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 1077 of 10600

Beta3-adrenergic receptor gene polymorphism is not associated with hypertension in NIDDM patients without nephropathy.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme | 1998-10-01 | PMID 9851671
Baba T, Nakajima S, Yajima Y
MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase.
European journal of biochemistry | 1998-11-15 | PMID 9851701
Bröker S, Meunier B, Rich P and 2 more
Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects.
The Journal of laboratory and clinical medicine | 1998-12-01 | PMID 9851733
Dilley A, Austin H, Hooper W C and 5 more
Additive effects of the mutations in the beta3-adrenergic receptor and uncoupling protein-1 genes on weight loss and weight maintenance in Finnish women.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851758
Fogelholm M, Valve R, Kukkonen-Harjula K and 4 more
Azoospermia associated with a mutation in the ligand-binding domain of an androgen receptor displaying normal ligand binding, but defective trans-activation.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851768
Wang Q, Ghadessy F J, Trounson A and 4 more
Mutation of the RET proto-oncogene is correlated with RET immunostaining in subpopulations of cells in sporadic medullary thyroid carcinoma.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851769
Eng C, Thomas G A, Neuberg D S and 7 more
Genes: RET
The frequency of an inactivating point mutation (566C-->T) of the human follicle-stimulating hormone receptor gene in four populations using allele-specific hybridization and time-resolved fluorometry.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851774
Jiang M, Aittomäki K, Nilsson C and 8 more
Genes: FSHR
Activating mutations of the Gs alpha gene are associated with low levels of Gs alpha protein in growth hormone-secreting tumors.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851782
Ballaré E, Mantovani S, Lania A and 3 more
The codon 213 of the 11beta-hydroxysteroid dehydrogenase type 2 gene is a hot spot for mutations in apparent mineralocorticoid excess.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851783
Rogoff D, Smolenicka Z, Bergadá I and 4 more
Molecular genotyping in Brazilian patients with the classical and nonclassical forms of 21-hydroxylase deficiency.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851787
Bachega T A, Billerbeck A E, Madureira G and 5 more
Evidences for an allelic variant of the human LC/CG receptor rather than a gene duplication: functional comparison of wild-type and variant receptors.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851790
Rodien P, Cetani F, Costagliola S and 5 more
Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptor.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851797
Wojcik J, Berg M A, Esposito N and 7 more
Genes: GHR
The Ala/Val98 polymorphism of the hepatocyte nuclear factor-1alpha gene contributes to the interindividual variation in serum C-peptide response during an oral glucose tolerance test: evidence from studies of 231 glucose-tolerant first degree relatives of type 2 diabetic probands.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851800
Urhammer S A, Hansen T, Ekstrøm C T and 2 more
Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: identification of several genetic variants.
The Journal of clinical endocrinology and metabolism | 1998-12-01 | PMID 9851804
Rosenkranz K, Hinney A, Ziegler A and 7 more
The effect of number of days in culture and plasminogen activator inhibitor-1 (PAI-1) 4G/5G genotype on PAI-1 antigen release by cultured human umbilical vein endothelial cells.
Thrombosis research | 1998-12-01 | PMID 9851810
McCormack L J, Semple J I, Stickland M H and 2 more
Association between polymorphisms in the fibrinogen alpha- and beta-genes on the post-trauma fibrinogen increase.
Thrombosis research | 1998-12-01 | PMID 9851811
Ferrer-Antunes C, de Maat M P, Palmeiro A and 2 more
The amn gene product is required in extraembryonic tissues for the generation of middle primitive streak derivatives.
Developmental biology | 1998-12-01 | PMID 9851841
Tomihara-Newberger C, Haub O, Lee H G and 3 more
Tinman function is essential for vertebrate heart development: elimination of cardiac differentiation by dominant inhibitory mutants of the tinman-related genes, XNkx2-3 and XNkx2-5.
Developmental biology | 1998-12-01 | PMID 9851852
Grow M W, Krieg P A
Heat stress-induced life span extension in yeast.
Experimental cell research | 1998-12-15 | PMID 9851879
Shama S, Lai C Y, Antoniazzi J M and 2 more
A human succinate-ubiquinone oxidoreductase CII-3 subunit gene ending in a polymorphic dinucleotide repeat is located within the sulfonylurea receptor (SUR) gene.
