Problems with determination of noncommunicating classes for Monte Carlo Markov chain applications in pedigree analysis.
Biometrics | 1998-06-01 | PMID 9629636
Jensen C S, Sheehan N
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 998 of 10600
[Relationship between pathogenicity of Schistosoma mansoni in mice and the susceptibility of the vector mollusk. IV--Infectiousness of miracidia].
Revista de saude publica | 1997-10-01 | PMID 9629726
Zanotti-Magalhães E M, Magalhães L A, de Carcalho J F
[Resistance of human immunodeficiency virus (HIV) to zidovudine. Genotypic analysis in strains isolated from Chilean patients].
Revista medica de Chile | 1998-01-01 | PMID 9629750
Vial P A, Vial C, Abarca K and 7 more
Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene.
Annals of neurology | 1998-06-01 | PMID 9629839
Cudkowicz M E, McKenna-Yasek D, Chen C and 2 more
Genes: SOD1
Amyloid myopathy: an underdiagnosed entity.
Annals of neurology | 1998-06-01 | PMID 9629841
Spuler S, Emslie-Smith A, Engel A G
Descriptive epidemiology of Creutzfeldt-Jakob disease in six European countries, 1993-1995. EU Collaborative Study Group for CJD.
Annals of neurology | 1998-06-01 | PMID 9629846
Will R G, Alperovitch A, Poser S and 8 more
Neuroanatomical and neurocognitive differences in a pair of monozygous twins discordant for strictly defined autism.
Annals of neurology | 1998-06-01 | PMID 9629848
Kates W R, Mostofsky S H, Zimmerman A W and 5 more
Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease.
Annals of neurology | 1998-06-01 | PMID 9629853
Shibuya S, Higuchi J, Shin R W and 2 more
Genes: PRNP
Simultaneous genotyping of alcohol dehydrogenase 2 (ADH2) and aldehyde dehydrogenase 2 (ALDH2) loci by amplified product length polymorphism (APLP) analysis.
Electrophoresis | 1998-05-01 | PMID 9629893
Aoshima T, Umetsu K, Yuasa I and 2 more
Genes: ALDH2
Population analysis of the collagen type IIalpha1 3' variable number of tandem repeat polymorphism by heteroduplex genotyping.
Electrophoresis | 1998-05-01 | PMID 9629894
Uitterlinden A G, Huang Q, Pols H A and 1 more
Screening of a highly polymorphic microsatellite for microheterogeneity in human identification.
Electrophoresis | 1998-05-01 | PMID 9629895
Miścicka-Sliwka D, Grzybowski T, Czarny J and 1 more
Detection of sequence variation in parasite ribosomal DNA by electrophoresis in agarose gels supplemented with a DNA-intercalating agent.
Electrophoresis | 1998-05-01 | PMID 9629896
Zhu X Q, Chilton N B, Gasser R B
Increasing incidence of meningococcal disease in Spain associated with a new variant of serogroup C.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 1998-02-01 | PMID 9629971
Berrón S, De La Fuente L, Martín E and 1 more
Use of pulsed field gel electrophoresis to determine the source of microbial contamination of central venous catheters.
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 1998-02-01 | PMID 9629976
Livesley M A, Tebbs S E, Moss H A and 3 more
HLA-DQB1 and DRB1 alleles in Egyptian children with steroid-sensitive nephrotic syndrome.
Pediatric nephrology (Berlin, Germany) | 1998-04-01 | PMID 9630045
Bakr A M, El-Chenawy F
Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis.
Clinical genetics | 1998-03-01 | PMID 9630070
Adams P C
Genes: HFE
DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome.
Clinical genetics | 1998-03-01 | PMID 9630071
Chan S Y, Wong V
Glucose-6-phosphatase gene (727G-->T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a.
Clinical genetics | 1998-03-01 | PMID 9630072
Lam C W, But W M, Shek C C and 6 more
Serum lipids and apolipoprotein E phenotypes in identical twins reared apart.
Clinical genetics | 1998-03-01 | PMID 9630073
Kervinen K, Kaprio J, Koskenvuo M and 2 more
Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene.
Clinical genetics | 1998-03-01 | PMID 9630075
Arduino C, Ferrone M, Brusco A and 4 more
Genes: CFTR
A novel missense mutation (402C-->T) in exon 1 in the EDA gene in a family with X-linked hypohidrotic ectodermal dysplasia.
