Human Prop-1: Cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency

FEBS Letters

Volumn 437, Issue 3, 1998, Pages 216-220

  Duquesnoy, Philippe ^a   Roy, Anne ^a   Dastot, Florence ^a   Ghali, Isis ^b   Teinturier, Cécile ^c   Netchine, Irène ^a   Cacheux, Valère ^a   Hafez, Mona ^b   Salah, Nermine ^b   Chaussain, Jean Louis ^c   Goossens, Michel ^a   Bougnères, Pierre ^c   Amselem, Serge ^a  

^a HENRI MONDOR HOSPITAL   (France)

^b Cairo University   (Egypt)

^c HÔPITAL SAINT VINCENT DE PAUL   (France)

Author keywords

Chromosomal localization; Combined pituitary hormone deficiency; Mutation; Prop 1

Indexed keywords

COMPLEMENTARY DNA; HYPOPHYSIS HORMONE; TRANSCRIPTION FACTOR;

ARTICLE; CLINICAL ARTICLE; DNA SEQUENCE; FAMILIAL DISEASE; GENE LOCATION; GENOME; HORMONE DEFICIENCY; HUMAN; MISSENSE MUTATION; MUTATION; PRIORITY JOURNAL;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 5; CLONING, MOLECULAR; CONSANGUINITY; COS CELLS; DNA MUTATIONAL ANALYSIS; DNA, COMPLEMENTARY; EXONS; HOMEODOMAIN PROTEINS; HUMANS; INTRONS; MICE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PITUITARY HORMONES;

EID: 0032561414     PISSN: 00145793     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-5793(98)01234-4     Document Type: Article

References (26)

1. Phillips, J. (1995) in: The Metabolic Basis of Inherited Diseases (Scriver, C., Ed.) pp. 3023-3044, McGraw-Hill, New York, NY.
2. Li S., Crenshaw E. III, Rawson E., Simmons D., Swanson L., Rosenfeld M. Nature. 347:1990;528-533.
3. Tang K., Bartke A., Gardiner C.S., Wagner T.E., Yun J.S. Endocrinology. 132:1993;2518-2524.
4. Bartke A., Goldman B.D., Bex F., Dalterio S. Endocrinology. 101:1977;1760-1766.
5. Andersen B., Pearse R.V. II, Jenne K., Sornson M., Lin S.C., Bartke A., Rosenfeld M.G. Dev. Biol. 172:1995;495-503.
6. Gage P.J., Brinkmeier M.L., Scarlett L.M., Knapp L.T., Camper S.A., Mahon K.A. Mol. Endocrinol. 10:1996;1570-1581.
7. Sornson M.W., et al. Nature. 384:1996;327-333.
8. Gehring W.J., Affolter M., Burglin T. Annu. Rev. Biochem. 63:1994;487-526.
9. Radovick S., Cohen L.E., Wondisford F.E. Horm. Res. 49:1998;30-36.
10. Wu W., et al. Nat. Genet. 18:1998;147-149.
11. Fofanova O., et al. J. Clin. Endocrinol. Metab. 83:1998;2601-2604.
12. Pinkel D., Straume T., Gray J.W. Proc. Natl. Acad. Sci. USA. 83:1986;2934-2938.
13. Ellis L., Clauser E., Morgan D., Edery M., Roth R., Rutter W. Cell. 45:1986;721-732.
14. Duquesnoy P., Sobrier M.-L., Amselem S., Goossens M. Proc. Natl. Acad. Sci. USA. 88:1991;10272-10276.
15. Kozak M. J. Biol. Chem. 266:1991;19867-19870.
16. Buckwalter M.S., Katz R.W., Camper S.A. Genomics. 10:1991;515-526.
17. Shapiro M.B., Senapathy P. Nucleic Acids Res. 15:1987;7155-7174.
18. Kappen C., Schughart K., Ruddle F.H. Genomics. 18:1993;54-70.
19. Mount S.M. Nucleic Acids Res. 10:1982;459-472.
20. Gage P.J., Roller M.L., Saunders T.L., Scarlett L.M., Camper S.A. Development. 122:1996;151-160.
21. Li H., Zeitler P.S., Valerius M.T., Small K., Potter S.S. EMBO J. 15:1996;714-724.
22. Sheng H.Z., et al. Science. 272:1996;1004-1007.
23. Sheng H.Z., Moriyama K., Yamashita T., Li H., Potter S.S., Mahon K.A., Westphal H. Science. 278:1997;1809-1812.
24. Topilko P., Schneider-Maunoury S., Levi G., Trembleau A., Gourdji D., Driancourt M.A., Rao C.V., Charnay P. Mol. Endocrinol. 12:1998;107-122.
25. Acampora D., et al. Development. 125:1998;1229-1239.
26. Dattani M.T., et al. Nat. Genet. 19:1998;125-133.