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Gastric metastases of oral carcinoma resulting from percutaneous endoscopic gastrostomy placement via the introducer technique.

Gastroenterology report

Teh JL, Wong RK, Gowans M, Shabbir A, Doshi B, Ong DE, Fan VT.
PMID: 24759969
Gastroenterol Rep (Oxf). 2013 Nov;1(3):211-3. doi: 10.1093/gastro/got027. Epub 2013 Oct 15.

INTRODUCTION. Tumour cell implantation is a rare complication in patients with head and neck cancers, who have undergone percutaneous endoscopic gastrostomy (PEG) tube placement. It has not been reported in patients who underwent a PEG insertion via the radiological...

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Teh JL, Wong RK, Gowans M, et al. Gastric metastases of oral carcinoma resulting from percutaneous endoscopic gastrostomy placement via the introducer technique. Gastroenterol Rep (Oxf). 2013;1(3):211-3doi: 10.1093/gastro/got027.
Teh, J. L., Wong, R. K., Gowans, M., Shabbir, A., Doshi, B., Ong, D. E., & Fan, V. T. (2013). Gastric metastases of oral carcinoma resulting from percutaneous endoscopic gastrostomy placement via the introducer technique. Gastroenterology report, 1(3), 211-3. https://doi.org/10.1093/gastro/got027
Teh, Jun Liang, et al. "Gastric metastases of oral carcinoma resulting from percutaneous endoscopic gastrostomy placement via the introducer technique." Gastroenterology report vol. 1,3 (2013): 211-3. doi: https://doi.org/10.1093/gastro/got027
Teh JL, Wong RK, Gowans M, Shabbir A, Doshi B, Ong DE, Fan VT. Gastric metastases of oral carcinoma resulting from percutaneous endoscopic gastrostomy placement via the introducer technique. Gastroenterol Rep (Oxf). 2013 Nov;1(3):211-3. doi: 10.1093/gastro/got027. Epub 2013 Oct 15. PMID: 24759969; PMCID: PMC3937992.
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Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus.

Journal of dental research

Awotoye W, Comnick C, Pendleton C, Zeng E, Alade A, Mossey PA, Gowans LJJ, Eshete MA, Adeyemo WL, Naicker T, Adeleke C, Busch T, Li M, Petrin A, Olotu J, Hassan M, Pape J, Miller SE, Donkor P, Anand D, Lachke SA, Marazita ML, Adeyemo AA, Murray JC, Albokhari D, Sobreira N, Butali A.
PMID: 34689653
J Dent Res. 2021 Oct 23;220345211046614. doi: 10.1177/00220345211046614. Epub 2021 Oct 23.

Risk loci identified through genome-wide association studies have explained about 25% of the phenotypic variations in nonsyndromic orofacial clefts (nsOFCs) on the liability scale. Despite the notable sex differences in the incidences of the different cleft types, investigation of...

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Awotoye W, Comnick C, Pendleton C, et al. Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. J Dent Res. 2021;220345211046614doi: 10.1177/00220345211046614.
Awotoye, W., Comnick, C., Pendleton, C., Zeng, E., Alade, A., Mossey, P. A., Gowans, L. J. J., Eshete, M. A., Adeyemo, W. L., Naicker, T., Adeleke, C., Busch, T., Li, M., Petrin, A., Olotu, J., Hassan, M., Pape, J., Miller, S. E., Donkor, P., Anand, D., Lachke, S. A., Marazita, M. L., Adeyemo, A. A., Murray, J. C., Albokhari, D., Sobreira, N., & Butali, A. (2021). Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. Journal of dental research, 220345211046614. https://doi.org/10.1177/00220345211046614
Awotoye, W, et al. "Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus." Journal of dental research vol. (2021): 220345211046614. doi: https://doi.org/10.1177/00220345211046614
Awotoye W, Comnick C, Pendleton C, Zeng E, Alade A, Mossey PA, Gowans LJJ, Eshete MA, Adeyemo WL, Naicker T, Adeleke C, Busch T, Li M, Petrin A, Olotu J, Hassan M, Pape J, Miller SE, Donkor P, Anand D, Lachke SA, Marazita ML, Adeyemo AA, Murray JC, Albokhari D, Sobreira N, Butali A. Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. J Dent Res. 2021 Oct 23;220345211046614. doi: 10.1177/00220345211046614. Epub 2021 Oct 23. PMID: 34689653.
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Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations.

