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標(biāo)題: Titlebook: Genetics of Male Infertility; A Case-Based Guide f Mohamed Arafa,Haitham Elbardisi,Ashok Agarwal Book 2020 Springer Nature Switzerland AG 2 [打印本頁(yè)]

作者: 劉興旺    時(shí)間: 2025-3-21 16:26
書目名稱Genetics of Male Infertility影響因子(影響力)




書目名稱Genetics of Male Infertility影響因子(影響力)學(xué)科排名




書目名稱Genetics of Male Infertility網(wǎng)絡(luò)公開度




書目名稱Genetics of Male Infertility網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Genetics of Male Infertility被引頻次




書目名稱Genetics of Male Infertility被引頻次學(xué)科排名




書目名稱Genetics of Male Infertility年度引用




書目名稱Genetics of Male Infertility年度引用學(xué)科排名




書目名稱Genetics of Male Infertility讀者反饋




書目名稱Genetics of Male Infertility讀者反饋學(xué)科排名





作者: 撫慰    時(shí)間: 2025-3-21 23:24
Schriftenreihe für den Au?enhandeldifferentiation is clear, we are unable to explain the etiology of DSD in most of the cases. A better understanding of the players involved in the process of testis differentiation is required for evolving strategies for diagnosis and management of DSDs.
作者: FUSE    時(shí)間: 2025-3-22 03:55

作者: 小淡水魚    時(shí)間: 2025-3-22 08:33
Die Suche nach Leben auf dem Mars,fects on the embryo, especially considering the profound remodeling to the sperm epigenome that is initiated at the pronuclear stage of development. Additionally, a better understanding of the effects of environmental insults to the sperm epigenome will aid in decreasing risk to the health of offspring.
作者: medieval    時(shí)間: 2025-3-22 10:48

作者: CUB    時(shí)間: 2025-3-22 16:23
The Molecular Genetics of Testis Determinationdifferentiation is clear, we are unable to explain the etiology of DSD in most of the cases. A better understanding of the players involved in the process of testis differentiation is required for evolving strategies for diagnosis and management of DSDs.
作者: CUB    時(shí)間: 2025-3-22 20:03
Mitochondrial Function and Male Infertility ensuring functional oxidative phosphorylation, are discussed by illustrating how single-point or serial mutations have the ability to infer male infertility. In this regard, the balance of redox reactions is therefore crucial in preventing oxidative stress.
作者: 助記    時(shí)間: 2025-3-23 00:25
The Sperm Epigenome and Potential Implications for the Developing Embryofects on the embryo, especially considering the profound remodeling to the sperm epigenome that is initiated at the pronuclear stage of development. Additionally, a better understanding of the effects of environmental insults to the sperm epigenome will aid in decreasing risk to the health of offspring.
作者: Afflict    時(shí)間: 2025-3-23 03:21
Chromosomal Translocations and Inversion in Male Infertilitygrees, and reattaches to the same chromosome. Moreover, the chapter aims to present the underlying mechanisms by which chromosomal translocations and inversions pave the way to male infertility, clinical presentations of related conditions, and management approach in cases of chromosomal abnormalities-induced male infertility.
作者: 萬(wàn)靈丹    時(shí)間: 2025-3-23 06:07

作者: inhibit    時(shí)間: 2025-3-23 12:53
Quantitative empirische Marktanalyse,pathways underlying male infertility. This chapter reviews these technologies and the discoveries they have led to and sets the scene for the transformation of infertile patient care in the era of next-generation sequencing.
作者: Ostrich    時(shí)間: 2025-3-23 14:59

作者: 哭得清醒了    時(shí)間: 2025-3-23 20:17

作者: Jocose    時(shí)間: 2025-3-23 23:08
Sperm DNA Fragmentation and Male Infertilitychapter elucidates?the molecular changes, specifically proteomic alterations, caused due to SDF. Moreover, the factors affecting sperm DNA integrity and the consequences of increased SDF are highlighted. It?also focusses on the importance of SDF testing and its impact on reproductive outcomes.
作者: acheon    時(shí)間: 2025-3-24 03:56
Molecular Regulation of Sperm Production Cascadee implementation of whole genome studies has added more candidates that need further in-depth research for dissecting their biological roles. In this chapter, we have summarized the genes important for spermatogonial stem cell renewal, meiosis, and spermiogenesis and the association of mutations in
作者: chalice    時(shí)間: 2025-3-24 07:42

