| Y-chromosome haplogroups and Azoospermia Factor (AZF) analysis in Tunisian infertile male. | Y-chromosome haplogroups and Azoospermia Factor (AZF) analysis in Tunisian infertile male.
Ghorbel M, Baklouti-Gargouri S, Keskes R, Sellami A, McElreavy K, Ammar-Keskes L. | 09/27/2024 |
| AZF microdeletion affects semen parameters, sex hormone levels, and chromosome karyotypes in infertile men in Xinjiang. | AZF microdeletion affects semen parameters, sex hormone levels, and chromosome karyotypes in infertile men in Xinjiang.
Han N, Liu X. | 09/27/2024 |
| [Analysis of copy number variation in AZF region of Y chromosome in patients with spermatogenic failure]. | [Analysis of copy number variation in AZF region of Y chromosome in patients with spermatogenic failure].
Gao H, Wang L, Song Y, Ma D, Nie R, Hu Y, He H, Zhang R, Wang S, Guo H. | 09/27/2024 |
| High incidence of AZF duplications in clan-structured Iranian populations detected through Y chromosome sequencing read depth analysis. | High incidence of AZF duplications in clan-structured Iranian populations detected through Y chromosome sequencing read depth analysis.
Hajiesmaeil M, Ravasini F, Risi F, Magnarini G, Olivieri A, D'Atanasio E, Galehdari H, Trombetta B, Cruciani F., Free PMC Article | 09/27/2024 |
| DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia. | DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia.
Dicke AK, Pilatz A, Wyrwoll MJ, Punab M, Ruckert C, Nagirnaja L, Aston KI, Conrad DF, Di Persio S, Neuhaus N, Fietz D, Laan M, Stallmeyer B, Tüttelmann F., Free PMC Article | 09/27/2024 |
| AZF gene microdeletions in azoospermic-oligozoospermic males. | AZF gene microdeletions in azoospermic-oligozoospermic males.
Lahoz Alonso R, Sienes Bailo P, César Márquez MÁ, Sánchez Torres JC, Albericio Portero JI, Sánchez Parrilla M, Suárez Broto MÁ, Rello Varas L, Izquierdo Álvarez S. | 09/27/2024 |
| We investigated partial deletion of AZFc region and DAZ copy number in a population of Iranian infertile men and normozoospermic controls. Partial AZFc deletions were not significantly different between the infertile and normozoospermic men. | Analysis of partial azoospermia factor c deletion and DAZ copy number in azoospermia and severe oligozoospermia.
Alimardanian L, Saliminejad K, Razi S, Ahani A. | 09/27/2024 |
| AZFd deletions were found to be significant (P < 0.05) in male infertility and it may be associated with other types of AZF deletions. | Association of azoospermia factor region deletions in infertile male subjects among Malaysians.
Hussein AA, Vasudevan R, Patimah I, Prashant N, Nora FA. | 09/27/2024 |
| genetic association study in population in China: Data suggest b2/b3 partial deletions (both deletion-only and deletion-duplication) in AZFc (azoospermia factor c region) are associated with infertility due to spermatogenic impairment (azoospermia). | Gene copy number alterations in the azoospermia-associated AZFc region and their effect on spermatogenic impairment.
Lu C, Jiang J, Zhang R, Wang Y, Xu M, Qin Y, Lin Y, Guo X, Ni B, Zhao Y, Diao N, Chen F, Shen H, Sha J, Xia Y, Hu Z, Wang X. | 09/27/2024 |
| male infertility is associated with partial AZFc duplications, but neither gr/gr nor b2/b3 deletions, suggesting that partial AZFc duplications rather than deletions are risk factors for male infertility in the Chinese-Yi population | Partial AZFc duplications not deletions are associated with male infertility in the Yi population of Yunnan Province, China.
Ye JJ, Ma L, Yang LJ, Wang JH, Wang YL, Guo H, Gong N, Nie WH, Zhao SH., Free PMC Article | 09/27/2024 |
| genetic association studies: Data from 4 unrelated azoospermic patients in France with Y chromosome deletions exclude HSFY1/HSF2 genes as factors in AZFb/P4 palindrome haplogroup required for spermatogenesis. | HSFY genes and the P4 palindrome in the AZFb interval of the human Y chromosome are not required for spermatocyte maturation.
Kichine E, Rozé V, Di Cristofaro J, Taulier D, Navarro A, Streichemberger E, Decarpentrie F, Metzler-Guillemain C, Lévy N, Chiaroni J, Paquis-Flucklinger V, Fellmann F, Mitchell MJ. | 09/27/2024 |
| The microdeletion of AZFb+c+d was one of the important causes of the high level of FSH. | [Relationship between follicle stimulating hormone and AZF microdeletion on Y chromosome in patients with azoospermia or severe oligozoospermia].
