correlative study on the expression of p53 and DNA ploidy in acute nonlymphocytic leukemia.
Journal of Tongji Medical University = Tong ji yi ke da xue xue bao | 1995-01-01 | PMID 8731941
Lin F R, Yao E G, Zuo L F and 4 more
[Genetic polymorphism of properdin factor B in the Han population in Chengdu, China].
Hua xi yi ke da xue xue bao = Journal of West China University of Medical Sciences = Huaxi yike daxue xuebao | 1995-12-01 | PMID 8732066
Chen G, Gou Q, Hou Y and 1 more
Cell cycle state, response to hemopoietic growth factors and retroviral vector-mediated transduction of human hemopoietic stem cells.
Gene therapy | 1996-04-01 | PMID 8732164
Knaän-Shanzer S, Valerio D, van Beusechem V W
Expression of mutant and wild-type gag proteins for gene therapy in HIV-1 infection.
Gene therapy | 1996-04-01 | PMID 8732168
Miele G, Lever A M
Clinical relevance of hepatitis C virus quasispecies.
Journal of viral hepatitis | 1995-01-01 | PMID 8732171
Enomoto N, Sato C
Analysis of hepatitis B virus precore variants in hepatitis B e antibody-positive patients treated with prednisone plus interferon.
Journal of viral hepatitis | 1995-01-01 | PMID 8732173
Lopez-Alcorocho J M, Cabrerizo M, Bartolome J and 2 more
Variations of hepatitis C virus NS5B sequence (nucleotides 8261-8566) do not correlate with response to interferon-alpha therapy.
Journal of viral hepatitis | 1995-01-01 | PMID 8732174
Nelson D R, Gray A H, Kolberg J A and 5 more
Hepatitis C virus genotypes in patients with chronic liver disease and haemodialysis patients from Saudi Arabia.
Journal of viral hepatitis | 1995-01-01 | PMID 8732175
al-Faleh F Z, Huraib S, Sbeih F and 6 more
The distribution of hepatitis C virus genotypes in Turkish patients.
Journal of viral hepatitis | 1995-01-01 | PMID 8732176
Abacioglu Y H, Davidson F, Tuncer S and 4 more
Thyroid peroxidase: experimental and clinical integration.
Endocrine journal | 1996-02-01 | PMID 8732446
Ohtaki S, Nakagawa H, Nakamura M and 1 more
Genes: TPO
Absence of mutations at codon 768 of the RET proto-oncogene in sporadic and hereditary pheochromocytomas.
Endocrine journal | 1996-02-01 | PMID 8732460
Yoshimoto K, Kimura T, Tanaka C and 3 more
Genes: RET
HLA-DQA1 and -DQB1 genotyping by PCR-RFLP, heteroduplex and homoduplex analysis.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics | 1996-04-01 | PMID 8732474
Teutsch S M, Bennetts B H, Castle M and 3 more
An apparent functional correlation between variations in amino acid residues in HLA-DR4.1 and 4.2 serological subtypes and oligonucleotide characterization.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics | 1996-04-01 | PMID 8732476
Lee T D, Lee A, Lai S and 3 more
Investigation of the association of major histocompatibility complex genes, including HLA class I, class II and TAP genes, with clinical forms of Crohn's disease.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics | 1996-04-01 | PMID 8732477
Hesresbach D, Alizadeh M, Bretagne J F and 6 more
Genes: TAP2
HLA-G polymorphism and allelic association with HLA-A in a Finnish population.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics | 1996-04-01 | PMID 8732478
Karhukorpi J, Ikäheimo I, Silvennoinen-Kassinen S and 1 more
TCR gene polymorphisms and autoimmune disease.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics | 1996-04-01 | PMID 8732480
Kay R A
Acute hyperinsulinaemia decreases cholesterol synthesis less in subjects with non-insulin-dependent diabetes mellitus than in non-diabetic subjects.
European journal of clinical investigation | 1996-04-01 | PMID 8732493
Naoumova R P, Cummings M H, Watts G F and 4 more
Single lung transplantation followed by contralateral bullectomy for bullous emphysema.
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation | 1996-04-01 | PMID 8732598
Kuno R, Kanter K R, Torres W E and 1 more
A modification of the APC resistance test and its application to the study of patients on coumarin therapy.
Thrombosis research | 1996-05-01 | PMID 8732625
Jorquera J I, Aznar J, Fernández M A and 3 more
Genes: APC
Clinical significance of activated protein C resistance as a potential marker for hypercoagulable state.
