Trichinella species and intraspecific varieties.
Wiadomosci parazytologiczne | 1992-01-01 | PMID 1299067
Britov V A
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 9607 of 10600
Neuro-oncogenesis. A review.
Romanian journal of neurology and psychiatry = Revue roumaine de neurologie et psychiatrie | 2000-01-01 | PMID 1299306
Dănăilă L
A correlation of the outcome of clinical in vitro fertilization with the inositol content and embryotrophic properties of human serum
1992-12-01 | PMID 1299385
Interleukin‐8 receptor‐mediated chemotaxis of normal human epidermal cells
1992-07-06 | PMID 1299623
[The significance of tumor heterogeneity in metastasis].
Voprosy onkologii | 1992-01-01 | PMID 1300732
Lobanov S L
Neurofibromin, a predominantly neuronal GTPase activating protein in the adult, is ubiquitously expressed during development
1992-11-01 | PMID 1301085
Towards the molecular localisation of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome
1992-01-01 | PMID 1301132
Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.
Human molecular genetics | 1992-04-01 | PMID 1301136
Zhang Z P, Falk G, Blombäck M and 2 more
Dinucleotide repeat polymorphism at the human c-myc oncogene locus (MYC).
Human molecular genetics | 1992-04-01 | PMID 1301140
Polymeropoulos M H, Xiao H, Merril C R
Genes: MYC
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
1992-01-01 | PMID 1301144
Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient.
Human molecular genetics | 1992-11-01 | PMID 1301174
Winnard A V, Jia-Hsu Y, Gibbs R A and 2 more
Genes: DMD
A polymorphic synonymous mutation (K54K) in the human 70 kD peroxisomal membrane protein gene (PMP1).
Human molecular genetics | 1992-11-01 | PMID 1301179
Gärtner J, Obie C, Moser H and 1 more
Identification of a missense mutation (S436R) in the acid sphingomyelinase gene from a Japanese patient with type B Niemann-Pick disease.
Human mutation | 1992-01-01 | PMID 1301192
Takahashi T, Desnick R J, Takada G and 1 more
Five mutations at the PAH locus account for almost 90% of PKU mutations in French-Canadians from eastern Quebec.
Human mutation | 1992-01-01 | PMID 1301193
John S W, Rozen R, Laframboise R and 2 more
Genes: PAH
The unstable and methylatable mutations causing the fragile X syndrome.
Human mutation | 1992-01-01 | PMID 1301206
Rousseau F, Heitz D, Mandel J L
[Genetic approaches to the study of meningococci].
Zhurnal mikrobiologii, epidemiologii i immunobiologii | 1992-01-01 | PMID 1301667
Kukhtevich E V
[Mid-face malignant T-cell lymphoma (old malignant granuloma). A series of 4 cases with immunophenotyping and genotype study].
Annales de dermatologie et de venereologie | 1992-01-01 | PMID 1301709
Wechsler J, Bagot M, Bosq J and 4 more
[Subcutaneous anaplastic Kil+ large cell lymphoma with clinical aspect of panniculitis].
Annales de dermatologie et de venereologie | 1992-01-01 | PMID 1301713
Grange F, Avril M F, Duvillard P and 4 more
Rejection of the "flying primate" hypothesis by phylogenetic evidence from the epsilon-globin gene.
Science (New York, N.Y.) | 1992-04-03 | PMID 1301735
Bailey W J, Slightom J L, Goodman M
Genetics in speech disorders.
Clinics in communication disorders | 1992-01-01 | PMID 1301905
Lewis B
Identification of genetic influences.
Clinics in communication disorders | 1992-01-01 | PMID 1301907
Smith S D
A novel beta-thalassemia mutation (G-->A) at the initiation codon of the beta-globin gene.
Human mutation | 1992-01-01 | PMID 1301952
Saba L, Meloni A, Sardu R and 4 more
Gaucher disease: four rare alleles encoding F213I, P289L, T323I, and R463C in type 1 variants.
