Identification and genetic analysis of wunen, a gene guiding Drosophila melanogaster germ cell migration.
Genetics | 1996-07-01 | PMID 8807296
Zhang N, Zhang J, Cheng Y and 1 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 747 of 10600
The genetics of reproductive isolation in the Drosophila simulans clade: X vs. autosomal effects and male vs. female effects.
Genetics | 1996-07-01 | PMID 8807297
Hollocher H, Wu C I
The Om (1E) mutation in Drosophila ananassae causes compound eye overgrowth due to tom retrotransposon-driven overexpression of a novel gene.
Genetics | 1996-07-01 | PMID 8807298
Juni N, Awasaki T, Yoshida K and 1 more
A genetic analysis of pannier, a gene necessary for viability of dorsal tissues and bristle positioning in Drosophila.
Genetics | 1996-07-01 | PMID 8807299
Heitzler P, Haenlin M, Ramain P and 2 more
The broom of the sorcerer's apprentice: the fine structure of a chromosomal region causing reproductive isolation between two sibling species of Drosophila.
Genetics | 1996-07-01 | PMID 8807300
Davis A W, Wu C I
Inversion monophyly in African anopheline malaria vectors.
Genetics | 1996-07-01 | PMID 8807303
García B A, Caccone A, Mathiopoulos K D and 1 more
Scalloped wings is the Lucilia cuprina Notch homologue and a candidate for the modifier of fitness and asymmetry of diazinon resistance.
Genetics | 1996-07-01 | PMID 8807304
Davies A G, Game A Y, Chen Z and 5 more
Species-specific segregation of gender-associated mitochondrial DNA types in an area where two mussel species (Mytilus edulis and M. trossulus) hybridize.
Genetics | 1996-07-01 | PMID 8807307
Saavedra C, Stewart D T, Stanwood R R and 1 more
Demographic genetics of brown trout (Salmo trutta) and estimation of effective population size from temporal change of allele frequencies.
Genetics | 1996-07-01 | PMID 8807308
Jorde P E, Ryman N
Mutator-induced mutations of the rf1 nuclear fertility restorer of T-cytoplasm maize alter the accumulation of T-urf13 mitochondrial transcripts.
Genetics | 1996-07-01 | PMID 8807309
Wise R P, Dill C L, Schnable P S
Evolution of anthocyanin biosynthesis in maize kernels: the role of regulatory and enzymatic loci.
Genetics | 1996-07-01 | PMID 8807310
Hanson M A, Gaut B S, Stec A O and 4 more
Realized sampling variances of estimates of genetic parameters and the difference between genetic and phenotypic correlations.
Genetics | 1996-07-01 | PMID 8807311
Koots K R, Gibson J P
The amount of DNA polymorphism maintained in a finite population when the neutral mutation rate varies among sites.
Genetics | 1996-07-01 | PMID 8807315
Tajima F
Comparing mutational variabilities.
Genetics | 1996-07-01 | PMID 8807316
Houle D, Morikawa B, Lynch M
Phenylketonuria in The Netherlands: 93% of the mutations are detected by single-strand conformation analysis.
Human heredity | 2000-01-01 | PMID 8807319
van der Sijs-Bos C J, Diepstraten C M, Juyn J A and 8 more
Genes: PAH
Human enzyme polymorphism in the Canary Islands. VII. G6PD Seattle in Canarians and North African Berbers.
Human heredity | 2000-01-01 | PMID 8807321
Cabrera V M, González P, Salo W L
G6PD NanKang (517 T-->C; 173 Phe-->Leu): a new Chinese G6PD variant associated with neonatal jaundice.
Human heredity | 2000-01-01 | PMID 8807322
Chen H L, Huang M J, Huang C S and 1 more
ABO, Rh and Kell frequency distribution in a sample population of Terni province, Italy.
Human heredity | 2000-01-01 | PMID 8807323
Cassetti M, Palazzesi G, Minestrini D and 2 more
Genes: ABO
Linkage study of Best's vitelliform macular dystrophy (VMD2) in a large North American family.
Human heredity | 2000-01-01 | PMID 8807324
Hou Y C, Richards J E, Bingham E L and 6 more
Genes: ROM1
Association between the p21 codon 31 A1 (arg) allele and lung cancer.
