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Steinmann P. 《Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology》1929,11(1):160-172
Ohne Zusammenfassung 相似文献
105.
Summary Root initiation at cuttings is inhibited by application of gibberellin. CCC does not antagonize this inhibition. However, CCC stimulates root initiation at cuttings of three different species of twining plants known to be rich in endogenous gibberellin. CCC seems to be an antagonist for endogenous but not for exogenous gibberellin, which suggests that CCC influences gibberellin biosynthesis. 相似文献
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B Lee E Vitale A Superti-Furga B Steinmann F Ramirez 《The Journal of biological chemistry》1991,266(8):5256-5259
We identified a splicing mutation in a patient with Ehlers-Danlos syndrome type IV, a heritable connective tissue disorder associated with dysfunctions of type III collagen. The mutation was first localized in the patient's type III procollagen mRNA by amplifying the reverse transcribed product in several overlapping fragments using the polymerase chain reaction. Amplified products spanning exon 24-26 sequences displayed two distinct fragments, one of normal size and the other lacking the 99 base pairs of exon 25. Sequencing of amplified genomic products identified a G to T transversion at position +5 of the splice donor site of intron 25 in one of the patient's procollagen III genes. Expression of allelic minigene constructs correlated the T for G substitution with skipping of exon 25 sequences. Like previously characterized splicing mutations in other collagen genes, lowering the temperature at which the patient's fibroblasts were incubated nearly abolished exon skipping. As a part of this study, we also identified a highly polymorphic, intronic DNA sequence whose different allelic forms can be detected easily by the polymerase chain reaction technique. 相似文献
107.
The structure of human collagen type IX and its organization in fetal and infant cartilage fibrils 总被引:1,自引:0,他引:1
P Bruckner M Mendler B Steinmann S Huber K H Winterhalter 《The Journal of biological chemistry》1988,263(32):16911-16917
Human collagen type IX was isolated from the media of organ cultures of fetal or infant hyaline cartilage. It consisted of three distinct, disulfide-bonded polypeptides of 115, 84, and 72 kDa, respectively. Digestion with chondroitinase ABC reduced the apparent molecular mass of the 115-kDa chain to about 65 kDa demonstrating that also human collagen type IX is a proteoglycan. In the electron microscope, the molecule had a rigid rod-like structure with characteristic kinks and with a globular domain at one end. Digestion of human collagen type IX with pepsin leads to somewhat heterogeneous fragments. Affinity-purified antibodies to the mixture of fragments specifically reacted with the fragment HMW without cross-reaction with chicken HMW. LMW of both species were recognized to the same low extent. Mechanically generated fibril fragments from human fetal cartilage were heterogeneous in diameter. Significantly, they could be immunostained for collagen type IX in a D-periodic pattern and regardless of the fibril diameter. Some fibrils were poorly labeled, again independently of the diameter. Therefore, the role of collagen type IX in cartilage probably is not to control directly the lateral growth during fibrillogenesis but rather to stabilize the fibril network. 相似文献
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G. Steinmann 《Molecular & general genetics : MGG》1910,3(1):98-103
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