Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Malgorzata Schmidt"'
Publikováno v:
Nonlinear Analysis: Theory, Methods & Applications. 21:501-515
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f2e39e8e474d473605820a60ce72d5d
https://doi.org/10.1016/0362-546x(93)90007-f
https://doi.org/10.1016/0362-546x(93)90007-f
Publikováno v:
Proceedings of the American Mathematical Society. 119:457-463
LetX1{X_1}andX2{X_2}be Banach spaces, and letX1×X2{X_1} \times {X_2}be equipped with thel1{l_1}-norm. If the first spaceX1{X_1}is uniformly convex in every direction, thenX1×X2{X_1} \times {X_2}has the fixed point property for nonexpansive mappings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f768af1a93cf8dee9ad6d404bdfa2f0b
https://doi.org/10.1090/s0002-9939-1993-1155601-9
https://doi.org/10.1090/s0002-9939-1993-1155601-9
Autor:
Paul Kalitsis, Malgorzata Schmidt, Louise Hills, Dean Foster, Julie Davies, Neil J. Fraser, Lucille Voullaire, Desirée du Sart, Margaret Leversha, Vida Petrovic, Rhonda Hutchinson
Publikováno v:
American Journal of Medical Genetics. 38:411-415
Over 30% of female carriers of the fragile X [fra(X)] syndrome are clinically affected. A nonrandom X chromosome inactivation in these cases could be a plausible explanation. A review of previous studies addressing this question showed inconclusive r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dbf4fcd4a8272c9ae4fd16974bc79b4
https://doi.org/10.1002/ajmg.1320380252
https://doi.org/10.1002/ajmg.1320380252
Autor:
Egbert Bakker, Ben A. Oostra, J. O. Van Hemel, Danielle Majoor-Krakauer, B.A. van Oost, Malgorzata Schmidt, David F. Callen
Publikováno v:
American Journal of Medical Genetics. 38:332-335
A new polymorphic DNA marker RN1, defining locus DXS369, was recently isolated. Using different somatic cell hybrids, RN1 was mapped between markers 4D-8 and U6.2. We have narrowed the localization of RN1 to the region between 4D-8 and FRAXA by genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b1848598468c3c5d454a8811ea54255
https://doi.org/10.1002/ajmg.1320380233
https://doi.org/10.1002/ajmg.1320380233
Autor:
Malgorzata Schmidt, Barbara R. Migeon
Publikováno v:
Proceedings of the National Academy of Sciences. 87:3685-3689
The two X chromosomes in mammalian females replicate asynchronously, the inactive later than the active one. Using BrdUrd-sensitive restriction and UV irradiation to identify newly synthesized DNA directly on Southern blots, and restriction fragment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5610856429f8109bf9edabddd67c880f
https://doi.org/10.1073/pnas.87.10.3685
https://doi.org/10.1073/pnas.87.10.3685
Autor:
Ian Jack, David M. Danks, Margaret Leversha, Malgorzata Schmidt, Desirée du Sart, Paul Kalitsis, Leslie J. Sheffield, Andrea Certoma, Kerry J. Fowler
Publikováno v:
Human Genetics. 84:347-352
A de novo interstitial deletion (X)(q27.1q27.3), between the loci DXS 105 and F8, has been found in a mentally retarded female. The deleted X chromosome is preferentially early replicating in fibroblasts, B cells and T cells, suggesting that the miss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085ec59e48f15f3f072f559809b89cad
https://doi.org/10.1007/bf00196232
https://doi.org/10.1007/bf00196232
Autor:
D. J. J. Halley, C. A. van Bennekom, Malgorzata Schmidt, Ben A. Oostra, D. Du Sart, Egbert Bakker, Arie P. T. Smits, B. Wieringa, P.E. Hupkes, B.A. van Oost, L.F. Perdon
Publikováno v:
Genomics. 6:129-132
DNA from a human-hamster hybrid cell line, 908-K1B17, containing a small terminal portion of the long arm of the human X chromosome as well as the pericentric region of 19q was used as starting material for the isolation of an X-chromosome-specific D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cca459334c7d8a129681ed9039af169
https://doi.org/10.1016/0888-7543(90)90457-6
https://doi.org/10.1016/0888-7543(90)90457-6
Autor:
Malgorzata Schmidt
Publikováno v:
American Journal of Medical Genetics. 64:166-168
We reviewed female interstitial deletions in the distal Xq and compared them to those reported in males. Most of the deletions were common to females and males, and they were scattered within Xq27 and proximal Xq. Six females had large deletions of 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a3b8ae3315bf8a74d0205f00fc6136e
https://doi.org/10.1002/(sici)1096-8628(19960712)64:1<166::aid-ajmg28>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19960712)64:1<166::aid-ajmg28>3.0.co
Autor:
Malgorzata Schmidt
Publikováno v:
American Journal of Medical Genetics. 64:163-165
We constructed a deletion map of the distal Xq, using previously reported male interstitial deletions within Xq27-Xqter. The map consists of 12 large interstitial deletions, ranging from 100-9,000 kb. All but one fall within Xq27{r_arrow}proximal Xq2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4d8ce9d864233efe7f81285645ad10a
https://doi.org/10.1002/(sici)1096-8628(19960712)64:1<163::aid-ajmg27>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19960712)64:1<163::aid-ajmg27>3.0.co
Autor:
Malgorzata Schmidt
Publikováno v:
American Journal of Medical Genetics. 43:279-281
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c9f24cd8ff903e8042dba15eeb8807d
https://doi.org/10.1002/ajmg.1320430143
https://doi.org/10.1002/ajmg.1320430143