Specific alterations of U1-C protein or U1 small nuclear RNA can eliminate the requirement of Prp28p, an essential DEAD box splicing factor.
Molecular cell | 2001-01-01 | PMID 11172727
Chen J Y, Stands L, Staley J P and 3 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.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 1479 of 10600
A combinatorial role of angiopoietin-1 and orphan receptor TIE1 pathways in establishing vascular polarity during angiogenesis.
Molecular cell | 2001-01-01 | PMID 11172728
Loughna S, Sato T N
Genes: TIE1
Opposite effects of the Hsp90 inhibitor Geldanamycin: induction of apoptosis in PC12, and differentiation in N2A cells.
FEBS letters | 2001-02-09 | PMID 11172804
López-Maderuelo M D, Fernández-Renart M, Moratilla C and 1 more
The dimerization motif of cytosolic sulfotransferases.
FEBS letters | 2001-02-09 | PMID 11172807
Petrotchenko E V, Pedersen L C, Borchers C H and 2 more
Multiple PIP2 binding sites in Kir2.1 inwardly rectifying potassium channels.
FEBS letters | 2001-02-09 | PMID 11172809
Soom M, Schönherr R, Kubo Y and 3 more
The role of a proline-induced broken-helix motif in alpha-helix 2 of Bacillus thuringiensis delta-endotoxins.
FEBS letters | 2001-02-09 | PMID 11172813
Arnold S, Curtiss A, Dean D H and 1 more
Low seminal plasma folate concentrations are associated with low sperm density and count in male smokers and nonsmokers.
Fertility and sterility | 2001-02-01 | PMID 11172823
Wallock L M, Tamura T, Mayr C A and 3 more
Neuroendocrine, polysomnographic and psychometric observations in healthy subjects at high familial risk for affective disorders: the current state of the 'Munich vulnerability study'.
Journal of affective disorders | 2001-01-01 | PMID 11172871
Krieg J C, Lauer C J, Schreiber W and 2 more
Genes: CRH
Molecular genetic and family studies in affective disorders: state of the art.
Journal of affective disorders | 2001-01-01 | PMID 11172873
Souery D, Rivelli S K, Mendlewicz J
Neurotransmitters and signal transduction processes in bipolar affective disorders: a synopsis.
Journal of affective disorders | 2001-01-01 | PMID 11172877
Ackenheil M
Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator gene.
Cancer genetics and cytogenetics | 2001-01-15 | PMID 11172908
Minelli A, Maserati E, Giudici G and 8 more
Are DNA mismatch repair deficiencies responsible for accumulation of genetic alterations in epithelial ovarian cancers?
Cancer genetics and cytogenetics | 2001-01-15 | PMID 11172909
Suzuki M, Ohwada M, Saga Y and 2 more
Detection and genotyping of GBV-C/HGV variants in China.
Virus research | 2001-03-01 | PMID 11172917
Lu L, Ng M H, Zhou B and 4 more
Nucleotide sequence and deduced amino acid sequence of the medium RNA segment of Oropouche, a Simbu serogroup virus: comparison with the middle RNA of Bunyamwera and California serogroup viruses.
Virus research | 2001-03-01 | PMID 11172919
Wang H, Beasley D W, Li L and 2 more
Highly diverse TTV population in infants and their mothers.
Virus research | 2001-03-01 | PMID 11172922
Sugiyama K, Goto K, Ando T and 3 more
The impact of pharmacogenetics for migraine.
European journal of pharmacology | 2001-02-09 | PMID 11173058
Ophoff R A, van den Maagdenberg A M, Roon K I and 2 more
Pharmacogenomics of neurodegenerative diseases.
European journal of pharmacology | 2001-02-09 | PMID 11173059
Maimone D, Dominici R, Grimaldi L M
The molecular biology of cancer.
Molecular aspects of medicine | 2000-12-01 | PMID 11173079
Bertram J S
Responsiveness to sucrose affects tactile and olfactory learning in preforaging honey bees of two genetic strains.
Behavioural brain research | 2001-04-08 | PMID 11173086
Scheiner R, Page R E, Erber J
Sex and U.
