Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Park S. Gerald"'
Autor:
Park S. Gerald, Henry J. Issenberg, Eveline E. Schneeberger, Samuel R. Schuster, Joanne M. McCormack
Publikováno v:
Journal of Ultrastructure Research. 73:34-43
Detailed ultrastructural analysis of the respiratory cilia of three male patients with the immotile-cilia syndrome is presented. They all had similar clinical manifestations, namely, situs inversus totalis, repeated respiratory infections, and sinusi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe813d1b317723b43f848201229228a8
https://doi.org/10.1016/0022-5320(80)90114-8
https://doi.org/10.1016/0022-5320(80)90114-8
Publikováno v:
Experimental Cell Research. 99:438-444
A late replicating X or Y chromosome can be detected by 33258 Hoechst staining and fluorescence microscopy in a large proportion of female or male mouse embryo cells, respectively, which have been cultured in medium containing 5-bromodeoxyuridine (BU
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12f0fe8cd0151702f9b78a545210299d
https://doi.org/10.1016/0014-4827(76)90604-2
https://doi.org/10.1016/0014-4827(76)90604-2
Autor:
Park S. Gerald
Publikováno v:
Pediatrics in Review. 3:333-340
The best known chromosomal abnormalities are alterations in the number of chromosomes. This type of chromosomal alteration is found in approximately 5% of all fetuses, most of whom are unable to survive pregnancy. Because of this selection process, o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e35d771a240ba89a6a66e4109863dd5
https://doi.org/10.1542/pir.3-10-333
https://doi.org/10.1542/pir.3-10-333
Autor:
Gail A. P. Bruns, Park S. Gerald
Publikováno v:
Biochemical Genetics. 14:1-17
The expression of the adenylate kinase isozymes and of phosphopyruvate hydratase was studied in man-mouse and man-hamster hybrid clones. Concordant segregation of the loci coding for AK-2 and PPH was observed in 54 of 55 primary hybrid clones, and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0aa6583573e3aa2b1439642c94a0f42c
https://doi.org/10.1007/bf00484869
https://doi.org/10.1007/bf00484869
Publikováno v:
Pediatrics. 74:883-886
The fragile-X syndrome, an X-linked form of mental retardation, is estimated to affect one in every 1,000 to 2,000 live-born male infants. Most commonly, fragile-X syndrome has been detected only after patients clearly demonstrate developmental delay
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61b927fe1027fad91082b09e01eca19
https://doi.org/10.1542/peds.74.5.883
https://doi.org/10.1542/peds.74.5.883
Publikováno v:
Chromosoma. 57:135-153
BrdU-33258 Hoechst techniques have been used to characterize DNA replication patterns in lymphocytes from hunam females with supernumerary or structurally abnormal X chromosomes. Fluorescence analysis permits identification of late replicating X chro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a2523fb545ab931375f0f63cad6dbb2
https://doi.org/10.1007/bf00292912
https://doi.org/10.1007/bf00292912
Autor:
Park S. Gerald, Zuheir L. Awdeh, John F. Crigler, Chester A. Alper, D. Raum, Edmond J. Yunis, E. Fleischnick
Publikováno v:
Annals of the New York Academy of Sciences. 458:28-35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda67ac41b367c39ed6bb07494cfe338
https://doi.org/10.1111/j.1749-6632.1985.tb14586.x
https://doi.org/10.1111/j.1749-6632.1985.tb14586.x
Publikováno v:
Retina. 3:121-125
A number of patients with retinoblastoma have a deletion of chromosome 13. Comparison of the deleted segments from different individuals reveals that all deletions involve chromosome band 13q14. This observation has lead to the hypothesis that in thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2058a1833517e84d1efeb0dd907c0cf4
https://doi.org/10.1097/00006982-198300320-00010
https://doi.org/10.1097/00006982-198300320-00010
Publikováno v:
Biochemical Genetics. 17:1031-1059
The segregation of human lysosomal arylsulfatase A (ARS-A) has been evaluated in 50 primary hybrid clones derived from four separate fusions involving WBCs from two unrelated individuals and three hamster cell lines. ARS-A was expressed in the hybrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeae65c489ad8e8a91c5f14a6be47cd7
https://doi.org/10.1007/bf00504344
https://doi.org/10.1007/bf00504344
Publikováno v:
Pediatrics. 66:716-719
Wilms tumor developed in five cousins in a family. Two with bilateral tumors have died, but three with unilateral lesions have survived. None of the patients had associated chromosome defects, aniridia, hemihypertrophy, or other anomalies. The patter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99479f6a65816fad054be8828f6a5ef2
https://doi.org/10.1542/peds.66.5.716
https://doi.org/10.1542/peds.66.5.716