Clinical genetics | 1998-03-01 | PMID 9630076
Hertz J M, Nørgaard Hansen K, Juncker I and 2 more
Genes: EDA
Deletion of chromosome 3q proximal region gives rise to a variable phenotype.
Clinical genetics | 1998-03-01 | PMID 9630079
Mackie Ogilvie C, Rooney S C, Hodgson S V and 1 more
C-cell hyperplasia and medullary thyroid carcinoma in patients routinely screened for serum calcitonin.
The American journal of surgical pathology | 1998-06-01 | PMID 9630179
Kaserer K, Scheuba C, Neuhold N and 4 more
The PHANTASTICA gene encodes a MYB transcription factor involved in growth and dorsoventrality of lateral organs in Antirrhinum.
Cell | 1998-05-29 | PMID 9630222
Waites R, Selvadurai H R, Oliver I R and 1 more
Genes: MYB
A mutant Drosophila homolog of mammalian Clock disrupts circadian rhythms and transcription of period and timeless.
Cell | 1998-05-29 | PMID 9630223
Allada R, White N E, So W V and 2 more
Genes: TIMELESS
CYCLE is a second bHLH-PAS clock protein essential for circadian rhythmicity and transcription of Drosophila period and timeless.
Cell | 1998-05-29 | PMID 9630224
Rutila J E, Suri V, Le M and 3 more
Genes: BMAL1
HTLV-I Tax protein binds to MEKK1 to stimulate IkappaB kinase activity and NF-kappaB activation.
Cell | 1998-05-29 | PMID 9630230
Yin M J, Christerson L B, Yamamoto Y and 6 more
Partial V(D)J recombination activity leads to Omenn syndrome.
Cell | 1998-05-29 | PMID 9630231
Villa A, Santagata S, Bozzi F and 9 more
The hereditary ataxias.
Journal of neuropathology and experimental neurology | 1998-06-01 | PMID 9630233
Koeppen A H
Genes: GAA
Modeling the tertiary interactions in the eukaryotic selenocysteine tRNA.
RNA (New York, N.Y.) | 1998-04-01 | PMID 9630244
Ioudovitch A, Steinberg S V
A comprehensive biochemical and genetic analysis of the yeast U1 snRNP reveals five novel proteins.
RNA (New York, N.Y.) | 1998-04-01 | PMID 9630245
Gottschalk A, Tang J, Puig O and 8 more
Genetic analysis of the U5-PBS of a novel HIV-1 reveals multiple interactions between the tRNA and RNA genome required for initiation of reverse transcription.
RNA (New York, N.Y.) | 1998-04-01 | PMID 9630246
Zhang Z, Kang S M, Li Y and 1 more
Mechanistic analysis of RNA synthesis by RNA-dependent RNA polymerase from two promoters reveals similarities to DNA-dependent RNA polymerase.
RNA (New York, N.Y.) | 1998-04-01 | PMID 9630251
Adkins S, Stawicki S S, Faurote G and 2 more
Epidemiological typing of klebsiellae with extended-spectrum beta-lactamases from European intensive care units.
The Journal of antimicrobial chemotherapy | 1998-05-01 | PMID 9630406
Yuan M, Aucken H, Hall L M and 2 more
A naturally occurring basically charged human follicle-stimulating hormone (FSH) variant inhibits FSH-induced androgen aromatization and tissue-type plasminogen activator enzyme activity in vitro.
Neuroendocrinology | 1998-03-01 | PMID 9630432
Timossi C M, Barrios de Tomasi J, Zambrano E and 2 more
Characterization of phenotypic alterations induced by 2,3,7,8-tetrachlorodibenzo-p-dioxin on thymocytes in vivo and its effect on apoptosis.
Toxicology and applied pharmacology | 1998-05-01 | PMID 9630460
Kamath A B, Nagarkatti P S, Nagarkatti M
Polymorphic insertions/deletions of both 1550nt and 100nt in two microsatellite-containing, LINE-related intronic regions of the rabbit kappa-casein gene.
Gene | 1998-06-15 | PMID 9630490
Hiripi L, Devinoy E, Rat P and 3 more
Promoter analysis of the human mismatch repair gene hMSH2.
