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Genital abnormalities in male patients with cystic fibrosis.

作者信息

Holsclaw D S, Perlmutter A D, Jockin H, Shwachman H

出版信息

J Urol. 1971 Oct;106(4):568-74. doi: 10.1016/s0022-5347(17)61343-0.

DOI:10.1016/s0022-5347(17)61343-0
PMID:4399160
Abstract
摘要

相似文献

1
Genital abnormalities in male patients with cystic fibrosis.
J Urol. 1971 Oct;106(4):568-74. doi: 10.1016/s0022-5347(17)61343-0.
2
[Malformations of Wolffian duct derived male genital organs (epididymis, vas deferens, seminal vesicules, ejaculatory ducts)].中肾管衍生男性生殖器官(附睾、输精管、精囊、射精管)的畸形
Prog Urol. 1997 Apr;7(2):262-9.
3
Cystic fibrosis and fertility.囊性纤维化与生育能力。
Br Med J. 1969 Aug 9;3(5666):356. doi: 10.1136/bmj.3.5666.356-c.
4
Abnormality of the epididymis and vas deferens in cystic fibrosis.囊性纤维化患者附睾和输精管的异常
Arch Pathol. 1969 Dec;88(6):569-80.
5
Increased incidence of inguinal hernia, hydrocele, and undescended testicle in males with cystic fibrosis.患有囊性纤维化的男性腹股沟疝、鞘膜积液和隐睾的发病率增加。
Pediatrics. 1971 Sep;48(3):442-5.
6
Genetic diseases of the seminal ducts.输精管遗传病
Biomed Pharmacother. 1998;52(5):197-203. doi: 10.1016/S0753-3322(98)80016-4.
7
[Obstructive azoospermia and malformations of seminal tract].[梗阻性无精子症与精道畸形]
Arch Ital Urol Androl. 1996 Dec;68(5):353-7.
8
Congenital anomalies of the seminal ducts.输精管道先天性异常。
Int Urol Nephrol. 1987;19(2):189-94. doi: 10.1007/BF02550472.
9
Clinical, andrological and genetic characteristics of patients with congenital bilateral absence of vas deferens (CBAVD).先天性双侧输精管缺如(CBAVD)患者的临床、男科学及遗传学特征
Arch Androl. 2006 Nov-Dec;52(6):471-7. doi: 10.1080/01485010600691993.
10
Congenital mesonephric defects in male infants with mucoviscidosis.患有黏液黏稠症的男婴的先天性中肾缺陷。
J Clin Pathol. 1969 Nov;22(6):725-30. doi: 10.1136/jcp.22.6.725.

引用本文的文献

1
A novel role for CFTR interaction with LH and FGF in azoospermia and epididymal maldevelopment caused by cryptorchidism.囊性纤维化跨膜传导调节因子(CFTR)与促黄体生成素(LH)和成纤维细胞生长因子(FGF)相互作用在隐睾症所致无精子症和附睾发育异常中的新作用。
Basic Clin Androl. 2022 Jun 21;32(1):10. doi: 10.1186/s12610-022-00160-0.
2
Congenital unilateral absence of the vas deferens with ipsilateral renal agenesis encountered during laparoscopic totally extraperitoneal inguinal hernia repair in an adult patient: A case report.成年患者腹腔镜完全腹膜外腹股沟疝修补术中发现先天性单侧输精管缺如伴同侧肾缺如:一例报告
Ann Med Surg (Lond). 2021 May 27;66:102449. doi: 10.1016/j.amsu.2021.102449. eCollection 2021 Jun.
3
Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.
携带致病性 CFTR 突变的非阻塞性无精子症男性中 CBAVD 的患病率-在 639 名非输精管结扎的非阻塞性无精子症男性队列中评估。
Andrology. 2021 Mar;9(2):588-598. doi: 10.1111/andr.12925. Epub 2020 Nov 7.
4
An atlas of human proximal epididymis reveals cell-specific functions and distinct roles for CFTR.人类近端附睾图谱揭示了 CFTR 的细胞特异性功能和不同作用。
Life Sci Alliance. 2020 Aug 27;3(11). doi: 10.26508/lsa.202000744. Print 2020 Nov.
5
SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens.SLC9A3 影响输精管发育并与台湾先天性双侧输精管缺如相关。
Biomed Res Int. 2019 Mar 10;2019:3562719. doi: 10.1155/2019/3562719. eCollection 2019.
6
SLC9A3 Protein Is Critical for Acrosomal Formation in Postmeiotic Male Germ Cells.SLC9A3 蛋白对于减数分裂后雄性生殖细胞顶体的形成至关重要。
Int J Mol Sci. 2017 Dec 29;19(1):103. doi: 10.3390/ijms19010103.
7
Loss of SLC9A3 decreases CFTR protein and causes obstructed azoospermia in mice.SLC9A3的缺失会降低CFTR蛋白水平,并导致小鼠梗阻性无精子症。
PLoS Genet. 2017 Apr 6;13(4):e1006715. doi: 10.1371/journal.pgen.1006715. eCollection 2017 Apr.
8
Meta-analyses of 4 CFTR variants associated with the risk of the congenital bilateral absence of the vas deferens.对4种与先天性双侧输精管缺如风险相关的CFTR变异体的荟萃分析。
J Clin Bioinforma. 2014 Aug 21;4:11. doi: 10.1186/2043-9113-4-11. eCollection 2014.
9
Letter from the editor: CFTR and male fertility-Impact beyond cystic fibrosis.编辑来信:囊性纤维化跨膜传导调节因子与男性生育——囊性纤维化之外的影响
Spermatogenesis. 2013 Jul 1;3(3):e26228. doi: 10.4161/spmg.26228. Epub 2013 Aug 29.
10
Assessing the Disease-Liability of Mutations in CFTR.评估 CFTR 突变的疾病致病变异。
Cold Spring Harb Perspect Med. 2012 Dec 1;2(12):a009480. doi: 10.1101/cshperspect.a009480.