Biomedical publications with connected research

Angiotensin-converting enzyme (ACE) gene polymorphism and the erythrocyte sodium-lithium countertransporter (SLC) phenotype in hypertension.

Journal of human hypertension | 1996-06-01 | PMID 8872813

Hardman T C, Wierzbicki A S, Croft P and 3 more

Genes: ACE

Genetic association between cytochrome P450IA1 gene and susceptibility to Parkinson's disease.

Journal of neural transmission (Vienna, Austria : 1996) | 1996-01-01 | PMID 8872868

Takakubo F, Yamamoto M, Ogawa N and 3 more

Epigenetic factors controlling the development of avian Purkinje neurons.

Journal of neuroscience methods | 1996-08-01 | PMID 8872882

Jeffrey P L, Meaney J, Tolhurst O and 1 more

Evidence against chronic antigen-specific T lymphocyte activation in myasthenia gravis.

Journal of neuroscience research | 1996-08-15 | PMID 8872911

Infante A J, Infante P D, Jackson C E and 7 more

Renal involvement in von Hippel-Lindau disease.

Kidney international | 1996-09-01 | PMID 8872970

Chauveau D, Duvic C, Chrétien Y and 6 more

Genes: VHL

New immunodeficient mouse strains bred by introducing beige and xid mutations into the KSN nude strain.

Laboratory animal science | 1996-08-01 | PMID 8872993

Ishigaki Y, Hayakawa J, Hashimoto N and 2 more

The development of the noradrenergic transmitter phenotype in postganglionic sympathetic neurons.

Neurochemical research | 1996-07-01 | PMID 8873087

Ernsberger U, Rohrer H

Role in fast inactivation of conserved amino acids in the IV/S4-S5 loop of the human muscle Na+ channel.

Neuroscience letters | 1996-08-16 | PMID 8873119

Mitrovic N, Lerche H, Heine R and 5 more

Purkinje cell loss and astrocytosis in the cerebellum in familial and sporadic Alzheimer's disease.

Neuroscience letters | 1996-08-16 | PMID 8873125

Fukutani Y, Cairns N J, Rossor M N and 1 more

Genes: APP

Decrease in exploratory behavior in naturally occurring cholecystokinin (CCK)-A receptor gene knockout rats.

Neuroscience letters | 1996-08-16 | PMID 8873132

Kobayashi S, Ohta M, Miyasaka K and 1 more

Genes: CCK

Neostriatal dopamine depletion and locomotor abnormalities due to the Albino Swiss rat agu mutation.

Neuroscience letters | 1996-08-09 | PMID 8873142

Campbell J M, Payne A P, Gilmore D P and 6 more

Genes: ECD

Superactivation of transglutaminase type 2 without change in enzyme level occurs during progressive neurodegeneration in the mnd mouse mutant.

Neuroscience letters | 1996-08-09 | PMID 8873145

Holmes F E, Haynes L W

Genetic polymorphism of thiopurine S-methyltransferase: clinical importance and molecular mechanisms.

Pharmacogenetics | 1996-08-01 | PMID 8873214

Krynetski E Y, Tai H L, Yates C R and 5 more

Genes: TPMT

Increased prevalence of the Taq I A1 allele of the dopamine receptor gene (DRD2) in obesity with comorbid substance use disorder: a preliminary report.

Pharmacogenetics | 1996-08-01 | PMID 8873216

Blum K, Braverman E R, Wood R C and 7 more

Genes: DRD2

Characterization and PCR-based detection of two different hybrid CYP2D7P/CYP2D6 alleles associated with the poor metabolizer phenotype.

Pharmacogenetics | 1996-08-01 | PMID 8873218

Daly A K, Fairbrother K S, Andreassen O A and 3 more

CYP2C19 genotyping and associated mephenytoin hydroxylation polymorphism in a Canadian Inuit population.

Pharmacogenetics | 1996-08-01 | PMID 8873219

Jurima-Romet M, Goldstein J A, LeBelle M and 4 more

The role of the CYP2C9-Leu359 allelic variant in the tolbutamide polymorphism.

Pharmacogenetics | 1996-08-01 | PMID 8873220

Sullivan-Klose T H, Ghanayem B I, Bell D A and 6 more

PCR-based genotyping for duplicated and deleted CYP2D6 genes.

Pharmacogenetics | 1996-08-01 | PMID 8873221

Johansson I, Lundqvist E, Dahl M L and 1 more

Neurofibromatosis type 2: a new mechanism of tumor suppression.