Gene | 1998-06-15 | PMID 9630578
Iwahashi Y, Ito E, Yanagisawa Y and 4 more
Diversity of sequence haplotypes associated with beta-thalassaemia mutations in Algeria: implications for their origin.
Gene | 1998-06-15 | PMID 9630612
Perrin P, Bouhassa R, Mselli L and 5 more
Characterization of the human mitochondrial aconitase gene (ACO2).
Gene | 1998-06-15 | PMID 9630632
Mirel D B, Marder K, Graziano J and 4 more
Genes: ACO2
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.
Biochimica et biophysica acta | 1998-04-28 | PMID 9630669
Yamamoto K, Sato H, Fujiyama Y and 2 more
Analysis of a naturally occurring mutation in sucrase-isomaltase: glutamine 1098 is not essential for transport to the surface of COS-1 cells.
Biochimica et biophysica acta | 1998-04-28 | PMID 9630686
Ouwendijk J, Peters W J, te Morsche R H and 4 more
Endogenous and ectopic expression of noggin suggests a conserved mechanism for regulation of BMP function during limb and somite patterning.
Developmental biology | 1998-05-15 | PMID 9630747
Capdevila J, Johnson R L
The cloche and spadetail genes differentially affect hematopoiesis and vasculogenesis.
Developmental biology | 1998-05-15 | PMID 9630750
Thompson M A, Ransom D G, Pratt S J and 17 more
The paternal effect gene ms(3)sneaky is required for sperm activation and the initiation of embryogenesis in Drosophila melanogaster.
Developmental biology | 1998-05-15 | PMID 9630751
Fitch K R, Wakimoto B T
Metabolism of warfarin enantiomers in Japanese patients with heart disease having different CYP2C9 and CYP2C19 genotypes.
Clinical pharmacology and therapeutics | 1998-05-01 | PMID 9630825
Takahashi H, Kashima T, Nomizo Y and 6 more
Influence of CYP2D6 polymorphism on the pharmacokinetics and pharmacodynamic of tolterodine.
Clinical pharmacology and therapeutics | 1998-05-01 | PMID 9630826
Brynne N, Dalén P, Alván G and 2 more
Detection of evolving viruses.
Nature biotechnology | 1996-04-01 | PMID 9630926
Lee Y, Yin J
Use of green fluorescent protein variants to monitor gene transfer and expression in mammalian cells.
Nature biotechnology | 1996-05-01 | PMID 9630951
Cheng L, Fu J, Tsukamoto A and 1 more
Pathway engineering for the production of aromatic compounds in Escherichia coli.
Nature biotechnology | 1996-05-01 | PMID 9630954
Flores N, Xiao J, Berry A and 2 more
Genes: PTS
Translational level is a critical factor for the secretion of heterologous proteins in Escherichia coli.
Nature biotechnology | 1996-05-01 | PMID 9630956
Simmons L C, Yansura D G
Development of friable embryogenic callus and embryogenic suspension culture systems in cassava (Manihot esculenta Crantz)
Nature biotechnology | 1996-06-01 | PMID 9630979
Taylor N J, Edwards M, Kiernan R J and 3 more
High efficiency transformation of maize (Zea mays L.) mediated by Agrobacterium tumefaciens.
Nature biotechnology | 1996-06-01 | PMID 9630983
Ishida Y, Saito H, Ohta S and 3 more
Genetic engineering of harvest index in tobacco through overexpression of a phytochrome gene.
Nature biotechnology | 1996-08-01 | PMID 9631038
Robson P R, McCormac A C, Irvine A S and 1 more
The molecular structure of green fluorescent protein.
Nature biotechnology | 1996-10-01 | PMID 9631087
Yang F, Moss L G, Phillips G N
Engineering human glycoprotein hormone superactive analogues.
Nature biotechnology | 1996-10-01 | PMID 9631089
Szkudlinski M W, Teh N G, Grossmann M and 2 more
Spontaneous change of a benign satellite RNA of cucumber mosaic virus to a pathogenic variant.
Nature biotechnology | 1996-10-01 | PMID 9631090
Palukaitis P, Roossinck M J
Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia.
Nature biotechnology | 1996-10-01 | PMID 9631093
Baron H, Fung S, Aydin A and 3 more
Diagnosis of sickle-cell disease by DNA analysis in Nigeria.
The Central African journal of medicine | 1997-12-01 | PMID 9631113
Adewole T A, Olukoya D K, Afonja A
Characterization of the viral population during primary HIV-1 infection.
