Found: 23
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(Symposium on Myxobacteria and Flavobacteria: Paper VI). Morphology and Morphogenesis of Sorangium compositum.
- Published in:
- Journal of Applied Microbiology, 1969, v. 32, n. 1, p. 24, doi. 10.1111/j.1365-2672.1969.tb02185.x
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- Publication type:
- Article
Fluorescence Detection of a Neurotoxic Astroglia-Released Factor using Gradient Liquid Chromatography after Precolumn Derivatization.
- Published in:
- Biomedical Chromatography, 1997, v. 11, n. 2, p. 93, doi. 10.1002/(SICI)1099-0801(199703)11:2<93::AID-BMC656>3.0.CO;2-J
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- Publication type:
- Article
Assisted oocyte activation does not overcome recurrent embryo developmental problems.
- Published in:
- Human Reproduction, 2023, v. 38, n. 5, p. 872, doi. 10.1093/humrep/dead051
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- Publication type:
- Article
TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo.
- Published in:
- 2022
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- Publication type:
- journal article
Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differences.
- Published in:
- 2021
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- Publication type:
- journal article
Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Protection of the small bowel with a silicone tissue expander prosthesis and a polyglycolic acid mesh during radiation therapy for cervical carcinoma.
- Published in:
- BJOG: An International Journal of Obstetrics & Gynaecology, 1994, v. 101, n. 6, p. 541, doi. 10.1111/j.1471-0528.1994.tb13159.x
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- Publication type:
- Article
Identification of von Willebrand disease type 1 in a patient with Ehlers-Danlos syndrome classic type.
- Published in:
- Haemophilia, 2016, v. 22, n. 4, p. e309, doi. 10.1111/hae.12931
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- Publication type:
- Article
Hearing loss in Waardenburg syndrome: a systematic review.
- Published in:
- Clinical Genetics, 2016, v. 89, n. 4, p. 416, doi. 10.1111/cge.12631
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- Publication type:
- Article
A Dutch family with progressive sensorineural hearing impairment linked to the DFNA2 region.
- Published in:
- European Archives of Oto-Rhino-Laryngology, 2000, v. 257, n. 2, p. 62, doi. 10.1007/PL00007511
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- Publication type:
- Article
Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 6, p. 1605, doi. 10.1007/s10815-024-03095-9
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- Publication type:
- Article
The Abcc6a Knockout Zebrafish Model as a Novel Tool for Drug Screening for Pseudoxanthoma Elasticum.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.822143
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- Publication type:
- Article
18q-syndrome with coeliac disease.
- Published in:
- 1999
- By:
- Publication type:
- case study
Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome.
- Published in:
- Human Mutation, 2004, v. 24, n. 2, p. 140, doi. 10.1002/humu.20070
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- Publication type:
- Article
Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population.
- Published in:
- Disease Markers, 2015, v. 2015, p. 1, doi. 10.1155/2015/458653
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- Publication type:
- Article
CARD15polymorphisms are associated with anti-Saccharomyces cerevisiaeantibodies in caucasian Crohn's disease patients.
- Published in:
- Clinical & Experimental Immunology, 2005, v. 140, n. 2, p. 354, doi. 10.1111/j.1365-2249.2005.02759.x
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- Publication type:
- Article
CPT-11 and concomitant hyperfractionated accelerated radiotherapy induce efficient local control in rectal cancer patients: results from a phase II.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Reproducibility of measurements of potential doubling time of tumour cells in the multicentre National Cancer Institute protocol T92-0045.
- Published in:
- British Journal of Cancer, 1999, v. 79, n. 2, p. 323, doi. 10.1038/sj.bjc.6690052
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- Publication type:
- Article
Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome.
- Published in:
- Science Translational Medicine, 2010, v. 2, n. 23, p. 1, doi. 10.1126/scitranslmed.3000488
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- Publication type:
- Article
The new Ghent criteria for Marfan syndrome: what do they change?
- Published in:
- Clinical Genetics, 2012, v. 81, n. 5, p. 433, doi. 10.1111/j.1399-0004.2011.01703.x
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- Publication type:
- Article
Utility of molecular analyses in the exploration of extreme intrafamilial variability in the Marfan syndrome.
- Published in:
- Clinical Genetics, 2007, v. 72, n. 3, p. 188, doi. 10.1111/j.1399-0004.2007.00845.x
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- Publication type:
- Article
Primary non-Hodgkin's lymphoma of the nasal cavity: prognostic significance of paranasal extension and the role of radiotherapy and chemotherapy.
- Published in:
- 1998
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- Publication type:
- journal article
Postoperative radiation therapy for rectal cancer: an interim analysis of a prospective, randomized multicenter trial in The Netherlands.
- Published in:
- 1992
- By:
- Publication type:
- clinical trial