Human mutation | 1992-01-01 | PMID 1301953
He G S, Grace M E, Grabowski G A
Rapid generation of region specific probes by chromosome microdissection and their application
1992-04-01 | PMID 1301994
Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene
1992-04-01 | PMID 1302000
Aberrant splicing of the CHM gene is a significant cause of choroideremia
1992-05-01 | PMID 1302003
Characterization of the myotonic dystrophy region predicts multiple protein isoform–encoding mRNAs
1992-07-01 | PMID 1302022
Kallmann syndrome due to a translocation resulting in an X/Y fusion gene
1992-08-01 | PMID 1302031
Adenovirus–mediated in vivo gene transfer and expression in normal rat liver
1992-08-01 | PMID 1302034
Pharmacogenetics of alcohol metabolism and alcoholism
1992-04-01 | PMID 1302043
[Genetics and cancer].
Gaceta medica de Mexico | 2000-01-01 | PMID 1302207
Carnevale A, Salamanca-Gómez F, Lisker R and 1 more
Perinatal Mortality and Prevalence of Major Congenital Malformations of Twins in Taipei City
1992-07-01 | PMID 1302430
Twins and genetic studies of man.
Acta geneticae medicae et gemellologiae | 1992-01-01 | PMID 1302432
Inouye E
A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients.
Human molecular genetics | 1992-12-01 | PMID 1302613
Zhang Z P, Falk G, Blombäck M and 2 more
Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family.
Human molecular genetics | 1992-12-01 | PMID 1302614
Farrar G J, Findlay J B, Kumar-Singh R and 4 more
Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA)
1992-12-01 | PMID 1302622
A novel mutation in the p53 gene in a Burkitt's lymphoma cell line.
Human molecular genetics | 1992-06-01 | PMID 1303181
Bhatia K, Gutierrez M I, Magrath I T
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutation.
Human molecular genetics | 1992-06-01 | PMID 1303182
Ahluwalia A, Corcoran C M, Vulliamy T J and 6 more
Standards for reporting alleles at highly polymorphic loci: a proposal.
Human molecular genetics | 1992-06-01 | PMID 1303183
Spurr N K
Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci.
Human molecular genetics | 1992-06-01 | PMID 1303184
Browne D, Barker D, Litt M
Microsatellite polymorphisms at the D11S554 and D11S569 loci.
Human molecular genetics | 1992-06-01 | PMID 1303185
Phromchotikul T, Browne D, Litt M
Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S43 locus.
Human molecular genetics | 1992-06-01 | PMID 1303186
Tagle D A, Blanchard-McQuate K L, Collins F S
The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat.
Human molecular genetics | 1992-06-01 | PMID 1303187
Wilcox E R, Rivolta M N, Ploplis B and 2 more
Genes: PAX3
Dinucleotide repeat polymorphism at the DXS178 locus.
Human molecular genetics | 1992-06-01 | PMID 1303188
Allen R C, Belmont J W
An Alu variable polyA repeat polymorphism upstream of L-myc at 1p32.
Human molecular genetics | 1992-06-01 | PMID 1303189
Mäkelä T P, Hellsten E, Vesa J and 2 more
A further tetranucleotide repeat polymorphism in the vWF gene.
Human molecular genetics | 1992-07-01 | PMID 1303199
Kimpton C, Walton A, Gill P
Dinucleotide repeat polymorphism at the human erythroid alpha-spectrin (SPTA1) mRNA gene detected using PCR.
Human molecular genetics | 1992-07-01 | PMID 1303200
Bodfish P, Warne D, Nyberg K and 1 more
Genes: SPTA1
Dinucleotide repeat polymorphism at the D18S37 locus.
Human molecular genetics | 1992-07-01 | PMID 1303201
Sharma V, Guo Z, Litt M
Dinucleotide repeat polymorphism at the D21S236 locus.