Human heredity | 2000-01-01 | PMID 8807325
Själander A, Birgander R, Rannug A and 3 more
Faster linkage analysis computations for pedigrees with loops or unused alleles.
Human heredity | 2000-01-01 | PMID 8807326
Schäffer A A
T cell receptor beta chain RFLP in Chinese, Indians and Malays from Singapore.
Human heredity | 2000-01-01 | PMID 8807327
Tan J A, Tay J S, Aziz N B and 1 more
Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core.
Human mutation | 1996-01-01 | PMID 8807330
Couch F J, Weber B L
Genes: BRCA1
Single base-pair substitutions in pathology and evolution: two sides to the same coin.
Human mutation | 1996-01-01 | PMID 8807332
Krawczak M, Cooper D N
A sensitive mutation screening strategy for Fabry disease: detection of nine mutations in the alpha-galactosidase A gene.
Human mutation | 1996-01-01 | PMID 8807334
Blanch L C, Meaney C, Morris C P
IDS gene-pseudogene exchange responsible for an intragenic deletion in a Hunter patient.
Human mutation | 1996-01-01 | PMID 8807335
Birot A M, Bouton O, Froissart R and 2 more
Genes: IDS
Neurofibromatosis type I gene mutation in a patient with features of LEOPARD syndrome.
Human mutation | 1996-01-01 | PMID 8807336
Wu R, Legius E, Robberecht W and 3 more
Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto-oncogene mutations.
Human mutation | 1996-01-01 | PMID 8807338
Kambouris M, Jackson C E, Feldman G L
Genes: RET
Characterization of different soluble TNF receptor (TNFR80) derivatives: positive influence of the intracellular domain on receptor/ligand interaction and TNF neutralization capacity.
Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research | 1996-06-01 | PMID 8807502
Moosmayer D, Wajant H, Gerlach E and 3 more
Genes: TNF
Passover eliminates gap junctional communication between neurons of the giant fiber system in Drosophila. off.
Journal of neurobiology | 1996-07-01 | PMID 8807527
Sun Y A, Wyman R J
Relationship between COL4A5 gene mutation and distribution of type IV collagen in male X-linked Alport syndrome. Japanese Alport Network.
Kidney international | 1996-07-01 | PMID 8807602
Naito I, Kawai S, Nomura S and 2 more
Nomenclature for human CYP2D6 alleles.
Pharmacogenetics | 1996-06-01 | PMID 8807658
Daly A K, Brockmöller J, Broly F and 13 more
Human cytochrome P450 2E1 (CYP2E1): from genotype to phenotype.
Pharmacogenetics | 1996-06-01 | PMID 8807659
Carrière V, Berthou F, Baird S and 3 more
A study of the dopamine D2 receptor gene in pathological gambling.
Pharmacogenetics | 1996-06-01 | PMID 8807661
Comings D E, Rosenthal R J, Lesieur H R and 5 more
Genes: DRD2
Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders.
Pharmacogenetics | 1996-06-01 | PMID 8807664
Lachman H M, Papolos D F, Saito T and 3 more
Genes: COMT
Glutathione S-transferase mu as a risk factor in bladder tumours.
Pharmacogenetics | 1996-06-01 | PMID 8807665
Okkels H, Sigsgaard T, Wolf H and 1 more
Genes: GSTM1
Evidence that poor metabolizers of (S)-mephenytoin could be identified by haplotypes of CYP2C19 in Japanese.
Pharmacogenetics | 1996-06-01 | PMID 8807668
Takakubo F, Kuwano A, Kondo I
Predominant p53 mutations in enzootic bovine leukemic cell lines.
Veterinary immunology and immunopathology | 1996-06-15 | PMID 8807776
Komori H, Ishiguro N, Horiuchi M and 2 more
Role of gyrA mutation and loss of OprF in the multiple antibiotic resistance phenotype of Pseudomonas aeruginosa G49.
FEMS microbiology letters | 1996-09-15 | PMID 8807797
Pumbwe L, Everett M J, Hancock R E and 1 more
Deletion of the putative effector region of Era, an essential GTP-binding protein in Escherichia coli, causes a dominant-negative phenotype.
