Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.
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Low levels of genetic divergence across geographically and linguistically diverse populations from India3' deletions cause aniridia by preventing PAX6 gene expressiondelta-Aminolevulinate dehydratase deficient porphyria: identification of the molecular lesions in a severely affected homozygotePaget disease of bone: mapping of two loci at 5q35-qter and 5q31.Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19Familial porphyria cutanea tarda: characterization of seven novel uroporphyrinogen decarboxylase mutations and frequency of common hemochromatosis alleles.A genomic screen of autism: evidence for a multilocus etiology.Linkage disequilibrium at the ADH2 and ADH3 loci and risk of alcoholismA global view of the OCA2-HERC2 region and pigmentationFabry disease: six gene rearrangements and an exonic point mutation in the alpha-galactosidase geneMutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouseDisruption of neurexin 1 associated with autism spectrum disorder.A SNP in a let-7 microRNA complementary site in the KRAS 3' untranslated region increases non-small cell lung cancer riskMolecular analysis of mutations in a patient with purine nucleoside phosphorylase deficiencyGenetic heterogeneity in benign familial neonatal convulsions: identification of a new locus on chromosome 8qA gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9A missense mutation (I278T) in the cystathionine beta-synthase gene prevalent in pyridoxine-responsive homocystinuria and associated with mild clinical phenotypeMutations in the lysosomal beta-galactosidase gene that cause the adult form of GM1 gangliosidosisAmerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineagesHuman beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic casesDefective gene in lactic acidosis: abnormal pyruvate dehydrogenase E1 alpha-subunit caused by a frame shiftA variant of Freeman-Sheldon syndrome maps to 11p15.5-pterDistinct early molecular responses to mutations causing vLINCL and JNCL presage ATP synthase subunit C accumulation in cerebellar cellsA Variant in a MicroRNA complementary site in the 3' UTR of the KIT oncogene increases risk of acral melanomaIdentical mutations in NOG can cause either tarsal/carpal coalition syndrome or proximal symphalangismUroporphyrinogen III synthase erythroid promoter mutations in adjacent GATA1 and CP2 elements cause congenital erythropoietic porphyriaAutophagy is disrupted in a knock-in mouse model of juvenile neuronal ceroid lipofuscinosisThe distribution and most recent common ancestor of the 17q21 inversion in humansHuntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study.Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosisDinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita.Complex patterns of linkage disequilibrium in the Huntington disease region.A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.Mutational analysis of patients with neurofibromatosis 2Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.DNA instability in replicating Huntington's disease lymphoblastsCongenital erythropoietic porphyria: a novel uroporphyrinogen III synthase branchpoint mutation reveals underlying wild-type alternatively spliced transcripts
P2860
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P2860
Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年学术文章
@wuu
1984年学术文章
@zh
1984年学术文章
@zh-cn
1984年学术文章
@zh-hans
1984年学术文章
@zh-my
1984年学术文章
@zh-sg
1984年學術文章
@yue
1984年學術文章
@zh-hant
name
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@en
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@nl
type
label
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@en
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@nl
prefLabel
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@en
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@nl
P356
P1433
P1476
Use of cyclosporin A in establ ...... man lymphoblastoid cell lines.
@en
P2093
M A Anderson
P304
P356
10.1007/BF02619631
P577
1984-11-01T00:00:00Z