作者: BINGE    時(shí)間: 2025-3-24 10:45

作者: 媒介    時(shí)間: 2025-3-24 17:38

作者: Obedient    時(shí)間: 2025-3-24 19:42

作者: 寬大    時(shí)間: 2025-3-25 01:16
Genetics of Vas Aplasiaon or two mild CFTR mutations. A proportion of CBAVD men (11–20%) suffer from concomitant urogenital abnormalities. CFTR mutations are generally not detected in these men, and other genetic causes are postulated. The type and severity of mutation vary with geography and ethnicity. Current ASRM, ACOG
作者: 牢騷    時(shí)間: 2025-3-25 03:55

作者: 制定    時(shí)間: 2025-3-25 09:24
Infertility and Cryptorchidismesticular descent, the location of the undescended testes can shed light on which processes were interrupted. There are a variety of genetic and environmental risk factors that can impact the precise timing and coordination of these processes, resulting in cryptorchidism. Understanding the pathophys
作者: 是貪求    時(shí)間: 2025-3-25 14:20
Kartagener and Immotile Cilia Syndromee of cilia, an abnormal ciliary structure may lead to the reduction or inability of the flagellum to adequately work; as a consequence, male infertility may occur. On the other hand, ciliary dysfunction may also occur in the fallopian tubes of affected women, leading to an increased risk of ectopic
作者: guardianship    時(shí)間: 2025-3-25 16:33
ts, mitochondrial function and DNA fragmentation. The clinical case material in part 3 illustrates real-world examples of genetic etiologies and the current diagnostic and therapeutic strategies for conditions 978-3-030-37974-2978-3-030-37972-8
作者: 泥沼    時(shí)間: 2025-3-25 22:49

作者: Hippocampus    時(shí)間: 2025-3-26 00:42

作者: SKIFF    時(shí)間: 2025-3-26 07:36

作者: 晚來(lái)的提名    時(shí)間: 2025-3-26 09:24
https://doi.org/10.1007/978-3-531-91527-2cts occurring during the first, the second or both meiotic divisions are consistently associated with large-headed spermatozoa. Patients presenting with a monomorphic teratozoospermia such as globozoospermia or macrospermia with more than 85% of the spermatozoa presenting this specific abnormality h
作者: JOG    時(shí)間: 2025-3-26 14:24

作者: etiquette    時(shí)間: 2025-3-26 17:54

作者: 宏偉    時(shí)間: 2025-3-26 22:20

作者: 反抗者    時(shí)間: 2025-3-27 04:25

作者: 易于交談    時(shí)間: 2025-3-27 07:53
https://doi.org/10.1007/978-3-662-63618-3e of cilia, an abnormal ciliary structure may lead to the reduction or inability of the flagellum to adequately work; as a consequence, male infertility may occur. On the other hand, ciliary dysfunction may also occur in the fallopian tubes of affected women, leading to an increased risk of ectopic
作者: 含糊    時(shí)間: 2025-3-27 12:20
Book 2020of genetic abnormalities on male infertility is the subject of part 2,covering sperm defects, mitochondrial function and DNA fragmentation. The clinical case material in part 3 illustrates real-world examples of genetic etiologies and the current diagnostic and therapeutic strategies for conditions
作者: 移動(dòng)    時(shí)間: 2025-3-27 14:38

作者: Infiltrate    時(shí)間: 2025-3-27 19:04
Molecular Regulation of Sperm Production Cascadeplex process involving the interplay of thousands of genes, of which about 1000 are testis enriched with about 200 signature genes. Such a complex spatiotemporal molecular interplay is mandatory for orchestrating the most diverse cellular changes beginning with mitosis, going through meiosis, and te
作者: 惡名聲    時(shí)間: 2025-3-28 01:35
Spermatozoal Chromatin Structure: Role in Sperm Functions and Fertilizationequired for normal embryo development. During spermiogenesis, the formation of mature spermatozoa results in an extreme compacted DNA in sperm nucleus with respect to somatic nucleus. To reach such compaction, a dramatic reorganization occurs in developing spermatids where the vast majority of somat
作者: 推測(cè)    時(shí)間: 2025-3-28 05:23

