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Academic Journal

A pilot study of LINE-1 copy number and telomere length with aging in human sperm.

  • Authors : Berteli TS; Department of Obstetrics and Gynecology, Langone Medical Center, New York University, 462, 1st Avenue, New York, NY, 10016, USA. .; Human Reproduction Division, Department of Gynecology and Obstetrics, Ribeirao Preto Medical School, University of Sao Paulo, Ribeirao Preto, SP, Brazil. .

Subjects: DNA Copy Number Variations* ; Semen*; Humans

  • Source: Journal of assisted reproduction and genetics [J Assist Reprod Genet] 2023 Aug; Vol. 40 (8), pp. 1845-1854. Date of Electronic Publication: 2023 Jun 29.Publisher: Springer Country of Publication: Netherlands NLM ID: 9206495 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos.

  • Authors : Tang F; Department of Obstetrics and Gynecology, Reproductive Medicine Center, The First Affiliated Hospital of Anhui Medical University, No 218 Jixi Road, Hefei, Anhui, China.; NHC Key Laboratory of Study on Abnormal Gametes and Reproductive Tract, Anhui Medical University, Hefei, Anhui, China.

Subjects: Azoospermia*/Azoospermia*/Azoospermia*/genetics ; DNA Copy Number Variations*; Female Azoospermia, Nonobstructive

  • Source: Journal of assisted reproduction and genetics [J Assist Reprod Genet] 2023 Jul; Vol. 40 (7), pp. 1689-1702. Date of Electronic Publication: 2023 Mar 03.Publisher: Springer Country of Publication: Netherlands NLM ID: 9206495 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Establishment of a prognostic model for melanoma based on necroptosis-related genes.

  • Authors : Sui X; Department of Traditional Chinese Medicine, Qilu Hospital of Shandong University, Jinan, 250012, China.; First College of Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, 250011, China.

Subjects: DNA Copy Number Variations* ; Melanoma*/Melanoma*/Melanoma*/genetics; Humans

  • Source: Functional & integrative genomics [Funct Integr Genomics] 2023 Jun 14; Vol. 23 (3), pp. 202. Date of Electronic Publication: 2023 Jun 14.Publisher: Springer Country of Publication: Germany NLM ID: 100939343 Publication Model: Electronic Cited Medium:

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Academic Journal

Deciphering the RNA-binding protein interaction with the mRNAs encoded from human chromosome 15q11.2 BP1-BP2 microdeletion region.

  • Authors : Biswal SR; Department of Life Science, National Institute of Technology (NIT), Rourkela, Odisha, 769008, India.; Singh M

Subjects: DNA Copy Number Variations* ; Chromosomes, Human*; Humans Duplication 15q11-q13 Syndrome

  • Source: Functional & integrative genomics [Funct Integr Genomics] 2023 May 23; Vol. 23 (2), pp. 174. Date of Electronic Publication: 2023 May 23.Publisher: Springer Country of Publication: Germany NLM ID: 100939343 Publication Model: Electronic Cited Medium:

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Academic Journal

Characterization of the Immune Infiltration Landscape and Identification of Prognostic Biomarkers for Esophageal Cancer.

  • Authors : Chen Y; Department of Thoracic Surgery, Fujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, Fujian, China.; Huang X

Subjects: DNA Copy Number Variations* ; Esophageal Neoplasms*/Esophageal Neoplasms*/Esophageal Neoplasms*/genetics ; Esophageal Neoplasms*/Esophageal Neoplasms*/Esophageal Neoplasms*/therapy

  • Source: Molecular biotechnology [Mol Biotechnol] 2023 Mar; Vol. 65 (3), pp. 361-383. Date of Electronic Publication: 2022 Jul 03.Publisher: Springer Country of Publication: Switzerland NLM ID: 9423533 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

An effect of large-scale deletions and duplications on transcript expression.

  • Authors : Mielczarek M; Wroclaw University of Environmental and Life Sciences, Kozuchowska 7, 51-631, Wroclaw, Poland. .; Frąszczak M

Subjects: Genome* ; DNA Copy Number Variations*; Animals

  • Source: Functional & integrative genomics [Funct Integr Genomics] 2022 Dec 23; Vol. 23 (1), pp. 19. Date of Electronic Publication: 2022 Dec 23.Publisher: Springer Country of Publication: Germany NLM ID: 100939343 Publication Model: Electronic Cited Medium:

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Academic Journal

Genomic testing for copy number and single nucleotide variants in spermatogenic failure.

  • Authors : Hardy J; Department of OBGYN and Reproductive Sciences, Magee-Womens Research Institute, School of Medicine, University of Pittsburgh, 204 Craft Avenue, Pittsburgh, PA, 15213, USA.; Pollock N

Subjects: DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics ; Oligospermia*/Oligospermia*/Oligospermia*/diagnosis ; Oligospermia*/Oligospermia*/Oligospermia*/geneticsAzoospermia, Nonobstructive

  • Source: Journal of assisted reproduction and genetics [J Assist Reprod Genet] 2022 Sep; Vol. 39 (9), pp. 2103-2114. Date of Electronic Publication: 2022 Jul 18.Publisher: Springer Country of Publication: Netherlands NLM ID: 9206495 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

DNA sequence features underlying large-scale duplications and deletions in human.

  • Authors : Kołomański M; Biostatistics Group, Department of Genetics, Wroclaw University of Environmental and Life Sciences, Wroclaw, Poland.; Szyda J

Subjects: DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics ; Genome-Wide Association Study*; Base Sequence

  • Source: Journal of applied genetics [J Appl Genet] 2022 Sep; Vol. 63 (3), pp. 527-533. Date of Electronic Publication: 2022 May 20.Publisher: Springer Country of Publication: England NLM ID: 9514582 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Genomic imbalance in euploid pregnancy loss.

  • Authors : Gu C; Department of Obstetrics and Gynecology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, 9 Jinsui Road, Tianhe District, Guangzhou, 510623, China. .; Li K

Subjects: Abortion, Spontaneous*/Abortion, Spontaneous*/Abortion, Spontaneous*/genetics ; DNA Copy Number Variations*/DNA Copy Number Variations*/DNA Copy Number Variations*/genetics; Aneuploidy

  • Source: Journal of assisted reproduction and genetics [J Assist Reprod Genet] 2022 Sep; Vol. 39 (9), pp. 2115-2124. Date of Electronic Publication: 2022 Jun 06.Publisher: Springer Country of Publication: Netherlands NLM ID: 9206495 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains.

  • Authors : Wan R; Department of Human Genetics, Hannover Medical School, Hannover, Germany.; Schieck M

Subjects: Chromosome Aberrations* ; DNA Copy Number Variations* ; Immune System Diseases*/Immune System Diseases*/Immune System Diseases*/genetics

  • Source: Journal of clinical immunology [J Clin Immunol] 2022 Jul; Vol. 42 (5), pp. 1083-1092. Date of Electronic Publication: 2022 Apr 29.Publisher: Springer Country of Publication: Netherlands NLM ID: 8102137 Publication Model: Print-Electronic Cited Medium:

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  • 1-10 of  266 results for ""DNA copy number variations""