<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>32(1)</volume><submitter>Hadziselimovic F</submitter><pubmed_abstract>Cryptorchidism occurs frequently in children with cystic fibrosis. Among boys with cryptorchidism and abrogated mini-puberty, the development of the epididymis and the vas deferens is frequently impaired. This finding suggests that a common cause underlies the abnormal development of Ad spermatogonia and the epididymis. The cystic fibrosis transmembrane conductance regulator (CFTR) is an ATP-binding cassette transporter protein that acts as a chloride channel. The CFTR gene has been associated with spermatogenesis and male fertility. In boys with cryptorchidism, prepubertal hypogonadotropic hypogonadism induces suboptimal expression of the ankyrin-like protein gene, ASZ1, the P-element induced wimpy testis-like gene, PIWIL, and CFTR. The abrogated expression of these gene leads to transpos</pubmed_abstract><journal>Basic and clinical andrology</journal><pagination>10</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9210799</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A novel role for CFTR interaction with LH and FGF in azoospermia and epididymal maldevelopment caused by cryptorchidism.</pubmed_title><pmcid>PMC9210799</pmcid><pubmed_authors>Hadziselimovic F</pubmed_authors><pubmed_authors>Stadler M</pubmed_authors><pubmed_authors>Verkauskas G</pubmed_authors></additional><is_claimable>false</is_claimable><name>A novel role for CFTR interaction with LH and FGF in azoospermia and epididymal maldevelopment caused by cryptorchidism.</name><description>Cryptorchidism occurs frequently in children with cystic fibrosis. Among boys with cryptorchidism and abrogated mini-puberty, the development of the epididymis and the vas deferens is frequently impaired. This finding suggests that a common cause underlies the abnormal development of Ad spermatogonia and the epididymis. The cystic fibrosis transmembrane conductance regulator (CFTR) is an ATP-binding cassette transporter protein that acts as a chloride channel. The CFTR gene has been associated with spermatogenesis and male fertility. In boys with cryptorchidism, prepubertal hypogonadotropic hypogonadism induces suboptimal expression of the ankyrin-like protein gene, ASZ1, the P-element induced wimpy testis-like gene, PIWIL, and CFTR. The abrogated expression of these gene leads to transpos</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-22T05:49:40.361Z</modification><creation>2024-11-21T05:02:17.055Z</creation></dates><accession>S-EPMC9210799</accession><cross_references><pubmed>35725394</pubmed><doi>10.1186/s12610-022-00160-0</doi></cross_references></HashMap>