Teratozoospermia: spotlight on the main genetic actors in the human

Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men

(2015) PierreF Ray et al.   ASIAN JOURNAL OF ANDROLOGY

Dynamics of Sun5 Localization during Spermatogenesis in Wild Type and Dpy19l2 Knock-Out Mice Indicates That Sun5 Is Not Involved in Acrosome Attachment to the Nuclear Envelope

(2015) Sandra Yassine et al.   PLoS One

CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation

(2014) Rim Hjeij et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations inRSPH1Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype

(2014) Michael R. Knowles et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Management of primary ciliary dyskinesia/Kartagener′s syndrome in infertile male patients and current progress in defining the underlying genetic mechanism

(2014) Ping Li et al.   ASIAN JOURNAL OF ANDROLOGY

Atg7 is required for acrosome biogenesis during spermatogenesis in mice

(2014) Hongna Wang et al.   CELL RESEARCH

First successful pregnancy in a globozoospermic patient having homozygous mutation in SPATA16

(2014) Nilay Karaca et al.   FERTILITY AND STERILITY

Prevalence of the Aurora kinase C c.144delC mutation in infertile Moroccan men

(2014) Abdelmajid Eloualid et al.   FERTILITY AND STERILITY

Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects

(2014) Alexandros Onoufriadis et al.   HUMAN MOLECULAR GENETICS

Meiotic segregation and sperm DNA fragmentation in Tunisian men with dysplasia of the fibrous sheath (DFS) associated with head abnormalities

(2014) H. Ghedir et al.   JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Dpy19l2-deficient globozoospermic sperm display altered genome packaging and DNA damage that compromises the initiation of embryo development

(2014) Sandra Yassine et al.   MOLECULAR HUMAN REPRODUCTION

Subcellular localization of phospholipase Cζ in human sperm and its absence in DPY19L2-deficient sperm are consistent with its role in oocyte activation

(2014) Jessica Escoffier et al.   MOLECULAR HUMAN REPRODUCTION

Selective Disruption of Aurora C Kinase Reveals Distinct Functions from Aurora B Kinase during Meiosis in Mouse Oocytes

(2014) Ahmed Z. Balboula et al.   PLoS Genetics

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia

(2013) Christina Austin-Tse et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in SPAG1 Cause Primary Ciliary Dyskinesia Associated with Defective Outer and Inner Dynein Arms

(2013) Michael R. Knowles et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry

(2013) Rim Hjeij et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects

(2013) Esther Kott et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in ZMYND10, a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms in Humans and Flies, Cause Primary Ciliary Dyskinesia

(2013) Daniel J. Moore et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6

(2013) Maimoona A. Zariwala et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia

(2013) Thassadite Dirami et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in DNAH1, which Encodes an Inner Arm Heavy Chain Dynein, Lead to Male Infertility from Multiple Morphological Abnormalities of the Sperm Flagella

(2013) Mariem Ben Khelifa et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease

(2013) Michael R. Knowles et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Disruption of a Spermatogenic Cell-Specific Mouse Enolase 4 (Eno4) Gene Causes Sperm Structural Defects and Male Infertility1

(2013) Noriko Nakamura et al.   BIOLOGY OF REPRODUCTION

Cell division: control of the chromosomal passenger complex in time and space

(2013) Armando van der Horst et al.   CHROMOSOMA

Reproductive outcomes in patients with male infertility because of Klinefelterʼs syndrome, Kartagenerʼs syndrome, round-head sperm, dysplasia fibrous sheath, and ‘stump’ tail sperm

(2013) S.A. Dávila Garza et al.   CURRENT OPINION IN OBSTETRICS & GYNECOLOGY

Gene therapy on the move

(2013) Kerstin B. Kaufmann et al.   EMBO Molecular Medicine

The coiled-coil domain containing protein CCDC151 is required for the function of IFT-dependent motile cilia in animals

(2013) Julie Jerber et al.   HUMAN MOLECULAR GENETICS

Founder Mutation inRSPH4AIdentified in Patients of Hispanic Descent with Primary Ciliary Dyskinesia

(2013) M. Leigh Anne Daniels et al.   HUMAN MUTATION

Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status

(2013) P. Kuentz et al.   HUMAN REPRODUCTION

A solid-state control system for dynein-based ciliary/flagellar motility

(2013) Stephen M. King   JOURNAL OF CELL BIOLOGY

Mutations ofNANOS1, a human homologue of theDrosophilamorphogen, are associated with a lack of germ cells in testes or severe oligo-astheno-teratozoospermia

