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Items: 1 to 20 of 39

1.

Absence of cytochrome b-245 in chronic granulomatous disease. A multicenter European evaluation of its incidence and relevance.

Segal AW, Cross AR, Garcia RC, Borregaard N, Valerius NH, Soothill JF, Jones OT.

N Engl J Med. 1983 Feb 3;308(5):245-51.

PMID:
6848934
2.

Organization and expression of eucaryotic split genes coding for proteins.

Breathnach R, Chambon P.

Annu Rev Biochem. 1981;50:349-83. Review. No abstract available.

PMID:
6791577
3.

Biogenesis of the acetylcholine receptor, a multisubunit integral membrane protein.

Merlie JP.

Cell. 1984 Mar;36(3):573-5. No abstract available.

PMID:
6697388
4.

Chronic granulomatous disease: a syndrome of phagocyte oxidase deficiencies.

Tauber AI, Borregaard N, Simons E, Wright J.

Medicine (Baltimore). 1983 Sep;62(5):286-309. Review.

PMID:
6353131
5.

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Feinberg AP, Vogelstein B.

Anal Biochem. 1983 Jul 1;132(1):6-13.

PMID:
6312838
6.

Polymorphic DNA region adjacent to the 5' end of the human insulin gene.

Bell GI, Karam JH, Rutter WJ.

Proc Natl Acad Sci U S A. 1981 Sep;78(9):5759-63.

7.

Defective polymorphonuclear-leukocyte function and chronic granulomatous disease in two female children.

Quie PG, Kaplan EL, Page AR, Gruskay FL, Malawista SE.

N Engl J Med. 1968 May 2;278(18):976-80. No abstract available.

PMID:
4868715
8.

Quantitative nitroblue tetrazolium test in chronic granulomatous disease.

Baehner RL, Nathan DG.

N Engl J Med. 1968 May 2;278(18):971-6. No abstract available.

PMID:
4384563
9.

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Francke U, Ochs HD, de Martinville B, Giacalone J, Lindgren V, Dist├Ęche C, Pagon RA, Hofker MH, van Ommen GJ, Pearson PL, et al.

Am J Hum Genet. 1985 Mar;37(2):250-67.

10.

Human von Willebrand factor (vWF): isolation of complementary DNA (cDNA) clones and chromosomal localization.

Ginsburg D, Handin RI, Bonthron DT, Donlon TA, Bruns GA, Latt SA, Orkin SH.

Science. 1985 Jun 21;228(4706):1401-6.

PMID:
3874428
11.
12.

The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245.

Teahan C, Rowe P, Parker P, Totty N, Segal AW.

Nature. 1987 Jun 25-Jul 1;327(6124):720-1.

PMID:
3600769
13.

The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex.

Dinauer MC, Orkin SH, Brown R, Jesaitis AJ, Parkos CA.

Nature. 1987 Jun 25-Jul 1;327(6124):717-20.

PMID:
3600768
14.

Heterogeneous mutations in the beta subunit common to the LFA-1, Mac-1, and p150,95 glycoproteins cause leukocyte adhesion deficiency.

Kishimoto TK, Hollander N, Roberts TM, Anderson DC, Springer TA.

Cell. 1987 Jul 17;50(2):193-202.

PMID:
3594570
16.

Building a multichain receptor: synthesis, degradation, and assembly of the T-cell antigen receptor.

Minami Y, Weissman AM, Samelson LE, Klausner RD.

Proc Natl Acad Sci U S A. 1987 May;84(9):2688-92.

17.

Platelet-derived growth factor A chain: gene structure, chromosomal location, and basis for alternative mRNA splicing.

Bonthron DT, Morton CC, Orkin SH, Collins T.

Proc Natl Acad Sci U S A. 1988 Mar;85(5):1492-6.

18.
19.

Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b.

Parkos CA, Dinauer MC, Walker LE, Allen RA, Jesaitis AJ, Orkin SH.

Proc Natl Acad Sci U S A. 1988 May;85(10):3319-23.

20.

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