Trends in genetics : TIG | 2001-02-01 | PMID 11173114
Kondrashov A S
Response to Kondrashov.
Trends in genetics : TIG | 2001-02-01 | PMID 11173115
Keightley P D, Eyre-Walker A
Somatic mosaicism and variable expressivity.
Trends in genetics : TIG | 2001-02-01 | PMID 11173116
Gottlieb B, Beitel L K, Trifiro M A
Too much of a good thing: mechanisms of gene action in Down syndrome.
Trends in genetics : TIG | 2001-02-01 | PMID 11173117
Reeves R H, Baxter L L, Richtsmeier J T
HLA complex genes in type 1 diabetes and other autoimmune diseases. Which genes are involved?
Trends in genetics : TIG | 2001-02-01 | PMID 11173119
Undlien D E, Lie B A, Thorsby E
Interaction between potential doubling time and TP53 mutation: predicting radiotherapy outcome in squamous cell carcinoma of the head and neck.
International journal of radiation oncology, biology, physics | 2001-02-01 | PMID 11173149
Alsner J, Høyer M, Sørensen S B and 1 more
Radiation-induced chromatid breaks as a predictor of breast cancer risk.
International journal of radiation oncology, biology, physics | 2001-02-01 | PMID 11173151
Buchholz T A, Wu X
Breast cancer after mantle irradiation for Hodgkin's disease: correlation of clinical, pathologic, and molecular features including loss of heterozygosity at BRCA1 and BRCA2.
International journal of radiation oncology, biology, physics | 2001-02-01 | PMID 11173152
Gaffney D K, Hemmersmeier J, Holden J and 5 more
Genes: BRCA1, BRCA2
A centuries-long epidemic of scrapie in British sheep?
Trends in microbiology | 2001-02-01 | PMID 11173245
Woolhouse M E, Coen P, Matthews L and 5 more
Atomic resolution structure of a mutant of the spectrin SH3 domain.
Acta crystallographica. Section D, Biological crystallography | 2001-02-01 | PMID 11173498
Berisio R, Viguera A, Serrano L and 1 more
Genetic mapping and allelic loss analysis in mouse thymic lymphomas of Helios and Aiolos belonging to the Ikaros gene family.
Japanese journal of cancer research : Gann | 2001-01-01 | PMID 11173542
Xu H, Wakabayashi Y, Okano H and 3 more
p53 protein accumulation and p53 gene mutation in colorectal cancer.
Pathology oncology research : POR | 2000-01-01 | PMID 11173660
Nasierowska-Guttmejer A, Trzeciak L, Nowacki M P and 1 more
Fusion genes in leukemia: an emerging network.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173830
Bohlander S K
Genes: ETV6, RUNX1, BCR, JAK2, PDGFRB
A high frequency of XO offspring from X(Paf)Y* male mice: evidence that the Paf mutation involves an inversion spanning the X PAR boundary.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173831
Burgoyne P S, Evans E P
TSPY variants in six loci on the human Y chromosome.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173833
Dechend F, Williams G, Skawran B and 4 more
A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173836
Dufke A, Eggermann K, Balg S and 3 more
Gonadal development and birth weight in X*X and X*Y females of the wood lemming, Myopus schisticolor.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173838
Fredga K, Setterfield L, Mittwoch U
Comparative genomic aspects of rat, mouse and human MHC class I gene regions.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173841
Günther E, Walter L
Chromosomes of the antelope genus Kobus (Artiodactyla, Bovidae): karyotypic divergence by centric fusion rearrangements.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173844
Kingswood S C, Kumamoto A T, Charter S J and 2 more
Clustering of FGFR2 gene mutations inpatients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses).
