Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 222

1.

The alpha 1-antitrypsin gene and its deficiency states.

Crystal RG.

Trends Genet. 1989 Dec;5(12):411-7. Review.

PMID:
2696185
2.

Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.

Crystal RG.

J Clin Invest. 1990 May;85(5):1343-52. Review. No abstract available.

3.

Molecular basis of the liver and lung disease associated with the alpha 1-antitrypsin deficiency allele Mmalton.

Curiel DT, Holmes MD, Okayama H, Brantly ML, Vogelmeier C, Travis WD, Stier LE, Perks WH, Crystal RG.

J Biol Chem. 1989 Aug 15;264(23):13938-45.

4.

Alpha 1-antitrypsin deficiency and augmentation therapy in emphysema.

Stoller JK.

Cleve Clin J Med. 1989 Oct;56(7):683-9. Review.

PMID:
2688991
5.

Alpha 1-antitrypsin deficiency and liver disease.

Birrer P, McElvaney NG, Chang-Stroman LM, Crystal RG.

J Inherit Metab Dis. 1991;14(4):512-25. Review.

PMID:
1749216
6.

Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele.

Curiel DT, Vogelmeier C, Hubbard RC, Stier LE, Crystal RG.

Mol Cell Biol. 1990 Jan;10(1):47-56.

7.

Emphysema associated with complete absence of alpha 1- antitrypsin in serum and the homozygous inheritance [corrected] of a stop codon in an alpha 1-antitrypsin-coding exon.

Satoh K, Nukiwa T, Brantly M, Garver RI Jr, Hofker M, Courtney M, Crystal RG.

Am J Hum Genet. 1988 Jan;42(1):77-83. Erratum in: Am J Hum Genet 1988 May;42(5):789.

8.

Molecular basis of alpha-1-antitrypsin deficiency.

Brantly M, Nukiwa T, Crystal RG.

Am J Med. 1988 Jun 24;84(6A):13-31. Review.

PMID:
3289385
9.

Alpha(1)-antitrypsin deficiency, liver disease and emphysema.

Parfrey H, Mahadeva R, Lomas DA.

Int J Biochem Cell Biol. 2003 Jul;35(7):1009-14. Review.

PMID:
12672469
10.

Alpha-1-antitrypsin deficiency: diagnosis and treatment.

Perlmutter DH.

Clin Liver Dis. 2004 Nov;8(4):839-59, viii-ix. Review.

PMID:
15464658
11.

[From gene disease; alpha1-antitrypsine deficiency].

Hiemstra PS, Stolk J.

Ned Tijdschr Geneeskd. 2003 Apr 19;147(16):758-60. Review. Dutch.

PMID:
12731467
12.

Alpha 1-antitrypsin deficiency: pathogenesis and treatment.

Crystal RG.

Hosp Pract (Off Ed). 1991 Feb 15;26(2):81-4, 88-9, 93-4. Review.

PMID:
1899256
13.

[Alpha-1 antitrypsin deficiency: diagnosis and treatment].

Camelier AA, Winter DH, Jardim JR, Barboza CE, Cukier A, Miravitlles M.

J Bras Pneumol. 2008 Jul;34(7):514-27. Review. Portuguese.

14.

The pallid mouse. A model of genetic alpha 1-antitrypsin deficiency.

Martorana PA, Brand T, Gardi C, van Even P, de Santi MM, Calzoni P, Marcolongo P, Lungarella G.

Lab Invest. 1993 Feb;68(2):233-41.

PMID:
8441253
15.

Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsin.

Curiel D, Brantly M, Curiel E, Stier L, Crystal RG.

J Clin Invest. 1989 Apr;83(4):1144-52. Erratum in: J Clin Invest 1989 Sep;84(3):following 1041.

16.

The alpha 1-antitrypsin gene and emphysema.

Perlmutter DH, Pierce JA.

Am J Physiol. 1989 Oct;257(4 Pt 1):L147-62. Review.

PMID:
2679136
17.

Z-type alpha 1-antitrypsin is less competent than M1-type alpha 1-antitrypsin as an inhibitor of neutrophil elastase.

Ogushi F, Fells GA, Hubbard RC, Straus SD, Crystal RG.

J Clin Invest. 1987 Nov;80(5):1366-74.

19.

[Alpha 1-antitrypsin deficiency: a review with special reference to the significance of heterozygous deficiency].

Schneider M, Pott G, Gerlach U.

Klin Wochenschr. 1986 Mar 3;64(5):197-205. German.

PMID:
3009960
20.

Molecular mechanisms of alpha1-antitrypsin null alleles.

Lee JH, Brantly M.

Respir Med. 2000 Aug;94 Suppl C:S7-11. Review.

PMID:
10954248
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk