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Unraveling non-genetic heterogeneity in cancer with dynamical models and computational tools
Nature Computational Science, 2023Maalavika Pillai +3 more
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Genetic heterogeneity of congenital glaucoma
Clinical Genetics, 1980Analysis of 126 families comprising 205 patients with congenital glaucoma demonstrates that in Gypsies this disease follows the pattern of autosomal recessive inheritance with complete penetrance, while in the non‐Gypsy population, its mode of inheritance is most probably multifactorial.
A, Gencík, A, Gencíková, A, Gerinec
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On the Genetic Heterogeneity of Juvenile Hyperglycemia
1979We have briefly discussed immunogenetic studies of families with hyperglycemia which suggest the existence of at least four types of the disease: a) juvenile, insulin-dependent, ketosis prone diabetes determined by an autosomal recessive gene with 50% penetrance and in linkage with the HLA; b) juvenile, insulin-dependent, ketosis prone diabetes ...
J, Barbosa, M M, Chern
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The Impact of Non-Genetic Heterogeneity on Cancer Cell Death
Critical reviews in biochemistry and molecular biology, 2017The goal of cancer chemotherapy is to induce homogeneous cell death within the population of targeted cancer cells. However, no two cells are exactly alike at the molecular level, and sensitivity to drug-induced cell death, therefore, varies within a ...
Z. Inde, S. Dixon
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Genetic heterogeneity of diabetes and HLA
Clinical Genetics, 1982Histocompatibility (HLA) antigens and genotypes B, D and DR were studied in a large sample of Caucasian insulin dependent diabetic (IDD) probands. The associations between IDD and B8, B15, Dw3, Dw4, DR3, and DR4 were measured by relative risks (RR) and delta values (δ). Both the homozygotes (B8/8: RR 10, B 15/15: RR 7, DR3/3: RR32, DR4/4: RR34) and the
J, Barbosa, F H, Bach, S S, Rich
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Further genetic heterogeneity in acatalasemia
ELECTROPHORESIS, 1997AbstractA T‐deletion at position 10 of exon 4 for catalase gene was reported as a novel mutation, causing a new genetic type of acatalasemia in Japan. This mutation, destroying a Hinf1 recognition site, was searched for in Hungarian acatalasemic (2) and hypocatalasemic (22) patients and in controls (27) by Hinf1 digestion and sequence analyses of a 203
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Cystinuria: Genetic Heterogeneity and Allelism
Science, 1966Studies of four stone-forming cystinuric subjects from three unrelated pedigrees indicated that each was heterozygous for two of the three described mutant genes producing cystinuria (I, II, III). Their genotypes were I-II, II-III, I-III, and I-III, respectively.
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Genetic testing in prostate cancer management: Considerations informing primary care
Ca-A Cancer Journal for Clinicians, 2022Mary-Ellen Taplin +2 more
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