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173845
Kress W, Collmann H, Büsse M and 2 more
Genes: FGFR2, FGFR1, FGFR3
An unusual FGFR1 mutation (fibroblast growth factor receptor 1 mutation) in a girl with non-syndromic trigonocephaly.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173846
Kress W, Petersen B, Collmann H and 1 more
Genes: FGFR1
Parent-offspring resemblance of palmar and plantar dermatoglyphic patterns in Down syndrome.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173849
Langenbeck U, Herzberger G, Kümmerle S
Expression of a candidate gene for the gonadoblastoma locus in gonadoblastoma and testicular seminoma.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173850
Lau Y, Chou P, Iezzoni J and 2 more
A distinctive phenotype associated with an interstitial deletion 6q14 contained within a de novo pericentric inversion 6 (p11.2q15).
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173855
Passarge E
Elevated DNA sequence diversity in the genomic region of the phosphatase PPP2R3L gene in the human pseudoautosomal region.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173861
Schiebel K, Meder J, Rump A and 6 more
Discrepancies in cytogenetic results between different tissues in two fetuses with Wolf- Hirschhorn syndrome.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173862
Schinzel A
Susceptibility genes: GSTM1 and GSTM3 as genetic risk factors in bladder cancer.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173863
Schnakenberg E, Breuer R, Werdin R and 2 more
Genes: GSTM3, GSTM1, GSTM5
Mutagen sensitivity of human lymphoblastoid cells with a BRCA1 mutation in comparison to ataxia telangiectasia heterozygote cells.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173867
Speit G, Trenz K, Schütz P and 2 more
Genes: BRCA1
Monozygotic twins of opposite sex.
Cytogenetics and cell genetics | 2000-01-01 | PMID 11173871
Wachtel S S, Somkuti S G, Schinfeld J S
Genes: SRY
Polymorphisms of the apolipoprotein E gene regulatory region and of the LDL receptor gene in late-onset Alzheimer's disease in relation to the plasma lipidic pattern.
Dementia and geriatric cognitive disorders | 2000-01-01 | PMID 11173876
Scacchi R, Gambina G, Martini M C and 5 more
Genes: APOE
APOE genotype: no influence on galantamine treatment efficacy nor on rate of decline in Alzheimer's disease.
Dementia and geriatric cognitive disorders | 2000-01-01 | PMID 11173877
Aerssens J, Raeymaekers P, Lilienfeld S and 3 more
Genes: APOE
Genetic association between Alzheimer disease and the alpha-synuclein gene.
Dementia and geriatric cognitive disorders | 2000-01-01 | PMID 11173882
Matsubara M, Yamagata H, Kamino K and 4 more
Cerebrospinal fluid tau levels increase with age in healthy individuals.
Dementia and geriatric cognitive disorders | 2000-01-01 | PMID 11173885
Blomberg M, Jensen M, Basun H and 2 more
Genes: APOE
Elevated serum total and LDL cholesterol in very old patients with Alzheimer's disease.
Dementia and geriatric cognitive disorders | 2000-01-01 | PMID 11173887
Lesser G, Kandiah K, Libow L S and 6 more
Existence of variant gamma delta T cells in Crohn's disease.
Digestion | 2001-01-01 | PMID 11173910
Ishiguro Y, Kanazawa H, Yamagata K and 2 more
Rumpshaker behaves like juvenile-lethal Plp mutations when combined with shiverer in double mutant mice.
Developmental neuroscience | 2001-01-01 | PMID 11173922
Billings-Gagliardi S, Nunnari J J, Wolf M K
Is intracytoplasmic sperm injection itself an indication to perform preimplantation genetic diagnosis (PGD)? About PGD, invasive prenatal diagnosis and genetic sonography.
Fetal diagnosis and therapy | 2000-01-01 | PMID 11173952
Ludwig M, Geipel A, Berg C and 3 more
Genes: PGD
Does higher concordance in monozygotic twins than in dizygotic twins suggest a genetic component?
Human heredity | 2001-01-01 | PMID 11173963
Guo S W
On estimating the proportion of variance in a phenotypic trait attributable to a measured locus.
Human heredity | 2001-01-01 | PMID 11173965
Wijsman E M, Nur N
Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from chile.
Human heredity | 2001-01-01 | PMID 11173967
Frank J, Aita V M, Ahmad W and 3 more
Absence of association between a variant of the mast cell chymase gene and atopic dermatitis in an Italian population.
