Analysis of eight STR loci in two Hungarian populations.
Forensic science international | 2000-09-11 | PMID 10978596
Egyed B, Füredi S, Angyal M and 4 more
Genes: FGA
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 1398 of 10600
Human autosomal short tandem repeat types in Jat Sikhs from North India.
Forensic science international | 2000-09-11 | PMID 10978597
Chattopadhyay P K, Cleef S, Duelmer M and 2 more
Reliability of SE33 typing by capillary electrophoresis.
Forensic science international | 2000-09-11 | PMID 10978598
Rothämel T, Kleemann W J, Tröger H D
Population genetics of ACTBP2 (SE33) in Western Saxony (Germany).
Forensic science international | 2000-09-11 | PMID 10978599
Lessig R, Edelmann J, Akkad Y
Haplotype frequencies and population data of nine Y-chromosomal STR polymorphisms in a German and a Chinese population.
Forensic science international | 2000-09-11 | PMID 10978601
Hidding M, Schmitt C
Distinguishing minisatellite mutation from non-paternity by MVR-PCR.
Forensic science international | 2000-09-11 | PMID 10978602
Tamaki K, Brenner C H, Jeffreys A J
Application of subpopulation theory to evaluation of DNA evidence.
Forensic science international | 2000-09-11 | PMID 10978603
Wolańska-Nowak P
The personal identification of many samples recovered from under the sea.
Forensic science international | 2000-09-11 | PMID 10978605
Mukaida M, Kimura H, Takada Y and 2 more
Genes: ABO
Is it possible to differentiate mtDNA by means of HVIII in samples that cannot be distinguished by sequencing the HVI and HVII regions?
Forensic science international | 2000-09-11 | PMID 10978608
Lutz S, Wittig H, Weisser H J and 8 more
Mitochondrial DNA in the Central European population. Human identification with the help of the forensic mt-DNA D-loop-base database.
Forensic science international | 2000-09-11 | PMID 10978611
Wittig H, Augustin C, Baasner A and 12 more
Association between LDLR polymorphism and diseases in the Japanese population: aging and distribution of the polymorphism.
Forensic science international | 2000-09-11 | PMID 10978614
Hara M, Takada A, Ro A and 2 more
Genes: LDLR
Evaluation of ABO and Lewis genotypes using primer extension preamplification.
Forensic science international | 2000-09-11 | PMID 10978615
Itoh Y, Kobayashi R
Genes: ABO
The conflict of understanding the genetic make-up of man and his knowledge of it.
Forensic science international | 2000-09-11 | PMID 10978664
Taupitz J
Enhanced 2-deoxy-D-ribose-induced-apoptosis, a phenotype of lymphocytes from old donors, is not observed in the Werner syndrome.
Experimental gerontology | 2000-08-01 | PMID 10978682
Battisti C, Formichi P, Tripodi S A and 3 more
Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer.
Hearing research | 2000-10-01 | PMID 10978835
Alagramam K N, Zahorsky-Reeves J, Wright C G and 4 more
Genes: ABR
Applications of recombinant DNA technology in gastrointestinal medicine and hepatology: basic paradigms of molecular cell biology. Part C: protein synthesis and post-translational processing in eukaryotic cells.
Canadian journal of gastroenterology = Journal canadien de gastroenterologie | 2000-01-01 | PMID 10978948
Wild G E, Papalia P, Ropeleski M J and 2 more
[Genetic diversity of mtDNA of domestic camels (C. bactrianus) in China].
Yi chuan xue bao = Acta genetica Sinica | 2000-01-01 | PMID 10979183
Quan J X, Zhang Y P, Han J L and 1 more
[Isolation and cytological identification of a desynaptic variant in rice].
Yi chuan xue bao = Acta genetica Sinica | 2000-01-01 | PMID 10979187
Yu H X, Cheng Z K, Gong Z Y and 1 more
High interleukin-10 production in first-degree relatives of patients with generalized but not cutaneous lupus erythematosus.
Journal of investigative medicine : the official publication of the American Federation for Clinical Research | 2000-09-01 | PMID 10979237
van der Linden M W, Westendorp R G, Sturk A and 2 more
Are fasting plasma homocyst(e)ine levels heritable? A study of normotensive twins.
Journal of investigative medicine : the official publication of the American Federation for Clinical Research | 2000-09-01 | PMID 10979240
Cesari M, Burlina A B, Narkiewicz K and 3 more
Genes: ACE
Genetic risk factors for coronary artery spasm: significance of endothelial nitric oxide synthase gene T-786-->C and missense Glu298Asp variants.
