Codon 972 polymorphism of the insulin receptor substrate-1 gene in impaired glucose tolerance and late-onset NIDDM.
Diabetes care | 1998-05-01 | PMID 9589236
Yamada K, Yuan X, Ishiyama S and 6 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 985 of 10600
Evaluation of the insertion/deletion ACE gene polymorphism as a risk factor for carotid artery intima-media thickening and hypertension in young type 1 diabetic patients.
Diabetes care | 1998-05-01 | PMID 9589251
Frost D, Pfohl M, Clemens P and 2 more
Genes: ACE
Variants of the fatty acid-binding protein 2 gene are not associated with coronary heart disease in nondiabetic subjects and in patients with NIDDM.
Diabetes care | 1998-05-01 | PMID 9589253
Saarinen L, Pulkkinen A, Kareinen A and 3 more
Genes: FABP2
Absence of association between genetic variation of the beta 3-adrenergic receptor and metabolic phenotypes in Oji-Cree.
Diabetes care | 1998-05-01 | PMID 9589254
Hegele R A, Harris S B, Hanley A J and 3 more
Genes: ADRB3
Genetic alterations in mouse lung tumors: implications for cancer chemoprevention.
Journal of cellular biochemistry. Supplement | 1997-01-01 | PMID 9589349
Herzog C R, Lubet R A, You M
Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis.
Journal of nephrology | 2000-01-01 | PMID 9589375
Bettinelli A, Vezzoli G, Colussi G and 3 more
p53 protein expression in non-Hodgkin's lymphomas is infrequently related to p53 gene mutations.
Pathology international | 1998-01-01 | PMID 9589459
Oka T, Sarker A B, Teramoto N and 2 more
Transforming growth factor beta type II receptor (TGF beta RII) mutation in gastric lymphoma without mutator phenotype.
Pathology international | 1998-02-01 | PMID 9589477
Yasumi K, Guo R J, Hanai H and 6 more
Genes: GCA
Sequence analysis of MHC class I alpha 2 domain exon variants in one diploid and two haploid Atlantic salmon pedigrees.
Animal genetics | 1997-12-01 | PMID 9589580
Grimholt U, Olsaker I, Lingaas F and 1 more
New microsatellite markers in chicken optimized for automated fluorescent genotyping.
Animal genetics | 1997-12-01 | PMID 9589584
Crooijmans R P, Dijkhof R J, van der Poel J J and 1 more
A single base transversion in the flanking region of an equine microsatellite locus affects amplification of one allele.
Animal genetics | 1997-12-01 | PMID 9589585
Eggleston-Stott M L, Delvalle A, Dileanis S and 2 more
Some new variants of serum protease inhibitors in Meishan pigs.
Animal genetics | 1997-12-01 | PMID 9589587
Stratil A, Cepica S, Cízová-Schröffelová D and 1 more
Molecular characterization of Chinese G6PD deficiency by using polymerase chain reaction/single strand conformation polymorphism.
The Kaohsiung journal of medical sciences | 1998-04-01 | PMID 9589612
Chen B H, Lin S R, Chiang C H and 1 more
Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptor.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589634
Grüters A, Schöneberg T, Biebermann H and 4 more
Genes: TSHR
Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589637
Sunthornthepvarakul T, Likitmaskul S, Ngowngarmratana S and 4 more
Assessment of Turner's syndrome by molecular analysis of the X chromosome in growth-retarded girls.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589641
Gicquel C, Gaston V, Cabrol S and 1 more
Immortalized human pituitary cells express glycoprotein alpha-subunit and thyrotropin beta (TSH beta).
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589662
Ham J, Webster J, Bond J A and 7 more
Genes: CHP2, TRH
Pronostic and therapeutic consequences of Gs alpha mutations in somatotroph adenomas.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589663
Barlier A, Gunz G, Zamora A J and 5 more
Constitutively active Gs alpha is associated with an increased phosphodiesterase activity in human growth hormone-secreting adenomas.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589667
Lania A, Persani L, Ballaré E and 3 more
A recurrent missense mutation in the KAL gene in patients with X-linked Kallmann's syndrome.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589672
Maya-Nuñez G, Zenteno J C, Ulloa-Aguirre A and 2 more
Genes: GAA
Congenital central hypothyroidism due to a homozygous mutation in the thyrotropin beta-subunit gene follows an autosomal recessive inheritance.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589689
Doeker B M, Pfäffle R W, Pohlenz J and 1 more
Genes: PRL, TRH
Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: are athyreosis and ectopic thyroid distinct entities?
