• 제목/요약/키워드: hereditary

검색결과 510건 처리시간 0.029초

ON THE DUALITY OF THE SPACE X AND THE ALGEBRA $C_p$(X)

  • Park, Sung-Ki
    • 대한수학회보
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    • 제36권4호
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    • pp.717-722
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    • 1999
  • The set of continuous maps of a space X to real usual space R equipped with the toplogy of pointwise convergence will be denoted by $C_p$(X). In this paper, we prove that; $C_p$(X) is hereditarily separable and hereditary Lindelof if and only if $X^n$ is hereditarily separable and hereditary Lindelof.

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LOWER AND UPPER FORMATION RADICAL OF NEAR-RINGS

  • Saxena, P.K.;Bhandari, M.C.
    • Kyungpook Mathematical Journal
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    • 제19권2호
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    • pp.205-211
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    • 1979
  • In this paper we continue the study of formation radical (F-radical) classes initiated in [3]. Hereditary and stronger properties of F-radical classes are discussed by giving construction for lower hereditary, lower stronger and lower strongly hereditary F-radical classes containing a given class M. It is shown that the Baer F-radical B is the lower strongly hereditary F-radical class containing the class of all nilpotent ideals and it is the upper radical class with $\{(I,\;N){\mid}N{\in}C,\;N\;is\;prime\}{\subset}SB$ where SB denotes the semisimple F-radical class of B and C is an arbitrary but fixed class of homomorphically closed near-rings. The existence of a largest F-radical class contained in a given class is examined using the concept of complementary F-radical introduced by Scott [5].

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Genetics of hereditary nephrotic syndrome: a clinical review

  • Ha, Tae-Sun
    • Clinical and Experimental Pediatrics
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    • 제60권3호
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    • pp.55-63
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    • 2017
  • Advances in podocytology and genetic techniques have expanded our understanding of the pathogenesis of hereditary steroid-resistant nephrotic syndrome (SRNS). In the past 20 years, over 45 genetic mutations have been identified in patients with hereditary SRNS. Genetic mutations on structural and functional molecules in podocytes can lead to serious injury in the podocytes themselves and in adjacent structures, causing sclerotic lesions such as focal segmental glomerulosclerosis or diffuse mesangial sclerosis. This paper provides an update on the current knowledge of podocyte genes involved in the development of hereditary nephrotic syndrome and, thereby, reviews genotype-phenotype correlations to propose an approach for appropriate mutational screening based on clinical aspects.

ON 𝜃-MODIFICATIONS OF GENERALIZED TOPOLOGIES VIA HEREDITARY CLASSES

  • Al-Omari, Ahmad;Modak, Shyamapada;Noiri, Takashi
    • 대한수학회논문집
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    • 제31권4호
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    • pp.857-868
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    • 2016
  • Let (X, ${\mu}$) be a generalized topological space (GTS) and $\mathcal{H}$ be a hereditary class on X due to $Cs{\acute{a}}sz{\acute{a}}r$ [8]. In this paper, we define an operator $()^{\circ}:\mathcal{P}(X){\rightarrow}\mathcal{P}(X)$. By setting $c^{\circ}(A)=A{\cup}A^{\circ}$ for every subset A of X, we define the family ${\mu}^{\circ}=\{M{\subseteq}X:X-M=c^{\circ}(X-M)\}$ and show that ${\mu}^{\circ}$ is a GT on X such that ${\mu}({\theta}){\subseteq}{\mu}^{\circ}{\subseteq}{\mu}^*$, where ${\mu}^*$ is a GT in [8]. Moreover, we define and investigate ${\mu}^{\circ}$-codense and strongly ${\mu}^{\circ}$-codense hereditary classes.

ON STRONGLY GORENSTEIN HEREDITARY RINGS

  • Hu, Kui;Kim, Hwankoo;Wang, Fanggui;Xu, Longyu;Zhou, Dechuan
    • 대한수학회보
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    • 제56권2호
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    • pp.373-382
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    • 2019
  • In this note, we mainly discuss strongly Gorenstein hereditary rings. We prove that for any ring, the class of SG-projective modules and the class of G-projective modules coincide if and only if the class of SG-projective modules is closed under extension. From this we get that a ring is an SG-hereditary ring if and only if every ideal is G-projective and the class of SG-projective modules is closed under extension. We also give some examples of domains whose ideals are SG-projective.