Journal of investigative medicine : the official publication of the American Federation for Clinical Research | 2000-09-01 | PMID 10979242
Yoshimura M, Yasue H, Nakayama M and 12 more
Nesting behavior of house mice (Mus domesticus) selected for increased wheel-running activity.
Behavior genetics | 2000-03-01 | PMID 10979598
Carter P A, Swallow J G, Davis S J and 1 more
Mice lacking PKC gamma exhibit decreased anxiety.
Behavior genetics | 2000-03-01 | PMID 10979601
Bowers B J, Collins A C, Tritto T and 1 more
Differential susceptibility to periodontitis in genetically selected Wistar rat lines that differ in their behavioral and endocrinological response to stressors.
Behavior genetics | 2000-03-01 | PMID 10979602
Breivik T, Sluyter F, Hof M and 1 more
Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinking rat lines.
Behavior genetics | 2000-03-01 | PMID 10979603
Foroud T, Bice P, Castelluccio P and 6 more
Power of selective genotyping in genetic association analyses of quantitative traits.
Behavior genetics | 2000-03-01 | PMID 10979604
Van Gestel S, Houwing-Duistermaat J J, Adolfsson R and 2 more
A note on the statistical power in extended twin designs.
Behavior genetics | 2000-03-01 | PMID 10979605
Posthuma D, Boomsma D I
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic.
Annals of internal medicine | 2000-09-05 | PMID 10979877
Beutler E, Felitti V, Gelbart T and 1 more
Genes: HFE
Diversity and prevalence of PorA types in Neisseria meningitidis serogroup B in the United States, 1992-1998.
The Journal of infectious diseases | 2000-10-01 | PMID 10979914
Sacchi C T, Whitney A M, Popovic T and 7 more
Sulfa or sulfone prophylaxis and geographic region predict mutations in the Pneumocystis carinii dihydropteroate synthase gene.
The Journal of infectious diseases | 2000-10-01 | PMID 10979917
Huang L, Beard C B, Creasman J and 8 more
Genes: DHPS
Differential host susceptibility to pulmonary infections with bacteria and fungi in mice deficient in myeloperoxidase.
The Journal of infectious diseases | 2000-10-01 | PMID 10979934
Aratani Y, Kura F, Watanabe H and 5 more
Genes: MPO
Analysis of the role of AML1-ETO in leukemogenesis, using an inducible transgenic mouse model.
Blood | 2000-09-15 | PMID 10979955
Rhoades K L, Hetherington C J, Harakawa N and 6 more
Protein A is the von Willebrand factor binding protein on Staphylococcus aureus.
Blood | 2000-09-15 | PMID 10979960
Hartleib J, Köhler N, Dickinson R B and 7 more
Reduced oncogenicity of p190 Bcr/Abl F-actin-binding domain mutants.
Blood | 2000-09-15 | PMID 10979970
Heisterkamp N, Voncken J W, Senadheera D and 6 more
Genes: BCR
The incidence of clonal T-cell receptor rearrangements in B-cell precursor acute lymphoblastic leukemia varies with age and genotype.
Blood | 2000-09-15 | PMID 10979974
Brumpt C, Delabesse E, Beldjord K and 8 more
Genes: PBX1, BCR, IGH
Somatostatin modulation of excitatory synaptic transmission between periventricular and arcuate hypothalamic nuclei in vitro.
Journal of neurophysiology | 2000-09-01 | PMID 10980019
Lanneau C, Peineau S, Petit F and 2 more
Genes: ARC, GHRH, GAL, NPY, POMC
Beta-catenin mutations are associated with a subset of low-stage hepatocellular carcinoma negative for hepatitis B virus and with favorable prognosis.
The American journal of pathology | 2000-09-01 | PMID 10980116
Hsu H C, Jeng Y M, Mao T L and 3 more
Mutations and copy number increase of HRAS in Spitz nevi with distinctive histopathological features.
The American journal of pathology | 2000-09-01 | PMID 10980135
Bastian B C, LeBoit P E, Pinkel D
Genes: HRAS
Topographical distributions of allelic loss in individual non-small-cell lung cancers.
The American journal of pathology | 2000-09-01 | PMID 10980137
Yatabe Y, Konishi H, Mitsudomi T and 2 more
Functional loss of ABCA1 in mice causes severe placental malformation, aberrant lipid distribution, and kidney glomerulonephritis as well as high-density lipoprotein cholesterol deficiency.