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589691
Gagné N, Parma J, Deal C and 2 more
Comparative genomic hybridization analysis of nonfunctioning pituitary tumors.
The Journal of clinical endocrinology and metabolism | 1998-05-01 | PMID 9589696
Daniely M, Aviram A, Adams E F and 5 more
Genes: MEN1
[Alpha-helix retention in prion proteins].
Genetika | 1998-02-01 | PMID 9589849
Kuznetsov I B, Morozov P S, Matushkin Iu G
[New phenotypic manifestation of the ad2 mutation in Saccharomyces cerevisiae yeast--the inability to grow on a synthetic medium with glycerol and hypoxanthine].
Genetika | 1998-02-01 | PMID 9589850
Zekhnov A M, Andreĭchuk Iu V, Domkin V D
[Identification of polygenes in the system achaete-scute in Drosophila melanogaster using cluster analysis].
Genetika | 1998-02-01 | PMID 9589853
Furman D P, Matushkin Iu G, Morozov P S
[Genetics of ketosis resistance in cattle].
Genetika | 1998-02-01 | PMID 9589856
Kochnev N N, Ernst L K, Petukhov V L and 3 more
[Analysis of polymorphism of the angiotensin gene in patients with ischemic heart disease and in a random sample from the Moscow population].
Genetika | 1998-02-01 | PMID 9589857
Shadrina M I, Slominskiĭ P A, Zhidko N I and 2 more
[Allelic polymorphism and analysis of haplotypes of the muscle protein kinase genes and haplotype analysis in residents of northwestern Russia and patients with myotonic dystrophy].
Genetika | 1998-02-01 | PMID 9589858
Malysheva O V, Ivashchenko T E, Vasil'eva T N and 2 more
Genes: DMPK
[Molecular analysis of a double hyperunstable system y(2ns)sc(me)].
Genetika | 1998-03-01 | PMID 9589862
Gracheva E M, Gauze M G, Mogila V A and 1 more
[Role of the lawc(p1) mutation in the regulation of the white locus expression in Drosophila].
Genetika | 1998-03-01 | PMID 9589863
Simonova O B, Petruk S F, Dzhagaeva I V and 1 more
[Ethanol inhibits recombination in somatic cells of gamma-irradiated larvae of Drosophila melanogaster].
Genetika | 1998-03-01 | PMID 9589864
Zakharenko L P, Zakharov I K
[Cloning of the gene leg-arista-wing complex and analysis of its mutant derivatives in Drosophila].
Genetika | 1998-03-01 | PMID 9589872
Petruk S F, Jagaeva I V, Soldatov A V and 1 more
Genomic imprinting and carcinogenesis.
Histology and histopathology | 1998-04-01 | PMID 9589901
Yun K
Genes: IGF2
Interactions between Epstein-Barr virus and the cell cycle control machinery.
Histology and histopathology | 1998-04-01 | PMID 9589903
Sinclair A J, Fenton M, Delikat S
Thymic anti-tumor effectors in mice cured of lymphoma by cyclophosphamide plus TNF-alpha therapy: phenotypic and functional characterization up to 20 months after initial tumor inoculation.
International journal of cancer | 1998-05-18 | PMID 9590137
Ehrke M J, Verstovsek S, Pocchiari S K and 6 more
Genes: TNF
Factors affecting the rate of iron mobilization during venesection therapy for genetic hemochromatosis.
American journal of hematology | 1998-05-01 | PMID 9590143
Adams P C
Two distinct truncated variants of ankyrin associated with hereditary spherocytosis.
American journal of hematology | 1998-05-01 | PMID 9590147
Hayette S, Carré G, Bozon M and 9 more
Genes: CGA
Expressions of p53 and PCNA do not correlate with the international index or early response to chemotherapy in non-Hodgkin's lymphoma.
American journal of hematology | 1998-05-01 | PMID 9590148
Sakai A, Oda K, Asaoku H and 4 more
Genes: PCNA
Juvenile myelomonocytic leukemia (JMML) with the hematologic phenotype of severe beta thalassemia.
American journal of hematology | 1998-05-01 | PMID 9590152
Honig G R, Suarez C R, Vida L N and 2 more
Hemophilia B in a female carrier due to skewed inactivation of the normal X-chromosome.
American journal of hematology | 1998-05-01 | PMID 9590153
Chan V, Chan V W, Yip B and 2 more
Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis.
Cell | 1998-05-01 | PMID 9590170
Chua P R, Roeder G S
Jak2 is essential for signaling through a variety of cytokine receptors.
