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- 2003
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Mark
Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism
(
- Contribution to journal › Article
-
Mark
Phosphorylation of the potyvirus capsid protein by protein kinase CK2 and its relevance for virus infection.
(
- Contribution to journal › Article
-
Mark
Dysfunctionality of a tobacco mosaic virus movement protein mutant mimicking threonine 104 phosphorylation.
(
- Contribution to journal › Article
-
Mark
Prevalence of hemochromatosis gene (HFE) mutations in Greece
(
- Contribution to journal › Article
-
Mark
Functional split and crosslinking of the membrane domain of the beta subunit of proton-translocating transhydrogenase from Escherichia coli
(
- Contribution to journal › Article
-
Mark
The Journal of Gene Medicine 2002 Young Investigator Award. European Society of Gene Therapy
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Temperature-controlled structural alterations of an RNA thermometer
(
- Contribution to journal › Article
- 2002
-
Mark
Uneven distribution of repetitive trinucleotide motifs in human immunoglobulin heavy variable genes
(
- Contribution to journal › Article
-
Mark
Improving the pathogenicity of a nematode-trapping fungus by genetic engineering of a subtilisin with nematotoxic activity.
(
- Contribution to journal › Article
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
A peptide methionine sulfoxide reductase highly expressed in photosynthetic tissue in Arabidopsis thaliana can protect the chaperone-like activity of a chloroplast-localized small heat shock protein.
(
- Contribution to journal › Article
-
Mark
Genetic variability in hepatitis B viruses.
(
- Contribution to journal › Scientific review
-
Mark
An androgen receptor gene mutation (E653K) in a family with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency as well as in partial androgen insensitivity.
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer.
(
- Contribution to journal › Article
-
Mark
Screening for MODY mutations, GAD antibodies, and type 1 diabetes--associated HLA genotypes in women with gestational diabetes mellitus.
(
- Contribution to journal › Article
-
Mark
Hepatitis B virus infection and genomic changes from a long-term perspective
2002)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Characterization of a naturally occurring mutation (L107I) in the HNF1 alpha (MODY3) gene.
(
- Contribution to journal › Article
-
Mark
Clinical and histopathological features of malignant melanoma in germline CDKN2A mutation families
(
- Contribution to journal › Article
-
Mark
TP53 protein expression analysis by luminometric immunoassay in comparison with gene mutation status and prognostic factors in early stage endometrial cancer
(
- Contribution to journal › Article
-
Mark
Malignant Melanoma in southern Sweden; Histopathology, Prognosis and Aetiology
2002)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Improved partitioning in aqueous two-phase system of tyrosine-tagged recombinant lactate dehydrogenase
(
- Contribution to journal › Article
-
Mark
Refractory anemia with ring sideroblasts associated with i(17q) and mutation of the TP53 gene
(
- Contribution to journal › Article
-
Mark
The fundamental prevalence of chronic myeloid leukemia-generating clonogenic cells in the light of the neutrality theory of evolution
(
- Contribution to journal › Article
-
Mark
Predictors of deterioration of lung function in cystic fibrosis.
(
- Contribution to journal › Article
- 2001
-
Mark
Haemophilia B mutations in Sweden: a population-based study of mutational heterogeneity
(
- Contribution to journal › Article
-
Mark
Molecular Genetic Alterations In Endometrial And Ovarian Cancers
2001)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas
(
- Contribution to journal › Article
-
Mark
Assembly of tapasin-associated MHC class I in the absence of the transporter associated with antigen processing (TAP)
(
- Contribution to journal › Article
-
Mark
A hypothesis about tumour development and the clinical features of hereditary breast cancers
(
- Contribution to journal › Article
-
Mark
Recombinant expression of N-terminal truncated mutants of the membrane bound mouse, rat and human flavoenzyme dihydroorotate dehydrogenase. : A versatile tool to rate inhibitor effects?
(
- Contribution to journal › Article
- 2000
-
Mark
Fusidic acid-resistant EF-G perturbs the accumulation of ppGpp
(
- Contribution to journal › Article
-
Mark
Molecular analysis of FRIGIDA, a major determinant of natural variation in Arabidopsis flowering time
(
- Contribution to journal › Article
-
Mark
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
(
- Contribution to journal › Article
-
Mark
Error-prone PCR of Vitreoscilla hemoglobin (VHb) to support the growth of microaerobic Escherichia coli
(
- Contribution to journal › Article
-
Mark
A hypersensitive estrogen receptor-alpha mutation in premalignant breast lesions
(
- Contribution to journal › Article
-
Mark
Absence of cystatin C mutation in sporadic cerebral amyloid angiopathy-related hemorrhage
(
- Contribution to journal › Article
-
Mark
Hereditary cystatin C amyloid angiopathy
2000) In Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 7(1). p.70-79(
- Contribution to journal › Scientific review
-
Mark
Somatic hypermutation in the absence of DNA-dependent protein kinase catalytic subunit (DNA-PK(cs)) or recombination-activating gene (RAG)1 activity
(
- Contribution to journal › Article
- 1999
-
Mark
An individual with a healthy phenotype in spite of a pathogenic LDL receptor mutation (C240F)
(
- Contribution to journal › Article
-
Mark
Factor V Q506 (resistance to activated protein C) and prognosis after acute coronary syndrome
(
- Contribution to journal › Article
-
Mark
Human glycogen synthase genes. Role in insulin resistance and hypoglycaemia
1999)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Mutation Analysis and Hypercholesterolemia: Studies in FH patients and in healthy middle-aged men with high, low, or increasing cholesterol levels during a six-year follow-up (the CRISS study).