Human heredity | 2001-01-01 | PMID 11173969
Pascale E, Tarani L, Meglio P and 5 more
Genes: MCC
P300 event-related potential amplitude as an endophenotype of alcoholism--evidence from the collaborative study on the genetics of alcoholism.
Journal of biomedical science | 2000-01-01 | PMID 11173979
Hesselbrock V, Begleiter H, Porjesz B and 2 more
Genes: DRD2
Nutritional factors in cerebral aging and dementia: epidemiological arguments for a role of oxidative stress.
Neuroepidemiology | 2001-02-01 | PMID 11174040
Deschamps V, Barberger-Gateau P, Peuchant E and 1 more
Evidence for an association between polymorphism in the serotonin-2A receptor variant (102T/C) and increment of N100 amplitude in schizophrenics treated with clozapine.
Neuropsychobiology | 2001-01-01 | PMID 11174050
Yu Y W, Tsai S J, Yang K H and 3 more
Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A-->G mitochondrial mutation.
ORL; journal for oto-rhino-laryngology and its related specialties | 2000-01-01 | PMID 11174059
Tono T, Kiyomizu K, Matsuda K and 4 more
Genetic susceptibility and severity of alopecia areata in human and animal models.
European journal of dermatology : EJD | 2000-01-01 | PMID 11174130
McElwee K, Freyschmidt-Paul P, Ziegler A and 2 more
Expression of vascular endothelial growth factor, basic fibroblast growth factor, and angiogenin immunoreactivity in asthmatic airways and its relationship to angiogenesis.
The Journal of allergy and clinical immunology | 2001-02-01 | PMID 11174196
Hoshino M, Takahashi M, Aoike N
Acquisition and alteration of adhesion molecules during cultured human mast cell differentiation.
The Journal of allergy and clinical immunology | 2001-02-01 | PMID 11174197
Tachimoto H, Hudson S A, Bochner B S
Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy.
American heart journal | 2001-02-01 | PMID 11174330
Lee W, Hwang T H, Kimura A and 6 more
Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome.
Journal of the American Academy of Dermatology | 2001-02-01 | PMID 11174374
Wanner M, Celebi J T, Peacocke M
Genes: PTEN
A novel KIT mutation results in piebaldism with progressive depigmentation.
Journal of the American Academy of Dermatology | 2001-02-01 | PMID 11174389
Richards K A, Fukai K, Oiso N and 1 more
Genes: KIT, MITF
UV-specific p53 and PTCH mutations in sporadic basal cell carcinoma of sun-exposed skin.
Journal of the American Academy of Dermatology | 2001-02-01 | PMID 11174390
Ratner D, Peacocke M, Zhang H and 2 more
ApaI polymorphisms of the vitamin D receptor predict bone density of the lumbar spine and not racial difference in bone density in young men.
The Journal of laboratory and clinical medicine | 2001-02-01 | PMID 11174470
Bell N H, Morrison N A, Nguyen T V and 2 more
Genes: VDR
Polymorphism of TP53 codon 72 and the risk of cervical cancer among Korean women.
American journal of obstetrics and gynecology | 2001-01-01 | PMID 11174479
Kim J W, Roh J W, Park N H and 3 more
Surfactant protein-A gene locus associated with recurrent otitis media.
The Journal of pediatrics | 2001-02-01 | PMID 11174628
Rämet M, Löfgren J, Alho O P and 1 more
Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study.
European journal of endocrinology | 2001-01-01 | PMID 11174835
Nguyen L, Niccoli-Sire P, Caron P and 8 more
Counterregulatory responses to hypoglycemia in patients with maturity-onset diabetes of the young caused by HNF-1alpha gene mutations (MODY3).
European journal of endocrinology | 2001-01-01 | PMID 11174836
Guenat E, Seematter G, Philippe J and 3 more
Aldosterone synthase deficiency type I with no documented homozygous mutations in the CYP11B2 gene.
European journal of endocrinology | 2001-01-01 | PMID 11174838
Wasniewska M, De Luca F, Valenzise M and 2 more
Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia.