Molecular genetics and metabolism | 1998-11-01 | PMID 9851882
Wohllk N, Thomas P M, Huang E and 1 more
At least six different mutations in HEXA gene cause Tay-Sachs disease among the Turkish population.
Molecular genetics and metabolism | 1998-11-01 | PMID 9851891
Ozkara H A, Navon R
Genes: HEXA, INS
A novel complex allele and two new point mutations in type 2 (acute neuronopathic) Gaucher disease.
Blood cells, molecules & diseases | 1998-12-01 | PMID 9851895
Sinclair G, Choy F Y, Humphries L
Hemochromatosis in Ireland and HFE.
Blood cells, molecules & diseases | 1998-12-01 | PMID 9851896
Ryan E, O'keane C, Crowe J
Genes: HFE
Celtic origin of the C282Y mutation of hemochromatosis.
Blood cells, molecules & diseases | 1998-12-01 | PMID 9851897
Lucotte G
Genes: HFE
Neuroendocrine and immune mediators in prostate cancer progression.
Frontiers in bioscience : a journal and virtual library | 1998-12-15 | PMID 9851913
Hoosein N M
Treatment of severe male infertility by micromanipulation-assisted fertilization: news and views.
Frontiers in bioscience : a journal and virtual library | 1998-12-15 | PMID 9851915
Tesarik J, Mendoza C, Greco E
Identification of alpha-dystroglycan as a receptor for lymphocytic choriomeningitis virus and Lassa fever virus.
Science (New York, N.Y.) | 1998-12-11 | PMID 9851928
Cao W, Henry M D, Borrow P and 7 more
The essential Gcd10p-Gcd14p nuclear complex is required for 1-methyladenosine modification and maturation of initiator methionyl-tRNA.
Genes & development | 1998-12-01 | PMID 9851972
Anderson J, Phan L, Cuesta R and 6 more
c-Cbl/Sli-1 regulates endocytic sorting and ubiquitination of the epidermal growth factor receptor.
Genes & development | 1998-12-01 | PMID 9851973
Levkowitz G, Waterman H, Zamir E and 6 more
Genes: EGF
A constitutively active epidermal growth factor receptor cooperates with disruption of G1 cell-cycle arrest pathways to induce glioma-like lesions in mice.
Genes & development | 1998-12-01 | PMID 9851974
Holland E C, Hively W P, DePinho R A and 1 more
Genes: EGFR, GFAP
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.
Genes & development | 1998-12-01 | PMID 9851976
Thorvaldsen J L, Duran K L, Bartolomei M S
Genes: DMD
A novel class of evolutionarily conserved genes defined by piwi are essential for stem cell self-renewal.
Genes & development | 1998-12-01 | PMID 9851978
Cox D N, Chao A, Baker J and 3 more
Genes: GSC
Drosophila Cyclin B3 is required for female fertility and is dispensable for mitosis like Cyclin B.
Genes & development | 1998-12-01 | PMID 9851980
Jacobs H W, Knoblich J A, Lehner C F
Suppression of an Hsp70 mutant phenotype in Saccharomyces cerevisiae through loss of function of the chromatin component Sin1p/Spt2p.
Journal of bacteriology | 1998-12-01 | PMID 9851990
Baxter B K, Craig E A
Complex metabolic phenotypes caused by a mutation in yjgF, encoding a member of the highly conserved YER057c/YjgF family of proteins.
Journal of bacteriology | 1998-12-01 | PMID 9851994
Enos-Berlage J L, Langendorf M J, Downs D M
The two-component regulators GacS and GacA influence accumulation of the stationary-phase sigma factor sigmaS and the stress response in Pseudomonas fluorescens Pf-5.
Journal of bacteriology | 1998-12-01 | PMID 9852008
Whistler C A, Corbell N A, Sarniguet A and 2 more
The first gene of the Bacillus subtilis clpC operon, ctsR, encodes a negative regulator of its own operon and other class III heat shock genes.
Journal of bacteriology | 1998-12-01 | PMID 9852015
Krüger E, Hecker M
A mutant of Mycobacterium smegmatis defective in dipeptide transport.
Journal of bacteriology | 1998-12-01 | PMID 9852030
Bhatt A, Green R, Coles R and 2 more
Identification and characterization of the Erwinia amylovora rpoS gene: RpoS is not involved in induction of fireblight disease symptoms.
Journal of bacteriology | 1998-12-01 | PMID 9852034
Anderson M, Pollitt C E, Roberts I S and 1 more
Affinity purification and partial characterization of a yeast multiprotein complex for nucleotide excision repair using histidine-tagged Rad14 protein.
