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1.
Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility.
Am J Hum Genet
; 107(2): 342-351, 2020 08 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32673564
2.
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
Am J Hum Genet
; 105(5): 1030-1039, 2019 11 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31630787
3.
The Ca2+ channel CatSper is not activated by cAMP/PKA signaling but directly affected by chemicals used to probe the action of cAMP and PKA.
J Biol Chem
; 295(38): 13181-13193, 2020 09 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-32703901
4.
The Male Fertility Gene Atlas: a web tool for collecting and integrating OMICS data in the context of male infertility.
Hum Reprod
; 35(9): 1983-1990, 2020 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-32766702
5.
Transcriptome analyses in infertile men reveal germ cell-specific expression and splicing patterns.
Life Sci Alliance
; 6(2)2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36446526
6.
Machine learning based prediction models in male reproductive health: Development of a proof-of-concept model for Klinefelter Syndrome in azoospermic patients.
Andrology
; 10(3): 534-544, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34914193
7.
Limitations of Nasal Nitric Oxide Measurement for Diagnosis of Primary Ciliary Dyskinesia with Normal Ultrastructure.
Ann Am Thorac Soc
; 19(8): 1275-1284, 2022 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35202559
8.
FSHB Genotype Identified as a Relevant Diagnostic Parameter Revealed by Cluster Analysis of Men With Idiopathic Infertility.
Front Endocrinol (Lausanne)
; 12: 780403, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34992580
9.
Does the FSHB c.-211G>T polymorphism impact Sertoli cell number and the spermatogenic potential in infertile patients?
Andrology
; 8(5): 1030-1037, 2020 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-32096339
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