human | Q5 |
P496 | ORCID iD | 0000-0002-7587-8227 |
P108 | employer | Hudson Institute of Medical Research | Q28224129 |
P735 | given name | Patrick | Q18002623 |
Patrick | Q18002623 | ||
P106 | occupation | researcher | Q1650915 |
P21 | sex or gender | male | Q6581097 |
Q90863048 | A step toward making human oocytes |
Q40372936 | Analysis of Esg1 expression in pluripotent cells and the germline reveals similarities with Oct4 and Sox2 and differences between human pluripotent cell lines |
Q51762787 | Atrial natriuretic peptide infusion in chronic heart failure in the rat. |
Q48568883 | Changing expression and subcellular distribution of karyopherins during murine oogenesis |
Q33847708 | Copy number variation in patients with disorders of sex development due to 46,XY gonadal dysgenesis |
Q40515250 | Differentiation of Fetal Male Germline and Gonadal Progenitor Cells Is Disrupted in Organ Cultures Containing Knockout Serum Replacement. |
Q50644594 | Dppa2 and Dppa4 are closely linked SAP motif genes restricted to pluripotent cells and the germ line. |
Q46892364 | Dynamic regulation of mitotic arrest in fetal male germ cells. |
Q71389339 | Evolution of the mammalian mitochondrial control region--comparisons of control region sequences between monotreme and therian mammals |
Q38103228 | Fine-tuning evolution: germ-line epigenetics and inheritance. |
Q37989113 | Germ cell sex and cell cycle. |
Q34696280 | Identifying disruptors of male germ cell development by small molecule screening in ex vivo gonad cultures. |
Q51910470 | Male fetal germ cell differentiation involves complex repression of the regulatory network controlling pluripotency. |
Q28506426 | Marker genes identify three somatic cell types in the fetal mouse ovary |
Q33933075 | Mitotic arrest in teratoma susceptible fetal male germ cells |
Q33770655 | Normalizing gene expression levels in mouse fetal germ cells. |
Q57086633 | Nuclear reprogramming—alchemy or analysis? |
Q48824967 | Nuclei of adult mammalian somatic cells are directly reprogrammed to oct-4 stem cell gene expression by amphibian oocytes. |
Q60938069 | Out of sight, out of mind? Germ cells and the potential impacts of epigenomic drugs |
Q37655408 | PRC2 is required for extensive reorganization of H3K27me3 during epigenetic reprogramming in mouse fetal germ cells. |
Q52668268 | Pharmacological inhibition of EZH2 disrupts the female germline epigenome. |
Q50591653 | Rapid and reliable determination of transgene zygosity in mice by multiplex ligation-dependent probe amplification. |
Q58711458 | Reduced PRC2 function alters male germline epigenetic programming and paternal inheritance |
Q38644268 | Refurbishing the germline epigenome: Out with the old, in with the new. |
Q47855408 | SOX8 expression during chick embryogenesis. |
Q34465741 | Sex, genes, and heat: triggers of diversity. |
Q28585371 | Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development |
Q33669167 | Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication |
Q62059567 | Temperature-dependent sex determination in the American alligator: expression of SF1, WT1 and DAX1 during gonadogenesis |
Q46404950 | Testis development, fertility, and survival in Ethanolamine kinase 2-deficient mice |
Q51714714 | The migrating gubernaculum grows like a "limb bud". |
Q39391328 | The proto-oncogene Ret is required for male foetal germ cell survival. |
Q46055761 | The rhox homeobox gene family shows sexually dimorphic and dynamic expression during mouse embryonic gonad development |
Q40337342 | Tob1 is expressed in developing and adult gonads and is associated with the P-body marker, Dcp2. |
Q38586384 | Transgenerational epigenetic inheritance: adaptation through the germline epigenome? |
Q39950385 | WNT/β-catenin and p27/FOXL2 differentially regulate supporting cell proliferation in the developing ovary. |