Trends in neurosciences | 1996-09-01 | PMID 8873351

Lutchman M, Rouleau G A

Evidence for a new type of O allele at the ABO locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion.

Vox sanguinis | 1996-01-01 | PMID 8873422

Olsson M L, Chester M A

Genes: ABO

Flavin adenine dinucleotide binding is the crucial step in alcohol oxidase assembly in the yeast Hansenula polymorpha.

Yeast (Chichester, England) | 1996-08-01 | PMID 8873445

Evers M E, Titorenko V, Harder W and 2 more

A useful colony colour phenotype associated with the yeast selectable/counter-selectable marker MET15.

Yeast (Chichester, England) | 1996-08-01 | PMID 8873447

Cost G J, Boeke J D

Characterization of the SAC3 gene of Saccharomyces cerevisiae.

Yeast (Chichester, England) | 1996-08-01 | PMID 8873450

Bauer A, Kölling R

Characterization of cwl1+, a gene from Schizosaccharomyces pombe whose overexpression causes cell lysis.

Yeast (Chichester, England) | 1996-08-01 | PMID 8873452

Godoy C, Arellano M, Diaz M and 2 more

Population structure of the yellow-footed rock-wallaby Petrogale xanthopus (Gray, 1854) inferred from mtDNA sequences and microsatellite loci.

Molecular ecology | 1996-10-01 | PMID 8873466

Pope L C, Sharp A, Moritz C

Clinical significance of the FV:Q506 mutation in unselected oncology patients.

The American journal of medicine | 1996-10-01 | PMID 8873512

Otterson G A, Monahan B P, Harold N and 3 more

Identification of histidine as an axial ligand to P700+.

Biochemistry | 1996-10-15 | PMID 8873594

Mac M, Tang X S, Diner B A and 2 more

Genetic polymorphism of methylenetetrahydrofolate reductase and myocardial infarction. A case-control study.

Circulation | 1996-10-15 | PMID 8873653

Schmitz C, Lindpaintner K, Verhoef P and 2 more

Failure to detect connexin43 mutations in 38 cases of sporadic and familial heterotaxy.

Circulation | 1996-10-15 | PMID 8873667

Gebbia M, Towbin J A, Casey B

The Asp9 Asn mutation in the lipoprotein lipase gene is associated with increased progression of coronary atherosclerosis. REGRESS Study Group, Interuniversity Cardiology Institute, Utrecht, The Netherlands. Regression Growth Evaluation Statin Study.

Circulation | 1996-10-15 | PMID 8873668

Jukema J W, van Boven A J, Groenemeijer B and 10 more

Genes: LPL

Determination of cytochrome P450 3A4/5 activity in vivo with dextromethorphan N-demethylation.

Clinical pharmacology and therapeutics | 1996-10-01 | PMID 8873685

Jones D R, Gorski J C, Haehner B D and 2 more

lem7, a novel temperature-sensitive Arabidopsis mutation that reversibly inhibits vegetative development.

Developmental biology | 1996-10-10 | PMID 8873758

Meisel L, Xie S, Lam E

Nonmyristoylated MARCKS complements some but not all of the developmental defects associated with MARCKS deficiency in mice.

Developmental biology | 1996-10-10 | PMID 8873759

Swierczynski S L, Siddhanti S R, Tuttle J S and 1 more

Genes: MARCKS

Cytoplasmic polyadenylation of activin receptor mRNA and the control of pattern formation in Xenopus development.

Developmental biology | 1996-10-10 | PMID 8873767

Simon R, Wu L, Richter J D

Genes: CPE

The origin, by mutation, of high level resistance to ceftazidime and cefotaxime in a clinical isolate of Enterobacter cloacae.

Journal of chemotherapy (Florence, Italy) | 1996-08-01 | PMID 8873831

Blahová J, Lesická-Hupková M, Králiková K and 2 more

Pneumocystis carinii: an atypical fungal micro-organism.

Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology | 2000-01-01 | PMID 8873881

Cailliez J C, Séguy N, Denis C M and 5 more

Colony phenotype switching in clinical and non-clinical isolates of Saccharomyces cerevisiae.

Journal of medical and veterinary mycology : bi-monthly publication of the International Society for Human and Animal Mycology | 2000-01-01 | PMID 8873885

Clemons K V, Hanson L C, Stevens D A

Comparison of different electrophoretic methods for digital typing of the MS32 (D1S8) locus.