FEMS microbiology letters | 1996-09-15 | PMID 8807801
Pillutla R C, Ahnn J, Inouye M
Cloning and characterization of chsD, a chitin synthase-like gene of Aspergillus fumigatus.
FEMS microbiology letters | 1996-09-15 | PMID 8807804
Mellado E, Specht C A, Robbins P W and 1 more
Comparative methodology to investigate the presence of Escherichia coli K-12 strains in environmental and human stool samples.
FEMS microbiology letters | 1996-09-15 | PMID 8807805
Blum G, Mühldorfer I, Kuhnert P and 2 more
Using evolutionary changes to achieve species-specific inhibition of enzyme action--studies with triosephosphate isomerase.
Chemistry & biology | 1995-12-01 | PMID 8807818
Gómez-Puyou A, Saavedra-Lira E, Becker I and 3 more
Loss of functional prion protein: a role in prion disorders?
Chemistry & biology | 1996-08-01 | PMID 8807894
Borchelt D R, Sisodia S S
Molecular basis for the binding of SH3 ligands with non-peptide elements identified by combinatorial synthesis.
Chemistry & biology | 1996-08-01 | PMID 8807900
Feng S, Kapoor T M, Shirai F and 2 more
Rearrangement/hypermutation/gene conversion: when, where and why?
Immunology today | 1996-02-01 | PMID 8808057
Weill J C, Reynaud C A
Thyroperoxidase microsatellite polymorphism in thyroid diseases.
Thyroid : official journal of the American Thyroid Association | 1995-12-01 | PMID 8808096
Pirro M T, De Filippis V, Di Cerbo A and 3 more
Genes: TPO
Involvement of the brain catecholaminergic system in the regulation of dominant behavior.
Pharmacology, biochemistry, and behavior | 1996-02-01 | PMID 8808133
Serova L I, Naumenko E V
Neonatal MSG reduces hypothalamic DA, beta-endorphin, and delays weight gain in genetically obese (A viable yellow/alpha) mice.
Pharmacology, biochemistry, and behavior | 1996-02-01 | PMID 8808153
Caputo F A, Ali S F, Wolff G L and 1 more
Genes: POMC
Genetic study of gold-salt-induced immune disorders in the rat.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1995-12-01 | PMID 8808209
Kermarrec N, Blanpied C, Pelletier L and 4 more
Genotype distribution and transmission of hepatitis C virus (HCV) in French haemodialysed patients.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1995-12-01 | PMID 8808220
Bouchardeau F, Chauveau P, Courouce A M and 1 more
Analysis of the murine Dtk gene identifies conservation of genomic structure within a new receptor tyrosine kinase subfamily.
Genomics | 1996-01-01 | PMID 8808274
Lewis P M, Crosier K E, Wood C R and 1 more
Relationship between the monosomy X phenotype and Y-linked ribosomal protein S4 (Rps4) in several species of mammals: a molecular evolutionary analysis of Rps4 homologs.
Genomics | 1996-01-01 | PMID 8808278
Omoe K, Endo A
A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197.
Genomics | 1996-01-01 | PMID 8808284
Auburger G, Ratzlaff T, Lunkes A and 9 more
Genes: KCNA1
Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs.
Genomics | 1996-01-01 | PMID 8808290
Kwok P Y, Deng Q, Zakeri H and 2 more
Genes: STS
The gene encoding p120cas, a novel catenin, localizes on human chromosome 11q11 (CTNND) and mouse chromosome 2 (Catns).
Genomics | 1996-01-01 | PMID 8808291
Reynolds A B, Jenkins N A, Gilbert D J and 4 more
Co-expression of fibroblastic, histiocytic and smooth muscle cell phenotypes on cultured adherent cells derived from human palatine tonsils: a morphological and immunocytochemical study.
Pathology international | 1995-12-01 | PMID 8808295
Honma M, Koizumi F, Wakaki K and 1 more
A fluorescent multiplex ARMS method for rapid mutation analysis.
Molecular and cellular probes | 1995-12-01 | PMID 8808316
Zschocke J, Graham C A
Variation in the fusion glycoprotein gene of human respiratory syncytial virus subgroup A.
