S78409[Secondary Source ID] - Search Results

1

Characterization and nucleotide sequences of the variable regions of a monoclonal antibody against alpha-fetoprotein.

Hong TH, Hsiao SC, Sheu WJ, Chang TH. Hong TH, et al. Hybridoma. 1992 Jun;11(3):339-50. doi: 10.1089/hyb.1992.11.339. Hybridoma. 1992. PMID: 1379974

2

Induction of endothelin-1 gene by angiotensin and vasopressin in endothelial cells.

Imai T, Hirata Y, Emori T, Yanagisawa M, Masaki T, Marumo F. Imai T, et al. Hypertension. 1992 Jun;19(6 Pt 2):753-7. doi: 10.1161/01.hyp.19.6.753. Hypertension. 1992. PMID: 1592477

3

On genetic components in autoimmunity: a critical review based on evolutionarily oriented rationality.

Epplen JT. Epplen JT. Hum Genet. 1992 Dec;90(4):331-41. doi: 10.1007/BF00220454. Hum Genet. 1992. PMID: 1483686 Review.

4

Human C-type natriuretic peptide. Characterization of the gene and peptide.

Ogawa Y, Nakao K, Nakagawa O, Komatsu Y, Hosoda K, Suga S, Arai H, Nagata K, Yoshida N, Imura H. Ogawa Y, et al. Hypertension. 1992 Jun;19(6 Pt 2):809-13. doi: 10.1161/01.hyp.19.6.809. Hypertension. 1992. PMID: 1339402

5

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G, et al. Dörk T, et al. Hum Genet. 1992 Feb;88(4):417-25. doi: 10.1007/BF00215676. Hum Genet. 1992. PMID: 1371263

6

HLA class II nucleotide sequences, 1992.

Marsh SG, Bodmer JG. Marsh SG, et al. Hum Immunol. 1992 Sep;35(1):1-17. doi: 10.1016/0198-8859(92)90090-a. Hum Immunol. 1992. PMID: 1478891

7

Molecular basis of group A xeroderma pigmentosum: a missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC gene.

Satokata I, Tanaka K, Okada Y. Satokata I, et al. Hum Genet. 1992 Mar;88(6):603-7. doi: 10.1007/BF02265282. Hum Genet. 1992. PMID: 1339397

8

A familial mutation in the testis-determining gene SRY shared by both sexes.

Jäger RJ, Harley VR, Pfeiffer RA, Goodfellow PN, Scherer G. Jäger RJ, et al. Hum Genet. 1992 Dec;90(4):350-5. doi: 10.1007/BF00220457. Hum Genet. 1992. PMID: 1483689

9

Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1 alpha subunit.

De Meirleir L, Lissens W, Vamos E, Liebaers I. De Meirleir L, et al. Hum Genet. 1992 Mar;88(6):649-52. doi: 10.1007/BF02265291. Hum Genet. 1992. PMID: 1551669

10

Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal.

Hawkins JR, Taylor A, Berta P, Levilliers J, Van der Auwera B, Goodfellow PN. Hawkins JR, et al. Hum Genet. 1992 Feb;88(4):471-4. doi: 10.1007/BF00215684. Hum Genet. 1992. PMID: 1339396

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

34 results

Search Page

Filters