Cargando…

Analysis of copy number variations of the autosomal genome in 156 patients with azoospermia

BACKGROUND: To analyze the relationship between copy number variations (CNVs) and azoospermia by analyzing the chromosome gene copy data of 156 patients with azoospermia. METHODS: A total of 156 azoospermia patients who were treated in our hospital from October 2018 to May 2021 were selected. Inform...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Yongjie, Shi, Dongmei, Zhang, Fan, Dai, Liang, Ma, Wenzhi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	AME Publishing Company 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177260/ https://www.ncbi.nlm.nih.gov/pubmed/35693722 http://dx.doi.org/10.21037/tau-22-301

Ejemplares similares

Analysis of copy number variation in men with non-obstructive azoospermia
por: Wyrwoll, M. J., et al.
Publicado: (2022)

Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia
por: Xin, Xing, et al.
Publicado: (2023)

Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia
por: Huang, Yuhua, et al.
Publicado: (2022)

Identifying Novel Copy Number Variants in Azoospermia Factor Regions and Evaluating Their Effects on Spermatogenic Impairment
por: Zhou, Ran, et al.
Publicado: (2019)

Initial Clinical Experience with NIPT for Rare Autosomal Aneuploidies and Large Copy Number Variations
por: Harasim, Thomas, et al.
Publicado: (2022)

Plasmodium copy number variation scan: gene copy numbers evaluation in haploid genomes
por: Beghain, Johann, et al.
Publicado: (2016)

Copy number variation in the bovine genome
por: Fadista, João, et al.
Publicado: (2010)

Copy Number Variation in the Horse Genome
por: Ghosh, Sharmila, et al.
Publicado: (2014)

Genomic characteristics of cattle copy number variations
por: Hou, Yali, et al.
Publicado: (2011)

Elusive Copy Number Variation in the Mouse Genome
por: Agam, Avigail, et al.
Publicado: (2010)

Genomic copy number variations in glaucomatous neurodegeneration
por: Mukhopadhyay, Arijit
Publicado: (2014)

Genomic copy number variation in Mus musculus
por: Locke, M Elizabeth O, et al.
Publicado: (2015)

Copy number variations in the genome of the Qatari population
por: Fakhro, Khalid A., et al.
Publicado: (2015)

Genomic copy number variation analysis in multiple system atrophy
por: Hama, Yuka, et al.
Publicado: (2017)

Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders
por: Tropeano, Maria, et al.
Publicado: (2013)

Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with RHO copy number variation
por: Kandoi, Sangeetha, et al.
Publicado: (2023)

Novel Population Specific Autosomal Copy Number Variation and Its Functional Analysis amongst Negritos from Peninsular Malaysia
por: Mokhtar, Siti Shuhada, et al.
Publicado: (2014)

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
por: Bai, Wei, et al.
Publicado: (2023)

Gliosarcoma: The Distinct Genomic Alterations Identified by Comprehensive Analysis of Copy Number Variations
por: Cheng, Chuan-dong, et al.
Publicado: (2022)

Copy Number Variation Analysis of Euploid Pregnancy Loss
por: Gu, Chongjuan, et al.
Publicado: (2022)

Analysis of genomic copy number variations through whole-genome scan in Chinese Qaidam cattle
por: Liu, Yangkai, et al.
Publicado: (2023)

X-CNV: genome-wide prediction of the pathogenicity of copy number variations
por: Zhang, Li, et al.
Publicado: (2021)

Copy number variation and genomic alterations in health and disease
por: Patrinos, George P, et al.
Publicado: (2009)

Novel origins of copy number variation in the dog genome
por: Berglund, Jonas, et al.
Publicado: (2012)

Potential Value of Genomic Copy Number Variations in Schizophrenia
por: Zhuo, Chuanjun, et al.
Publicado: (2017)

Early Breast Cancer Evolution by Autosomal Broad Copy Number Alterations
por: Larsen, Joseph R., et al.
Publicado: (2022)

Genome-Wide Analysis of Copy Number Variation in Type 1 Diabetes
por: Grayson, Britney L., et al.
Publicado: (2010)

Genomic Structural Diversity in Local Goats: Analysis of Copy-Number Variations
por: Di Gerlando, Rosalia, et al.
Publicado: (2020)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Copy number variations and stroke
por: Colaianni, Valeria, et al.
Publicado: (2016)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

Copy Number Variation and Osteoporosis
por: Lovšin, Nika
Publicado: (2023)

Genome-Wide Identification of Copy Number Variations in Chinese Holstein
por: Jiang, Li, et al.
Publicado: (2012)

Genome-wide association analysis reveals 6 copy number variations associated with the number of cervical vertebrae in Pekin ducks
por: Xu, Yaxi, et al.
Publicado: (2022)

MSX2 copy number increase and craniosynostosis: copy number variation detected by array comparative genomic hybridization
por: de Oliveira Pelegrino, Karla, et al.
Publicado: (2012)

Mapping copy number variation by population scale genome sequencing
por: Mills, Ryan E., et al.
Publicado: (2011)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

Genome-wide patterns of copy number variation in the Chinese yak genome
por: Zhang, Xiao, et al.
Publicado: (2016)

Analysis of Copy Number Variation in the Whole Genome of Normal-Haired and Long-Haired Tianzhu White Yaks
por: Meng, Guangyao, et al.
Publicado: (2022)

Population-genetic nature of copy number variations in the human genome
por: Kato, Mamoru, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_eg0j5taaid0fuh60fvlef941qo