The Journal of biological chemistry | 1998-12-18 | PMID 9852079
Rodriguez K, Talamantez J, Huang W and 6 more
Interaction of ZPR1 with translation elongation factor-1alpha in proliferating cells.
The Journal of cell biology | 1998-12-14 | PMID 9852145
Gangwani L, Mikrut M, Galcheva-Gargova Z and 1 more
Genes: ZPR1, EGF
Distinct mutants of retrograde intraflagellar transport (IFT) share similar morphological and molecular defects.
The Journal of cell biology | 1998-12-14 | PMID 9852153
Piperno G, Siuda E, Henderson S and 3 more
Role of polo kinase and Mid1p in determining the site of cell division in fission yeast.
The Journal of cell biology | 1998-12-14 | PMID 9852154
Bähler J, Steever A B, Wheatley S and 4 more
Morphogenesis beyond cytokinetic arrest in Saccharomyces cerevisiae.
The Journal of cell biology | 1998-12-14 | PMID 9852155
Jiménez J, Cid V J, Cenamor R and 4 more
Gap junction-mediated cell-cell communication modulates mouse neural crest migration.
The Journal of cell biology | 1998-12-14 | PMID 9852163
Huang G Y, Cooper E S, Waldo K and 3 more
Reduction of platelet phospholipase C-delta1 activity in Alzheimer's disease associated with a specific apolipoprotein E genotype (epsilon3/epsilon3).
International journal of molecular medicine | 1998-01-01 | PMID 9852204
Matsushima H, Shimohama S, Kawamata J and 3 more
Correlation of activated monocytes or B cells with T lymphocyte subsets in patients with Graves' disease.
International journal of molecular medicine | 1998-01-01 | PMID 9852205
González A, Calleja A, Santiago E and 3 more
Interferon-gamma receptor deficiency: relationship between genotype, environment, and phenotype (Review).
International journal of molecular medicine | 1998-02-01 | PMID 9852244
Lamhamedi S, Jouanguy E, Altare F and 2 more
DNA mismatch repair genes and their association with colorectal cancer (Review).
International journal of molecular medicine | 1998-02-01 | PMID 9852252
Whitehouse A, Meredith D M, Markham A F
Determination of p53 protein and high-risk human papillomavirus DNA in carcinomas of the renal pelvis and ureter.
International journal of molecular medicine | 1998-04-01 | PMID 9852285
Kuwahara M, Fujisaki N, Kagawa S and 2 more
CD46 (membrane cofactor protein of complement, measles virus receptor): structural and functional divergence among species (review).
International journal of molecular medicine | 1998-05-01 | PMID 9852300
Seya T, Nomura M, Murakami Y and 3 more
Abnormal cortical development; towards elucidation of the LIS1 gene product function (review).
International journal of molecular medicine | 1998-05-01 | PMID 9852306
Reiner O, Sapir T
Allelic status of 1p, 14q, and 22q and NF2 gene mutations in sporadic schwannomas.
International journal of molecular medicine | 1998-05-01 | PMID 9852312
Leone P E, Bello M J, Mendiola M and 6 more
Genetic and epigenetic alterations of the estrogen receptor gene and hormone independence in human breast cancer.
Oncology | 1998-12-01 | PMID 9852397
Iwase H, Omoto Y, Iwata H and 3 more
Requirement of estrogen receptor expression and function for [12Val] K-Ras-mediated NIH3T3 cell transformation.
Oncology | 1998-12-01 | PMID 9852401
Kato K, Sakamoto T, Wake N
Rapid detection of genetic mutations associated with haemochromatosis.
Vox sanguinis | 1998-01-01 | PMID 9852416
Guttridge M G, Thompson J, Worwood M and 1 more
Genes: HFE
Synaptic physiology and ultrastructure in comatose mutants define an in vivo role for NSF in neurotransmitter release.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1998-12-15 | PMID 9852561
Kawasaki F, Mattiuz A M, Ordway R W
Genes: NSF
NSF function in neurotransmitter release involves rearrangement of the SNARE complex downstream of synaptic vesicle docking.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1998-12-15 | PMID 9852562
Tolar L A, Pallanck L
Genes: NSF, SDS
Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1998-12-15 | PMID 9852570
Morrill J A, Brown R H, Cannon S C
Rhythmic properties of the hamster suprachiasmatic nucleus in vivo.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1998-12-15 | PMID 9852606
Yamazaki S, Kerbeshian M C, Hocker C G and 2 more
p53 and protein kinase C independent induction of growth arrest and apoptosis by bryostatin 1 in a highly metastatic mammary epithelial cell line: In vitro versus in vivo activity.