Virus genes | 1995-01-01 | PMID 8808333
Plows D J, Pringle C R
Dominant negative expression of a cytoplasmically deleted mutant of XB/U-cadherin disturbs mesoderm migration during gastrulation in Xenopus laevis.
Mechanisms of development | 1996-01-01 | PMID 8808407
Kühl M, Finnemann S, Binder O and 1 more
Graded effect of tailless on posterior gut development: molecular basis of an allelic series of a nuclear receptor gene.
Mechanisms of development | 1996-01-01 | PMID 8808411
Diaz R J, Harbecke R, Singer J B and 3 more
Assessment of a mutation in the H5 domain of Girk2 as a candidate for the weaver mutation.
Genome research | 1995-12-01 | PMID 8808466
Mjaatvedt A E, Cabin D E, Cole S E and 3 more
A novel in vivo method to detect DNA sequence variation.
Genome research | 1995-12-01 | PMID 8808468
Faham M, Cox D R
Accurate and absolute quantitative measurement of gene expression by single-tube RT-PCR and HPLC.
Genome research | 1995-12-01 | PMID 8808471
Hayward-Lester A, Oefner P J, Sabatini S and 1 more
Genetic and nongenetic factors for moderate hyperhomocyst(e)inemia.
Atherosclerosis | 1996-01-26 | PMID 8808490
Kang S S, Wong P W
The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia.
Atherosclerosis | 1996-01-26 | PMID 8808493
Hoffer M J, Bredie S J, Boomsma D I and 7 more
Genes: LPL
Women have a larger and less atherogenic low density lipoprotein particle size than men.
Atherosclerosis | 1996-01-26 | PMID 8808495
Nikkilä M, Pitkäjärvi T, Koivula T and 7 more
Triglycerides and HDL-cholesterol as risk factors for ischemic heart disease. Results from the Québec cardiovascular study.
Atherosclerosis | 1996-01-26 | PMID 8808500
Lamarche B, Després J P, Moorjani S and 3 more
DnaSP, DNA sequence polymorphism: an interactive program for estimating population genetics parameters from DNA sequence data.
Computer applications in the biosciences : CABIOS | 1995-12-01 | PMID 8808578
Rozas J, Rozas R
Protein secondary structure prediction by the analysis of variation and conservation in multiple alignments.
Computer applications in the biosciences : CABIOS | 1995-12-01 | PMID 8808579
Tuckwell D S, Humphries M J, Brass A
Using a measure of structural variation to define a core for the globins.
Computer applications in the biosciences : CABIOS | 1995-12-01 | PMID 8808580
Gerstein M, Altman R B
Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.
American journal of human genetics | 1996-10-01 | PMID 8808592
Pérez Jurado L A, Peoples R, Kaplan P and 2 more
Genes: ELN
Premature chain termination is a unifying mechanism for COL1A1 null alleles in osteogenesis imperfecta type I cell strains.
American journal of human genetics | 1996-10-01 | PMID 8808594
Willing M C, Deschenes S P, Slayton R L and 1 more
RNA-based mutation screening in hereditary nonpolyposis colorectal cancer.
American journal of human genetics | 1996-10-01 | PMID 8808596
Kohonen-Corish M, Ross V L, Doe W F and 7 more
Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene.
American journal of human genetics | 1996-10-01 | PMID 8808597
Huang C H, Chen Y, Reid M and 1 more
Genes: RHCE, RHD
A high frequency of distinct ATM gene mutations in ataxia-telangiectasia.
American journal of human genetics | 1996-10-01 | PMID 8808599
Wright J, Teraoka S, Onengut S and 4 more
Genes: ATM
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.
American journal of human genetics | 1996-10-01 | PMID 8808601
Collier D A, Barrett T G, Curtis D and 4 more
Genes: DRD5
Evidence for a major retinitis pigmentosa locus on 19q13.4 (RP11) and association with a unique bimodal expressivity phenotype.
American journal of human genetics | 1996-10-01 | PMID 8808602
Al-Maghtheh M, Vithana E, Tarttelin E and 5 more
Genetic homogeneity of autoimmune polyglandular disease type I.
American journal of human genetics | 1996-10-01 | PMID 8808604
Björses P, Aaltonen J, Vikman A and 16 more
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.
