标题
Teratozoospermia: spotlight on the main genetic actors in the human
作者
关键词
-
出版物
HUMAN REPRODUCTION UPDATE
Volume 21, Issue 4, Pages 455-485
出版商
Oxford University Press (OUP)
发表日期
2015-04-19
DOI
10.1093/humupd/dmv020
参考文献
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注意：仅列出部分参考文献，下载原文获取全部文献信息。- 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
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- (2013) Alexandros Onoufriadis et al. JOURNAL OF MEDICAL GENETICS
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- (2013) Tomo Funaki et al. MOLECULAR BIOLOGY OF THE CELL
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- (2013) Falk F.R. Buettner et al. MOLECULAR CELL
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- (2013) F. Zhu et al. MOLECULAR HUMAN REPRODUCTION
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- (2013) Maureen Wirschell et al. NATURE GENETICS
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- (2013) Aarti Tarkar et al. NATURE GENETICS
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- (2013) Ali Zekri et al. ONCOLOGY RESEARCH
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- (2013) Amjad Horani et al. PEDIATRIC RESEARCH
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- (2013) Amjad Horani et al. PLoS One
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- (2012) Amjad Horani et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2012) Esther Kott et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (2012) Michael R. Knowles et al. AMERICAN JOURNAL OF HUMAN GENETICS
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- (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
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- (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
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- (2008) Alberto Tejera et al. FERTILITY AND STERILITY
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- (2008) Peter Satir et al. HISTOCHEMISTRY AND CELL BIOLOGY
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- (2008) P. H. Vogt et al. INTERNATIONAL JOURNAL OF ANDROLOGY
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- (2008) Khanh Huy Bui et al. JOURNAL OF CELL BIOLOGY
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- (2008) Sook-Young Yoon et al. JOURNAL OF CLINICAL INVESTIGATION
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- (2008) Heymut Omran et al. NATURE
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- (2008) Martin M Matzuk et al. NATURE MEDICINE
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- (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
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