International journal of molecular medicine | 1998-06-01 | PMID 9852625
Wang H, Mohammad R M, Werdell J and 1 more
A heterozygous frameshift mutation of the PTEN/MMAC1 gene in a patient with Lhermitte-Duclos disease - only the mutated allele was expressed in the cerebellar tumor.
International journal of molecular medicine | 1998-06-01 | PMID 9852626
Iida S, Tanaka Y, Fujii H and 4 more
Genes: PTEN
Mutation analysis of the phenylalanine hydroxylase gene and its clinical implications in two Japanese patients with non-phenylketonuria hyperphenylalaninemia.
Journal of human genetics | 1998-01-01 | PMID 9852673
Kibayashi M, Nagao M, Chiba S
Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysis.
Journal of human genetics | 1998-01-01 | PMID 9852674
Peng C T, Wu J Y, Tsai C H and 2 more
Mitochondrial DNA mutations in Japanese patients with optic neuropathy unassociated with a mutation at nucleotide position 11,778.
Journal of human genetics | 1998-01-01 | PMID 9852675
Matsumoto M, Hayasaka S, Hotta Y and 6 more
Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population.
Journal of human genetics | 1998-01-01 | PMID 9852676
Yamagata H, Nakagawa M, Johnson K and 1 more
A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFA alpha) locus.
Journal of human genetics | 1998-01-01 | PMID 9852684
Tsukamoto K, Ohta N, Shirai Y and 1 more
Genes: TNF
Isolation and radiation hybrid mapping of a dinucleotide repeat polymorphism at the human calcium-sensing receptor (CASR) locus.
Journal of human genetics | 1998-01-01 | PMID 9852685
Tsukamoto K, Watanabe I, Shiba T and 1 more
Genes: CASR
A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5.
Journal of human genetics | 1998-01-01 | PMID 9852686
Miura K, Masuzaki H, Ishimaru T and 2 more
Genes: IGF2
Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locus.
Journal of human genetics | 1998-01-01 | PMID 9852688
Tsukamoto K, Watanabe I, Shiba T and 1 more
Genes: PGR
A highly polymorphic CA repeat marker at the human interleukin 6 receptor (IL6R) locus.
Journal of human genetics | 1998-01-01 | PMID 9852689
Tsukamoto K, Ohta N, Shirai Y and 1 more
Exogenous estrogen may exacerbate thrombophilia, impair bone healing and contribute to development of chronic facial pain.
Cranio : the journal of craniomandibular practice | 1998-07-01 | PMID 9852807
Glueck C J, McMahon R E, Bouquot J E and 1 more
Constitutive and barbital-induced expression of the Cyp6a2 allele of a high producer strain of CYP6A2 in the genetic background of a low producer strain.
Gene | 1998-10-09 | PMID 9852951
Dombrowski S M, Krishnan R, Witte M and 4 more
Germ cell-specific enhancer activity of a repeated element in a variable region of the mouse genome.
Gene | 1998-10-09 | PMID 9852953
Sage J, Martin L, Rassoulzadegan M and 1 more
New alternatively spliced variants of calmodulin-dependent protein kinase II from rabbit liver.
Gene | 1998-10-09 | PMID 9852955
Takeuchi M, Fujisawa H
Isolation of an Arabidopsis thaliana cDNA by complementation of a yeast abc1 deletion mutant deficient in complex III respiratory activity.
Gene | 1998-10-09 | PMID 9852956
Cardazzo B, Hamel P, Sakamoto W and 2 more
Cloning and characterization of Planctomyces limnophilus rpoN: complementation of a Salmonella typhimurium rpoN mutant strain.
Gene | 1998-10-09 | PMID 9852960
Leary B A, Ward-Rainey N, Hoover T R
Deletion-pattern analysis of alpha-particle and X-ray induced mutations at the HPRT locus of V79 Chinese hamster cells.
Mutation research | 1998-11-03 | PMID 9852989
Schmidt P, Kiefer J
In situ detection of frameshift mutations in mouse cells.