American journal of human genetics | 1996-10-01 | PMID 8808605
Filosa S, Giacometti N, Wangwei C and 6 more
Analysis of meiotic segregation, using single-sperm typing: meiotic drive at the myotonic dystrophy locus.
American journal of human genetics | 1996-10-01 | PMID 8808606
Leeflang E P, McPeek M S, Arnheim N
Search for unstable DNA in schizophrenia families with evidence for genetic anticipation.
American journal of human genetics | 1996-10-01 | PMID 8808607
Petronis A, Bassett A S, Honer W G and 6 more
Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set.
American journal of human genetics | 1996-10-01 | PMID 8808608
Bowen T, Guy C, Speight G and 6 more
Identifying marker typing incompatibilities in linkage analysis.
American journal of human genetics | 1996-10-01 | PMID 8808612
Stringham H M, Boehnke M
Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes.
American journal of human genetics | 1996-10-01 | PMID 8808613
Zhang H, Risch N
Interchromosomal transfer of epigenetic states in Ascobolus: transfer of DNA methylation is mechanistically related to homologous recombination.
Cell | 1996-09-20 | PMID 8808621
Colot V, Maloisel L, Rossignol J L
Autocatalytic subunit processing couples active site formation in the 20S proteasome to completion of assembly.
Cell | 1996-09-20 | PMID 8808631
Chen P, Hochstrasser M
The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults.
Cell | 1996-09-20 | PMID 8808632
Lemaitre B, Nicolas E, Michaut L and 2 more
A novel receptor-mediated nuclear protein import pathway.
Cell | 1996-09-20 | PMID 8808633
Pollard V W, Michael W M, Nakielny S and 3 more
Polymorphism of acute-phase serum amyloid A isoforms and amyloid resistance in wild-type Mus musculus czech.
Clinical immunology and immunopathology | 1996-10-01 | PMID 8808637
Cathcart E S, Carreras I, Elliott-Bryant R and 3 more
The Ig(kappa) enhancer influences the ratio of Ig(kappa) versus Ig(lambda) B lymphocytes.
Immunity | 1996-09-01 | PMID 8808679
Gorman J R, van der Stoep N, Monroe R and 3 more
Cytotoxic T cell-resistant variants are selected in a virus-induced demyelinating disease.
Immunity | 1996-09-01 | PMID 8808680
Pewe L, Wu G F, Barnett E M and 2 more
Beta2 integrins and ICAM-1 are involved in establishment of the intestinal mucosal T cell compartment.
Immunity | 1996-09-01 | PMID 8808681
Huleatt J W, Lefrançois L
Apoptosis in human papillomavirus16 E7-, but not E6-immortalized human uroepithelial cells.
Oncogene | 1996-09-19 | PMID 8808685
Puthenveettil J A, Frederickson S M, Reznikoff C A
Genes: BAX
RB1 oncosuppressor gene over-expression inhibits tumor progression and induces melanogenesis in metastatic melanoma cells.
Oncogene | 1996-09-19 | PMID 8808691
Valente P, Melchiori A, Paggi M G and 6 more
Transcriptional activation potential of normal and tumor-associated myb isoforms does not correlate with their ability to block GCSF-induced terminal differentiation of murine myeloid precursor cells.
Oncogene | 1996-09-19 | PMID 8808694
Patel G, Tantravahi R, Oh I H and 1 more
Novel, activated RAS mutations alter protein-protein interactions.
Oncogene | 1996-09-19 | PMID 8808695
Dalley B K, Cannon J F
Transition of human papillomavirus type 16 and 18 transfected human foreskin keratinocytes towards immortality: activation of telomerase and allele losses at 3p, 10p, 11q and/or 18q.
Oncogene | 1996-09-19 | PMID 8808699
Steenbergen R D, Walboomers J M, Meijer C J and 5 more
The inhibition of cyclin B1 gene transcription in quiescent NIH3T3 cells is mediated by an E-box.
Oncogene | 1996-09-19 | PMID 8808703
Farina A, Gaetano C, Crescenzi M and 4 more
A PAb240+ conformation of wild type p53 binds DNA.
Oncogene | 1996-09-19 | PMID 8808704
McLure K G, Lee P W