The American journal of pathology | 2000-09-01 | PMID 10980140
Christiansen-Weber T A, Voland J R, Wu Y and 5 more
Genes: ABCA1
T(-786)--> C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with myocardial infarction, especially without coronary organic stenosis.
The American journal of cardiology | 2000-09-15 | PMID 10980213
Nakayama M, Yasue H, Yoshimura M and 11 more
Common polymorphism in the promoter of the CD14 monocyte receptor gene is associated with acute myocardial infarction in Japanese men.
The American journal of cardiology | 2000-09-15 | PMID 10980225
Shimada K, Watanabe Y, Mokuno H and 3 more
Aggregates of mutant protein appear progressively in dendrites, in periaxonal processes of oligodendrocytes, and in neuronal and astrocytic perikarya of mice expressing the SOD1(G93A) mutation of familial amyotrophic lateral sclerosis.
Journal of the neurological sciences | 2000-08-15 | PMID 10980307
Stieber A, Gonatas J O, Gonatas N K
Genes: SOD1
Progressive muscular atrophy variant of familial amyotrophic lateral sclerosis (PMA/ALS).
Journal of the neurological sciences | 2000-08-15 | PMID 10980308
Cervenakova L, Protas I I, Hirano A and 9 more
Genes: SOD1
Walker-Warburg syndrome is genetically distinct from Fukuyama type congenital muscular dystrophy.
Journal of the neurological sciences | 2000-08-15 | PMID 10980312
Chadani Y, Kondoh T, Kamimura N and 7 more
Immune responses of Nile tilapia (Oreochromis niloticus L.) clones: I. Non-specific responses.
Developmental and comparative immunology | 2001-01-01 | PMID 10980318
Sarder M R, Thompson K D, Penman D J and 1 more
Serotonin transporter gene regulatory region polymorphism (5-HTTLPR), [3H]paroxetine binding in healthy control subjects and alcohol-dependent patients and their relationships to impulsivity.
Psychiatry research | 2000-09-25 | PMID 10980326
Preuss U W, Soyka M, Bahlmann M and 5 more
Genes: HTT
Mapping of the HLA-linked genes controlling the susceptibility to Takayasu's arteritis.
International journal of cardiology | 2000-08-31 | PMID 10980346
Kimura A, Ota M, Katsuyama Y and 5 more
Genes: MICA
Association of HLA-DRB1*1602 and DRB1*1001 with Takayasu arteritis in Colombian mestizos as markers of Amerindian ancestry.
International journal of cardiology | 2000-08-31 | PMID 10980348
Salazar M, Varela A, Ramirez L A and 5 more
DNA sequencing of HLA-B alleles in Mexican patients with Takayasu arteritis.
International journal of cardiology | 2000-08-31 | PMID 10980349
Vargas-Alarcón G, Zúñiga J, Gamboa R and 7 more
Diversity of alleles encoding HLA-B40: relative frequencies in united states populations and description of five novel alleles.
Human immunology | 2000-08-01 | PMID 10980391
Pimtanothai N, Rizzuto G A, Slack R and 7 more
Early age of disease onset in African American type 1 diabetes patients is associated with DQB1*0201 allele.
Human immunology | 2000-08-01 | PMID 10980392
Berka N, Bland G N, Gause D P and 4 more
Relative frequencies of DRB1*11 alleles and their DRB3 associations in five major population groups in a United States bone marrow registry.
Human immunology | 2000-08-01 | PMID 10980393
Tang T F, Huang A Y, Pappas A and 4 more
Increased frequency of HLA class II alleles DRB1*0301 and DQB1*0201 in Lambert-Eaton myasthenic syndrome without associated cancer.
Human immunology | 2000-08-01 | PMID 10980394
Parsons K T, Kwok W W, Gaur L K and 1 more
Participation of stress-inducible systems and enzymes involved in BER and NER in the protection of Escherichia coli against cumene hydroperoxide.
Mutation research | 2000-09-15 | PMID 10980410
Asad L M, Medeiros D C, Felzenszwalb I and 2 more
A new X-ray sensitive CHO cell mutant of ionizing radiation group 7,XR-C2, that is defective in DSB repair but has only a mild defect in V(D)J recombination.
Mutation research | 2000-09-15 | PMID 10980412
Errami A, Overkamp W J, He D M and 7 more
Transcriptional mechanisms of chondrocyte differentiation.