(2013) Kamila Kusz-Zamelczyk et al.   JOURNAL OF MEDICAL GENETICS

Combined exome and whole-genome sequencing identifies mutations inARMC4as a cause of primary ciliary dyskinesia with defects in the outer dynein arm

(2013) Alexandros Onoufriadis et al.   JOURNAL OF MEDICAL GENETICS

The Arf GAP SMAP2 is necessary for organized vesicle budding from the trans-Golgi network and subsequent acrosome formation in spermiogenesis

(2013) Tomo Funaki et al.   MOLECULAR BIOLOGY OF THE CELL

C. elegans DPY-19 Is a C-Mannosyltransferase Glycosylating Thrombospondin Repeats

(2013) Falk F.R. Buettner et al.   MOLECULAR CELL

DPY19L2 gene mutations are a major cause of globozoospermia: identification of three novel point mutations

(2013) F. Zhu et al.   MOLECULAR HUMAN REPRODUCTION

The nexin-dynein regulatory complex subunit DRC1 is essential for motile cilia function in algae and humans

(2013) Maureen Wirschell et al.   NATURE GENETICS

DYX1C1 is required for axonemal dynein assembly and ciliary motility

(2013) Aarti Tarkar et al.   NATURE GENETICS

Gene Amplification and Overexpression of Aurora-C in Breast and Prostate Cancer Cell Lines

(2013) Ali Zekri et al.   ONCOLOGY RESEARCH

Picking up speed: advances in the genetics of primary ciliary dyskinesia

(2013) Amjad Horani et al.   PEDIATRIC RESEARCH

LRRC6 Mutation Causes Primary Ciliary Dyskinesia with Dynein Arm Defects

(2013) Amjad Horani et al.   PLoS One

CCDC65 Mutation Causes Primary Ciliary Dyskinesia with Normal Ultrastructure and Hyperkinetic Cilia

(2013) Amjad Horani et al.   PLoS One

Fine Characterisation of a Recombination Hotspot at the DPY19L2 Locus and Resolution of the Paradoxical Excess of Duplications over Deletions in the General Population

(2013) Charles Coutton et al.   PLoS Genetics

Whole-Exome Capture and Sequencing Identifies HEATR2 Mutation as a Cause of Primary Ciliary Dyskinesia

(2012) Amjad Horani et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Loss-of-Function Mutations in LRRC6 , a Gene Essential for Proper Axonemal Assembly of Inner and Outer Dynein Arms, Cause Primary Ciliary Dyskinesia

(2012) Esther Kott et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia without Randomization of Left-Right Body Asymmetry

(2012) Heike Olbrich et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Exome Sequencing Identifies Mutations in CCDC114 as a Cause of Primary Ciliary Dyskinesia

(2012) Michael R. Knowles et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Splice-Site Mutations in the Axonemal Outer Dynein Arm Docking Complex Gene CCDC114 Cause Primary Ciliary Dyskinesia

(2012) Alexandros Onoufriadis et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Molecular cytogenetic and genetic aspects of globozoospermia: a review

(2012) A. Perrin et al.   ANDROLOGIA

Mechanisms for recurrent and complex human genomic rearrangements

(2012) Pengfei Liu et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Absence of Dpy19l2, a new inner nuclear membrane protein, causes globozoospermia in mice by preventing the anchoring of the acrosome to the nucleus

(2012) V. Pierre et al.   DEVELOPMENT

SPACA1-deficient male mice are infertile with abnormally shaped sperm heads reminiscent of globozoospermia

(2012) Y. Fujihara et al.   DEVELOPMENT

Primary ciliary dyskinesia, an orphan disease

(2012) Mieke Boon et al.   EUROPEAN JOURNAL OF PEDIATRICS

European Association of Urology Guidelines on Male Infertility: The 2012 Update

(2012) Andreas Jungwirth et al.   EUROPEAN UROLOGY

Cell division control by the Chromosomal Passenger Complex

(2012) Maike S. van der Waal et al.   EXPERIMENTAL CELL RESEARCH

Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots

(2012) Elias ElInati et al.   HUMAN MOLECULAR GENETICS

SEPT12mutations cause male infertility with defective sperm annulus

(2012) Yung-Che Kuo et al.   HUMAN MUTATION

Mutations inCCDC39andCCDC40are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms

(2012) Dinu Antony et al.   HUMAN MUTATION

Acrosomal biogenesis in human globozoospermia: immunocytochemical, ultrastructural and proteomic studies