Cell | 1998-05-01 | PMID 9590173
Parganas E, Wang D, Stravopodis D and 9 more
Jak2 deficiency defines an essential developmental checkpoint in definitive hematopoiesis.
Cell | 1998-05-01 | PMID 9590174
Neubauer H, Cumano A, Müller M and 3 more
Genes: LIF
Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression.
Cell | 1998-05-01 | PMID 9590178
Nachtigal M W, Hirokawa Y, Enyeart-VanHouten D L and 3 more
Odorant receptor localization to olfactory cilia is mediated by ODR-4, a novel membrane-associated protein.
Cell | 1998-05-01 | PMID 9590179
Dwyer N D, Troemel E R, Sengupta P and 1 more
ACE gene polymorphism in childhood IgA nephropathy: association with clinicopathologic findings.
American journal of kidney diseases : the official journal of the National Kidney Foundation | 1998-05-01 | PMID 9590186
Tanaka R, Iijima K, Murakami R and 3 more
Genes: ACE
Affinity maturation in Lyn kinase-deficient mice with defective germinal center formation.
Journal of immunology (Baltimore, Md. : 1950) | 1998-05-15 | PMID 9590225
Kato J, Motoyama N, Taniuchi I and 4 more
HLA-E surface expression depends on binding of TAP-dependent peptides derived from certain HLA class I signal sequences.
Journal of immunology (Baltimore, Md. : 1950) | 1998-05-15 | PMID 9590243
Lee N, Goodlett D R, Ishitani A and 2 more
A mouse model for Prader-Willi syndrome imprinting-centre mutations.
Nature genetics | 1998-05-01 | PMID 9590284
Yang T, Adamson T E, Resnick J L and 6 more
Genes: SNRPN
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
Nature genetics | 1998-05-01 | PMID 9590285
Heiss N S, Knight S W, Vulliamy T J and 5 more
Genes: DKC1
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome.
Nature genetics | 1998-05-01 | PMID 9590287
Dreyer S D, Zhou G, Baldini A and 5 more
Genes: NPS
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
Nature genetics | 1998-05-01 | PMID 9590290
Verhoeven K, Van Laer L, Kirschhofer K and 17 more
Genes: TECTA
SMN oligomerization defect correlates with spinal muscular atrophy severity.
Nature genetics | 1998-05-01 | PMID 9590291
Lorson C L, Strasswimmer J, Yao J M and 6 more
Genes: SMN1
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome).
Nature genetics | 1998-05-01 | PMID 9590292
Belin V, Cusin V, Viot G and 7 more
Genes: SHOX
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis.
Nature genetics | 1998-05-01 | PMID 9590293
Shears D J, Vassal H J, Goodman F R and 5 more
Genes: SHOX
PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis.
Nature genetics | 1998-05-01 | PMID 9590296
Macchia P E, Lapi P, Krude H and 11 more
Genes: PAX8, TSHR
Correction of disease-causing CBS mutations in yeast.
Nature genetics | 1998-05-01 | PMID 9590298
Shan X, Kruger W D
Genes: CBS
Mutations in the integrin alpha7 gene cause congenital myopathy.
Nature genetics | 1998-05-01 | PMID 9590299
Hayashi Y K, Chou F L, Engvall E and 14 more
Genes: ITGA7
Association of the INS VNTR with size at birth. ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood.
Nature genetics | 1998-05-01 | PMID 9590300
Dunger D B, Ong K K, Huxtable S J and 8 more
Genes: INS
Rapid capillary zone electrophoresis in isoelectric histidine buffer: high resolution of the poly-T tract allelic variants in intron 8 of the CFTR gene.
Clinical chemistry | 1998-05-01 | PMID 9590360
Gelfi C, Perego M, Righetti P G and 4 more
Genes: CFTR
Ultrarapid drug metabolism: PCR-based detection of CYP2D6 gene duplication.
Clinical chemistry | 1998-05-01 | PMID 9590361
Steijns L S, Van Der Weide J
A homogeneous fluorescence assay for PCR amplicons: its application to real-time, single-tube genotyping.
Clinical chemistry | 1998-05-01 | PMID 9590362
Whitcombe D, Brownie J, Gillard H L and 4 more
Biological variations and genetic reference values for apolipoprotein E serum concentrations: results from the STANISLAS cohort study.
Clinical chemistry | 1998-05-01 | PMID 9590368
Vincent-Viry M, Schiele F, Gueguen R and 3 more
Flow cytometry with a monoclonal antibody to the low density lipoprotein receptor compared with gene mutation detection in diagnosis of heterozygous familial hypercholesterolemia.