Matrix biology : journal of the International Society for Matrix Biology | 2000-09-01 | PMID 10980415
de Crombrugghe B, Lefebvre V, Behringer R R and 3 more
GSK3, a master switch regulating cell-fate specification and tumorigenesis.
Current opinion in genetics & development | 2000-10-01 | PMID 10980428
Kim L, Kimmel A R
Imprinting: focusing on the center.
Current opinion in genetics & development | 2000-10-01 | PMID 10980434
Ben-Porath I, Cedar H
The Conradi-Hünermann-Happle syndrome is caused by mutations in the gene that encodes a 8- 7 sterol isomerase and is biochemically related to the CHILD syndrome.
European journal of dermatology : EJD | 2000-08-01 | PMID 10980461
Traupe H, Has C
Genes: NSDHL
"Sporadic" dystrophic epidermolysis bullosa: a new dominant or mitis recessive mutation?
European journal of dermatology : EJD | 2000-08-01 | PMID 10980463
Vaccaro M, Moretti G, Guarneri F and 2 more
Oligodendrocyte-type 2 astrocyte-derived trophic factors increase survival of developing dopamine neurons through the inhibition of apoptotic cell death.
The Journal of comparative neurology | 2000-10-09 | PMID 10980489
Sortwell C E, Daley B F, Pitzer M R and 3 more
Activating and inactivating mutations in the human GNAS1 gene.
Human mutation | 2000-09-01 | PMID 10980525
Aldred M A, Trembath R C
Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.
Human mutation | 2000-09-01 | PMID 10980526
Rabionet R, Gasparini P, Estivill X
Genes: GJB2, GJB3, GJB1, GJB6
Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans.
Human mutation | 2000-09-01 | PMID 10980527
Drost J B, Scaringe W A, Jaloma-Cruz A R and 4 more
Mutational analysis of GLUT1 (SLC2A1) in Glut-1 deficiency syndrome.
Human mutation | 2000-09-01 | PMID 10980529
Wang D, Kranz-Eble P, De Vivo D C
Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia.
Human mutation | 2000-09-01 | PMID 10980530
Laake K, Jansen L, Hahnemann J M and 13 more
Genes: ATM
Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extension.
Human mutation | 2000-09-01 | PMID 10980532
Gérard B, Ginet N, Matthijs G and 7 more
Genes: SMN1, SMN2
Mutations in familial porphyria cutanea tarda: two novel and two previously described for hepatoerythropoietic porphyria.
Human mutation | 2000-09-01 | PMID 10980536
Mendez M, Rossetti M V, De Siervi A and 2 more
Novel mutations in the myocilin gene in Japanese glaucoma patients.
Human mutation | 2000-09-01 | PMID 10980537
Kubota R, Mashima Y, Ohtake Y and 12 more
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations.
Human mutation | 2000-09-01 | PMID 10980539
Lira M G, Mottes M, Pignatti P F and 6 more
Genes: ABCD1
MEFV mutations in Behçet's disease.
Human mutation | 2000-09-01 | PMID 10980540
Touitou I, Magne X, Molinari N and 10 more
Genes: MEFV
BRCA1 mutation analysis in breast/ovarian cancer families from Greece.
Human mutation | 2000-09-01 | PMID 10980541
Konstantopoulou I, Kroupis C, Ladopoulou A and 12 more
Genes: BRCA1
Sequence variation within the RPGR gene: evidence for a founder complex allele.
Human mutation | 2000-09-01 | PMID 10980543
Zito I, Morris A, Tyson P and 6 more
Genes: RPGR
Two distinct Alu-mediated deletions of the human ABO-secretor (FUT2) locus in Samoan and Bangladeshi populations.
Human mutation | 2000-09-01 | PMID 10980544
Pang H, Fujitani N, Soejima M and 4 more
Genes: FUT2, ABO, FUT1
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1.
Human mutation | 2000-09-01 | PMID 10980545
Girodon-Boulandet E, Pantel J, Cazeneuve C and 9 more
A -96C-->T mutation in the promoter of the collagen type VII gene (COL7A1) abolishing transcription in a patient affected by recessive dystrophic epidermolysis bullosa.
Human mutation | 2000-09-01 | PMID 10980546
Gardella R, Barlati S, Zoppi N and 2 more
An association study of polymorphisms in the alpha-antichymotrypsin gene for Alzheimer disease in Han-Chinese.
Human mutation | 2000-09-01 | PMID 10980547
Meng G, Yuan J, An L and 5 more
Analysis of CAG and CCG repeats in Huntingtin gene among HD patients and normal populations of India.