Oral diseases

Li M, Olotu J, Buxo-Martinez CJ, Mossey PA, Anand D, Busch T, Alade A, Gowans LJJ, Eshete M, Adeyemo WL, Naicker T, Awotoye WO, Gupta S, Adeleke C, Bravo V, Huang S, Adamson OO, Toraño AM, Bello CA, Soto M, Soto M, Ledesma R, Marquez M, Cordero JF, Lopez-Del Valle LM, Salcedo MI, Debs N, Petrin A, Malloy H, Elhadi K, James O, Ogunlewe MO, Abate F, Hailu A, Mohammed I, Gravem P, Deribew M, Gesses M, Hassan M, Pape J, Obiri-Yeboah S, Arthur FKN, Oti AA, Donkor P, Marazita ML, Lachke SA, Adeyemo AA, Murray JC, Butali A.
PMID: 34061439
Oral Dis. 2021 Jun 01; doi: 10.1111/odi.13932. Epub 2021 Jun 01.

OBJECTIVES: Cleft lip with/without cleft palate and cleft palate only is congenital birth defects where the upper lip and/or palate fail to fuse properly during embryonic facial development. Affecting ~1.2/1000 live births worldwide, these orofacial clefts impose significant social...

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Li M, Olotu J, Buxo-Martinez CJ, et al. Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. Oral Dis. 2021;doi: 10.1111/odi.13932.
Li, M., Olotu, J., Buxo-Martinez, C. J., Mossey, P. A., Anand, D., Busch, T., Alade, A., Gowans, L. J. J., Eshete, M., Adeyemo, W. L., Naicker, T., Awotoye, W. O., Gupta, S., Adeleke, C., Bravo, V., Huang, S., Adamson, O. O., Toraño, A. M., Bello, C. A., Soto, M., Soto, M., Ledesma, R., Marquez, M., Cordero, J. F., Lopez-Del Valle, L. M., Salcedo, M. I., Debs, N., Petrin, A., Malloy, H., Elhadi, K., James, O., Ogunlewe, M. O., Abate, F., Hailu, A., Mohammed, I., Gravem, P., Deribew, M., Gesses, M., Hassan, M., Pape, J., Obiri-Yeboah, S., Arthur, F. K. N., Oti, A. A., Donkor, P., Marazita, M. L., Lachke, S. A., Adeyemo, A. A., Murray, J. C., & Butali, A. (2021). Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. Oral diseases, . https://doi.org/10.1111/odi.13932
Li, Mary, et al. "Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations." Oral diseases vol. (2021). doi: https://doi.org/10.1111/odi.13932
Li M, Olotu J, Buxo-Martinez CJ, Mossey PA, Anand D, Busch T, Alade A, Gowans LJJ, Eshete M, Adeyemo WL, Naicker T, Awotoye WO, Gupta S, Adeleke C, Bravo V, Huang S, Adamson OO, Toraño AM, Bello CA, Soto M, Soto M, Ledesma R, Marquez M, Cordero JF, Lopez-Del Valle LM, Salcedo MI, Debs N, Petrin A, Malloy H, Elhadi K, James O, Ogunlewe MO, Abate F, Hailu A, Mohammed I, Gravem P, Deribew M, Gesses M, Hassan M, Pape J, Obiri-Yeboah S, Arthur FKN, Oti AA, Donkor P, Marazita ML, Lachke SA, Adeyemo AA, Murray JC, Butali A. Variant analyses of candidate genes in orofacial clefts in multi-ethnic populations. Oral Dis. 2021 Jun 01; doi: 10.1111/odi.13932. Epub 2021 Jun 01. PMID: 34061439.
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Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus.

Journal of dental research

Awotoye W, Comnick C, Pendleton C, Zeng E, Alade A, Mossey PA, Gowans LJJ, Eshete MA, Adeyemo WL, Naicker T, Adeleke C, Busch T, Li M, Petrin A, Olotu J, Hassan M, Pape J, Miller SE, Donkor P, Anand D, Lachke SA, Marazita ML, Adeyemo AA, Murray JC, Albokhari D, Sobreira N, Butali A.
PMID: 34689653
J Dent Res. 2021 Oct 23;220345211046614. doi: 10.1177/00220345211046614. Epub 2021 Oct 23.