On n-Amitsur Rings

  • Ochirbat, Baatar;Mendes, Deolinda I.C.;Tumurbat, Sodnomkhorloo
    • Kyungpook Mathematical Journal
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    • 제60권4호
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    • pp.711-721
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    • 2020
  • The concepts of an Amitsur ring and a hereditary Amitsur ring, which were introduced and studied by S. Tumurbat in a recent paper, are generalized. For a positive integer n, a ring A is said to be an n-Amitsur ring if γ(A[Xn]) = (γ(A[Xn]) ∩ A)[Xn] for all radicals γ, where A[Xn] is the polynomial ring over A in n commuting indeterminates. If a ring A satisfies the above equation for all hereditary radicals γ, then A is said to be a hereditary n-Amitsur ring. Characterizations and examples of these rings are provided. Moreover, new radicals associated with n-Amitsur rings are introduced and studied. One of these is a special radical and its semisimple class is polynomially extensible.

SOME RESULTS ON 2-STRONGLY GORENSTEIN PROJECTIVE MODULES AND RELATED RINGS

  • Dong Chen;Kui Hu
    • 대한수학회보
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    • 제60권4호
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    • pp.895-903
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    • 2023
  • In this paper, we give some results on 2-strongly Gorenstein projective modules and related rings. We first investigate the relationship between strongly Gorenstein projective modules and periodic modules and then give the structure of modules over strongly Gorenstein semisimple rings. Furthermore, we prove that a ring R is 2-strongly Gorenstein hereditary if and only if every ideal of R is Gorenstein projective and the class of 2-strongly Gorenstein projective modules is closed under extensions. Finally, we study the relationship between 2-Gorenstein projective hereditary and 2-Gorenstein projective semisimple rings, and we also give an example to show the quotient ring of a 2-Gorenstein projective hereditary ring is not necessarily 2-Gorenstein projective semisimple.

Cationic Trypsinogen N29I 유전자 변이에 의한 유전 췌장염 1례 (A case of hereditary pancreatitis with a N29I mutation in the cationic trypsinogen gene)

  • 신지연;오대성;류정민;심정옥;박지숙;고재성;서정기
    • Clinical and Experimental Pediatrics
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    • 제49권10호
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    • pp.1111-1115
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    • 2006
  • 유전성 췌장염은 비교적 젊은 연령에서 다른 이유 없이 반복적으로 급성 췌장염으로 나타나는데 나이가 들면서 만성 췌장염으로 이행된다. 동일 가계 내에 2세대 이상에 걸쳐서 3명 이상의 췌장염 환자가 있을 때 진단이 가능하며 이와 관련된 유전자로 trypsinogen을 만드는 PRSS1 유전자 변이(R122H, N29I)가 가장 대표적으로 알려져 있다. 저자들은 3세부터 반복적인 췌장염으로 입원 치료를 했던 15세 환아와 반복적 췌장염을 앓은 환아모, 환아 동생을 대상으로 CT 유전자의 exon 2, 3의 염기 서열을 분석하여 환아와 환아모에서 국내 처음으로 N29I 변이를 경험하였기에 보고하는 바이다.

장액성 난소암 환자의 유전성 난소암에 대한 지식 및 불안정도 (Knowledge and Anxiety Related to Hereditary Ovarian Cancer in Serous Ovarian Cancer Patients)

  • 이상희;이향규;임명철;김수
    • 여성건강간호학회지
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    • 제25권4호
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    • pp.365-378
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    • 2019
  • Purpose: The awareness of hereditary breast and ovarian cancer (HBOC) and BRCA testing is increasing in Korea. Compared to the sizable research on HBOC knowledge among breast cancer women, studies in the ovarian cancer population are limited. This paper aimed to investigate the level of knowledge of hereditary ovarian cancer and anxiety in women diagnosed with serous ovarian cancer in Korea and determine differences in the knowledge and anxiety according to whether genetic testing was undertaken and whether BRCA1 or BRCA2 mutations were present. Methods: Using a descriptive research design, a cross-sectional survey was conducted on 100 women diagnosed with serous ovarian cancer at N hospital in Gyeonggi-do, Korea, from July to November 2018. The collected data were analyzed by descriptive statistics, independent t-tests, one-way analysis of variance, and Pearson's correlation coefficient using the SPSS 21.0 program. Results: The hereditary ovarian cancer-related knowledge score was mid-level (mean score 8.90±3.29 out of a total of 17), as was the state anxiety level was mid-level (mean score 47.96±3.26 out of possible score range of 20-80). Genetic knowledge of hereditary ovarian cancer was associated with age, education, occupation, genetic counseling, and BRCA mutations. There were no statistically significant factors related to anxiety and there were no statistically significant correlations between knowledge level and anxiety. Conclusion: More comprehensive education on gene-related cancer is needed for ovarian cancer patients, especially for items with low knowledge scores. A genetic counseling protocol should be developed to allow more patients to alleviate their anxiety through genetic counseling.