AIDS (London, England) | 1998-05-28 | PMID 9631136
Karlsson A C, Lindbäck S, Gaines H and 1 more
In vitro selective elimination of HIV-infected cells from peripheral blood in AIDS patients by the immunotoxin DAB389CD4.
AIDS (London, England) | 1998-05-28 | PMID 9631138
Martín-Serrano J, Folgueira L, Laín de Lera T and 6 more
Pneumocystis carinii mutations associated with sulfa and sulfone prophylaxis failures in AIDS patients.
AIDS (London, England) | 1998-05-28 | PMID 9631140
Kazanjian P, Locke A B, Hossler P A and 5 more
Genes: DHPS
Production of rat salivary cystatin S variant polypeptides in Escherichia coli.
Archives of oral biology | 1998-03-01 | PMID 9631169
Bedi G S, Zhou T, Bedi S K
Sibling similarities in the tempo of human tooth mineralization.
Archives of oral biology | 1998-03-01 | PMID 9631173
Merwin D R, Harris E F
Sequence analysis of mitochondrial DNA hypervariable regions using infrared fluorescence detection.
BioTechniques | 1998-06-01 | PMID 9631201
Steffens D L, Roy R
The functional significance of multimerization in ion channels.
Current opinion in structural biology | 1998-04-01 | PMID 9631291
Tierney M L, Stowell M H
Spontaneous inflammatory bowel disease in multiple mutant mouse lines: association with colonization by Helicobacter hepaticus.
Helicobacter | 1998-06-01 | PMID 9631303
Foltz C J, Fox J G, Cahill R and 4 more
Confirmation that a T-to-C mutation at 9176 in mitochondrial DNA is an additional candidate mutation for Leigh's syndrome.
Neuromuscular disorders : NMD | 1998-05-01 | PMID 9631394
Makino M, Horai S, Goto Y and 1 more
Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings.
Neuromuscular disorders : NMD | 1998-05-01 | PMID 9631397
Topaloğlu H, Talim B, Vignier N and 6 more
Genes: LAMA2
LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3.
Neuromuscular disorders : NMD | 1998-05-01 | PMID 9631401
Bönnemann C G, Wong J, Ben Hamida C and 3 more
Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscle.
Neuromuscular disorders : NMD | 1998-05-01 | PMID 9631403
Lane R J, Barrett M C, Taylor D J and 2 more
Novel splice variants of the voltage-sensitive sodium channel alpha subunit.
Neuroreport | 1998-05-11 | PMID 9631410
Oh Y, Waxman S G
Polymorphism in the promoter region of the alpha 2A adrenergic receptor gene and mood disorders.
Neuroreport | 1998-05-11 | PMID 9631415
Ohara K, Nagai M, Tani K and 3 more
Low activity allele of catechol-o-methyltransferase gene and Japanese unipolar depression.
Neuroreport | 1998-05-11 | PMID 9631418
Ohara K, Nagai M, Suzuki Y and 1 more
Genes: COMT
Mannan-binding lectin in human serum, cerebrospinal fluid and brain tissue and its role in Alzheimer's disease.
Neuroreport | 1998-05-11 | PMID 9631454
Lanzrein A S, Jobst K A, Thiel S and 4 more
Absence of PhIP adducts, p53 and Apc mutations, in rats fed a cooked beef diet containing a high level of heterocyclic amines.
Nutrition and cancer | 1998-01-01 | PMID 9631495
Shen C L, Purewal M, San Francisco S and 1 more
Serum resistance in bvg-regulated mutants of Bordetella pertussis.
FEMS microbiology letters | 1998-06-01 | PMID 9631546
Fernandez R C, Weiss A A
Coupling site-directed mutagenesis with high-level expression: large scale production of mutant porins from E. coli.
FEMS microbiology letters | 1998-06-01 | PMID 9631547
Prilipov A, Phale P S, Van Gelder P and 2 more
The dynamics of maternal-effect selfish genetic elements.
Journal of theoretical biology | 1998-03-21 | PMID 9631565
Smith N G
The paradoxical dynamics of prion disease latency.
Journal of theoretical biology | 1998-04-21 | PMID 9631573
Payne R J, Krakauer D C
A structured, minimal parameter model of the central nitrogen metabolism in Saccharomyces cerevisiae: the prediction of the behavior of mutants.