European journal of human genetics : EJHG | 2000-12-01 | PMID 11175279
Jonasson J, Juvonen V, Sistonen P and 8 more
Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples.
European journal of human genetics : EJHG | 2000-12-01 | PMID 11175281
Olsson C, Waldenström E, Westermark K and 2 more
mtDNA hypervariable region II (HVII) sequences in human evolution studies.
European journal of human genetics : EJHG | 2000-12-01 | PMID 11175285
Salas A, Lareu V, Calafell F and 2 more
Allelic association is increased by correlation of effective family size.
European journal of human genetics : EJHG | 2000-12-01 | PMID 11175287
Austerlitz F, Heyer E
Genes: EFS
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175293
Matsumoto N, Leventer R J, Kuc J A and 9 more
Genes: DCX
Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175294
Tiecke F, Katzke S, Booms P and 12 more
Genes: FBN1
Haplogroup-specific deviation from the stepwise mutation model at the microsatellite loci DYS388 and DYS392.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175295
Nebel A, Filon D, Hohoff C and 3 more
Y chromosome analysis reveals a sharp genetic boundary in the Carpathian region.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175296
Stefan M, Stefanescu G, Gavrila L and 4 more
Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175297
Irrthum A, Brouillard P, Enjolras O and 6 more
An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175298
Radhakrishna U, Senol S, Herken H and 5 more
Frequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutations.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175299
Witsch-Baumgartner M, Ciara E, Löffler J and 11 more
Genes: DHCR7
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175300
Mansour I, Delague V, Cazeneuve C and 15 more
Genes: MEFV
Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175302
Moilanen J S, Majamaa K
Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Dutch family: evidence for a TNFRSF1A mutation with reduced penetrance.
European journal of human genetics : EJHG | 2001-01-01 | PMID 11175303
Aganna E, Aksentijevich I, Hitman G A and 5 more
Genes: TNF
Comparisons of HIV-1 viral sequences in brain, choroid plexus and spleen: potential role of choroid plexus in the pathogenesis of HIV encephalitis.
Journal of neurovirology | 2000-12-01 | PMID 11175322
Chen H, Wood C, Petito C K
Enhanced tumorigenicity caused by truncation of the extracellular domain of GP125/CD98 heavy chain.
Oncogene | 2000-12-14 | PMID 11175335
Hara K, Kudoh H, Enomoto T and 2 more
Functional evidence for an ovarian cancer tumor suppressor gene on chromosome 22 by microcell-mediated chromosome transfer.
Oncogene | 2000-12-14 | PMID 11175342
Kruzelock R P, Cuevas B D, Wiener J R and 8 more
Identification of novel hypoxia dependent and independent target genes of the von Hippel-Lindau (VHL) tumour suppressor by mRNA differential expression profiling.
Oncogene | 2000-12-14 | PMID 11175344
Wykoff C C, Pugh C W, Maxwell P H and 2 more
Genes: VHL
NO activation of fos promoter elements requires nuclear translocation of G-kinase I and CREB phosphorylation but is independent of MAP kinase activation.
Oncogene | 2000-12-14 | PMID 11175347
Gudi T, Casteel D E, Vinson C and 2 more
Mouse models in the study of the Ets family of transcription factors.
Oncogene | 2000-12-18 | PMID 11175360
Bartel F O, Higuchi T, Spyropoulos D D
Ets factors and regulation of the extracellular matrix.
Oncogene | 2000-12-18 | PMID 11175362
Trojanowska M
[Clinical and nutritional aspects in patients with cystic fibrosis: 20 years of follow-up in the Clinical Hospital-Federal University of Minas Gerais (HC-UFMG)].
Revista da Associacao Medica Brasileira (1992) | 2000-01-01 | PMID 11175567
Reis F J, Oliveira M C, Penna F J and 3 more
Helicobacter pylori genotyping from positive CLOtests in patients with duodenal ulcer.
Revista do Hospital das Clinicas | 2000-01-01 | PMID 11175575
Mattar R, Laudanna A A