Electrophoresis | 1996-08-01 | PMID 8874052

Rodriguez-Calvo M S, Bellas S, Soto J L and 2 more

Rapid detection of sequence polymorphisms in the human mitochondrial DNA control region by polymerase chain reaction and single-strand conformation analysis in mutation detection enhancement gels.

Electrophoresis | 1996-08-01 | PMID 8874053

Alonso A, Martin P, Albarran C and 2 more

Salivary glands, cellular evolution, and adaptive radiation in mammals.

European journal of morphology | 1996-08-01 | PMID 8874089

Phillips C J, Tandler B

Minimal region of loss at 13q14 in B-cell chronic lymphocytic leukemia.

Blood | 1996-10-15 | PMID 8874210

Bullrich F, Veronese M L, Kitada S and 4 more

Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemia.

Blood | 1996-10-15 | PMID 8874222

Manabe J, Arya R, Sumimoto H and 4 more

Interphase cytogenetic analysis of serous ovarian tumors of low malignant potential: comparison with serous cystadenomas and invasive serous carcinomas.

Laboratory investigation; a journal of technical methods and pathology | 1996-10-01 | PMID 8874380

Diebold J, Deisenhofer I, Baretton G B and 6 more

Genes: MYC

In vitro production and transplantation of immunologically active skin equivalents.

Laboratory investigation; a journal of technical methods and pathology | 1996-10-01 | PMID 8874382

Rouabhia M

p53 mutations in Hodgkin's disease.

Laboratory investigation; a journal of technical methods and pathology | 1996-10-01 | PMID 8874383

Chen W G, Chen Y Y, Kamel O W and 2 more

Genes: MDM2

Molecular epidemiology of deletions and mutations of the latent membrane protein 1 oncogene of the Epstein-Barr virus in posttransplant lymphoproliferative disorders.

Laboratory investigation; a journal of technical methods and pathology | 1996-10-01 | PMID 8874388

Smir B N, Hauke R J, Bierman P J and 4 more

Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease).

Muscle & nerve | 1996-11-01 | PMID 8874401

Kobayashi H, Garcia C A, Tay P N and 1 more

Molecular characterization of the segment 2 gene of epizootic hemorrhagic disease virus serotype 2: gene sequence and genetic diversity.

Virology | 1996-10-15 | PMID 8874517

Cheney I W, Yamakawa M, Roy P and 2 more

Independent evolution of the env and pol genes of HIV-1 during zidovudine therapy.

AIDS (London, England) | 1996-09-01 | PMID 8874622

Brown A J, Cleland A

Identification of multiple HIV-1 cytotoxic T-cell epitopes presented by human leukocyte antigen B35 molecules.

AIDS (London, England) | 1996-09-01 | PMID 8874623

Shiga H, Shioda T, Tomiyama H and 8 more

Phenotypic alterations of neuropeptide Y, vasoactive intestinal peptide and choline acetyltransferase in rat cultured chromaffin cells as effected by nerve growth factor and glucocorticoid.

Archives of histology and cytology | 1996-08-01 | PMID 8874753

Morimoto M, Morita N, Ichikawa T and 1 more

Genes: NGF, VIP, NPY

Genotypes and alkaloid contents of Datura metel varieties.

Biological & pharmaceutical bulletin | 1996-08-01 | PMID 8874823

Hiraoka N, Tashimo K, Kinoshita C and 1 more

Effect of CYP2C polymorphisms on the pharmacokinetics of phenytoin in Japanese patients with epilepsy.

Biological & pharmaceutical bulletin | 1996-08-01 | PMID 8874828

Hashimoto Y, Otsuki Y, Odani A and 4 more

Dopamine D2 receptor (DRD2) gene and susceptibility to posttraumatic stress disorder: a study and replication.

Biological psychiatry | 1996-09-01 | PMID 8874837

Comings D E, Muhleman D, Gysin R

Genes: DRD2

Elevated serum Lp(a) concentration and the rare apo(a) phenotype in a patient with myocardial infarction.

Clinical cardiology | 1996-09-01 | PMID 8874999

Hibino T, Sakuma N, Hashimoto T and 4 more

Cytometry of cyclin proteins.

Cytometry | 1996-09-01 | PMID 8875049

Darzynkiewicz Z, Gong J, Juan G and 2 more

Genes: CDK4

Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish population.

European journal of human genetics : EJHG | 1996-01-01 | PMID 8875184

Monrós E, Cañizares J, Moltó M D and 10 more

Relative frequency, heterogeneity and geographic clustering of PKU mutations in Norway.

