Repetitive DNA sequences in the human Y chromosome and male infertility

Y Xu, Q Pang - Frontiers in Cell and Developmental Biology, 2022 - frontiersin.org
The male-specific Y chromosome, which is well known for its diverse and complex repetitive
sequences, has different sizes, genome structures, contents and evolutionary trajectories …

Y chromosome microdeletions in Chinese men with infertility: prevalence, phenotypes, and intracytoplasmic sperm injection outcomes

D Chen, G Fan, X Zhu, Q Chen, X Chen, F Gao… - Reproductive Biology …, 2023 - Springer
Background The incidence of Y chromosome microdeletions varies among men with
infertility across regions and ethnicities worldwide. However, comprehensive …

AZF gene microdeletions in azoospermic–oligozoospermic males

RL Alonso, PS Bailo, MÁC Márquez, JCS Torres… - … Clínica (English Edition), 2023 - Elsevier
Background and objective The presence of microdeletions in the Y-chromosome
azoospermia factor (AZF) region (YCMs) is considered the most frequent genetic cause of …

Detection of partial and/or complete Y chromosome microdeletions of azoospermia factor a (AZFa) sub‐region in infertile Iraqi patients with azoospermia and severe …

MT S. Al‐Ouqaili, SK Al‐Ani, R Alaany… - Journal of Clinical …, 2022 - Wiley Online Library
Background This study aimed to analyze the incidence of azoospermia factor a (AZFa)
microdeletions in the Y chromosome and their association with male infertility in a …

Detection of AZF microdeletions and analysis of reproductive hormonal profiles in Hainan men undergoing assisted reproductive technology

Q He, Y Zhang, M Song, Y Zhou, D Lin, Y Ma, F Sun… - BMC urology, 2024 - Springer
Background Male infertility has become a global health problem, and genetic factors are one
of the essential causes. Y chromosome microdeletion is the leading genetic factor cause of …

Identification of novel homozygous missense and deletion mutations manifesting oligospermia infertility in Kashmiri population

S Aslam, Z Zhang, Z Latif - The Journal of Gene Medicine, 2024 - Wiley Online Library
Background Human male infertility has a lot of known molecular components that have an
accurate diagnosis, such as Y chromosome deletion and monogenic causes. Only 4% of all …

西南地区男性不育患者染色体异常的分析研究.

姜柯安, 景鹏伟, 李道云, 陈霞… - Chinese Journal of …, 2022 - search.ebscohost.com
摘要目的研究西南地区男性不育患者的染色体异常的发生率和类型袁为临床诊断和治疗提供
依据遥方法回顾性分析2017 年8 月至2020 年11 月来我院就诊的男性不育患者3657 …

Microdeleciones del gen AZF en varones azoospérmicos-oligozoospérmicos

RL Alonso, PS Bailo, MÁC Márquez, JCS Torres… - Medicina Clínica, 2023 - Elsevier
Antecedentes y objetivo La presencia de microdeleciones en las regiones del factor de
azoospermia (AZF) del cromosoma Y (YCM) se considera la causa genética más frecuente …

Estimating chromosome sizes from karyotype images enables validation of de novo genome assemblies

M Pippel, A Ludwig, A Dibrov, E Myers - 2023 - researchsquare.com
Owing to decreased costs over time, the genomes of an increasing number of species are
being sequenced. However, chromosome-scale genome assembly is affected by scaffolding …

Prevalence of Y Chromosome Microdeletions among Saudi Infertile Men at King Faisal Specialist Hospital and Research Center (A Cohort Study from 2019 to 2020)

SAA Hamed - 2022 - search.proquest.com
Genetic causes of infertility get attention in the last decades, after performing human
genome project and NGS technologies there are many new discoveries of new mutations …