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[PDF] Top 20 Mutations of the p53 Gene in Nasal NKT-Cell Lymphoma

Has 10000 "Mutations of the p53 Gene in Nasal NKT-Cell Lymphoma" found on our website. Below are the top 20 most common "Mutations of the p53 Gene in Nasal NKT-Cell Lymphoma".

Mutations of the p53 Gene in Nasal NKT-Cell Lymphoma

Mutations of the p53 Gene in Nasal NKT-Cell Lymphoma

... asal lymphoma frequently shows a polymorphous pattern of proliferation, consisting of large atypical cells, small lymphocytes, plasma cells, benign looking macrophages occasionally showing with ... Lihat dokumen lengkap

7

Mutations of p53, c-kit, K-ras, and β-Catenin Gene in Non-Hodgkin’s Lymphoma of Adrenal Gland - e-Repository BATAN

Mutations of p53, c-kit, K-ras, and β-Catenin Gene in Non-Hodgkin’s Lymphoma of Adrenal Gland - e-Repository BATAN

... Malignant lymphoma of the adrenal gland is a rare disease, usually with diffuse large cell morphol- ogy and B-cell immunophenotype, and often associated with Epstein-Barr virus ... Lihat dokumen lengkap

8

ANTICANCER ACTIVITY OF CALANONE ON HeLa CELL LINE | Ekowati | Indonesian Journal of Chemistry 21467 40553 1 PB

ANTICANCER ACTIVITY OF CALANONE ON HeLa CELL LINE | Ekowati | Indonesian Journal of Chemistry 21467 40553 1 PB

... one of the most common cancers in ...role in the development of essentially all cases of cervical carcinoma ...drugs of several different classes to destroy cells ... Lihat dokumen lengkap

5

Microsatellite Instability and k-ras, p53 Mutations in Thyroid Lymphoma

Microsatellite Instability and k-ras, p53 Mutations in Thyroid Lymphoma

... k-ras mutations Detected mutations of p53 and k-ras genes are summarized in Table ...Four of 19 cases (21.1%) had mutations at exon 1 of the k-ras ... Lihat dokumen lengkap

7

Diffuse Large B-Cell Lymphoma Complicated by Small Bowel Obstruction after Radiotherapy: a Case Study | Safitri | Journal of the Medical Sciences (Berkala ilmu Kedokteran) 12478 33321 1 PB

Diffuse Large B-Cell Lymphoma Complicated by Small Bowel Obstruction after Radiotherapy: a Case Study | Safitri | Journal of the Medical Sciences (Berkala ilmu Kedokteran) 12478 33321 1 PB

... affects the small bowel or, after pelvic radiotherapy, the ...contribute in individual patients. It may develop as a result of benign causes such as changes in intestinal transit, ... Lihat dokumen lengkap

9

A LEECH IN THE NASAL CAVITY.

A LEECH IN THE NASAL CAVITY.

... shown in the nasal ...dislodged in the nasopharynx, examination of the patient under general anesthesia may be required, especially in small ...children. In ... Lihat dokumen lengkap

5

MOLECULAR ANALYSIS OF INDONESIAN LCA PATIENTS AND IN VITRO SPLICE CORRECTION FOR CEP290-ASSOCIATED LCA - Diponegoro University | Institutional Repository (UNDIP-IR)

MOLECULAR ANALYSIS OF INDONESIAN LCA PATIENTS AND IN VITRO SPLICE CORRECTION FOR CEP290-ASSOCIATED LCA - Diponegoro University | Institutional Repository (UNDIP-IR)

... Centrosomal-ciliary gene CEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital ... Lihat dokumen lengkap

5

Analysis of KRAS2 Gene Mutations in Colorectal Cancer Patients in Malaysia - Diponegoro University | Institutional Repository (UNDIP-IR)

Analysis of KRAS2 Gene Mutations in Colorectal Cancer Patients in Malaysia - Diponegoro University | Institutional Repository (UNDIP-IR)

... and the second leading cause of cancer death in the Western ...is the commonest cancer among men and the third most common cancer among women in ...43% of ... Lihat dokumen lengkap

1

Directory UMM :Data Elmu:jurnal:B:Brain Research:Vol885.Issue1.2000:

Directory UMM :Data Elmu:jurnal:B:Brain Research:Vol885.Issue1.2000:

... for p53-mediated modulation of neuronal viability has been suggested by the finding that p53 expression is increased in damaged neurons in models of ischemia and ... Lihat dokumen lengkap

5

Identification of point mutations in Glucose-6-Phosphate Dehydrogenase gene in Timor Island people : A preliminary report

Identification of point mutations in Glucose-6-Phosphate Dehydrogenase gene in Timor Island people : A preliminary report

... [r] ... Lihat dokumen lengkap

4

Bibliography | Clinical Research Centre

Bibliography | Clinical Research Centre

... from the pilot study on the National Cancer Patient Registry--Cervical ...Adequacy of cellular material in split-sampling of cervical scrapings for routine cancer screening: an analysis ... Lihat dokumen lengkap

12

Gene Therapy Using Adeno-Associated Virus Vectors

Gene Therapy Using Adeno-Associated Virus Vectors

... IX in the serum for 4 to 9 weeks in the two ...However, in contrast to what was observed in animal models, the serum concentration went back to baseline ...rise in ... Lihat dokumen lengkap

11

NKX2.5, GATA4 and TBX1 gene mutations on Tetralogy Fallot.