European journal of human genetics : EJHG | 1996-01-01 | PMID 8875186

Eiken H G, Knappskog P M, Boman H and 4 more

Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX.

European journal of human genetics : EJHG | 1996-01-01 | PMID 8875187

Korvatska E, Munier F L, Zografos L and 6 more

Genes: LOX, SPARC

Fabry disease: fourteen alpha-galactosidase A mutations in unrelated families from the United Kingdom and other European countries.

European journal of human genetics : EJHG | 1996-01-01 | PMID 8875188

Davies J P, Eng C M, Hill J A and 4 more

The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2.

European journal of human genetics : EJHG | 1996-01-01 | PMID 8875189

Peelen T, Cornelis R S, van Vliet M and 7 more

Genes: BRCA1, BRCA2

Biomarker expression in prostatic intraepithelial neoplasia.

European urology | 1996-01-01 | PMID 8875196

Myers R B, Grizzle W E

Genes: PCNA

Molecular events in the early phases of prostate carcinogenesis.

European urology | 1996-01-01 | PMID 8875197

Magi-Galluzzi C, Loda M

Role of the basal cells in premalignant changes of the human prostate: a stem cell concept for the development of prostate cancer.

European urology | 1996-01-01 | PMID 8875201

Bonkhoff H

A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction.

Gene therapy | 1996-09-01 | PMID 8875228

Dorin J R, Farley R, Webb S and 6 more

Genes: CFTR

Genomic instability in 1p and human malignancies.

Genes, chromosomes & cancer | 1996-08-01 | PMID 8875235

Schwab M, Praml C, Amler L C

Role of genomic instability in meningioma progression.

Genes, chromosomes & cancer | 1996-08-01 | PMID 8875241

Simon M, Kokkino A J, Warnick R E and 3 more

Down syndrome genetics: unravelling a multifactorial disorder.

Human molecular genetics | 1996-01-01 | PMID 8875245

Hernandez D, Fisher E M

The presenilin genes: a new gene family involved in Alzheimer disease pathology.

Human molecular genetics | 1996-01-01 | PMID 8875251

Cruts M, Hendriks L, Van Broeckhoven C

Molecular genetics of Bloom's syndrome.

Human molecular genetics | 1996-01-01 | PMID 8875252

Ellis N A, German J

Genes: BLM, FES

Mismatch repair defects in human carcinogenesis.

Human molecular genetics | 1996-01-01 | PMID 8875255

Eshleman J R, Markowitz S D

Recent advances in understanding of genetic susceptibility to breast cancer.

Human molecular genetics | 1996-01-01 | PMID 8875258

Stratton M R

Genes: BRCA2, BRCA1

Phylogenetic tree-building.

International journal for parasitology | 1996-06-01 | PMID 8875305

Morrison D A

Mapping the adhesive domains of the myelin Po protein.

Journal of neuroscience research | 1996-09-01 | PMID 8875317

Zhang K, Merazga Y, Filbin M T

Prion protein genotype and pathological phenotype studies in sporadic Creutzfeldt-Jakob disease.

Neuropathology and applied neurobiology | 1996-08-01 | PMID 8875462

MacDonald S T, Sutherland K, Ironside J W

Plastic phenotype of human oligodendroglial tumour cells in vitro.

Neuropathology and applied neurobiology | 1996-08-01 | PMID 8875464

Tenenbaum L, Teugels E, Dogusan Z and 2 more

Genes: GFAP

Association of hepatitis C virus and hepatocellular carcinoma in the United States.

Princess Takamatsu symposia | 1995-01-01 | PMID 8875608

Reid A E, Liang T J

Genetic heterogeneity of the hepatitis C virus.

Princess Takamatsu symposia | 1995-01-01 | PMID 8875612

Bukh J, Miller R H, Purcell R H

Structure and selection of hepatitis B virus variants during the natural course of infection and interferon therapy.

Princess Takamatsu symposia | 1995-01-01 | PMID 8875626

Günther S, Miska S, Meisel H and 1 more

Cytotoxic T lymphocyte responses in hepatitis C virus infection.

Princess Takamatsu symposia | 1995-01-01 | PMID 8875627

Imawari M, Kita H, Moriyama T and 2 more

Association of cytotoxic T lymphocyte (CTL) escape mutations with persistent hepatitis C virus (HCV) infection.

