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Autor:
Jaroslav Cervenka
Publikováno v:
Journal of Dental Research. 81:444-445
Autor:
Burton L. Shapiro
Publikováno v:
American Journal of Medical Genetics. 47:161-162
Autor:
B. Nijmeijer, Carl J. Witkop, J. W. N. Akkerman, James G. White, S. M. Gerritsen, J. J. Sixma
Publikováno v:
Scandinavian Journal of Haematology. 18:249-256
A Dutch kindred with the Hermansky-Pudlak syndrome (HPS) is described. We show for the first time evidence of a lowered platelet 5-hydroxytryptamine content in obligate heterozygotes. Platelet ATP and ADP levels and ATP/ADP ratio were normal in these
Publikováno v:
Clinical Genetics. 15:17-21
The prevalence of squamous cell carcinoma of the skin in albinos reaches approximately 90 % in patients over 20 years of age in the vicinity of Enugu, Nigeria. Chromosome breaks and sister chromatid exchanges (SCE) were evaluated in tyrosinase-positi
Publikováno v:
Clinical Genetics. 17:259-270
Seventy-nine Nigerian oculocutaneous albinos were investigated. Fifty-six had typical tyrosinase-positive albinism (TPA) and 23 had brown albinism (BA), a new oculocutaneous type. The TPA were characterized by localized but no generalized skin pigmen
Autor:
Susan Castronuovo, Carl J. Witkop, Bruce Wolf, John W. Simon, Paul L. Jenkins, Albert M. Morier, Gillray L. Kandel
Publikováno v:
American Journal of Ophthalmology. 111:419-426
We studied the albinotic characteristics in 13 members of a white family (age range, 2 to 73 years), which were graded according to severity and were correlated with visual acuity. Clinical, electrophysiologic, and biochemical characteristics of this
Autor:
E. J. Walter Bowie, Marlys D. Krumwiede, Elizabeth A. Plumhoff, James G. White, Carl J. Witkop, Jane Swanson
Publikováno v:
American journal of hematology. 44(4)
A study of 565 Puerto Rican patients with storage pool deficient (SPD) Hermansky-Pudlak syndrome (HPS) demonstrated that most HPS patients had minor bleeding episodes while others had repeated, severe hemorrhagic episodes requiring transfusion. The s
We have determined a molecular defect to be the likely basis for inactivity of the tyrosinase (EC 1.14.18.1) from a patient with tyrosinase-negative oculocutaneous albinism. A single base (thymine) was inserted in exon 5 of the tyrosinase gene follow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4f1f349ea3789ab794c2c4e306f333
https://europepmc.org/articles/PMC51854/
https://europepmc.org/articles/PMC51854/