Wang XQ, Zhang HY, Qi QW, Zhao J, Xu L. | 09/27/2024 |
| Deletion of sY255 and sY254 as well as sY157 is the most common pattern of AZFc microdeletion in the Chinese Han population. | [Sequence tagged sites of AZFc microdeletion in Chinese Han population].
Wu Q, Wang H, Liu YL, Xu Y, Wang P, Shi HJ, Feng Y. | 09/27/2024 |
| percentage of microdeletions in the AZF region is low in Slovak azoospermic patients, but important from a prognostic view. | Incidence of microdeletions in the AZF region of the Y chromosome in Slovak patients with azoospermia.
Behulova R, Varga I, Strhakova L, Bozikova A, Gabrikova D, Boronova I, Repiska V. | 09/27/2024 |
| results from genetic screening in the Netherlands: identification of partial AZF deletions in c region resulting from non-homologous recombination; one deletion, the P3c deletion, seems to be associated with increased sperm count | A novel partial deletion of the Y chromosome azoospermia factor c region is caused by non-homologous recombination between palindromes and may be associated with increased sperm counts.
Noordam MJ, van Daalen SK, Hovingh SE, Korver CM, van der Veen F, Repping S. | 09/27/2024 |
| High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermia. | High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermia.
Mirfakhraie R, Mirzajani F, Kalantar SM, Montazeri M, Salsabili N, Pourmand GR, Houshmand M. | 09/27/2024 |
| A comprehensive analysis of AZF structure and gene content was undertaken. | Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility?
Navarro-Costa P, Plancha CE, Gonçalves J., Free PMC Article | 09/27/2024 |
| analysis of the loss of the AZFc region due to a human Y-chromosome microdeletion in infertile male patients | Loss of the AZFc region due to a human Y-chromosome microdeletion in infertile male patients.
Pandey LK, Pandey S, Gupta J, Saxena AK. | 09/27/2024 |
| there could be an association between the AZFc region and Klinefelter syndrome | The azoospermia factor locus-c region was found to be related to Klinefelter syndrome in Turkish patients.
Ceylan C, Ceylan GG, Serel TA. | 09/27/2024 |
| partial AZFc deletions might not play a role in predisposing genetic background for the phenotype of azoospermic Klinefelter syndrome subjects. | Genetic association between AZF region polymorphism and Klinefelter syndrome.
Hadjkacem-Loukil L, Ghorbel M, Bahloul A, Ayadi H, Ammar-Keskes L. | 09/27/2024 |
| Both the b2/b3 partial deletion and the DAZ3/4+CDY1a deletion pattern were associated with spermatogenic failure. | The b2/b3 subdeletion shows higher risk of spermatogenic failure and higher frequency of complete AZFc deletion than the gr/gr subdeletion in a Chinese population.
Lu C, Zhang J, Li Y, Xia Y, Zhang F, Wu B, Wu W, Ji G, Gu A, Wang S, Jin L, Wang X. | 09/27/2024 |
| Antioncogenic roles of USP9Y and DDX3Y in lung cancer: USP9Y stabilizes DDX3Y by preventing its degradation through deubiquitination. | Antioncogenic roles of USP9Y and DDX3Y in lung cancer: USP9Y stabilizes DDX3Y by preventing its degradation through deubiquitination.
Xiu L, Ma B, Ding L. | 02/8/2024 |
| This is the first research investigating the utility of TTTY15-USP9Y in prostate cancer detection | Clinical utility of a novel urine-based gene fusion TTTY15-USP9Y in predicting prostate biopsy outcome.
Zhu Y, Ren S, Jing T, Cai X, Liu Y, Wang F, Zhang W, Shi X, Chen R, Shen J, Lu J, Xu C, Wang H, Wang H, Wang Y, Liu B, Li Y, Fang Z, Guo F, Qiao M, Shen D, Lu X, Gao X, Hou J, Sun Y. | 06/28/2016 |
| An impact of the identified polymorphism on discrimination of alleles of the M46 locus with various techniques was discussed, and solutions ensuring correctness of the genotyping results were proposed. | [Identification of a novel Y-SNP in the USP9Y gene and its impact on genotyping alleles of the M46 locus].
Rebała K, Tsybovsky IS, Mikulich AI, Szczerkowska Z. | 06/22/2013 |
| Findings indicated that AZF microdeletion and chromosomal abnormality should be important causes of male infertility. | [A genetic study on microdeletion of azoospermia factor region on Y chromosome of azoospermia and oligozoospermia patients].
Cai ZM, Xiao XS, Liu XY, Wang YQ. | 01/21/2010 |