Risk loci identified through genome-wide association studies have explained about 25% of the phenotypic variations in nonsyndromic orofacial clefts (nsOFCs) on the liability scale. Despite the notable sex differences in the incidences of the different cleft types, investigation of...

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Awotoye W, Comnick C, Pendleton C, et al. Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. J Dent Res. 2021;220345211046614doi: 10.1177/00220345211046614.
Awotoye, W., Comnick, C., Pendleton, C., Zeng, E., Alade, A., Mossey, P. A., Gowans, L. J. J., Eshete, M. A., Adeyemo, W. L., Naicker, T., Adeleke, C., Busch, T., Li, M., Petrin, A., Olotu, J., Hassan, M., Pape, J., Miller, S. E., Donkor, P., Anand, D., Lachke, S. A., Marazita, M. L., Adeyemo, A. A., Murray, J. C., Albokhari, D., Sobreira, N., & Butali, A. (2021). Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. Journal of dental research, 220345211046614. https://doi.org/10.1177/00220345211046614
Awotoye, W, et al. "Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus." Journal of dental research vol. (2021): 220345211046614. doi: https://doi.org/10.1177/00220345211046614
Awotoye W, Comnick C, Pendleton C, Zeng E, Alade A, Mossey PA, Gowans LJJ, Eshete MA, Adeyemo WL, Naicker T, Adeleke C, Busch T, Li M, Petrin A, Olotu J, Hassan M, Pape J, Miller SE, Donkor P, Anand D, Lachke SA, Marazita ML, Adeyemo AA, Murray JC, Albokhari D, Sobreira N, Butali A. Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. J Dent Res. 2021 Oct 23;220345211046614. doi: 10.1177/00220345211046614. Epub 2021 Oct 23. PMID: 34689653.
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Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes.

Molecular genetics & genomic medicine

Gowans LJJ, Al Dhaheri N, Li M, Busch T, Obiri-Yeboah S, Oti AA, Sabbah DK, Arthur FKN, Awotoye WO, Alade AA, Twumasi P, Agbenorku P, Plange-Rhule G, Naicker T, Donkor P, Murray JC, Sobreira NLM, Butali A.
PMID: 33719213
Mol Genet Genomic Med. 2021 Apr;9(4):e1655. doi: 10.1002/mgg3.1655. Epub 2021 Mar 14.

BACKGROUND: Orofacial clefts (OFCs) are congenital malformations of the face and palate, with an incidence of 1 per 700 live births. Clubfoot or congenital talipes equinovarus (CTEV) is a three-dimensional abnormality of the leg, ankle, and feet that leads...

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Gowans LJJ, Al Dhaheri N, Li M, et al. Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes. Mol Genet Genomic Med. 2021;9(4):e1655doi: 10.1002/mgg3.1655.
Gowans, L. J. J., Al Dhaheri, N., Li, M., Busch, T., Obiri-Yeboah, S., Oti, A. A., Sabbah, D. K., Arthur, F. K. N., Awotoye, W. O., Alade, A. A., Twumasi, P., Agbenorku, P., Plange-Rhule, G., Naicker, T., Donkor, P., Murray, J. C., Sobreira, N. L. M., & Butali, A. (2021). Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes. Molecular genetics & genomic medicine, 9(4), e1655. https://doi.org/10.1002/mgg3.1655
Gowans, Lord J J, et al. "Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes." Molecular genetics & genomic medicine vol. 9,4 (2021): e1655. doi: https://doi.org/10.1002/mgg3.1655
Gowans LJJ, Al Dhaheri N, Li M, Busch T, Obiri-Yeboah S, Oti AA, Sabbah DK, Arthur FKN, Awotoye WO, Alade AA, Twumasi P, Agbenorku P, Plange-Rhule G, Naicker T, Donkor P, Murray JC, Sobreira NLM, Butali A. Co-occurrence of orofacial clefts and clubfoot phenotypes in a sub-Saharan African cohort: Whole-exome sequencing implicates multiple syndromes and genes. Mol Genet Genomic Med. 2021 Apr;9(4):e1655. doi: 10.1002/mgg3.1655. Epub 2021 Mar 14. PMID: 33719213; PMCID: PMC8123728.
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Enhanced T Cell Responses Induced by a Necrotic Dendritic Cell Vaccine, Expressing HCV NS3.