(2012) C. Alvarez Sedo et al.   HUMAN REPRODUCTION

MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia

(2012) C. Coutton et al.   HUMAN REPRODUCTION

Identification of a new recurrent Aurora kinase C mutation in both European and African men with macrozoospermia

(2012) M. Ben Khelifa et al.   HUMAN REPRODUCTION

Novel mutations in calcium/calmodulin-dependent protein kinase IV (CAMK4) gene in infertile men

(2012) A. Khattri et al.   INTERNATIONAL JOURNAL OF ANDROLOGY

Delineation ofCCDC39/CCDC40mutation spectrum and associated phenotypes in primary ciliary dyskinesia

(2012) Sylvain Blanchon et al.   JOURNAL OF MEDICAL GENETICS

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms

(2012) Jennifer R Panizzi et al.   NATURE GENETICS

Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia

(2012) Hannah M Mitchison et al.   NATURE GENETICS

The chromosomal passenger complex (CPC): from easy rider to the godfather of mitosis

(2012) Mar Carmena et al.   NATURE REVIEWS MOLECULAR CELL BIOLOGY

RPGRmutations might cause reduced orientation of respiratory cilia

(2012) Zuzanna Bukowy-Bieryłło et al.   PEDIATRIC PULMONOLOGY

SEPTIN12 Genetic Variants Confer Susceptibility to Teratozoospermia

(2012) Ying-Hung Lin et al.   PLoS One

Maternally recruited Aurora C kinase is more stable than Aurora B to support mouse oocyte maturation and early development

(2012) K. Schindler et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Head and flagella subcompartmental proteomic analysis of human spermatozoa

(2012) Mark A. Baker et al.   PROTEOMICS

Sperm macrocephaly syndrome in a patient without AURKC mutations and with a history of recurrent miscarriage

(2012) Emanuela Molinari et al.   REPRODUCTIVE BIOMEDICINE ONLINE

A Recurrent Deletion of DPY19L2 Causes Infertility in Man by Blocking Sperm Head Elongation and Acrosome Formation

(2011) Radu Harbuz et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Primary Ciliary Dyskinesia Caused by Homozygous Mutation in DNAL1, Encoding Dynein Light Chain 1

(2011) Masha Mazor et al.   AMERICAN JOURNAL OF HUMAN GENETICS

DPY19L2 Deletion as a Major Cause of Globozoospermia

(2011) Isabelle Koscinski et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Tales of the Tail and Sperm Head AchesChanging concepts on the prognostic significance of sperm pathologies affecting the head, neck and tail

(2011) Héctor E Chemes et al.   ASIAN JOURNAL OF ANDROLOGY

Male infertility: Pathogenesis and clinical diagnosis

(2011) Csilla Krausz   BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM

Loss of SPEF2 Function in Mice Results in Spermatogenesis Defects and Primary Ciliary Dyskinesia1

(2011) Anu Sironen et al.   BIOLOGY OF REPRODUCTION

1001 model organisms to study cilia and flagella

(2011) Laetitia Vincensini et al.   BIOLOGY OF THE CELL

Dpy19l1, a multi-transmembrane protein, regulates the radial migration of glutamatergic neurons in the developing cerebral cortex

(2011) K. Watanabe et al.   DEVELOPMENT

Genetic disruption of aurora B uncovers an essential role for aurora C during early mammalian development

(2011) G. Fernandez-Miranda et al.   DEVELOPMENT

Hsp90b1 knockout targeted to male germline: a mouse model for globozoospermia

(2011) Christophe Audouard et al.   FERTILITY AND STERILITY

Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD

(2011) Jane S. Lucas et al.   HUMAN MUTATION

A role for Aurora C in the chromosomal passenger complex during human preimplantation embryo development

(2011) Margarida Avo Santos et al.   HUMAN REPRODUCTION

Successful childbirth after intracytoplasmic morphologically selected sperm injection without assisted oocyte activation in a patient with globozoospermia

(2011) N. Sermondade et al.   HUMAN REPRODUCTION

Confirmation de la forte prévalence au Maroc de la mutation homozygote c.144delC du gène aurora kinase C (AURKC) dans les tératozoospermies avec spermatozoïdes macrocéphales

(2011) F. El Kerch et al.   JOURNAL DE GYNECOLOGIE OBSTETRIQUE ET BIOLOGIE DE LA REPRODUCTION

Morphology of Partial Globozoospermia

(2011) A. H. Dam et al.   JOURNAL OF ANDROLOGY

Cryoelectron tomography of radial spokes in cilia and flagella

(2011) Gaia Pigino et al.   JOURNAL OF CELL BIOLOGY

Aberrantly expressed AURKC enhances the transformation and tumourigenicity of epithelial cells