Human molecular genetics | 1992-07-01 | PMID 1303202
Sharma V, de Jong P, Yokobata K and 1 more
Dinucleotide repeat polymorphism at the D3S1229 locus.
Human molecular genetics | 1992-07-01 | PMID 1303203
Xiao H, Merril C R, Polymeropoulos M H
Dinucleotide repeat polymorphism at the D5S356 locus.
Human molecular genetics | 1992-07-01 | PMID 1303204
Polymeropoulos M H, Xiao H, Merril C R
Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells
1992-01-01 | PMID 1303206
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions.
Human molecular genetics | 1992-08-01 | PMID 1303213
Saad F A, Vitiello L, Merlini L and 3 more
Improving the polymorphism content of the 3' UTR of the human IGF2R gene.
Human molecular genetics | 1992-08-01 | PMID 1303214
Hol F A, Geurds M P, Hamel B C and 1 more
Dinucleotide repeat polymorphism at the D4S251 locus.
Human molecular genetics | 1992-08-01 | PMID 1303215
Petrukhin K E, Modyanov N N, Gilliam T C
Dinucleotide repeat polymorphism at the D21S65 locus.
Human molecular genetics | 1992-08-01 | PMID 1303216
Goto J, Tassone F, Demczuk S and 4 more
Additional polymorphism at a CHR 9 reference locus (D9S12).
Human molecular genetics | 1992-08-01 | PMID 1303217
Yuille M A, Goudie D R, Affara N A and 1 more
Dinucleotide repeat polymorphism at the human gene for the brain-derived neurotrophic factor (BDNF).
Human molecular genetics | 1992-08-01 | PMID 1303218
Pröschel M, Saunders A, Roses A D and 1 more
Genes: BDNF
Dinucleotide repeat polymorphism in the human estrogen receptor (ESR) gene.
Human molecular genetics | 1992-08-01 | PMID 1303219
del Senno L, Aguiari G L, Piva R
Clinical conundrums in fragile X syndrome.
Nature genetics | 1992-06-01 | PMID 1303227
Hagerman R
The peripheral myelin gene PMP–22/GAS–3 is duplicated in Charcot–Marie–Tooth disease type 1A
1992-06-01 | PMID 1303229
The peripheral myelin protein gene PMP–22 is contained within the Charcot–Marie–Tooth disease type 1A duplication
1992-06-01 | PMID 1303230
Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy
1992-06-01 | PMID 1303233
Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
1992-06-01 | PMID 1303234
A Null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa
1992-06-01 | PMID 1303237
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene
1992-06-01 | PMID 1303239
Molecular evolution of the human interleukin–8 receptor gene cluster
1992-09-01 | PMID 1303245
Genetic dissection of autoimmune type I diabetes in the BB rat
1992-09-01 | PMID 1303251
Physical linkage of two mammalian imprinted genes, H19 and insulin–like growth factor 2
1992-09-01 | PMID 1303252
A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome
1992-10-01 | PMID 1303262
Norrie disease is caused by mutations in an extracellular protein resembling C–terminal globular domain of mucins
1992-10-01 | PMID 1303264
More missense in amyloid gene
1992-12-01 | PMID 1303275
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader–Willi syndrome region
1992-12-01 | PMID 1303276
Structure of the X–linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome
1992-12-01 | PMID 1303284
Mapping of a gene predisposing to early–onset Alzheimer's disease to chromosome 14q24.3
1992-12-01 | PMID 1303290
A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene
1992-12-01 | PMID 1303291
Relevance of haptoglobin in clinical medicine.
Folia histochemica et cytobiologica | 1992-01-01 | PMID 1303900
Dobryszycka W
[Genetic basis of early aging].
Archives francaises de pediatrie | 1992-12-01 | PMID 1304162
Piussan C
Polymerase chain reaction.