Journal of theoretical biology | 1998-04-21 | PMID 9631574
van Riel N A, Giuseppin M L, TerSchure E G and 1 more
Coevolutionary chase in two-species systems with applications to mimicry.
Journal of theoretical biology | 1998-04-21 | PMID 9631575
Gavrilets S, Hastings A
Scientific progress in understanding oral and pharyngeal cancers.
Journal of the American Dental Association (1939) | 1998-06-01 | PMID 9631611
Winn D M, Diehl S R, Horowitz A M and 3 more
Using mitochondrial and nuclear DNA markers to reconstruct human evolution.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1998-02-01 | PMID 9631658
Jorde L B, Bamshad M, Rogers A R
Dual functions of DNA repair genes: molecular, cellular, and clinical implications.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1998-02-01 | PMID 9631660
Lehmann A R
Underground metabolism.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1998-02-01 | PMID 9631663
D'Ari R, Casadesús J
Serologic and virologic profiles of hepatitis C infection in renal transplant candidates. New England Organ Bank Hepatitis C Study Group.
American journal of kidney diseases : the official journal of the National Kidney Foundation | 1998-06-01 | PMID 9631834
Natov S N, Lau J Y, Bouthot B A and 5 more
Genetic polymorphism of cytochrome P450s, CYP2C19, and CYP2C9 in a Japanese population.
Therapeutic drug monitoring | 1998-06-01 | PMID 9631918
Kimura M, Ieiri I, Mamiya K and 2 more
Tryptophan metabolism in male Sardinian alcohol-preferring (sP) and -non-preferring (sNP) rats.
Alcohol and alcoholism (Oxford, Oxfordshire) | 2000-01-01 | PMID 9632047
Bano S, Morgan C J, Badawy A A and 5 more
Serotonin is reduced in the frontal cortex of Sardinian ethanol-preferring rats.
Alcohol and alcoholism (Oxford, Oxfordshire) | 2000-01-01 | PMID 9632048
Devoto P, Colombo G, Stefanini E and 1 more
Expression of costimulatory molecule CD80 on peripheral blood T cells in patients with systemic lupus erythematosus.
The Journal of rheumatology | 1998-06-01 | PMID 9632068
Takasaki Y, Ogaki M, Abe K and 7 more
Association of HLA class I and class II alleles with myositis in Japanese patients.
The Journal of rheumatology | 1998-06-01 | PMID 9632072
Furuya T, Hakoda M, Higami K and 5 more
Association of primary antiphospholipid syndrome with inherited activated protein C resistance.
The Journal of rheumatology | 1998-06-01 | PMID 9632093
Picillo U, De Lucia D, Palatiello E and 4 more
Cloning and characterization of a Dictyostelium gene encoding a small GTPase of the Rab11 family.
Journal of cellular biochemistry | 1998-07-01 | PMID 9632105
Dragoi I A, O'Halloran T J
Ras, but not Src, transformation of RIE-1 epithelial cells is dependent on activation of the mitogen-activated protein kinase cascade.
Oncogene | 1998-05-01 | PMID 9632133
Oldham S M, Cox A D, Reynolds E R and 3 more
Genes: EGF
Oculocerebrorenal syndrome of Lowe: three mutations in the OCRL1 gene derived from three patients with different phenotypes.
American journal of medical genetics | 1998-06-05 | PMID 9632163
Kawano T, Indo Y, Nakazato H and 2 more
Genes: OCRL
Efficient, robust, and unified method for mapping complex traits (I): two-point linkage analysis.
American journal of medical genetics | 1998-06-05 | PMID 9632166
Zhao L P, Quiaoit F, Hsu L and 1 more
Yield of mtDNA mutation analysis in 2,000 patients.
American journal of medical genetics | 1998-06-05 | PMID 9632169
Liang M H, Wong L J
Random X inactivation in a girl with a balanced t(X;9) and an abnormal phenotype.
American journal of medical genetics | 1998-06-05 | PMID 9632170
Wolff D J, Schwartz S, Montgomery T and 1 more
Genes: FMR1
Evidence for complex nuclear inheritance in a pedigree with nonsyndromic deafness due to a homoplasmic mitochondrial mutation.
American journal of medical genetics | 1998-06-05 | PMID 9632174
Bykhovskaya Y, Shohat M, Ehrenman K and 8 more