(2011) Jen-Hui Tsou et al.   JOURNAL OF PATHOLOGY

A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis

(2011) M. Ben Khelifa et al.   MOLECULAR HUMAN REPRODUCTION

Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men

(2011) Alexander N. Yatsenko et al.   MOLECULAR HUMAN REPRODUCTION

Sperm flagella: comparative and phylogenetic perspectives of protein components

(2011) K. Inaba   MOLECULAR HUMAN REPRODUCTION

Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome

(2011) Frank Tüttelmann et al.   PLoS One

Overexpression of Active Aurora-C Kinase Results in Cell Transformation and Tumour Formation

(2011) Jabbar Khan et al.   PLoS One

Mutations ofDNAH11in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

(2011) Michael R Knowles et al.   THORAX

Analysis of Sperm Aneuploidies and DNA Fragmentation in Patients With Globozoospermia or With Abnormal Acrosomes

(2011) Sonia Brahem et al.   UROLOGY

Anomalous distribution of nuclear basic proteins in round-headed human spermatozoa: Anormale Verteilung basischer Kern-Proteine in menschlichen rundköpfigen Spermatozoen

(2010) Y. Blanchard et al.   ANDROLOGIA

Biochemical and Genetic Investigation of Round-headed Spermatozoa in Infertile Men including two Brothers and their Father

(2010) S. FLÖRKE-GERLOFF et al.   ANDROLOGIA

Notulae seminologicae. 2. The ‘short tail’ and ‘stump’ defect in human spermatozoa

(2010) B. Baccetti et al.   ANDROLOGIA

Structural Variation in the Human Genome and its Role in Disease

(2010) Paweł Stankiewicz et al.   Annual Review of Medicine

A newly discovered mutation in PICK1 in a human with globozoospermia

(2010) Gang Liu et al.   ASIAN JOURNAL OF ANDROLOGY

The making of abnormal spermatozoa: cellular and molecular mechanisms underlying pathological spermiogenesis

(2010) Hector E. Chemes et al.   CELL AND TISSUE RESEARCH

Centromere localization of INCENP-Aurora B is sufficient to support spindle checkpoint function

(2010) Markus Becker et al.   CELL CYCLE

Protein kinase CK2 and new binding partners during spermatogenesis

(2010) Nadja Mannowetz et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

TMF/ARA160: A key regulator of sperm development

(2010) Tal Lerer-Goldshtein et al.   DEVELOPMENTAL BIOLOGY

Oocyte activation, phospholipase C zeta and human infertility

(2010) J. Kashir et al.   HUMAN REPRODUCTION UPDATE

Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy

(2010) F. Tüttelmann et al.   INTERNATIONAL JOURNAL OF ANDROLOGY

The chromosome passenger complex is required for fidelity of chromosome transmission and cytokinesis in meiosis of mouse oocytes

(2010) B. Sharif et al.   JOURNAL OF CELL SCIENCE

Aurora-C Kinase Deficiency Causes Cytokinesis Failure in Meiosis I and Production of Large Polyploid Oocytes in Mice

(2010) Kuo-Tai Yang et al.   MOLECULAR BIOLOGY OF THE CELL

SPAG4L/SPAG4L-2 are testis-specific SUN domain proteins restricted to the apical nuclear envelope of round spermatids facing the acrosome

(2010) C. Frohnert et al.   MOLECULAR HUMAN REPRODUCTION

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

(2010) Anita Becker-Heck et al.   NATURE GENETICS

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

(2010) Anne-Christine Merveille et al.   NATURE GENETICS

Mammalian Sperm Head Formation Involves Different Polarization of Two Novel LINC Complexes

(2010) Eva Göb et al.   PLoS One

Tubulin polyglutamylation is essential for airway ciliary function through the regulation of beating asymmetry

(2010) K. Ikegami et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

From ultrastructural flagellar sperm defects to the health of babies conceived by ICSI

(2010) Patricia Fauque et al.   REPRODUCTIVE BIOMEDICINE ONLINE

Prdm9 Controls Activation of Mammalian Recombination Hotspots

(2010) E. D. Parvanov et al.   SCIENCE

Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination

(2010) S. Myers et al.   SCIENCE

PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice

(2010) F. Baudat et al.   SCIENCE

Tubulin Tyrosine Ligase–Like 1 Deficiency Results in Chronic Rhinosinusitis and Abnormal Development of Spermatid Flagella in Mice