NKX2.5, GATA4 and TBX1 gene mutations on Tetralogy Fallot.

... found. The anatomical changes are ventricular septal defect, overriding aorta, pulmonal stenosis and right ventricle ...hypertrophy. The etiology is related to environment, gene and the ... Lihat dokumen lengkap

9

HUBUNGAN IMUNOTERAPI DOSIS ESKALASI TERHADAP PERUBAHAN RASIO IL-4 IFN-Y DAN PERBAIKAN GEJALA KLINIK PENDERITA RINITIS ALERGI - Diponegoro University | Institutional Repository (UNDIP-IR)

HUBUNGAN IMUNOTERAPI DOSIS ESKALASI TERHADAP PERUBAHAN RASIO IL-4 IFN-Y DAN PERBAIKAN GEJALA KLINIK PENDERITA RINITIS ALERGI - Diponegoro University | Institutional Repository (UNDIP-IR)

... 33. Hamid QA, Schotman E, Jacobson MR, Walker SM, Durham SR. Increases in IL-12 messenger RNA cells accompany inhibition of allergen-induced late skin responses after successful grass pollen immunotherapy. ... Lihat dokumen lengkap

3

Directory UMM :Data Elmu:jurnal:I:Insect Biochemistry and Molecular Biology:Vol30.Issue10.Oct2000:

Directory UMM :Data Elmu:jurnal:I:Insect Biochemistry and Molecular Biology:Vol30.Issue10.Oct2000:

... S5 of domain II (Williamson et al., 1996). The house fly sodium channel carrying these two mutations is much less sensitive to the pyrethroid cismethrin than the wild-type when ... Lihat dokumen lengkap

7

Mutation Analysis Of Mitochondrial Dna Control Regions: A Study On Ectoderm Tissues.

Mutation Analysis Of Mitochondrial Dna Control Regions: A Study On Ectoderm Tissues.

... solution of 1 x TAE (tris-acetate ...all the agarose dissolves, then left at room temperature. After the agarose solution temperature reaches 50-60 °C, added 2  l into EtBr 10  ...turning ... Lihat dokumen lengkap

15

NKX2.5, GATA4 and TBX1 gene mutations on Tetralogy Fallot.

NKX2.5, GATA4 and TBX1 gene mutations on Tetralogy Fallot.

... found. The anatomical changes are ventricular septal defect, overriding aorta, pulmonal stenosis and right ventricle ...hypertrophy. The etiology is related to environment, gene and the ... Lihat dokumen lengkap

9

10.1128CMR.00008-08. 2008, 21(4):583. DOI: Clin. Microbiol. Rev. Shyam Daya and Kenneth I. Berns - Clin. Microbiol. Rev. 2008 Daya 583 93

10.1128CMR.00008-08. 2008, 21(4):583. DOI: Clin. Microbiol. Rev. Shyam Daya and Kenneth I. Berns - Clin. Microbiol. Rev. 2008 Daya 583 93

... made in the use of AAV vectors for human gene therapy, several developments are likely to enhance the potential utility of the ...system. The host immune response ... Lihat dokumen lengkap

12

08 Cervical Cancer Clinical

08 Cervical Cancer Clinical

... 52. Tran NT, Taylor R, Choe SI, et al. Knowledge, attitude and practice (KAP) concerning cervical cancer and screening among rural and urban female healthcare practitioners in the Democratic People's ... Lihat dokumen lengkap

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MOLECULAR GENETIC ANALYSIS OF NON SYNDROMIC RETINITIS PIGMENTOSA IN INDONESIA USING HIGH RESOLUTION HOMOZYGOSITY MAPPING - Diponegoro University | Institutional Repository (UNDIP-IR)

MOLECULAR GENETIC ANALYSIS OF NON SYNDROMIC RETINITIS PIGMENTOSA IN INDONESIA USING HIGH RESOLUTION HOMOZYGOSITY MAPPING - Diponegoro University | Institutional Repository (UNDIP-IR)

... (46) Collin RW, van den Born LI, Klevering BJ, de Castro Miro M., Littink KW, Arimadyo K, et al. High-resolution homozygosity mapping is a powerful tool to detect novel mutations causative for autosomal recessive ... Lihat dokumen lengkap

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