These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 36708028)

  • 1. Population-based genetic analysis in infertile men reveals novel mutations of ADAD family members in patients with impaired spermatogenesis.
    Dai S; Liu M; Liu M; Jiang C; Yang Y; Han H; Yang Y; Jiang X; Shen Y
    Hum Mol Genet; 2023 May; 32(11):1814-1825. PubMed ID: 36708028
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ADAD1 and ADAD2, testis-specific adenosine deaminase domain-containing proteins, are required for male fertility.
    Snyder E; Chukrallah L; Seltzer K; Goodwin L; Braun RE
    Sci Rep; 2020 Jul; 10(1):11536. PubMed ID: 32665638
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Biallelic mutations in RNA-binding protein ADAD2 cause spermiogenic failure and non-obstructive azoospermia in humans.
    Shi B; Shah W; Liu L; Gong C; Zhou J; Abbas T; Ma H; Zhang H; Yang M; Zhang Y; Ullah N; Mahammad Z; Khan M; Murtaza G; Ali A; Khan R; Sha J; Yuan Y; Shi Q
    Hum Reprod Open; 2023; 2023(3):hoad022. PubMed ID: 37325547
    [TBL] [Abstract][Full Text] [Related]  

  • 4. ADAD2 functions in spermiogenesis and piRNA biogenesis in mice.
    Lu Y; Nagamori I; Kobayashi H; Kojima-Kita K; Shirane K; Chang HY; Nishimura T; Koyano T; Yu Z; Castañeda JM; Matsuyama M; Kuramochi-Miyagawa S; Matzuk MM; Ikawa M
    Andrology; 2023 May; 11(4):698-709. PubMed ID: 36698249
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sequencing of the
    Wen Y; Wang X; Zheng R; Dai S; Li J; Yang Y; Shen Y
    J Med Genet; 2023 Apr; 60(4):380-390. PubMed ID: 35973810
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice.
    Zhang B; Khan I; Liu C; Ma A; Khan A; Zhang Y; Zhang H; Kakakhel MBS; Zhou J; Zhang W; Li Y; Ali A; Jiang X; Murtaza G; Khan R; Zubair M; Yuan L; Khan M; Wang L; Zhang F; Wang X; Ma H; Shi Q
    Clin Genet; 2021 Jan; 99(1):176-186. PubMed ID: 33070343
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermia.
    Wang W; Su L; Meng L; He J; Tan C; Yi D; Cheng D; Zhang H; Lu G; Du J; Lin G; Zhang Q; Tu C; Tan YQ
    Hum Reprod; 2023 Jul; 38(7):1399-1411. PubMed ID: 37192818
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia.
    Oud MS; Okutman Ö; Hendricks LAJ; de Vries PF; Houston BJ; Vissers LELM; O'Bryan MK; Ramos L; Chemes HE; Viville S; Veltman JA
    Hum Reprod; 2020 Jan; 35(1):240-252. PubMed ID: 31985809
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.
    Liu R; Yan Z; Fan Y; Qu R; Chen B; Li B; Wu L; Wu H; Mu J; Zhao L; Wang W; Dong J; Zeng Y; Li Q; Wang L; Sang Q; Zhang Z; Kuang Y
    Hum Reprod; 2022 Jun; 37(7):1394-1405. PubMed ID: 35551387
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel CCDC39 mutation causes multiple morphological abnormalities of the flagella in a primary ciliary dyskinesia patient.
    Chen D; Liang Y; Li J; Zhang X; Zheng R; Wang X; Zhang H; Shen Y
    Reprod Biomed Online; 2021 Nov; 43(5):920-930. PubMed ID: 34674941
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel mutation in DNAH17 is present in a patient with multiple morphological abnormalities of the flagella.
    Zheng R; Sun Y; Jiang C; Chen D; Yang Y; Shen Y
    Reprod Biomed Online; 2021 Sep; 43(3):532-541. PubMed ID: 34373205
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Biallelic
    Hu T; Meng L; Tan C; Luo C; He WB; Tu C; Zhang H; Du J; Nie H; Lu GX; Lin G; Tan YQ
    J Med Genet; 2023 Feb; 60(2):144-153. PubMed ID: 35387802
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biallelic mutations in spermatogenesis and centriole-associated 1 like (
    Li YZ; Li N; Liu WS; Sha YW; Wu RF; Tang YL; Zhu XS; Wei XL; Zhang XY; Wang YF; Lu ZX; Zhang FX
    Asian J Androl; 2022; 24(1):67-72. PubMed ID: 34213489
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Whole-exome sequencing of a cohort of infertile men reveals novel causative genes in teratozoospermia that are chiefly related to sperm head defects.
    Li Y; Wang Y; Wen Y; Zhang T; Wang X; Jiang C; Zheng R; Zhou F; Chen D; Yang Y; Shen Y
    Hum Reprod; 2021 Dec; 37(1):152-177. PubMed ID: 34791246
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel compound heterozygous variants of DNAH17 in a Chinese infertile man with multiple morphological abnormalities of sperm flagella.
    Liu Z; Wang C; Ni F; Yang F; Wei H; Li T; Wang J; Wang B
    Andrologia; 2022 Nov; 54(10):e14553. PubMed ID: 35932098
    [TBL] [Abstract][Full Text] [Related]  

  • 16. IQUB deficiency causes male infertility by affecting the activity of p-ERK1/2/RSPH3.
    Zhang Z; Zhou H; Deng X; Zhang R; Qu R; Mu J; Liu R; Zeng Y; Chen B; Wang L; Sang Q; Bao S
    Hum Reprod; 2023 Jan; 38(1):168-179. PubMed ID: 36355624
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
    Dong FN; Amiri-Yekta A; Martinez G; Saut A; Tek J; Stouvenel L; Lorès P; Karaouzène T; Thierry-Mieg N; Satre V; Brouillet S; Daneshipour A; Hosseini SH; Bonhivers M; Gourabi H; Dulioust E; Arnoult C; Touré A; Ray PF; Zhao H; Coutton C
    Am J Hum Genet; 2018 Apr; 102(4):636-648. PubMed ID: 29606301
    [TBL] [Abstract][Full Text] [Related]  

  • 18. PRSS55 is a novel potential causative gene for human male infertility.
    Liu M; Jiang C; Zhang X; Zhang G; Liu M; Zheng R; Yang Y; Shen Y
    Reprod Biomed Online; 2022 Sep; 45(3):553-562. PubMed ID: 35821214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
    Okutman O; Boivin M; Muller J; Charlet-Berguerand N; Viville S
    Hum Reprod; 2023 Feb; 38(2):306-314. PubMed ID: 36524333
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Linking human Dead end 1 (DND1) variants to male infertility employing zebrafish embryos.
    Westerich KJ; Reinecke S; Emich J; Wyrwoll MJ; Stallmeyer B; Meyer M; Oud MS; Fietz D; Pilatz A; Kliesch S; Reichman-Fried M; Tarbashevich K; Limon T; Stehling M; Friedrich C; Tüttelmann F; Raz E
    Hum Reprod; 2023 Apr; 38(4):655-670. PubMed ID: 36807972
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.