Princess Takamatsu symposia | 1995-01-01 | PMID 8875628

Weiner A J, Erickson A L, Kansopon J and 4 more

Multivariate analysis of HLA loci in conjunction with a thyrotropin receptor codon 52 polymorphism in conferring risk of Graves' disease.

Thyroid : official journal of the American Thyroid Association | 1996-08-01 | PMID 8875744

Cuddihy R M, Schaid D S, Bahn R S

Is there a negative TRE in the luciferase reporter cDNA?

Thyroid : official journal of the American Thyroid Association | 1996-08-01 | PMID 8875755

Maia A L, Harney J W, Larsen P R

Biological markers for the clinical diagnosis of Alzheimer's disease.

The Tohoku journal of experimental medicine | 1996-06-01 | PMID 8875763

Arai H

The mitochondrial DNA molecule of Sumatran orangutan and a molecular proposal for two (Bornean and Sumatran) species of orangutan.

Journal of molecular evolution | 1996-11-01 | PMID 8875856

Xu X, Arnason U

The complete mitochondrial DNA (mtDNA) of the donkey and mtDNA comparisons among four closely related mammalian species-pairs.

Journal of molecular evolution | 1996-11-01 | PMID 8875857

Xu X, Gullberg A, Arnason U

A new mouse mutation causing male sterility and histoincompatibility.

Mammalian genome : official journal of the International Mammalian Genome Society | 1996-11-01 | PMID 8875885

Ward-Bailey P F, Johnson K R, Handel M A and 2 more

Genes: CAST

Pigs with the dominant white coat color phenotype carry a duplication of the KIT gene encoding the mast/stem cell growth factor receptor.

Mammalian genome : official journal of the International Mammalian Genome Society | 1996-11-01 | PMID 8875890

Johansson Moller M, Chaudhary R, Hellmén E and 3 more

Genes: KIT, ALB, PDGFRA

Isolation of Ewingella americana from the cultivated mushroom, Agaricus bisporus.

Current microbiology | 1996-11-01 | PMID 8875916

Inglis P W, Peberdy J F

Structure of the p53 tumor suppressor bound to the ankyrin and SH3 domains of 53BP2.

Science (New York, N.Y.) | 1996-11-08 | PMID 8875926

Gorina S, Pavletich N P

CKI1, a histidine kinase homolog implicated in cytokinin signal transduction.

Science (New York, N.Y.) | 1996-11-08 | PMID 8875940

Kakimoto T

Mutations in the ligand-binding domain of the kit receptor: an uncommon site in human piebaldism.

The Journal of investigative dermatology | 1996-11-01 | PMID 8875953

Fleischman R A, Gallardo T, Mi X

Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex.

The Journal of investigative dermatology | 1996-11-01 | PMID 8875963

Jonkman M F, Heeres K, Pas H H and 8 more

Genes: KRT14

Effects of ectopic overexpression of p21(WAF1/CIP1) on aneuploidy and the malignant phenotype of human brain tumor cells.

Oncogene | 1996-10-03 | PMID 8875977

Chen J, Willingham T, Shuford M and 4 more

Genes: CDK2

BRCA1 germline mutational spectrum in Italian families from Tuscany: a high frequency of novel mutations.

Oncogene | 1996-10-03 | PMID 8875986

Caligo M A, Ghimenti C, Cipollini G and 9 more

Genes: BRCA1

Electric-field-induced Schiff-base deprotonation in D85N mutant bacteriorhodopsin.

Proceedings of the National Academy of Sciences of the United States of America | 1996-10-15 | PMID 8876185

Kolodner P, Lukashev E P, Ching Y C and 1 more

Microtubules mediate mitochondrial distribution in fission yeast.

Proceedings of the National Academy of Sciences of the United States of America | 1996-10-15 | PMID 8876193

Yaffe M P, Harata D, Verde F and 3 more

Cell cycling and patterned cell proliferation in the Drosophila wing during metamorphosis.

Proceedings of the National Academy of Sciences of the United States of America | 1996-10-15 | PMID 8876197

Milán M, Campuzano S, García-Bellido A

Common endocrine and genetic mechanisms of behavioral development in male and worker honey bees and the evolution of division of labor.

Proceedings of the National Academy of Sciences of the United States of America | 1996-10-15 | PMID 8876203

Giray T, Robinson G E

Molecular clock or erratic evolution? A tale of two genes.

Proceedings of the National Academy of Sciences of the United States of America | 1996-10-15 | PMID 8876205

Ayala F J, Barrio E, Kwiatowski J