Identification of the homologous beige and Chediak-Higashi syndrome genes

scientific article

Identification of the homologous beige and Chediak-Higashi syndrome genes is …
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scholarly articleQ13442814

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P6179Dimensions Publication ID1052215483
P356DOI10.1038/382262A0
P932PMC publication ID2893578
P698PubMed publication ID8717042
P5875ResearchGate publication ID14485449

P50authorCharlie HodgmanQ42801875
Stephen F KingsmoreQ47815897
P2093author name stringM Lovett
D Chotai
J A Ashley
J C Detter
M D Barbosa
Q A Nguyen
R C Solari
S J Brandt
S M Blaydes
V T Tchernev
P2860cites workIdentification of a protein that interacts with tubulin dimers and increases the catastrophe rate of microtubulesQ43410846
Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion.Q48082303
An algorithm for protein secondary structure prediction based on class prediction.Q52591620
The Rab Protein Family: Genetic Mapping of Six Rab Genes in the MouseQ57186295
Complementation analysis of Chediak-Higashi Syndrome: The same gene may be responsible for the defect in all patients and speciesQ59565703
Further developments of protein secondary structure prediction using information theory. New parameters and consideration of residue pairsQ68541267
Thiol proteinase inhibitors reverse the increased protein kinase C down-regulation and concanavalin A cap formation in polymorphonuclear leukocytes from Chediak-Higashi syndrome (beige) mouseQ68588091
The thiol proteinase inhibitors improve the abnormal rapid down-regulation of protein kinase C and the impaired natural killer cell activity in (Chediak-Higashi syndrome) beige mouseQ69347557
Stathmin interaction with a putative kinase and coiled-coil-forming protein domainsQ24561441
Stathmin: a relay phosphoprotein for multiple signal transduction?Q28250666
Loss of cytotoxic T lymphocyte function in Chediak-Higashi syndrome arises from a secretory defect that prevents lytic granule exocytosisQ28301479
Granulocyte function in the Chediak-Higashi syndrome of miceQ28504555
The origin and fate of large dense bodies in beige mouse fibroblasts. Lysosomal fusion and exocytosisQ28591716
Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) miceQ28592567
Defective T-cell response in beige mutant miceQ28594447
Combining evolutionary information and neural networks to predict protein secondary structureQ29614392
A positive selection vector for cloning high molecular weight DNA by the bacteriophage P1 system: improved cloning efficacyQ31122225
Correction of characteristic abnormalities of microtubule function and granule morphology in Chediak-Higashi syndrome with cholinergic agonistsQ35200718
Protein isoprenylation and methylation at carboxyl-terminal cysteine residuesQ35671041
Turnover of kidney beta-glucuronidase in normal and Chédiak-Higashi (beige) miceQ36058677
Construction of a large-insert yeast artificial chromosome library of the mouse genomeQ36767726
SOPM: a self-optimized method for protein secondary structure predictionQ38568739
Concanavalin A cap formation on polymorphonuclear leukocytes of normal and beige (Chediak-Higashi) miceQ39917301
The Chediak-Higashi syndrome: studies in four patients and a review of the literatureQ40018532
Lysosomal enzyme activities in Chediak-Higashi syndrome: evaluation of lymphoblastoid cell lines and review of the literature.Q40672765
The beige mutation in the mouse selectively impairs natural killer cell functionQ40713185
On the analysis of the pathophysiology of Chediak-Higashi syndrome. Defects expressed by cultured melanocytes.Q41456445
The giant organelles in beige and Chediak-Higashi fibroblasts are derived from late endosomes and mature lysosomesQ41512888
P2507corrigendum / erratumErratum: Identification of the homologous beige and Chediak–Higashi syndrome genesQ60085428
P433issue6588
P407language of work or nameEnglishQ1860
P921main subjectChediak-Higashi syndromeQ934034
P304page(s)262-265
P577publication date1996-07-01
P1433published inNatureQ180445
P1476titleIdentification of the homologous beige and Chediak-Higashi syndrome genes
P478volume382