Clinical chemistry | 1998-05-01 | PMID 9590369
Raungaard B, Heath F, Brorholt-Petersen J U and 2 more
Coding sequence and exon/intron organization of the canine CLN3 (Batten disease) gene and its exclusion as the locus for ceroid-lipofuscinosis in English setter dogs.
Journal of neuroscience research | 1998-05-01 | PMID 9590435
Shibuya H, Liu P C, Katz M L and 3 more
Genes: CLN3
Simulated microgravity conditions enhance differentiation of cultured PC12 cells towards the neuroendocrine phenotype.
In vitro cellular & developmental biology. Animal | 1998-04-01 | PMID 9590505
Lelkes P I, Galvan D L, Hayman G T and 5 more
Genes: PNMT
Cytological compartmentalization in the staggerer cerebellum, as revealed by calbindin immunohistochemistry for Purkinje cells.
The Journal of comparative neurology | 1998-05-25 | PMID 9590549
Nakagawa S, Watanabe M, Isobe T and 2 more
Cosegregation of the Tnfalpha locus with cardiovascular phenotypes in the F2 generation of a New Zealand genetically hypertensive and Brown Norway cross.
Clinical and experimental pharmacology & physiology | 2000-01-01 | PMID 9590569
Harris E L, Grigor M R, Thompson C M
Enhanced macrophage uptake of lipoprotein(a) after Ca2+-induced aggregate-formation.
Lipids | 1998-04-01 | PMID 9590626
Tanaka S, Yashiro A, Tasaki H and 1 more
Recombinant gene products of two natural variants of the human cytidine deaminase gene confer different deamination rates of cytarabine in vitro.
Experimental hematology | 1998-05-01 | PMID 9590659
Kirch H C, Schröder J, Hoppe H and 3 more
Salmonella typhi uses CFTR to enter intestinal epithelial cells.
Nature | 1998-05-07 | PMID 9590693
Pier G B, Grout M, Zaidi T and 6 more
Genes: CFTR
[DNA-diagnosis of bulbospinal muscular atrophy (Kennedy's disease)].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova | 1997-01-01 | PMID 9591063
Malygina N A, Kazakov A E, Dubchak L V
High-throughput screening for known mutations by automated analysis of single sequencing reactions.
BioTechniques | 1998-05-01 | PMID 9591134
Kristensen T, Kristensen V N, Børresen-Dale A L
Effect of early vs. late administration of 4-hydroxyphenylretinamide (4-HPR) on N-methyl-N-nitrosourea (MNU)-induced mammary tumorigenesis.
Journal of cellular biochemistry. Supplement | 1997-01-01 | PMID 9591198
Crist K A, Wang Y, Lubet R A and 3 more
Genes: HPR, PCNA
Effects of soy protein isolate (SPI) and casein on the postprandial lipemia in normolipidemic men.
Journal of nutritional science and vitaminology | 1998-02-01 | PMID 9591239
Shige H, Ishikawa T, Higashi K and 10 more
Prevalence of factor V Leiden in African-Americans.
Research communications in molecular pathology and pharmacology | 1998-03-01 | PMID 9591328
Mack R, Samaan P, Podolak I and 1 more
Genes: APC
[The cytological characteristics of the cells of the multilayer squamous epithelium of the cervix uteri in relation to the association of the pathological processes with the human papilloma virus].
TSitologiia i genetika | 2000-01-01 | PMID 9591341
Isakova L M, Ganina K P, Ivanova I M and 1 more
[Interlocus associations and their variability in cattle].
TSitologiia i genetika | 2000-01-01 | PMID 9591347
Oblap R V, Zhuravel' E V, Glazko G V
[An approach to genetic monitoring via a genetic registry].
TSitologiia i genetika | 2000-01-01 | PMID 9591349
Baryliak I R, Bohatyr'ova R V, Buzhiievs'ka T I and 2 more
A sedimentation equilibrium study of platypus insulin: the HB10D mutant does not associate beyond dimer.
Biophysical chemistry | 1998-03-30 | PMID 9591358
Nourse A, Jeffrey P D
Advance in the Rh blood group system.
Nihon hoigaku zasshi = The Japanese journal of legal medicine | 1998-02-01 | PMID 9591398
Kajii E
Genes: RHCE, RHD
Subtyping of D11S488 STR alleles by single-strand conformation polymorphism (SSCP) analysis in two cases of disputed parentage.
