Related references
Note: Only part of the references are listed.Copy number variation associated with meiotic arrest in idiopathic male infertility
Stefanie Eggers et al.
FERTILITY AND STERILITY (2015)
How successful is TESE-ICSI in couples with non-obstructive azoospermia?
V. Vloeberghs et al.
HUMAN REPRODUCTION (2015)
Male infertility and its genetic causes
Toshinobu Miyamoto et al.
JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH (2015)
Genetics of male infertility: from research to clinic
Csilla Krausz et al.
REPRODUCTION (2015)
BRDT gene sequence in human testicular pathologies and the implication of its single nucleotide polymorphism (rs3088232) on fertility
S. Barda et al.
ANDROLOGY (2014)
Genetic Variants in Meiotic Program Initiation Pathway Genes Are Associated with Spermatogenic Impairment in a Han Chinese Population
Chuncheng Lu et al.
PLOS ONE (2013)
Identification and molecular characterization of the mammalian α-kleisin RAD21L
Cristina Gutierrez-Caballero et al.
CELL CYCLE (2011)
The cohesin subunit RAD21L functions in meiotic synapsis and exhibits sexual dimorphism in fertility
Yurema Herran et al.
EMBO JOURNAL (2011)
A new meiosis-specific cohesin complex implicated in the cohesin code for homologous pairing
Kei-ichiro Ishiguro et al.
EMBO REPORTS (2011)
RAD21L, a novel cohesin subunit implicated in linking homologous chromosomes in mammalian meiosis
Jibak Lee et al.
JOURNAL OF CELL BIOLOGY (2011)
The biology of infertility: research advances and clinical challenges
Martin M. Matzuk et al.
NATURE MEDICINE (2008)
Azoospermia in patients heterozygous for a mutation in SYCP3
T Miyamoto et al.
LANCET (2003)
Segregating sister genomes: The molecular biology of chromosome separation
K Nasmyth
SCIENCE (2002)
Criteria predicting the absence of spermatozoa in the Sertoli cell-only syndrome can be used to improve success rates of sperm retrieval
R Anniballo et al.
HUMAN REPRODUCTION (2000)
Share Paper