Mutation research | 1998-11-03 | PMID 9852990
Cao J, DePrimo S E, Hersh M N and 1 more
Mutation of the uracil DNA glycosylase gene detected in glioblastoma.
Mutation research | 1998-11-03 | PMID 9852992
Moon Y W, Park W S, Vortmeyer A O and 5 more
Genes: UNG
Mitochondrial DNA rearrangements, including partial duplications, occur in young and old rat tissues.
Mutation research | 1998-11-03 | PMID 9852994
Moore C A, Gudikote J, Van Tuyle G C
[Apolipoprotein E and its alleles in healthy subjects and in atherosclerosis].
Annales de biologie clinique | 2000-01-01 | PMID 9853024
Couderc R, Bailleul S
[Is microalbuminuria, an early marker of clinical nephropathy, also a cardiovascular risk factor?].
Annales de biologie clinique | 2000-01-01 | PMID 9853026
Raynaud E, Brun J F, Fédou C and 3 more
[Genes and intra-uterine growth retardation].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1998-01-01 | PMID 9853079
Jeanpierre M
[Phenotype-genotype relations in growth hormone insensitivity].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1998-01-01 | PMID 9853085
Savage M O, Woods K A, Clark A J and 1 more
Genes: SDS, IGFBP3
[Activating mutations of the TSH receptor: a synthesis highlighting certain pediatric aspects].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1998-01-01 | PMID 9853087
Polak M
[Activating mutations of the gonadotrophin receptors].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1998-01-01 | PMID 9853088
Beck-Peccoz P, Persani L, Romoli R and 2 more
[Activating mutations of the parathyroid hormone and parathyroid hormone related peptide].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1998-01-01 | PMID 9853089
David L
Genes: PTH
A preliminary report: frequency of A-T heterozygotes among prostate cancer patients with severe late responses to radiation therapy.
The cancer journal from Scientific American | 2000-01-01 | PMID 9853138
Hall E J, Schiff P B, Hanks G E and 5 more
Genes: ATM
Genetic polymorphisms of the renin-angiotensin system and the outcome of focal segmental glomerulosclerosis in children.
Kidney international | 1998-12-01 | PMID 9853248
Frishberg Y, Becker-Cohen R, Halle D and 10 more
Genes: ACE
Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
Kidney international | 1998-12-01 | PMID 9853249
Igarashi T, Günther W, Sekine T and 9 more
Genes: CLCN5
Platelet-activating factor acetylhydrolase gene mutation in Japanese nephrotic children.
Kidney international | 1998-12-01 | PMID 9853251
Xu H, Iijima K, Shiozawa S and 7 more
AVPR2 variants and V2 vasopressin receptor function in nephrogenic diabetes insipidus.
Kidney international | 1998-12-01 | PMID 9853256
Wildin R S, Cogdell D E, Valadez V
Genes: AVPR2, AVP
Nephroprotection by long-term ACE inhibition with ramipril in spontaneously hypertensive stroke prone rats.
Kidney international | 1998-12-01 | PMID 9853269
Linz W, Becker R H, Schölkens B A and 3 more
Genes: ACE
pH-dependent growth retardation of Escherichia coli caused by overproduction of Na+/H+ antiporter.
Biological & pharmaceutical bulletin | 1998-11-01 | PMID 9853399
Inoue H, Noumi T, Shimomura T and 3 more
Identification of proteins whose amounts are altered by mutation in the pgsA gene of Escherichia coli.
Biological & pharmaceutical bulletin | 1998-11-01 | PMID 9853401
Ohba A, Inoue R, Akimitsu N and 2 more
Preferential involvement of excitatory neurons in medial temporal lobe in schizophrenia.
Lancet (London, England) | 1998-11-21 | PMID 9853440
Harrison P J, Eastwood S L
Genotype phenotype correlation in achondroplasia and hypochondroplasia.
The Journal of bone and joint surgery. British volume | 1998-11-01 | PMID 9853502
Matsui Y, Yasui N, Kimura T and 3 more
Genes: FGFR3
Lipofectamine and related cationic lipids strongly improve adenoviral infection efficiency of primitive human hematopoietic cells.
Human gene therapy | 1998-11-20 | PMID 9853516
Byk T, Haddada H, Vainchenker W and 1 more
Stable and inheritable changes in genotype and phenotype of albino melanocytes induced by an RNA-DNA oligonucleotide.
Nature biotechnology | 1998-12-01 | PMID 9853616
Alexeev V, Yoon K