Frontiers in microbiology

Mekonnen ZA, Masavuli MG, Yu W, Gummow J, Whelan DM, Al-Delfi Z, Torresi J, Gowans EJ, Grubor-Bauk B.
PMID: 33343515
Front Microbiol. 2020 Nov 24;11:559105. doi: 10.3389/fmicb.2020.559105. eCollection 2020.

A vaccine that induces potent, broad and sustained cell-mediated immunity, resulting in effective memory has the potential to restrict hepatitis C (HCV) virus infection. Early, multi-functional CD4

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Mekonnen ZA, Masavuli MG, Yu W, et al. Enhanced T Cell Responses Induced by a Necrotic Dendritic Cell Vaccine, Expressing HCV NS3. Front Microbiol. 2020;11:559105doi: 10.3389/fmicb.2020.559105.
Mekonnen, Z. A., Masavuli, M. G., Yu, W., Gummow, J., Whelan, D. M., Al-Delfi, Z., Torresi, J., Gowans, E. J., & Grubor-Bauk, B. (2020). Enhanced T Cell Responses Induced by a Necrotic Dendritic Cell Vaccine, Expressing HCV NS3. Frontiers in microbiology, 11559105. https://doi.org/10.3389/fmicb.2020.559105
Mekonnen, Zelalem A, et al. "Enhanced T Cell Responses Induced by a Necrotic Dendritic Cell Vaccine, Expressing HCV NS3." Frontiers in microbiology vol. 11 (2020): 559105. doi: https://doi.org/10.3389/fmicb.2020.559105
Mekonnen ZA, Masavuli MG, Yu W, Gummow J, Whelan DM, Al-Delfi Z, Torresi J, Gowans EJ, Grubor-Bauk B. Enhanced T Cell Responses Induced by a Necrotic Dendritic Cell Vaccine, Expressing HCV NS3. Front Microbiol. 2020 Nov 24;11:559105. doi: 10.3389/fmicb.2020.559105. eCollection 2020. PMID: 33343515; PMCID: PMC7739890.
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DESCRIPTIVE PROFILE OF SHOULDER RANGE OF MOTION AND STRENGTH IN YOUTH ATHLETES PARTICIPATING IN OVERHEAD SPORTS.

International journal of sports physical therapy

Oliver GD, Downs JL, Barbosa GM, Camargo PR.
PMID: 33344026
Int J Sports Phys Ther. 2020 Dec;15(6):1090-1098. doi: 10.26603/ijspt20201090.

BACKGROUND: The unilateral and repetitive nature of overhead sports, often result in a biomechanical overload of the upper extremity. Understanding the musculoskeletal shoulder range of motion (ROM) and strength patterns in the youth sports of baseball, softball, and tennis...

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Oliver GD, Downs JL, Barbosa GM, et al. DESCRIPTIVE PROFILE OF SHOULDER RANGE OF MOTION AND STRENGTH IN YOUTH ATHLETES PARTICIPATING IN OVERHEAD SPORTS. Int J Sports Phys Ther. 2020;15(6):1090-1098doi: 10.26603/ijspt20201090.
Oliver, G. D., Downs, J. L., Barbosa, G. M., & Camargo, P. R. (2020). DESCRIPTIVE PROFILE OF SHOULDER RANGE OF MOTION AND STRENGTH IN YOUTH ATHLETES PARTICIPATING IN OVERHEAD SPORTS. International journal of sports physical therapy, 15(6), 1090-1098. https://doi.org/10.26603/ijspt20201090
Oliver, Gretchen D, et al. "DESCRIPTIVE PROFILE OF SHOULDER RANGE OF MOTION AND STRENGTH IN YOUTH ATHLETES PARTICIPATING IN OVERHEAD SPORTS." International journal of sports physical therapy vol. 15,6 (2020): 1090-1098. doi: https://doi.org/10.26603/ijspt20201090
Oliver GD, Downs JL, Barbosa GM, Camargo PR. DESCRIPTIVE PROFILE OF SHOULDER RANGE OF MOTION AND STRENGTH IN YOUTH ATHLETES PARTICIPATING IN OVERHEAD SPORTS. Int J Sports Phys Ther. 2020 Dec;15(6):1090-1098. doi: 10.26603/ijspt20201090. PMID: 33344026; PMCID: PMC7727435.
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Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report.

