Pages that link to "Q44477270"
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The following pages link to Magnus Nordenskjöld (Q44477270):
Displaying 50 items.
- Molecular characterization of human telomerase reverse transcriptase-immortalized human fibroblasts by gene expression profiling: activation of the epiregulin gene (Q24300102) (← links)
- Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C beta 3 gene (PLCB3) (Q24318469) (← links)
- Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (Q24536183) (← links)
- Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors (Q24558744) (← links)
- Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients (Q24684113) (← links)
- FISH-mapping of a 100-kb terminal 22q13 deletion (Q28205575) (← links)
- Sequence analysis of the granulysin and granzyme B genes in familial hemophagocytic lymphohistiocytosis (Q28217729) (← links)
- Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway (Q28246648) (← links)
- Different NK cell-activating receptors preferentially recruit Rab27a or Munc13-4 to perforin-containing granules for cytotoxicity (Q28256255) (← links)
- Human estrogen receptor beta-gene structure, chromosomal localization, and expression pattern (Q28256533) (← links)
- Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis (Q28256832) (← links)
- Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis (Q28291167) (← links)
- Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C beta 3 gene on chromosomal region 11q13 (Q28291977) (← links)
- High expression of the EGFR in fibroadenomas compared to breast carcinomas (Q28306778) (← links)
- 4th Pediatric Allergy and Asthma Meeting (PAAM) (Q28818630) (← links)
- Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma (Q30502386) (← links)
- The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language (Q30515982) (← links)
- A high degree of aneuploidy in frozen-thawed human preimplantation embryos (Q30728731) (← links)
- Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes (Q30990642) (← links)
- Complete characterization of a large marker chromosome by reverse and forward chromosome painting (Q31043510) (← links)
- A case of acute lymphoblastic leukemia, near-triploidy, and poor outcome: characterization by fluorescence in situ hybridization using chromosome-specific libraries from all human chromosomes (Q32178725) (← links)
- Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus (Q33189562) (← links)
- Global expression profiling in atopic eczema reveals reciprocal expression of inflammatory and lipid genes (Q33395681) (← links)
- Isolation of anonymous, polymorphic DNA fragments from human chromosome 22q12-qter (Q33493313) (← links)
- Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome Patients (Q33571640) (← links)
- A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking (Q33632254) (← links)
- Knowledge and Attitudes Regarding Non-Invasive Prenatal Testing (NIPT) and Preferences for Risk Information among High School Students in Sweden (Q33634135) (← links)
- Gossypol induces DNA strand breaks in human fibroblasts and sister chromatid exchanges in human lymphocytes in vitro. (Q33671238) (← links)
- Genetic studies of thymic carcinoids in multiple endocrine neoplasia type 1 (Q33673648) (← links)
- Birt-Hogg-Dubé renal tumors are genetically distinct from other renal neoplasias and are associated with up-regulation of mitochondrial gene expression (Q33772820) (← links)
- Mitotic recombination of chromosome 17 in astrocytomas (Q33851092) (← links)
- Tumor suppressor genes (TSG). (Q33851873) (← links)
- Ehlers-Danlos syndrome with severe early-onset periodontal disease (EDS-VIII) is a distinct, heterogeneous disorder with one predisposition gene at chromosome 12p13. (Q33905913) (← links)
- The biology of inherited cancer. (Q34019570) (← links)
- Filaggrin genotype determines functional and molecular alterations in skin of patients with atopic dermatitis and ichthyosis vulgaris (Q34099095) (← links)
- Characterization of stem-like cells in mucoepidermoid tracheal paediatric tumor (Q34206687) (← links)
- Cloning of a novel, anonymous gene from a megabase-range YAC and cosmid contig in the neurofibromatosis type 2/meningioma region on human chromosome 22q12. (Q34344723) (← links)
- Assignment of the human FAU gene to a subregion of chromosome 11q13. (Q34357941) (← links)
- Cloning and characterization of a novel human gene related to vascular endothelial growth factor (Q34407476) (← links)
- Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitis (Q34493827) (← links)
- Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13 (Q34614026) (← links)
- Elevated expression and genetic association links the SOCS3 gene to atopic dermatitis (Q34658329) (← links)
- Birt-Hogg-Dubé syndrome: diagnosis and management (Q35015888) (← links)
- Prenatal diagnosis: molecular genetics and cytogenetics (Q35021963) (← links)
- Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance (Q35165436) (← links)
- Linkage analysis with markers on 17q in 29 Swedish breast cancer families (Q35194225) (← links)
- Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH). (Q35194867) (← links)
- Molecular cytogenetic approach to the diagnosis of splenic lymphoma: a case report of blastoid mantle cell lymphoma (Q35198933) (← links)
- Detection of human cytomegalovirus in medulloblastomas reveals a potential therapeutic target (Q35370135) (← links)
- Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH). (Q35449077) (← links)