Search Results - "chromosome"

Iranian Azeri's Y-Chromosomal Diversity in the Context of Turkish-Speaking Populations of the Middle East by L Andonian, S Rezaie, A Margaryan, DD Farhud, K Mohammad, K Holakouie Naieni, MR Khorramizadeh, MH Sanati, M Jamali, P Bayatian, L Yepiskoposyan

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Chromosome 2q gain and epigenetic silencing of GATA3 in microglandular adenosis of the breast by Martin Radner, Jana Lisa vanLuttikhuizen, Stephan Bartels, Janin Bublitz, Isabel Grote, Luisa Rieger, Henriette Christgen, Helge Stark, Christopher Werlein, Marcel Lafos, Doris Steinemann, Ulrich Lehmann, Matthias Christgen, Hans Kreipe

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Prenatal Diagnosis of a Fetus with Ring Chromosomal 15 by Two- and Three-Dimensional Ultrasonography by Ingrid Schwach Werneck Britto, Sandra Regina Silva Herbest, Giselle Darahem Tedesco, Carolina Leite Drummond, Luiz Claudio Silva Bussamra, Edward Araujo Júnior, Rodrigo Ruano, Simone Hernandez Ruano, José Mendes Aldrighi

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BRCA-mutated gastric adenocarcinomas are associated with chromosomal instability and responsiveness to platinum-based chemotherapy by Ji Hyun Oh, Chang Ohk Sung, Hyung-Don Kim, Sung-Min Chun, Jihun Kim

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Chapter 17 Visualization and Functional Analysis of Spindle Actin and Chromosome Segregation in Mammalian Oocytes by Mogessie, Binyam

Subjects: “…Actin, Microtubules, Chromosomes, Meiosis, Oocytes, Eggs, Spindle, Fertility, High-resolution live microscopy…”
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Clinical, cytogenetic and molecular analyses of a rare case with ring chromosome 15 and review of the literature by Hui-Yuan Shao, Hong-Ling Wang, Hong Wu, Xiao-Yan Liu, Zong-Yu Miao

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Hyponatremia: An Unusual Presentation in a Neonate With Chromosome 1q21.1 Deletion Syndrome by Bakri Alzarka, Bakri Alzarka, Rachel Usala, Matthew T. Whitehead, Matthew T. Whitehead, Sun-Young Ahn, Sun-Young Ahn

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Chromosome abnormalities in embryos derived from microsurgical epididymal sperm aspiration and testicular sperm extraction by Shao-Ping Fred Weng, Mark W. Surrey, Hal C. Danzer, David L. Hill, Pau-Chung Chen, Tsung-Chieh Jackson Wu

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Lack of Association Between Partial Y chromosome AZFc-gr/gr Deletions and Male Infertility by Muhsin Jamil Abdulwahid, Mustafa Saber Al-Attar

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UBE2C Is a Potential Biomarker of Intestinal-Type Gastric Cancer With Chromosomal Instability by Jun Zhang, Xinyu Liu, Guanzhen Yu, Guanzhen Yu, Lei Liu, Jiejun Wang, Xiaoyu Chen, Yuhai Bian, Yuan Ji, Xiaoyan Zhou, Yinan Chen, Jun Ji, Zhen Xiang, Lei Guo, Jingyuan Fang, Yihong Sun, Hui Cao, Zhenggang Zhu, Yingyan Yu

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Philadelphia chromosome detection in chronic myeloid leukemia: Utility of phytohemagglutinin-stimulated peripheral blood culture by Man Updesh Singh Sachdeva, Neelam Varma, Kamer Singh Rana, Subhash Varma

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Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome by Masatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, Maki Ogawa, Fumihiko Suzuki, Takema Kato, Shunsuke Miyai, Rie Kawamura, Hidehito Inagaki, Hiroki Kurahashi, Jun Murotsuki

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Interstitial Deletions of the Short Arm of Chromosome 4 in a Patient With Mental Retardation and Focal Seizure by Pen-Hua Su, Inn-Chi Lee, Jia-Yuh Chen, Suh-Jen Chen, Ju-Shan Yu, Teng-Fu Tsao

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Frontline Blinatumomab in Older Adults with Philadelphia Chromosome-Negative B-Cell Acute Lymphoblastic Leukemia by Sandrine Niyongere, Gabriela Sanchez-Petitto, Jack Masur, Maria R. Baer, Vu H. Duong, Ashkan Emadi

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Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China by Xiaomei Luo, Hong Zhu, Lili Wang, Bing Xiao, Yanjie Fan, Hui Ye, Xiaomin Ying, Wenjuan Qiu, Huiwen Zhang, Lianshu Han, Xuefan Gu, Yongguo Yu, Lei Wang

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Microdeletion on chromosome 8p23.1 in a familial form of severe Buruli ulcer. by Quentin B Vincent, Aziz Belkadi, Cindy Fayard, Estelle Marion, Ambroise Adeye, Marie-Françoise Ardant, Christian R Johnson, Didier Agossadou, Lazaro Lorenzo, Julien Guergnon, Christine Bole-Feysot, Jeremy Manry, Patrick Nitschké, Ioannis Theodorou, Jean-Laurent Casanova, Laurent Marsollier, Annick Chauty, Laurent Abel, Alexandre Alcaïs, Franco-Beninese Buruli Research Group

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Rare chromosomal abnormalities: Can they be identified using conventional first trimester combined screening methods? by Daniel Kane, Mary E. D'Alton, Fergal D. Malone

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A dicentric Y chromosome resulting from pericentric inversion between the centromere and Yq heterochromatin by Long-Ching Kuan, Mei-Tsz Su, Ming Chen, Pao-Lin Kuo, Tsung-Cheng Kuo

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Roles of regulator of chromosome condensation 2 in cancer: Beyond its regulatory function in cell cycle by Ali Calderon-Aparicio, Ann Bode

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Skeletal and dental abnormalities in patients with sex chromosome aberrations: a systematic case-based review by Dawid Gruszczyński, Kacper Nijakowski, Anna Wolska-Bułach, Katarzyna Lacka

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