1999)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Cancer risks in BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Origin of mutation in sporadic cases of haemophilia A
(
- Contribution to journal › Article
-
Mark
Search for MODY and Type 2 diabetes genes
1999)(
- Thesis › Doctoral thesis (compilation)
- 1998
-
Mark
BRCA1-positive patients are small for gestational age compared with their unaffected relatives
(
- Contribution to journal › Article
-
Mark
Mutations in the low-density lipoprotein receptor gene in Swedish familial hypercholesterolaemia patients: clinical expression and treatment response
(
- Contribution to journal › Article
-
Mark
Detection of alterations in all three exons of the peripherin/RDS gene in Swedish patients with retinitis pigmentosa using an efficient DGGE system
(
- Contribution to journal › Article
-
Mark
Mutation screening of the BTK gene in 56 families with X-linked agammaglobulinemia (XLA): 47 unique mutations without correlation to clinical course
(
- Contribution to journal › Article
-
Mark
Analysis of Swedish male breast cancer family data : a simple way to incorporate a common sibling effect
(
- Contribution to journal › Article
-
Mark
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect
(
- Contribution to journal › Article
-
Mark
Caracterización genómica de la cepa cubana de efecto citopático ligero
(
- Contribution to journal › Article
-
Mark
Parathyroid MEN1 gene mutations in relation to clinical characteristics of nonfamilial primary hyperparathyroidism
(
- Contribution to journal › Article
- 1997
-
Mark
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
(
- Contribution to journal › Article
-
Mark
Identification of TP53 gene mutations in uterine corpus cancer with short follow-up
(
- Contribution to journal › Article
-
Mark
Crystal structure of ferrochelatase: the terminal enzyme in heme biosynthesis
(
- Contribution to journal › Article
-
Mark
Resistance to activated protein C a novel risk factor for venous thrombosis
1997)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Tumour biological features of BRCA1-induced breast and ovarian cancer
(
- Contribution to journal › Article
-
Mark
Bernard-Soulier syndrome Karlstad : Trp 498-->Stop mutation resulting in a truncated glycoprotein Ib alpha that contains part of the transmembranous domain
(
- Contribution to journal › Article
-
Mark
The factor VR5O6Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance : Clinical implications
(
- Contribution to journal › Scientific review
-
Mark
A cluster of missense mutations at Arg356 of human steroid 21-hydroxylase may impair redox partner interaction
(
- Contribution to journal › Article
-
Mark
An estrogen receptor mutant with strong hormone-independent activity from a metastatic breast cancer
(
- Contribution to journal › Article
-
Mark
The tumor suppressor gene p53 can mediate transforming growth [corrected] factor beta1-induced differentiation of leukemic cells independently of activation of the retinoblastoma protein
(
- Contribution to journal › Article
- 1996
-
Mark
Genetic heterogeneity of hepatitis B and D viruses in chronic infection
1996)(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic predisposition to breast cancer
(
- Contribution to journal › Article
-
Mark
The dynamic structure of EF-G studied by fusidic acid resistance and internal revertants
(
- Contribution to journal › Article
-
Mark
Four novel mutations in deficiency of coagulation factor XIII: Consequences to expression and structure of the A-subunit
(
- Contribution to journal › Article
-
Mark
Prevalence of factor V gene mutation amongst myocardial infarction patients and healthy controls is higher in Sweden than in other countries
(
- Contribution to journal › Article
-
Mark
Activated protein C resistance as a basis for venous thrombosis.
(
- Contribution to journal › Article
-
Mark
Somatic mutation of immunoglobulin V genes in vitro
(
- Contribution to journal › Article
- 1995
-
Mark
TP53 mutations and breast cancer prognosis : particularly poor survival rates for cases with mutations in the zinc-binding domains
(
- Contribution to journal › Article
- 1994
-
Mark
Bacillus subtilis HemY is a peripheral membrane protein essential for protoheme IX synthesis which can oxidize coproporphyrinogen III and protoporphyrinogen IX
(
- Contribution to journal › Article
- 1992
-
Mark
Cloning and characterization of the Bacillus subtilis hemEHY gene cluster, which encodes protoheme IX biosynthetic enzymes
(
- Contribution to journal › Article
-
Mark
Nuclear colocalization of c-myc protein and hsp70 in cells transfected with human wild-type and mutant c-myc genes
(
- Contribution to journal › Article
- 1990
-
Mark
The incidence and distribution of CpG----TpG transitions in the coagulation factor IX gene. A fresh look at CpG mutational hotspots
(
- Contribution to journal › Article
-
Mark
Two factor IX mutations in the family of an isolated haemophilia B patient : direct carrier diagnosis by amplification mismatch detection (AMD)
(
- Contribution to journal › Article
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