Nihon hoigaku zasshi = The Japanese journal of legal medicine | 1998-02-01 | PMID 9591402
Fukuda M, Tamaki Y
Genes: FGA
Mutation frequency of cystic fibrosis transmembrane regulator is not increased in oligozoospermic male candidates for intracytoplasmic sperm injection.
Fertility and sterility | 1998-05-01 | PMID 9591500
Tuerlings J H, Mol B, Kremer J A and 6 more
Genes: CFTR
Malignant transformation of recurrent respiratory papillomatosis associated with integrated human papillomavirus type 11 DNA and mutation of p53.
The Laryngoscope | 1998-05-01 | PMID 9591556
Rady P L, Schnadig V J, Weiss R L and 2 more
Identification of a 910-kb region of common allelic loss in chromosome bands 16q24.1-q24.2 in human lung cancer.
Genes, chromosomes & cancer | 1998-05-01 | PMID 9591628
Sato M, Mori Y, Sakurada A and 7 more
Cervical intraepithelial neoplasia III shows frequent allelic loss in 3p and 6p.
Genes, chromosomes & cancer | 1998-05-01 | PMID 9591635
Rader J S, Gerhard D S, O'Sullivan M J and 4 more
Mechanism of cyclin D1 (CCND1, PRAD1) overexpression in human cancer cells: analysis of allele-specific expression.
Genes, chromosomes & cancer | 1998-05-01 | PMID 9591636
Hosokawa Y, Arnold A
Genes: CCND1
Atomic force microscopy of crystalline insulins: the influence of sequence variation on crystallization and interfacial structure.
Biophysical journal | 1998-05-01 | PMID 9591647
Yip C M, Brader M L, DeFelippis M R and 1 more
Using 2-step PCR and restriction endonuclease digestion to detect K-ras mutation in paraffin-embedded tissues: is it reliable?
Journal of clinical laboratory analysis | 1998-01-01 | PMID 9591704
Su W C, Chow N H, Huang C H and 1 more
The conjoint trait of low high-density lipoprotein cholesterol and high triglycerides in adolescent black and white males.
Metabolism: clinical and experimental | 1998-05-01 | PMID 9591740
Morrison J A, Barton B A, Biro F M and 1 more
Genes: DBP
Lack of interaction of apolipoprotein E phenotype with the lipoprotein response to lovastatin or gemfibrozil in patients with primary hypercholesterolemia.
Metabolism: clinical and experimental | 1998-05-01 | PMID 9591747
Sanllehy C, Casals E, Rodriguez-Villar C and 4 more
Serum paraoxonase activity and its relationship to diabetic complications in patients with non-insulin-dependent diabetes mellitus.
Metabolism: clinical and experimental | 1998-05-01 | PMID 9591753
Ikeda Y, Suehiro T, Inoue M and 6 more
The Trp64Arg mutation of the beta3-adrenergic receptor is associated with hyperglycemia and current body mass index in Jamaican women.
Metabolism: clinical and experimental | 1998-05-01 | PMID 9591756
McFarlane-Anderson N, Bennett F, Wilks R and 4 more
Angiotensin-1-converting enzyme (ACE) gene polymorphism, plasma ACE levels, and their association with the metabolic syndrome and electrocardiographic coronary artery disease in Pima Indians.
Metabolism: clinical and experimental | 1998-05-01 | PMID 9591757
Nagi D K, Foy C A, Mohamed-Ali V and 3 more
Genes: ACE, CAD, DBP
Expression of the adenocarcinoma-related antigen recognized by monoclonal antibody 44-3A6 in salivary gland neoplasias.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery | 1998-05-01 | PMID 9591857
Bentz B G, Haines G K, vonSchlegell A S and 3 more
Heat shock protein and p53 expression in head and neck squamous cell carcinoma.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery | 1998-05-01 | PMID 9591858
Gandour-Edwards R, Trock B J, Gumerlock P and 1 more
Angiotensin-converting enzyme gene polymorphism in systemic hypertension.
The American journal of cardiology | 1998-01-15 | PMID 9591915
Abbud Z A, Wilson A C, Cosgrove N M and 1 more
Genes: ACE
Influence of donor and recipient genotypes on CYP2D6 phenotype after liver transplantation: a study of mutations CYP2D6*3 and CYP2D6*4.
European journal of clinical pharmacology | 1998-03-01 | PMID 9591930
Monek O, Paintaud G, Bechtel Y and 3 more
The HLA phenotype in slipped capital femoral epiphysis.
Journal of pediatric orthopedics | 2000-01-01 | PMID 9592005
Günal I, Ateş E