European journal of human genetics : EJHG | 2000-09-01 | PMID 10980573
Pramanik S, Basu P, Gangopadhaya P K and 9 more
Structural interpretation of mutations in phenylalanine hydroxylase protein aids in identifying genotype-phenotype correlations in phenylketonuria.
European journal of human genetics : EJHG | 2000-09-01 | PMID 10980574
Jennings I G, Cotton R G, Kobe B
Genes: PAH
Increased frequency of CFTR gene mutations in sarcoidosis: a case/control association study.
European journal of human genetics : EJHG | 2000-09-01 | PMID 10980579
Bombieri C, Luisetti M, Belpinati F and 5 more
Genes: CFTR
A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease.
European journal of human genetics : EJHG | 2000-09-01 | PMID 10980580
Griseri P, Sancandi M, Patrone G and 6 more
Genes: RET
Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene.
European journal of human genetics : EJHG | 2000-09-01 | PMID 10980581
Homberger A, Linnebank M, Winter C and 4 more
Genes: MTHFR
Novel p53 splice site mutations in three families with Li-Fraumeni syndrome.
Oncogene | 2000-08-31 | PMID 10980596
Verselis S J, Rheinwald J G, Fraumeni J F and 1 more
Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line.
Oncogene | 2000-08-31 | PMID 10980605
Ohira M, Kageyama H, Mihara M and 21 more
Genes: PEX14, CORT, MYCN, PGD
Human breast carcinoma desmoplasia is PDGF initiated.
Oncogene | 2000-09-07 | PMID 10980609
Shao Z M, Nguyen M, Barsky S H
UVDDB p127-binding modulates activities and intracellular distribution of hepatitis B virus X protein.
Oncogene | 2000-09-07 | PMID 10980617
Sitterlin D, Bergametti F, Transy C
Correct binding of viral X protein to UVDDB-p127 cellular protein is critical for efficient infection by hepatitis B viruses.
Oncogene | 2000-09-07 | PMID 10980618
Sitterlin D, Bergametti F, Tiollais P and 2 more
The BRCA2 activation domain associates with and is phosphorylated by a cellular protein kinase.
Oncogene | 2000-09-07 | PMID 10980621
Milner J, Fuks F, Hughes-Davies L and 1 more
Genes: BRCA2
BCL-1 rearrangements and p53 mutations in atypical chronic lymphocytic leukemia with t(11;14)(q13;q32).
Haematologica | 2000-09-01 | PMID 10980628
De Angeli C, Gandini D, Cuneo A and 6 more
Inhibition of RhoA by p120 catenin.
Nature cell biology | 2000-09-01 | PMID 10980705
Anastasiadis P Z, Moon S Y, Thoreson M A and 4 more
Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.
Neurology | 2000-09-12 | PMID 10980727
Karadimas C L, Greenstein P, Sue C M and 8 more
The alpha2-macroglobulin gene in AD: a population-based study and meta-analysis.
Neurology | 2000-09-12 | PMID 10980733
Koster M N, Dermaut B, Cruts M and 9 more
Genes: APOE
Intrafamilial variability in hereditary spastic paraplegia associated with an SPG4 gene mutation.
Neurology | 2000-09-12 | PMID 10980739
Santorelli F M, Patrono C, Fortini D and 6 more
IgG Fc-receptor polymorphisms in Guillain-Barré syndrome.
Neurology | 2000-09-12 | PMID 10980740
Vedeler C A, Raknes G, Myhr K M and 1 more
Description of a new mutation in rhodopsin, Pro23Ala, and comparison with electroretinographic and clinical characteristics of the Pro23His mutation.
Archives of ophthalmology (Chicago, Ill. : 1960) | 2000-09-01 | PMID 10980774
Oh K T, Weleber R G, Lotery A and 3 more
Genes: ERG
Gene therapy for restenosis.
Current cardiology reports | 2000-01-01 | PMID 10980867
Smith R C, Walsh K
Molecular genetics of hypertrophic cardiomyopathy.
Current cardiology reports | 2000-03-01 | PMID 10980884
Towbin J A
Natural history of hypertrophic cardiomyopathy.
Current cardiology reports | 2000-03-01 | PMID 10980885
Elliott P M
Genetic abnormalities responsible for dilated cardiomyopathy.
Current cardiology reports | 2000-09-01 | PMID 10980917
Towbin J A, Bowles N E