Molecular cytogenetics

Haj R, Jackson K, Torchia BA, Shaffer LG, Bejjani BA, Gowans GC, Ruff MW.
PMID: 19128483
Mol Cytogenet. 2009 Jan 07;2:2. doi: 10.1186/1755-8166-2-2.

BACKGROUND: Complex chromosome rearrangements (CCRs), which involve more than two breakpoints on two or more chromosomes, are uncommon occurrences. Although most CCRs appear balanced at the level of the light microscope, many demonstrate cryptic, submicroscopic imbalances at the translocation...

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Haj R, Jackson K, Torchia BA, et al. Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report. Mol Cytogenet. 2009;2:2doi: 10.1186/1755-8166-2-2.
Haj, R., Jackson, K., Torchia, B. A., Shaffer, L. G., Bejjani, B. A., Gowans, G. C., & Ruff, M. W. (2009). Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report. Molecular cytogenetics, 22. https://doi.org/10.1186/1755-8166-2-2
Haj, Roland, et al. "Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report." Molecular cytogenetics vol. 2 (2009): 2. doi: https://doi.org/10.1186/1755-8166-2-2
Haj R, Jackson K, Torchia BA, Shaffer LG, Bejjani BA, Gowans GC, Ruff MW. Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report. Mol Cytogenet. 2009 Jan 07;2:2. doi: 10.1186/1755-8166-2-2. PMID: 19128483; PMCID: PMC2654037.
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Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

Naicker T, Adeleke CC, Alade A, Mossey PA, Awotoye WA, Busch TD, Li M, Olotu J, Gowans LJJ, Aldous C, Butali A.
PMID: 34459660
Cleft Palate Craniofac J. 2021 Aug 30;10556656211038453. doi: 10.1177/10556656211038453. Epub 2021 Aug 30.

OBJECTIVE: The etiology of cleft palate (CP) is poorly understood compared with that of cleft lip with or without palate (CL ± P). Recently, variants in Grainyhead like transcription factor 3 (DESIGN: We sequenced the exons of SETTING: The...

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Naicker T, Adeleke CC, Alade A, et al. Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate. Cleft Palate Craniofac J. 2021;10556656211038453doi: 10.1177/10556656211038453.
Naicker, T., Adeleke, C. C., Alade, A., Mossey, P. A., Awotoye, W. A., Busch, T. D., Li, M., Olotu, J., Gowans, L. J. J., Aldous, C., & Butali, A. (2021). Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 10556656211038453. https://doi.org/10.1177/10556656211038453
Naicker, Thirona, et al. "Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate." The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association vol. (2021): 10556656211038453. doi: https://doi.org/10.1177/10556656211038453
Naicker T, Adeleke CC, Alade A, Mossey PA, Awotoye WA, Busch TD, Li M, Olotu J, Gowans LJJ, Aldous C, Butali A. Novel GRHL3 Variants in a South African Cohort With Cleft Lip and Palate. Cleft Palate Craniofac J. 2021 Aug 30;10556656211038453. doi: 10.1177/10556656211038453. Epub 2021 Aug 30. PMID: 34459660.
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Targeting protein arginine methyltransferase 5 (PRMT5) suppresses radiation-induced neuroendocrine differentiation and sensitizes prostate cancer cells to radiation.

Molecular cancer therapeutics

Owens JL, Beketova E, Liu S, Shen Q, Pawar JS, Asberry AM, Yang J, Deng X, Elzey BD, Ratliff TL, Cheng L, Choo CR, Citrin DE, Polascik TJ, Wang B, Huang J, Li C, Wan J, Hu CD.
PMID: 35027481
Mol Cancer Ther. 2022 Jan 13; doi: 10.1158/1535-7163.MCT-21-0103. Epub 2022 Jan 13.

Prostate cancer remains the second leading cause of cancer death among American men. Radiation therapy (RT) is a potentially curative treatment for localized prostate cancer, and failure to control localized disease contributes to the majority of prostate cancer deaths....

