First African case report of hypoparathyroidism, deafness and renal dysplasia (HDR) syndrome due to inverted duplication and deletion of chromosome 10p by Tumelo M. Satekge, Glenrose Rikhotso, Bianca Rossouw, Bronwyn Dillon, Fiona Baine-Savanhu

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Detection of Chromosome X;18 Breakpoints and Translocation of the Xq22.3;18q23 Regions Resulting in Variable Fertility Phenotypes by Attila Szvetko, Nicole Martin, Chris Joy, Andrea Hayward, Bob Watson, Andrew Cary, Stephen Withers

“…We describe a familial pattern of gonosomal-autosomal translocation between the X and 18 chromosomes, balanced and unbalanced forms, in male and female siblings. …”
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A chromosomal reference genome sequence for the malaria mosquito, Anopheles maculipalpis, Giles, 1902 [version 1; peer review: 2 approved] by Shane A. McCarthy, Damon-Lee B. Pointon, Ying Sims, James W. Torrance, Marcela Uliano-Silva, Martin G. Wagah, Diego Ayala, Jonathan M. D. Wood, Joanna C. Collins, Harriet F. Johnson, Ksenia Krasheninnikova, Mara K. N. Lawniczak, Haynes Heaton, Alan Tracey, Katharina von Wyschetzki, Alex Makunin, Daniel E. Neafsey, Boris K. Makanga, Lemonde B. A. Bouafou, Sarah E. Pelan, Nil Rahola

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Frequent variations and phylogenetic relationships within the genus Secale identified by ND-FISH according to the genome-wide universal oligonucleotides chromosome probes by Zhi Li, Zhi Li, Zhi Li, Zixin Sun, Zixin Sun, Tianheng Ren, Tianheng Ren, Tianheng Ren

“…The evolution of rye chromosomes can be analyzed by the variation degree of different probes on rye chromosomes.MethodsAll materials were identified by non-denaturing fluorescence in situ hybridization (ND-FISH). …”
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Insights into the evolution and fruit color change‐related genes of chromosome doubled sweet cherry from an updated complete T2T genome assembly by Xin Zhang, Xuwei Duan, Jing Wang, Xiaoming Zhang, Guohua Yan, Chuanbao Wu, Yu Zhou, Kaichun Zhang

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Peer Review of “Identifying Safeguards Disabled by Epstein-Barr Virus Infections in Genomes From Patients With Breast Cancer: Chromosomal Bioinformatics Analysis”

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Retracted: A Newborn with Genital Ambiguity, 45,X/46,XY Mosaicism, a Jumping Chromosome Y, and Congenital Adrenal Hyperplasia by Case Reports in Endocrinology

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Chromosome-level genome reference of the Caucasian dwarf goby Knipowitschia cf. caucasica, a new alien Gobiidae invading the River Rhine by Schoenle, Alexandra, Guiglielmoni, Nadège, Mainz, Tobias, Greve, Carola, Hamadou, Alexander Ben, Heermann, Lisa, Borcherding, Jost, Waldvogel, Ann-Marie

“…We assembled a high-quality chromosome-scale reference genome of Knipowitschia cf. caucasica by combining PacBio, Omni-C and Illumina technologies. …”
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Peer Review of “Identifying Safeguards Disabled by Epstein-Barr Virus Infections in Genomes From Patients With Breast Cancer: Chromosomal Bioinformatics Analysis”

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Cytogenetics of Oryctes nasicornis L. (Coleoptera: Scarabaeidae: Dynastinae) with Emphasis on Its Neochromosomes and Asynapsis Inducing Premature Bivalent and Chromosome Splits at Meiosis by B. Dutrillaux, A. M. Dutrillaux

“…The chromosomes of specimens of Oryctes nasicornis from three locations in France and two locations in Greece were studied. …”
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Rad3 decorates critical chromosomal domains with gammaH2A to protect genome integrity during S-Phase in fission yeast. by Sophie Rozenzhak, Eva Mejía-Ramírez, Jessica S Williams, Lana Schaffer, Jennifer A Hammond, Steven R Head, Paul Russell

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The development and study of common wheat introgression lines derived from the synthetic form RS7 by R. O. Davoyan, I. V. Bebyakina, E. R. Davoyan, D. S. Mikov, Yu. S. Zubanova, D. M. Boldakov, E. D. Badaeva, I. G. Adonina, E. A. Salina, A. N. Zinchenko

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«The Mechanism of Mendelian Heredity» (The 100th anniversary of the first publication of the book by the group of T.H. Morgan) by E. B. Muzrukova

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A comparative study of dual marker test vs ultrasonography markers for detection of chromosomal abnormalities in patients attending a tertiary care center by S. Sailaja, Bindu Reddy Pamulapati

“… ABSTRACT Background It becomes important to detect chromosomal abnormalities prenatally and early in the pregnancy. …”
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Complex epilepsy phenotype associated with chromosome 2q24.2‐q24.3 deletion involving sodium channel gene cluster by Rima Madan, Fiorella S. Guido, Nicole Brescia

“…Abstract Objective The 2q24.2‐24.3 chromosome region encodes sodium channel genes important in severe childhood epilepsy, notably SCN1A linked to Dravet syndrome (DS). …”
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Molecular Monitoring in Adult Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia with the Variant e13a3 BCR-ABL1 Fusion by Mireille Crampe, Laura Kearney, David O’Brien, C. Larry Bacon, Derville O’Shea, Stephen E. Langabeer

“…Monitoring BCR-ABL1 transcript levels in patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) is a widely adopted method to assess response to therapy. …”
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Co-infection of HSV-1 amplicons containing the XPC gene and a human artificial chromosome vector into primary XPC deficient fibroblast cells by Daniela Moralli, Avi Smith, Jonathan Garlick, Kenneth H. Kraemer, Zoia L. Monaco

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Chromosome 15q13.1q13.2 microdeletion in a foetus with severe congenital heart defects: A case report by Thi Ha Vu, Thi Hai Hoang, Thi Sim Nguyen, Khanh Dung Ho, Thi Kim Phuong Doan

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Putative evolution of Myxococcus fulvus 124B02 plasmid pMF1 from a chromosomal segment in another Myxococcus species by Shruti Jain, Gaurav Sharma

“…We further reported that all pMF1 plasmid genes depict homology with Myxococcus stipitatus CYD1 draft genome (contig 28) and a chromosomal segment of M. stipitatus DSM14675 in a syntenic manner, implying the presence of plasmid-like structure in M. stipitatus CYD1, integrated into its chromosome. …”
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Alien introgressions and chromosomal rearrangements do not affect the activity of gliadin-coding genes in hybrid lines of Triticum aestivum L. × Aegilops columnaris Zhuk by A. Yu. Novoselskaya-Dragovich, A. A. Yankovskaya, E. D. Badaeva

“…Using chromosome C-banding and electrophoresis of grain storage proteins, gliadins, 17 Triticum aestivumAegilops columnaris lines with substitutions of chromosomes of homoeologous groups 1 and 6 were examined. …”
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