The National medical journal of India | 2000-01-01 | PMID 1304285
Ramesh R, Munshi A, Panda S K
Oncogenes and tumor suppressor genes--two different looks of the same gene?
Roumanian archives of microbiology and immunology | 2000-01-01 | PMID 1304831
Călin G
Dextromethorphan O-demethylation in a large number of French Caucasian families.
Pharmacogenetics | 1992-06-01 | PMID 1306113
Vincent-Viry M, Fournier B, Siest G and 1 more
Flow cytometry in the clinical laboratory. Principles, applications and problems.
Annales de biologie clinique | 1992-01-01 | PMID 1306962
Ruiz-Arguelles A
Mutation in codon 713 of the β amyloid precursor protein gene presenting with schizophrenia
1992-07-01 | PMID 1307241
Mismatch PCR: a rapid method to screen for the Pro207-->Leu mutation in the lipoprotein lipase (LPL) gene.
Human molecular genetics | 1992-10-01 | PMID 1307255
Bijvoet S M, Hayden M R
Genes: LPL
Kenny–Caffey syndrome in two sibs born to consanguineous parents: Evidence for an autosomal recessive variant
1992-01-01 | PMID 1308349
9qh+ variant band in two families.
American journal of medical genetics | 1992-01-01 | PMID 1308354
Roland B, Chernos J E, Cox D M
Head circumference of children with Down syndrome (0–36 months)
1992-01-01 | PMID 1308367
Pentalogy of Cantrell and associated midline anomalies: A possible ventral midline developmental field
1992-01-01 | PMID 1308371
[Gene amplification for the diagnosis of HIV infection].
Revue roumaine de virologie (Bucharest, Romania : 1990) | 2000-01-01 | PMID 1308433
Cernescu C, Ruţă S
Brazilian urease-positive strains of Vibrio parahaemolyticus carry genetic potential to produce the TDH-related hemolysin.
Memorias do Instituto Oswaldo Cruz | 2000-01-01 | PMID 1308550
Magalhães M, Takeda Y, Magalhães V and 1 more
Mutations in the insulin receptor and their effect on glucose transport.
Transactions of the Association of American Physicians | 1992-01-01 | PMID 1308998
Longo N, Langley S D, Griffin L D and 1 more
The molecular basis of glucocorticoid-remediable aldosteronism, a Mendelian cause of human hypertension.
Transactions of the Association of American Physicians | 1992-01-01 | PMID 1309006
Lifton R P, Dluhy R G, Powers M and 2 more
Possibilities of DNA analysis for the detection of predisposition to thrombotic disease.
Annals of the New York Academy of Sciences | 1992-12-04 | PMID 1309054
Thomas A E, Green F R, Dawson S J and 7 more
Structural organization, expression, and functional characterization of the murine cytomegalovirus immediate-early gene 3
1992-01-01 | PMID 1309246
EBNA1 can link the enhancer element to the initiator element of the Epstein-Barr virus plasmid origin of DNA replication
1992-01-01 | PMID 1309258
Genes homologous to ubiquitin-conjugating proteins and eukaryotic transcription factor SII in African swine fever virus
1992-01-01 | PMID 1309282
The use of selective mutagenesis to study the pathogenesis of gram-positive bacterial diseases.
The Journal of laboratory and clinical medicine | 1992-01-01 | PMID 1309377
Proctor R A
Simultaneous herpes simplex types 1 and 2 keratitis in acquired immunodeficiency syndrome.
American journal of ophthalmology | 1992-01-15 | PMID 1309408
Rosenwasser G O, Greene W H
Importance of primer selection for the detection of hepatitis C virus RNA with the polymerase chain reaction assay.
1992-01-01 | PMID 1309604
Ongoing enterovirus-induced myocarditis is associated with persistent heart muscle infection: quantitative analysis of virus replication, tissue damage, and inflammation.
1992-01-01 | PMID 1309611