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Owens JL, Beketova E, Liu S, et al. Targeting protein arginine methyltransferase 5 (PRMT5) suppresses radiation-induced neuroendocrine differentiation and sensitizes prostate cancer cells to radiation. Mol Cancer Ther. 2022;doi: 10.1158/1535-7163.MCT-21-0103.
Owens, J. L., Beketova, E., Liu, S., Shen, Q., Pawar, J. S., Asberry, A. M., Yang, J., Deng, X., Elzey, B. D., Ratliff, T. L., Cheng, L., Choo, C. R., Citrin, D. E., Polascik, T. J., Wang, B., Huang, J., Li, C., Wan, J., & Hu, C. D. (2022). Targeting protein arginine methyltransferase 5 (PRMT5) suppresses radiation-induced neuroendocrine differentiation and sensitizes prostate cancer cells to radiation. Molecular cancer therapeutics, . https://doi.org/10.1158/1535-7163.MCT-21-0103
Owens, Jake L, et al. "Targeting protein arginine methyltransferase 5 (PRMT5) suppresses radiation-induced neuroendocrine differentiation and sensitizes prostate cancer cells to radiation." Molecular cancer therapeutics vol. (2022). doi: https://doi.org/10.1158/1535-7163.MCT-21-0103
Owens JL, Beketova E, Liu S, Shen Q, Pawar JS, Asberry AM, Yang J, Deng X, Elzey BD, Ratliff TL, Cheng L, Choo CR, Citrin DE, Polascik TJ, Wang B, Huang J, Li C, Wan J, Hu CD. Targeting protein arginine methyltransferase 5 (PRMT5) suppresses radiation-induced neuroendocrine differentiation and sensitizes prostate cancer cells to radiation. Mol Cancer Ther. 2022 Jan 13; doi: 10.1158/1535-7163.MCT-21-0103. Epub 2022 Jan 13. PMID: 35027481.
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Care of Eyes of New Born.

Journal of the National Medical Association

Gowens HL.
PMID: 20891713
J Natl Med Assoc. 1919 Jan;11(1):6-7.

No abstract available.

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Gowens HL. Care of Eyes of New Born. J Natl Med Assoc. 1919;11(1):6-7
Gowens, H. L. (1919). Care of Eyes of New Born. Journal of the National Medical Association, 11(1), 6-7.
Gowens, H L. "Care of Eyes of New Born." Journal of the National Medical Association vol. 11,1 (1919): 6-7.
Gowens HL. Care of Eyes of New Born. J Natl Med Assoc. 1919 Jan;11(1):6-7. PMID: 20891713; PMCID: PMC2621761.
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Interleukin polymorphisms in aggressive periodontitis: A literature review.

Journal of Indian Society of Periodontology

Maney P, Owens JL.
PMID: 26015661
J Indian Soc Periodontol. 2015 Mar-Apr;19(2):131-41. doi: 10.4103/0972-124X.145787.

Aggressive periodontitis (AgP), occurs in a younger age group (≤35 years) and is associated with the rapid destruction of periodontal attachment and supporting bone. Genetic polymorphisms are allelic variants that occur in at least 1% of the population that...

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Maney P, Owens JL. Interleukin polymorphisms in aggressive periodontitis: A literature review. J Indian Soc Periodontol. 2015;19(2):131-41doi: 10.4103/0972-124X.145787.
Maney, P., & Owens, J. L. (2015). Interleukin polymorphisms in aggressive periodontitis: A literature review. Journal of Indian Society of Periodontology, 19(2), 131-41. https://doi.org/10.4103/0972-124X.145787
Maney, Pooja, and Owens, Jessica Leigh. "Interleukin polymorphisms in aggressive periodontitis: A literature review." Journal of Indian Society of Periodontology vol. 19,2 (2015): 131-41. doi: https://doi.org/10.4103/0972-124X.145787
Maney P, Owens JL. Interleukin polymorphisms in aggressive periodontitis: A literature review. J Indian Soc Periodontol. 2015 Mar-Apr;19(2):131-41. doi: 10.4103/0972-124X.145787. PMID: 26015661; PMCID: PMC4439620.
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Showing 13 to 24 of 66 entries