(2010) P. Vogel et al.   VETERINARY PATHOLOGY

Loss-of-Function Mutations in the Human Ortholog of Chlamydomonas reinhardtii ODA7 Disrupt Dynein Arm Assembly and Cause Primary Ciliary Dyskinesia

(2009) Philippe Duquesnoy et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects

(2009) Niki Tomas Loges et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in Radial Spoke Head Protein Genes RSPH9 and RSPH4A Cause Primary Ciliary Dyskinesia with Central-Microtubular-Pair Abnormalities

(2009) Victoria H. Castleman et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Copy Number Variation in Human Health, Disease, and Evolution

(2009) Feng Zhang et al.   Annual Review of Genomics and Human Genetics

High prevalence of primary ciliary dyskinesia in a British Asian population

(2009) C O'Callaghan et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Expression of SPEF2 During Mouse Spermatogenesis and Identification of IFT20 as an Interacting Protein1

(2009) Anu Sironen et al.   BIOLOGY OF REPRODUCTION

Meig1 deficiency causes a severe defect in mouse spermatogenesis

(2009) Yehuda Salzberg et al.   DEVELOPMENTAL BIOLOGY

The functional significance of centrosomes in mammalian meiosis, fertilization, development, nuclear transfer, and stem cell differentiation

(2009) Heide Schatten et al.   ENVIRONMENTAL AND MOLECULAR MUTAGENESIS

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population

(2009) K. Dieterich et al.   HUMAN MOLECULAR GENETICS

Reduced amounts and abnormal forms of phospholipase C zeta (PLC ) in spermatozoa from infertile men

(2009) E. Heytens et al.   HUMAN REPRODUCTION

PICK1 deficiency causes male infertility in mice by disrupting acrosome formation

(2009) Nan Xiao et al.   JOURNAL OF CLINICAL INVESTIGATION

Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia

(2009) M Failly et al.   JOURNAL OF MEDICAL GENETICS

Male infertility caused by spermiogenic defects: Lessons from gene knockouts

(2009) Wei Yan   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Genome-wide association study of bipolar disorder in European American and African American individuals

(2009) E N Smith et al.   MOLECULAR PSYCHIATRY

Complete globozoospermia associated with PLCζ deficiency treated with calcium ionophore and ICSI results in pregnancy

(2009) S.L. Taylor et al.   REPRODUCTIVE BIOMEDICINE ONLINE

ICSI: Where We Have Been and Where We Are Going

(2009) Gianpiero Palermo et al.   SEMINARS IN REPRODUCTIVE MEDICINE

DNAI2 Mutations Cause Primary Ciliary Dyskinesia with Defects in the Outer Dynein Arm

(2008) Niki Tomas Loges et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Clinical pregnancies and livebirths achieved by intracytoplasmic injection of round headed acrosomeless spermatozoa with and without oocyte activation in familial globozoospermia: case report

(2008) Enver K. Dirican et al.   ASIAN JOURNAL OF ANDROLOGY

Nocturnal Activation of Aurora C in Rat Pineal Gland: Its Role in the Norepinephrine-Induced Phosphorylation of Histone H3 and Gene Expression

(2008) D. M. Price et al.   ENDOCRINOLOGY

Study of aneuploidy in large-headed, multiple-tailed spermatozoa: case report and review of the literature

(2008) Aurore Perrin et al.   FERTILITY AND STERILITY

Successful pregnancy and childbirth after intracytoplasmic sperm injection with calcium ionophore oocyte activation in a globozoospermic patient

(2008) Alberto Tejera et al.   FERTILITY AND STERILITY

Structure and function of mammalian cilia

(2008) Peter Satir et al.   HISTOCHEMISTRY AND CELL BIOLOGY

The AZF proteins

(2008) P. H. Vogt et al.   INTERNATIONAL JOURNAL OF ANDROLOGY

Molecular architecture of inner dynein arms in situ inChlamydomonas reinhardtiiflagella

(2008) Khanh Huy Bui et al.   JOURNAL OF CELL BIOLOGY

Human sperm devoid of PLC, zeta 1 fail to induce Ca2+ release and are unable to initiate the first step of embryo development

(2008) Sook-Young Yoon et al.   JOURNAL OF CLINICAL INVESTIGATION

Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins

(2008) Heymut Omran et al.   NATURE

The biology of infertility: research advances and clinical challenges

(2008) Martin M Matzuk et al.   NATURE MEDICINE

The chromosomal passenger complex and the spindle assembly checkpoint: kinetochore-microtubule error correction and beyond

(2008) Gerben Vader et al.   Cell Division

Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused byDNAH11mutations

(2007) Georg C. Schwabe et al.   HUMAN MUTATION