作者: 開始從未    時(shí)間: 2025-3-28 07:23

作者: 母豬    時(shí)間: 2025-3-28 12:11
Genetic Evaluation of Male Infertilitybnormalities to the very recent discovery of point mutations disrupting spermatogenesis, it is clear that a substantial number of patients suffer from genetic abnormalities. However, the discovery of these causes has largely been limited by the resolutions of the technologies used for patient assess
作者: 勉強(qiáng)    時(shí)間: 2025-3-28 17:27
Genetic Basis of Sperm Morphologic Defects: Head Defects and Body and Tail Defectsell as clinicians. Among multifactorial aetiology which contributes to male infertility, genetic abnormalities play an important role of risk factor and cannot be ignored. Therefore, recognising and understanding how genetic abnormalities influence male infertility is the foremost agenda of most res
作者: 通知    時(shí)間: 2025-3-28 19:37

作者: Aura231    時(shí)間: 2025-3-29 00:16
Sperm DNA Fragmentation and Male Infertilityination status determine the extent of DNA damage. Oxidative stress due to increased levels of reactive oxygen species in the seminal fluid damages sperm DNA. Several tests have been introduced into the clinical laboratory settings to assess the sperm chromatin integrity and the extent of SDF. This
作者: 可商量    時(shí)間: 2025-3-29 05:51

作者: Veneer    時(shí)間: 2025-3-29 08:28

作者: Terrace    時(shí)間: 2025-3-29 12:21
Chromosomal Translocations and Inversion in Male Infertility of chromosomal abnormalities. An array of functional gene expressions determines normal testicular development and robust spermatogenesis. In case of any anomalies in these genes, testicular dysgenesis as well as spermatogenic arrest may occur leading to a comprised state of male fertility. The pre
作者: 隨意    時(shí)間: 2025-3-29 15:34

作者: Restenosis    時(shí)間: 2025-3-29 22:45

作者: 比目魚    時(shí)間: 2025-3-30 02:11
Infertility and Cryptorchidismwall to the scrotum. It is one of the most frequent congenital birth defects in male children and represents an important risk factor for infertility and testicular cancer. Approximately 2–4% of full-term newborns are born with at least one cryptorchid testis. In preterm births, the rate increases t
作者: 熱情贊揚(yáng)    時(shí)間: 2025-3-30 04:09
Kartagener and Immotile Cilia Syndromemong its genetic causes and deserves special attention, as it is accompanied by many complications that may severely affect the patient’s quality of life. PCD was first reported by Kartagener in 1933, when they described four patients presenting with the triad of chronic sinusitis, bronchiectasis, a
作者: somnambulism    時(shí)間: 2025-3-30 08:21
978-3-030-37974-2Springer Nature Switzerland AG 2020
作者: 搜尋    時(shí)間: 2025-3-30 15:47
Die Krisendiskussion um die Alterssicherung,nthesis, Sertoli cell function, androgen receptor, and other hormonal influences, such as estrogen. Congenital or acquired causes of endocrine dysfunction can affect spermatogenesis and male fertility. The purpose of this chapter is to discuss the endocrine regulation of spermatogenesis with consideration of its genetic basis.
作者: Cumbersome    時(shí)間: 2025-3-30 18:45

作者: Arable    時(shí)間: 2025-3-30 22:27
Mohamed Arafa,Haitham Elbardisi,Ashok AgarwalA comprehensive and case-based overview of the genetic basis of male infertility, discussing molecular bases and consequences of genetic abnormalities.Presents current clinical tools for diagnosis and
作者: 禁止    時(shí)間: 2025-3-31 04:01

作者: 圓桶    時(shí)間: 2025-3-31 06:31

作者: indemnify    時(shí)間: 2025-3-31 10:03
Der Markendiamant in der Praxis,plex process involving the interplay of thousands of genes, of which about 1000 are testis enriched with about 200 signature genes. Such a complex spatiotemporal molecular interplay is mandatory for orchestrating the most diverse cellular changes beginning with mitosis, going through meiosis, and te
作者: conflate    時(shí)間: 2025-3-31 16:14





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