Found: 23
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Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Dupilumab in Healthy Adult Subjects.
- Published in:
- Clinical Pharmacology in Drug Development, 2020, v. 9, n. 6, p. 742, doi. 10.1002/cpdd.798
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- Publication type:
- Article
AMEERA-1 phase 1/2 study of amcenestrant, SAR439859, in postmenopausal women with ER-positive/HER2-negative advanced breast cancer.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31668-8
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- Publication type:
- Article
Identification of a submicroscopic deletion of SHH associated with the holoprosencephaly spectrum by array-based CGH.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Holoprosencephaly: from Homer to Hedgehog.
- Published in:
- Clinical Genetics, 1998, v. 53, n. 3, p. 155, doi. 10.1111/j.1399-0004.1998.tb02666.x
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- Publication type:
- Article
Production of Interleukin-6 and a Cytolytic T Lymphocyte Differentiation Factor by Mononuclear Cells.
- Published in:
- Annals of the New York Academy of Sciences, 1989, v. 557, n. 1, p. 576, doi. 10.1111/j.1749-6632.1989.tb24071.x
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- Publication type:
- Article
Development of Cytolytic T Lymphocytes in Thymus Culture Requires a Cytokine Sharing Homology with IL-6<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1989, v. 557, n. 1, p. 396, doi. 10.1111/j.1749-6632.1989.tb24032.x
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- Publication type:
- Article
Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2018, v. 178, n. 2, p. 175, doi. 10.1002/ajmg.c.31622
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- Publication type:
- Article
Chromosome 1p36.22p36.21 duplications/triplication causes Setleis syndrome (focal facial dermal dysplasia type III).
- Published in:
- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 5, p. 1061, doi. 10.1002/ajmg.a.36973
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- Publication type:
- Article
SONIC HEDGEHOG mutations causing human holoprosencephaly impair neural patterning activity.
- Published in:
- Human Genetics, 2003, v. 113, n. 2, p. 170, doi. 10.1007/s00439-003-0950-4
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- Publication type:
- Article
Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome.
- Published in:
- Human Genetics, 2002, v. 111, n. 4/5, p. 421, doi. 10.1007/s00439-002-0803-6
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- Publication type:
- Article
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
- Published in:
- 2002
- By:
- Publication type:
- Erratum
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
- Published in:
- Human Genetics, 2002, v. 110, n. 4, p. 297, doi. 10.1007/s00439-002-0695-5
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- Publication type:
- Article
Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly.
- Published in:
- Human Genetics, 2001, v. 109, n. 1, p. 1, doi. 10.1007/s004390100537
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- Publication type:
- Article
A Quantitative Systems Pharmacology Platform to Investigate the Impact of Alirocumab and Cholesterol-Lowering Therapies on Lipid Profiles and Plaque Characteristics.
- Published in:
- Gene Regulation & Systems Biology, 2017, n. 11, p. 1, doi. 10.1177/1177625017710941
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- Publication type:
- Article
What Syndrome Is This?
- Published in:
- Pediatric Dermatology, 2007, v. 24, n. 1, p. 90, doi. 10.1111/j.1525-1470.2007.00344.x
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- Publication type:
- Article
TGIF, a gene associated with human brain defects, regulates neuronal development.
- Published in:
- Developmental Dynamics, 2006, v. 235, n. 6, p. 1482
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- Publication type:
- Article
Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 15, p. 4443, doi. 10.1093/hmg/ddv180
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- Publication type:
- Article
Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators.
- Published in:
- 2000
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- Publication type:
- journal article
Spectrum of MLL2 ( ALR) mutations in 110 cases of Kabuki syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 7, p. 1511, doi. 10.1002/ajmg.a.34074
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- Publication type:
- Article
Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays.
- Published in:
- Human Mutation, 2006, v. 27, n. 5, p. 467, doi. 10.1002/humu.20322
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- Publication type:
- Article
The mutational spectrum of the Sonic Hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 13, p. 2479, doi. 10.1093/hmg/8.13.2479
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- Publication type:
- Article
Bioequivalence Study Comparing Fixed-Dose Combination of Clopidogrel and Aspirin with Coadministration of Individual Formulations in Chinese Subjects Under Fed Conditions: A Phase I, Open-Label, Randomized, Crossover Study.
- Published in:
- Advances in Therapy, 2020, v. 37, n. 11, p. 4660, doi. 10.1007/s12325-020-01486-9
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- Publication type:
- Article
Implementation of a Reference-Scaled Average Bioequivalence Approach for Highly Variable Acetylsalicylic Acid in Fixed-Dose Combination with Clopidogrel Versus Enteric Aspirin in Chinese Subjects Under Fasting Conditions: A Phase 1, Open-Label, Randomized, Crossover Study.
- Published in:
- 2020
- By:
- Publication type:
- journal article