Thrombosis research | 1996-05-01 | PMID 8732627
Sakata T, Kario K, Katayama Y and 3 more
Genes: APC
Effect of 1-beta-D-arabinofuranosylcytosine on apoptosis and differentiation in human monocytic leukemia cells (U937) expressing a c-Jun dominant-negative mutant protein (TAM67).
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research | 1996-05-01 | PMID 8732670
Grant S, Freemerman A J, Birrer M J and 5 more
No association between the Gly971Arg variant of the insulin receptor substrate 1 gene and NIDDM in the Taiwanese population.
Diabetes care | 1996-05-01 | PMID 8732707
Chuang L M, Lai C S, Yeh J I and 3 more
Role of mitochondrial DNA tRNA leucine and glucagon receptor missense mutations in Utah white diabetic patients.
Diabetes care | 1996-05-01 | PMID 8732719
Elbein S C, Hoffman M D
A compound heterozygote for hepatic lipase gene mutations Leu334-->Phe and Thr383-->Met: correlation between hepatic lipase activity and phenotypic expression.
Journal of lipid research | 1996-04-01 | PMID 8732782
Knudsen P, Antikainen M, Ehnholm S and 8 more
Analysis of ENV V3 sequences from HIV-1-infected brain indicates restrained virus expression throughout the disease.
Journal of medical virology | 1996-05-01 | PMID 8732858
Di Stefano M, Gray F, Leitner T and 1 more
Distribution of HCV genotypes among blood donors, patients with chronic liver disease, hepatocellular carcinoma, and patients on maintenance hemodialysis in Korea.
Journal of medical virology | 1996-05-01 | PMID 8732860
Lee D S, Sung Y C, Whang Y S
Molecular characterization of Camberwell virus and sequence variation in ORF3 of small round-structured (Norwalk-like) viruses.
Journal of medical virology | 1996-05-01 | PMID 8732863
Cauchi M R, Doultree J C, Marshall J A and 1 more
Familial clustering of abdominal visceral fat and total fat mass: the Québec Family Study.
Obesity research | 1996-05-01 | PMID 8732959
Rice T, Pérusse L, Bouchard C and 1 more
Molecular basis of androgen insensitivity.
Steroids | 1996-04-01 | PMID 8732995
Brinkmann A, Jenster G, Ris-Stalpers C and 4 more
Mineralocorticoids, salt and high blood pressure.
Steroids | 1996-04-01 | PMID 8732997
Gómez-Sánchez E P, Zhou M, Gomez-Sanchez C E
The 11 beta-hydroxysteroid dehydrogenase type II enzyme: biochemical consequences of the congenital R337C mutation.
Steroids | 1996-04-01 | PMID 8733000
Ferrari P, Obeyesekere V R, Li K and 2 more
A clinician looks at androgen resistance.
Steroids | 1996-04-01 | PMID 8733002
Balducci R, Ghirri P, Brown T R and 5 more
Molecular basis of glucocorticoid-resistant syndromes.
Steroids | 1996-04-01 | PMID 8733004
Werner S, Brönnegård M
I/D polymorphism of the angiotensin-converting enzyme gene does not predict isolated systolic or systolic-diastolic hypertension in the elderly.
Journal of human hypertension | 1996-03-01 | PMID 8733034
Johnson A G, Simons L A, Friedlander Y and 3 more
Genes: ACE
Mutation analysis in 24 French patients with glycogen storage disease type 1a.
Journal of medical genetics | 1996-05-01 | PMID 8733042
Chevalier-Porst F, Bozon D, Bonardot A M and 4 more
Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia.
Journal of medical genetics | 1996-05-01 | PMID 8733045
Lee H H, Chao H T, Ng H T and 1 more
FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male.
Journal of medical genetics | 1996-05-01 | PMID 8733046
Wang Z, Taylor A K, Bridge J A
Genes: FMR1
Arginine-164-tryptophan substitution in connexin32 associated with X linked dominant Charcot-Marie-Tooth disease.
Journal of medical genetics | 1996-05-01 | PMID 8733054
Oterino A, Montón F I, Cabrera V M and 3 more
Analysis of GLRA1 in hereditary and sporadic hyperekplexia: a novel mutation in a family cosegregating for hyperekplexia and spastic paraparesis.
Journal of medical genetics | 1996-05-01 | PMID 8733061
Elmslie F V, Hutchings S M, Spencer V and 4 more
Genes: GLRA1
Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3.
Journal of medical genetics | 1996-05-01 | PMID 8733062
Llewellyn D H, Scobie G A, Urquhart A J and 4 more
Genes: AIP