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Movement of Organisms Modified or Produced Through Genetic Engineering; Notice of Proposed Exemptions

The Federal Register / FIND, 2023, Vol.88 (219), p.78285

2023

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De nove Philadelphia chromosome-positive myelodysplastic syndromes with complex karyotype and p230 BCR::ABL fusion transcript: a case report with a literature review

Hematology, 2023, Vol.28 (1)

2023

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A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal cases

Systems Biology in Reproductive Medicine, 2023, Vol.ahead-of-print (ahead-of-print), p.1-7

2023

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A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities

Fetal and Pediatric Pathology, 2021, Vol.40 (3), p.256-261

2021

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A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature

The Journal of Maternal-Fetal & Neonatal Medicine, 2021, Vol.34 (17), p.2918-2922

2021

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First description of karyotypes and localization of ribosomal genes in two sand lances (Uranoscopiformes: Ammodytidae); small sand-eel (Ammodytes tobianus Linnaeus, 1758) and great sand-eel (Hyperoplus lanceolatus Le Sauvage, 1824)

Marine Biology Research, 2019, Vol.15 (8-9), p.523-529

2019

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The effect of ionomycin-induced oocyte activation on multiple morphological abnormalities of the sperm flagella

Systems Biology in Reproductive Medicine, 2023, Vol.69 (3), p.245-254

2023

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The effect of early life stress on the cognitive phenotype of children with an extra X chromosome (47,XXY/47,XXX)

Child Neuropsychology, 2018, Vol.24 (2), p.277-286

2018

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Rich maternal and paternal genetic diversity and divergent lineage composition in wild yak (Bos mutus)

Animal Biotechnology, 2022, Vol.33 (6), p.1382-1386

2022

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High prevalence of maternal mosaic monosomy X in pregnant women in Vietnam

The Journal of Maternal-Fetal & Neonatal Medicine, 2023, Vol.36 (1)

2023

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Quantitative assessment of chromosome instability induced through chemical disruption of mitotic progression

Cell Cycle, 2016, Vol.15 (13), p.1706-1714

2016

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HDAC6 inhibition disrupts maturational progression and meiotic apparatus assembly in mouse oocytes

Cell Cycle, 2018, Vol.17 (5), p.550-556

2018

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Hmga1 null mouse embryonic fibroblasts display downregulation of spindle assembly checkpoint gene expression associated to nuclear and karyotypic abnormalities

Cell Cycle, 2016, Vol.15 (6), p.812-818

2016

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Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome

Ophthalmic Genetics, 2023, Vol.44 (2), p.198-203

2023

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Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype

Gynecological Endocrinology, 2021, Vol.37 (4), p.377-381

2021

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Comparative evaluation of autosomal STRs and X-chromosome STRs as a complement of autosomal STRs in kinship testing in Southern Han Chinese

Annals of Human Biology, 2021, Vol.48 (1), p.66-69

2021

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Retinoschisis and Hyperopia Associated with Partial Monosomy of 6q and Partial Trisomy of 11q

Ophthalmic Genetics, 2014, Vol.35 (2), p.107-111

2014

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Probe the function of histone lysine 36 methylation using histone H3 lysine 36 to methionine mutant transgene in mammalian cells

Cell Cycle, 2017, Vol.16 (19), p.1781-1789

2017

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Movement of Organisms Modified or Produced Through Genetic Engineering; Notice of Exemptions

The Federal Register / FIND, 2021, Vol.86 (135), p.37988

2021

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The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype

Systems Biology in Reproductive Medicine, 2015, Vol.61 (6), p.398-402

2015

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Protease dead separase inhibits chromosome segregation and RAB-11 vesicle trafficking

Cell Cycle, 2017, Vol.16 (20), p.1902-1917

2017

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Life-history chronicle for a patient with the recently described chromosome 4q21 microdeletion syndrome

American Journal of Medical Genetics Part A, 2012, Vol.158A (10), p.2606-2609

2012

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Ring chromosome 7 in a child with T-cell acute lymphoblastic leukemia with myeloid markers

Baylor University Medical Center Proceedings, 2021, Vol.34 (2), p.302-304

2021

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Direct duplication of the Y chromosome with normal phenotype - incidental finding in two cases

Andrologia, 2013, Vol.45 (2), p.140-144

2013

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Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11

American Journal of Medical Genetics Part A, 2013, Vol.161A (1), p.179-184

2013

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Movement of Organisms Modified or Produced Through Genetic Engineering; Notice of Proposed Exemptions

De nove Philadelphia chromosome-positive myelodysplastic syndromes with complex karyotype and p230 BCR::ABL fusion transcript: a case report with a literature review

A rare ring chromosome 21 abnormality is associated with azoospermia in two different phenotypically normal cases

A Case of a Derivative Chromosome: der(Y)t(Y;18)Pat with Congenital Abnormalities

A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature

First description of karyotypes and localization of ribosomal genes in two sand lances (Uranoscopiformes: Ammodytidae); small sand-eel (Ammodytes tobianus Linnaeus, 1758) and great sand-eel (Hyperoplus lanceolatus Le Sauvage, 1824)

The effect of ionomycin-induced oocyte activation on multiple morphological abnormalities of the sperm flagella

The effect of early life stress on the cognitive phenotype of children with an extra X chromosome (47,XXY/47,XXX)

Rich maternal and paternal genetic diversity and divergent lineage composition in wild yak (Bos mutus)

High prevalence of maternal mosaic monosomy X in pregnant women in Vietnam

Quantitative assessment of chromosome instability induced through chemical disruption of mitotic progression

HDAC6 inhibition disrupts maturational progression and meiotic apparatus assembly in mouse oocytes

Hmga1 null mouse embryonic fibroblasts display downregulation of spindle assembly checkpoint gene expression associated to nuclear and karyotypic abnormalities

Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosome

Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype

Comparative evaluation of autosomal STRs and X-chromosome STRs as a complement of autosomal STRs in kinship testing in Southern Han Chinese

Retinoschisis and Hyperopia Associated with Partial Monosomy of 6q and Partial Trisomy of 11q

Probe the function of histone lysine 36 methylation using histone H3 lysine 36 to methionine mutant transgene in mammalian cells

Movement of Organisms Modified or Produced Through Genetic Engineering; Notice of Exemptions

The first case of a small supernumerary marker chromosome derived from chromosome 10 in an adult woman with an apparently normal phenotype

Protease dead separase inhibits chromosome segregation and RAB-11 vesicle trafficking

Life-history chronicle for a patient with the recently described chromosome 4q21 microdeletion syndrome

Ring chromosome 7 in a child with T-cell acute lymphoblastic leukemia with myeloid markers

Direct duplication of the Y chromosome with normal phenotype - incidental finding in two cases

Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11

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