Publication date
1992 (1451)
 
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References
Significance of the detection of Epstein-Barr virus DNA in lymph nodes in patients with Hodgkin's disease
Knecht H., Joske D. J., Bachmann E., Sahli R., Odermatt B. F., 1992/11. Leukemia and Lymphoma, 8 (4-5) pp. 319-25.
[DOI][WoS][Pmid][serval:BIB_C5B51755364F]
Von den Indianern wirklich etwas lernen...
Kunz Marco, 1992/11. Basler Zeitung 213 p. 61.
[serval:BIB_A364DCA65DB0]
A single amino acid exchange transfers VP16-induced positive control from the Oct-1 to the Oct-2 homeo domain.
Lai J.S., Cleary M.A., Herr W., 1992/11. Genes and Development, 6 (11) pp. 2058-2065.
[WoS][Pmid][serval:BIB_379B170DFF7E]
Controlled preparation of the endometrium with exogenous oestradiol and progesterone: a novel regimen not using a gonadotrophin-releasing hormone agonist
Lelaidier C., de Ziegler D., Gaetano J., Hazout A., Fernandez H., Frydman R., 1992/11. Human Reproduction, 7 (10) pp. 1353-6. Peer-reviewed.
[WoS][Pmid][serval:BIB_73E24D77B9B3]
Les communes suisses face aux nouveaux espaces européens
Leresche Jean-Philippe, 1992/11. Die Stadt/les villes 6 pp. 16-19.
[serval:BIB_CA89C84273FD]
The effect of ultraviolet B irradiation and urocanic acid isomers on dendritic cell migration
Moodycliffe A. M., Kimber I., Norval M., 1992/11. Immunology, 77 (3) pp. 394-9.
[WoS][Pmid][serval:BIB_368F93EAF873]
Lox2, a putative leech segment identity gene, is expressed in the same segmental domain in different stem cell lineages
Nardelli-Haefliger D., Shankland M., 1992/11. Development, 116 (3) pp. 697-710.
[WoS][Pmid][serval:BIB_2A2B0125F224]
Approche diagnostique d'un patient asthmatique. [Diagnostic approach in an asthmatic patient]
Pecoud A., 1992/11. Revue Médicale de la Suisse Romande, 112 (11) pp. 977-9.
[Pmid][serval:BIB_BFF8319A1819]
Complementary DNA Cloning and Sequence Analysis of a Pathogen-Induced Putative Peroxidase from Rice
Reimmann C., Ringli C., Dudler R., 1992/11. Plant Physiology, 100 (3) pp. 1611-1612.
[DOI][WoS][Pmid][serval:BIB_1DCEF2973A71]
Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy
Richard I., Broux O., Hillaire D., Cherif D., Fougerousse F., Cohen D., Beckmann J. S., 1992/11. Human Molecular Genetics, 1 (8) pp. 621-4.
[DOI][WoS][Pmid][serval:BIB_D0E125CCDEC8]