Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Chandra R. Samuel"'
Autor:
Jaganathan Suganya, Smita B Kujur, Kamala Selvaraj, Muthiah S. Suruli, Geetha Haripriya, Chandra R. Samuel
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 7, Pp GC05-GC10 (2015)
Background and Objective: Male infertility has been associated with aneuploidies and structural chromosomal abnormalities, Yq microdeletions and specific gene mutations and/or polymorphisms. Besides genetic factors, any block in sperm delivery, en
Externí odkaz:
https://doaj.org/article/abd953197b484329a4b886d7e89726fa
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 6, Pp QD01-QD03 (2017)
Fragile sites represent regions of chromatin that fail to compact during mitosis. Based on the prevalence and pattern of inheritance they are classified as rare fragile sites or common fragile sites. Rare fragile sites either occur spontaneously or
Externí odkaz:
https://doaj.org/article/2d72619c15484431b795bd529620c99a
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 12, Pp GD01-GD03 (2016)
Spontaneous abortion or loss of fetus prior to 20 weeks of gestation is observed in 15-20% of clinically recognized pregnancies. Recurrent Miscarriage (RM) is defined as three or more consecutive pregnancy losses and it affects 1-2% of women. Parent
Externí odkaz:
https://doaj.org/article/b8e98d3014f94eba939e2a3c18a6dda4
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Objective: Multiple myeloma (MM) is a clinically and genetically heterogeneous plasma cell neoplasm. The prognosis of MM patients is dependent on several factors including the patient’s age, the stage of disease and genetic alterations. This study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d8e20ecd0ab60ac3b9d42d41f750aa9
https://pubmed.ncbi.nlm.nih.gov/30678438
https://pubmed.ncbi.nlm.nih.gov/30678438
Autor:
Muthiah S. Suruli, Kamala Selvaraj, Jaganathan Suganya, Geetha Haripriya, Chandra R Samuel, Smita B. Kujur
Publikováno v:
British Journal of Medicine and Medical Research. 13:1-10
Aim: Yq microdeletions involving the azoospermia factor (AZF) region are the second most frequent genetic cause of spermatogenic failure next to Klinefelter syndrome. These deletions occur in about 10-15 percent of men with azoospermia and severe oli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ea6d24926d32caec15c2d577dd5745e
https://doi.org/10.9734/bjmmr/2016/24208
https://doi.org/10.9734/bjmmr/2016/24208
Autor:
Chandra R Samuel, Prabu Pandurangan, Nithya Mohan, Perumal Govindasamy, Anil Tarigopula, Charles Sharchil, Rama Mani
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 2, Pp GC01-GC05 (2018)
Introduction: Multiple Myeloma (MM) is a cytogenetically heterogeneous haematologic malignancy characterised by uncontrolled proliferation of clonal plasma cells within the bone marrow. TP53 gene inactivation is considered as an independent prognosti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3f00ca52ad4a52d5ff931983d0fc6d0
https://doi.org/10.7860/jcdr/2018/34222.11170
https://doi.org/10.7860/jcdr/2018/34222.11170
Autor:
Patricia Teixeira, Lin Li, Atalia Shtorch-Asor, Mara Santos Córdoba, Quentin Hauet, Marcos L.M. Morris, Albert David, Bertrand Isidor, Xuan Huang, Cristina T.N. Medina, Nicolas Joram, Qun Fang, Yanmin Luo, Iris Ferrari, Reuven Sharony, Jayarama S. Kadandale, Olivier Baron, Deenadayalu Anuradha, Ido Laish, Shaobin Lin, Linhuan Huang, Tal Biron-Shental, Laurianne Le Gloan, Chloé Arfeuille, Pauline Arnaud, Maria Gisele dos Santos, Ambika Srikanth, Chandra R Samuel, Faruk Hadziselimovic, Beatriz R. Versiani, Dana Sadeh-Mestechkin, Nadine Hanna, Pooja S. Kulshreshtha, Catherine Boileau, Juliana F. Mazzeu, Meirav Keiser, Satz Mengensatzproduktion, Bénédicte Romefort, Martin Poot, Druckerei Stückle, José Eduardo Baroneza, Aliza Amiel, Aswini Sivasankaran, Ana Carolina S. Fonseca, Véronique Gournay, Silviene Fabiana de Oliveira, Erika L. Freitas, Nadir Benbrik, Liege L. Roese, Carla Rosenberg, Aline Pic-Taylor
Publikováno v:
Molecular Syndromology. 6:I-VI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::929367282db9f15b4543c59f0432368f
https://doi.org/10.1159/000444613
https://doi.org/10.1159/000444613
Autor:
Qun Fang, Bertrand Isidor, Catherine Boileau, Juliana F. Mazzeu, Meirav Keiser, Dana Sadeh-Mestechkin, Cristina T.N. Medina, Nadine Hanna, Pooja S. Kulshreshtha, Erika L. Freitas, Bénédicte Romefort, Quentin Hauet, Olivier Baron, Ambika Srikanth, Tal Biron-Shental, Reuven Sharony, Atalia Shtorch-Asor, Laurianne Le Gloan, Deenadayalu Anuradha, Xuan Huang, Mara Santos Córdoba, Marcos L.M. Morris, Martin Poot, Satz Mengensatzproduktion, Chandra R Samuel, Shaobin Lin, José Eduardo Baroneza, Aliza Amiel, Chloé Arfeuille, Jayarama S. Kadandale, Albert David, Silviene Fabiana de Oliveira, Patricia Teixeira, Iris Ferrari, Carla Rosenberg, Liege L. Roese, Lin Li, Maria Gisele dos Santos, Linhuan Huang, Aswini Sivasankaran, Ana Carolina S. Fonseca, Aline Pic-Taylor, Druckerei Stückle, Yanmin Luo, Faruk Hadziselimovic, Pauline Arnaud, Véronique Gournay, Beatriz R. Versiani, Nadir Benbrik, Ido Laish, Nicolas Joram
Publikováno v:
Molecular Syndromology. 6:304-335
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4513ad8a744a6ab6376b0f1c5f48f500
https://doi.org/10.1159/000444288
https://doi.org/10.1159/000444288
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 6, Pp QD01-QD03 (2017)
Fragile sites represent regions of chromatin that fail to compact during mitosis. Based on the prevalence and pattern of inheritance they are classified as rare fragile sites or common fragile sites. Rare fragile sites either occur spontaneously or c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32fa3c5d8f807ac61d66f641a61da1e5
https://doi.org/10.7860/jcdr/2017/26545.10043
https://doi.org/10.7860/jcdr/2017/26545.10043
Autor:
Lakshmi Rao Kandukuri, Chandra R Samuel, Aswini Sivasankaran, Deenadayalu Anuradha, Murthy Kanakavalli
Publikováno v:
Cytogenetic and genome research. 148(2-3)
Ring chromosomes have been described for all human chromosomes and are typically associated with physical and/or mental abnormalities resulting from a deletion of the terminal ends of both chromosome arms. This report describes the presence of a ring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::132304e19799e9ed69936c207039601a
https://pubmed.ncbi.nlm.nih.gov/27222354
https://pubmed.ncbi.nlm.nih.gov/27222354