Found: 29
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A randomized study of docetaxel and dexamethasone with low- or high-dose estramustine for patients with advanced hormone-refractory prostate cancer.
- Published in:
- BJU International, 2006, v. 98, n. 3, p. 580, doi. 10.1111/j.1464-410X.2006.06324.x
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- Publication type:
- Article
Universal Cardiac Induction of Human Pluripotent Stem Cells in Two and Three-Dimensional Formats: Implications for In Vitro Maturation.
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- Stem Cells, 2015, v. 33, n. 5, p. 1456, doi. 10.1002/stem.1964
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- Publication type:
- Article
Rotational motion and rheotaxis of human sperm do not require functional CatSper channels and transmembrane Ca<sup>2+</sup> signaling.
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- EMBO Journal, 2020, v. 39, n. 4, p. 1, doi. 10.15252/embj.2019102363
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- Article
Astrocyte pathology in a human neural stem cell model of frontotemporal dementia caused by mutant TAU protein.
- Published in:
- Scientific Reports, 2017, p. 42991, doi. 10.1038/srep42991
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- Publication type:
- Article
Derivation and Expansion Using Only Small Molecules of Human Neural Progenitors for Neurodegenerative Disease Modeling.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059252
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- Article
Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019426
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- Publication type:
- Article
Promoter CpG hypermethylation and downregulation of DICE1 expression in prostate cancer.
- Published in:
- Oncogene, 2005, v. 24, n. 44, p. 6667, doi. 10.1038/sj.onc.1208824
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- Article
Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 1012, doi. 10.1038/ejhg.2012.290
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- Article
Parental mosaicism of JAG1 mutations in families with Alagille syndrome.
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- European Journal of Human Genetics, 2001, v. 9, n. 7, p. 559, doi. 10.1038/sj.ejhg.5200671
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- Article
Parental mosaicism of JAG1 mutations in families with Alagille syndrome.
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- European Journal of Human Genetics, 2001, v. 9, n. 3, p. 209, doi. 10.1038/sj.ejhg.5200613
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- Publication type:
- Article
Aberrations of the X chromosome as cause of male infertility.
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- European Journal of Endocrinology, 2017, v. 177, n. 5, p. R249, doi. 10.1530/EJE-17-0246
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- Article
Mutational Analysis of GNAQ and GNA11 to Aid Therapy Management of a Choroidal Melanoma Metastatic to the Contralateral Orbit.
- Published in:
- JAMA Ophthalmology, 2013, v. 131, n. 6, p. 812, doi. 10.1001/jamaophthalmol.2013.1921
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- Article
WWC2 expression in the testis: Implications for spermatogenesis and male fertility.
- Published in:
- FASEB Journal, 2023, v. 37, n. 5, p. 1, doi. 10.1096/fj.202200960R
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- Publication type:
- Article
Gain of androgen receptor gene copies in primary prostate cancer due to X chromosome polysomy.
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- Prostate, 2004, v. 59, n. 1, p. 59, doi. 10.1002/pros.10356
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- Publication type:
- Article
The first versatile human iPSC-based model of ectopic virus induction allows new insights in RNA-virus disease.
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- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72966-9
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- Publication type:
- Article
The human RHOX gene cluster: target genes and functional analysis of gene variants in infertile men.
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- Human Molecular Genetics, 2016, v. 25, n. 22, p. 4898, doi. 10.1093/hmg/ddw313
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- Publication type:
- Article
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
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- Journal of Assisted Reproduction & Genetics, 2017, v. 34, n. 5, p. 683, doi. 10.1007/s10815-017-0900-z
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- Article
Azoospermia and ring chromosome 9-a case report.
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- 2015
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- Publication type:
- Report
Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case report.
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- 2013
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- Publication type:
- Report
High incidence of familial breast cancer segregates with constitutional t(11;22)(q23;q11).
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- Genes, Chromosomes & Cancer, 2006, v. 45, n. 10, p. 945, doi. 10.1002/gcc.20358
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- Publication type:
- Article
Extrinsic immune cell-derived, but not intrinsic oligodendroglial factors contribute to oligodendroglial differentiation block in multiple sclerosis.
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- Acta Neuropathologica, 2020, v. 140, n. 5, p. 715, doi. 10.1007/s00401-020-02217-8
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- Publication type:
- Article
Genetic Variants of DICE1/INTS6 in German Prostate Cancer Families with Linkage to 13q14.
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- Urologia Internationalis, 2015, v. 95, n. 4, p. 386, doi. 10.1159/000366229
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- Publication type:
- Article
Cardiogenic programming of human pluripotent stem cells by dose-controlled activation of EOMES.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02812-6
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- Publication type:
- Article
Retrospective diagnosis and subsequent prenatal diagnosis of Nijmegen breakage syndrome.
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- Prenatal Diagnosis, 2004, v. 24, n. 2, p. 111, doi. 10.1002/pd.803
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- Publication type:
- Article
Severe, very early onset preeclampsia in a Covid 19-positive woman with a twin pregnancy presenting with a hydatidiform mole and coexisting normal fetus: a case report.
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- Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1340905
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- Publication type:
- Article
A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.
- Published in:
- 2005
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- Publication type:
- Letter
Identification of 36 novel Jagged1 (JAG1) mutations in patients with Alagille syndrome.
- Published in:
- Human Mutation, 2003, v. 21, n. 1, p. 100, doi. 10.1002/humu.9102
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- Publication type:
- Article
Initial experience with [18F]DPA-714 TSPO-PET to image inflammation in primary angiitis of the central nervous system.
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- European Journal of Nuclear Medicine & Molecular Imaging, 2020, v. 47, n. 9, p. 2131, doi. 10.1007/s00259-019-04662-4
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- Publication type:
- Article
Cardiac Subtype-Specific Modeling of K<sub>v</sub>1.5 Ion Channel Deficiency Using Human Pluripotent Stem Cells.
- Published in:
- Frontiers in Physiology, 2017, p. 1, doi. 10.3389/fphys.2017.00469
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- Article