Related references
Note: Only part of the references are listed.X-Linked TEX11 Mutations, Meiotic Arrest, and Azoospermia in Infertile Men
Alexander N. Yatsenko et al.
NEW ENGLAND JOURNAL OF MEDICINE (2015)
Excess of Rare Variants in Genes that are Key Epigenetic Regulators of Spermatogenesis in the Patients with Non-Obstructive Azoospermia
Zesong Li et al.
SCIENTIFIC REPORTS (2015)
A Mouse Geneticist's Practical Guide to CRISPR Applications
Priti Singh et al.
GENETICS (2015)
Applying Gold Standards to In-Vitro-Derived Germ Cells
Mary Ann Handel et al.
CELL (2014)
A general framework for estimating the relative pathogenicity of human genetic variants
Martin Kircher et al.
NATURE GENETICS (2014)
Ensembl 2014
Paul Flicek et al.
NUCLEIC ACIDS RESEARCH (2014)
Association analysis identifies new risk loci for non-obstructive azoospermia in Chinese men
Zhibin Hu et al.
NATURE COMMUNICATIONS (2014)
Two Families with Normosmic Congenital Hypogonadotropic Hypogonadism and Biallelic Mutations in KISS1R (KISS1 Receptor): Clinical Evaluation and Molecular Characterization of a Novel Mutation
Frederic Brioude et al.
PLOS ONE (2013)
Human Spermatogenic Failure Purges Deleterious Mutation Load from the Autosomes and Both Sex Chromosomes, including the Gene DMRT1
Alexandra M. Lopes et al.
PLOS GENETICS (2013)
Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients
Toshinobu Miyamoto et al.
ASIAN JOURNAL OF ANDROLOGY (2012)
Loss of Cyclin-Dependent Kinase 2 (CDK2) Inhibitory Phosphorylation in a CDK2AF Knock-In Mouse Causes Misregulation of DNA Replication and Centrosome Duplication
Hui Zhao et al.
MOLECULAR AND CELLULAR BIOLOGY (2012)
Predicting the functional impact of protein mutations: application to cancer genomics
Boris Reva et al.
NUCLEIC ACIDS RESEARCH (2011)
Mutation analysis of three genes in patients with maturation arrest of spermatogenesis and couples with recurrent miscarriages
K. Stouffs et al.
REPRODUCTIVE BIOMEDICINE ONLINE (2011)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Identification of Potentially Damaging Amino Acid Substitutions Leading to Human Male Infertility
Anastasia Kuzmin et al.
BIOLOGY OF REPRODUCTION (2009)
The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population
Klaus Dieterich et al.
HUMAN MOLECULAR GENETICS (2009)
Functional Annotations Improve the Predictive Score of Human Disease-Related Mutations in Proteins
Remo Calabrese et al.
HUMAN MUTATION (2009)
LMTK2 and PARP-2 gene polymorphism and azoospermia secondary to meiotic arrest
Naoko Sakugawa et al.
JOURNAL OF ASSISTED REPRODUCTION AND GENETICS (2009)
CDK2 is required for proper homologous pairing, recombination and sex-body formation during male mouse meiosis
Alberto Viera et al.
JOURNAL OF CELL SCIENCE (2009)
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
Prateek Kumar et al.
NATURE PROTOCOLS (2009)
Mouse TEX15 is essential for DNA double-strand break repair and chromosomal synapsis during male meiosis
Fang Yang et al.
JOURNAL OF CELL BIOLOGY (2008)
The biology of infertility: research advances and clinical challenges
Martin M. Matzuk et al.
NATURE MEDICINE (2008)
Homozygous mutation in SPATA16 is associated with male infertility in human globozoospermia
Anika H. D. M. Dam et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
SNAP: predict effect of non-synonymous polymorphisms on function
Yana Bromberg et al.
NUCLEIC ACIDS RESEARCH (2007)
A dominant, recombination-defective allele of Dmc1 causing male-specific sterility
Laura A. Bannister et al.
PLOS BIOLOGY (2007)
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility
Klaus Dieterich et al.
NATURE GENETICS (2007)
Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information
E. Capriotti et al.
BIOINFORMATICS (2006)
Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest
Hisashi Sato et al.
JOURNAL OF HUMAN GENETICS (2006)
Positional cloning and characterization of mouse mei8, a disrupted allele of the meiotic cohesin Rec8
LA Bannister et al.
GENESIS (2004)
Methods for quantifying follicular numbers within the mouse ovary
M Myers et al.
REPRODUCTION (2004)
Cdk2 knockout mice are viable
C Berthet et al.
CURRENT BIOLOGY (2003)
Cyclin-dependent kinase 2 is essential for meiosis but not for mitotic cell division in mice
S Ortega et al.
NATURE GENETICS (2003)
PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification
PD Thomas et al.
NUCLEIC ACIDS RESEARCH (2003)
Novel meiosis-specific isoform of mammalian SMC1
E Revenkova et al.
MOLECULAR AND CELLULAR BIOLOGY (2001)
Y chromosome microdeletions and alterations of spermatogenesis
C Foresta et al.
ENDOCRINE REVIEWS (2001)
Share Paper
