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Genetic Variants in the TBC1D2B Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 16, p. 8867, doi. 10.3390/ijms25168867
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- Article
Hormone Replacement Therapy in Breast Cancer Survivors.
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- Breast Journal, 1997, v. 3, n. 2, p. 63, doi. 10.1111/j.1524-4741.1997.tb00142.x
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- Article
Postnatal Ontogeny of the Cranial Base and Craniofacial Skeleton in Male C57BL/6J Mice: A Reference Standard for Quantitative Analysis.
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- Frontiers in Physiology, 2016, p. 1, doi. 10.3389/fphys.2015.00417
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- Article
Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico.
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- Frontiers in Physiology, 2015, v. 6, p. 1, doi. 10.3389/fphys.2015.00092
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- Article
Evaluation and integration of disparate classification systems for clefts of the lip.
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- Frontiers in Physiology, 2014, v. 5, p. 1, doi. 10.3389/fphys.2014.00163
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- Article
Genetic evidence for conserved non-coding element function across species-the ears have it.
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- Frontiers in Physiology, 2014, v. 4/5, p. 1, doi. 10.3389/fphys.2014.00007
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- Article
Lack of association between the A118G polymorphism of the mu opioid receptor gene (OPRM1) and opioid dependence: A meta-analysis.
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- Pharmacogenomics & Personalized Medicine, 2009, v. 2, p. 9
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- Article
Isl1 Controls Patterning and Mineralization of Enamel in the Continuously Renewing Mouse Incisor.
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- Journal of Bone & Mineral Research, 2017, v. 32, n. 11, p. 2219, doi. 10.1002/jbmr.3202
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- Article
Inhibition of Notch Signaling During Mouse Incisor Renewal Leads to Enamel Defects.
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- Journal of Bone & Mineral Research, 2016, v. 31, n. 1, p. 152, doi. 10.1002/jbmr.2591
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- Article
Cerebral perfusion characteristics show differences in younger versus older children with sickle cell anaemia: Results from a multiple-inflow-time arterial spin labelling study.
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- NMR in Biomedicine, 2018, v. 31, n. 6, p. 1, doi. 10.1002/nbm.3915
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- Article
A micro-computed tomography-based comparison of the canal transportation and centering ability of ProTaper Universal rotary and WaveOne reciprocating files.
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- Quintessence International, 2014, v. 45, n. 2, p. 101, doi. 10.3290/j.qi.a30998
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- Article
TRIM18 is a critical regulator of viral myocarditis and organ inflammation.
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- Journal of Biomedical Science, 2022, v. 29, n. 1, p. 1, doi. 10.1186/s12929-022-00840-z
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- Article
Hypomyelination, hypodontia and craniofacial abnormalities in a Polr3b mouse model of leukodystrophy.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 12, p. 5070, doi. 10.1093/brain/awad249
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- Article
Rare Genetic Variants in Human APC Are Implicated in Mesiodens and Isolated Supernumerary Teeth.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 5, p. 4255, doi. 10.3390/ijms24054255
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- Article
A Founder Intronic Variant in P3H1 Likely Results in Aberrant Splicing and Protein Truncation in Patients of Karen Descent with Osteogenesis Imperfecta Type VIII.
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- Genes, 2023, v. 14, n. 2, p. 322, doi. 10.3390/genes14020322
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- Article
SERPINB3 , Adult-Onset Immunodeficiency, and Generalized Pustular Psoriasis.
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- Genes, 2023, v. 14, n. 2, p. 266, doi. 10.3390/genes14020266
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- Article
Loss of Function TGFBR2 Variant as a Contributing Factor in Generalized Pustular Psoriasis and Adult-Onset Immunodeficiency.
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- Genes, 2023, v. 14, n. 1, p. 103, doi. 10.3390/genes14010103
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- Publication type:
- Article
A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and Palate.
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- Genes, 2020, v. 11, n. 8, p. 903, doi. 10.3390/genes11080903
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- Article
CDH1 Mutation Distribution and Type Suggests Genetic Differences between the Etiology of Orofacial Clefting and Gastric Cancer.
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- Genes, 2020, v. 11, n. 4, p. 1, doi. 10.3390/genes11040391
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- Article
A very high density microsatellite map (1 STR / 41 kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical region.
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- European Journal of Human Genetics, 1998, v. 6, n. 4, p. 406, doi. 10.1038/sj.ejhg.5200203
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- Article
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 12, p. 6358, doi. 10.3390/ijms25126358
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- Article
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 10, p. 5179, doi. 10.3390/ijms25105179
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- Article
Genome-Wide Association Studies in Dogs and Humans Identify ADAMTS20 as a Risk Variant for Cleft Lip and Palate.
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- PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005059
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- Article
Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice.
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- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002278
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- Article
Maternal Ethanol Consumption Alters the Epigenotype and the Phenotype of Offspring in a Mouse Model.
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- PLoS Genetics, 2010, v. 6, n. 1, p. 1, doi. 10.1371/journal.pgen.1000811
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- Article
Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08520-7
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- Article
Differences in Oral Structure and Tissue Interactions during Mouse vs. Human Palatogenesis: Implications for the Translation of Findings from Mice.
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- Frontiers in Physiology, 2017, v. 8, p. 1, doi. 10.3389/fphys.2017.00154
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- Publication type:
- Article
Branch-Based Model for the Diameters of the Pulmonary Airways: Accounting for Departures From Self-Consistency and Registration Errors.
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- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2012, v. 295, n. 6, p. 1027, doi. 10.1002/ar.22476
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- Article
Perspectives and challenges in advancing research into craniofacial anomalies.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 4, p. 213, doi. 10.1002/ajmg.c.31383
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- Article
Intra- and Intersexual swim bladder dimorphisms in the plainfin midshipman fish ( Porichthys notatus): Implications of swim bladder proximity to the inner ear for sound pressure detection.
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- Journal of Morphology, 2017, v. 278, n. 11, p. 1458, doi. 10.1002/jmor.20724
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- Article
Digging adaptation in insectivorous subterranean eutherians. The enigma of M esoscalops montanensis unveiled by geometric morphometrics and finite element analysis.
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- Journal of Morphology, 2015, v. 276, n. 10, p. 1157, doi. 10.1002/jmor.20405
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- Article
The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4.
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- Mammalian Genome, 2023, v. 34, n. 3, p. 453, doi. 10.1007/s00335-023-09999-8
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- Article
Altering maternal calcium and phosphorus dietary intake induces persistent sex‐specific changes in the dentition of the offspring.
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- Orthodontics & Craniofacial Research, 2024, v. 27, n. 3, p. 403, doi. 10.1111/ocr.12742
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- Article
Altering osteoclast numbers using CTSK models in utero affects mice offspring craniofacial morphology.
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- Orthodontics & Craniofacial Research, 2023, v. 26, n. 3, p. 338, doi. 10.1111/ocr.12614
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- Article
Altering calcium and phosphorus levels in utero affects adult mouse mandibular morphology.
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- 2019
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- Publication type:
- journal article
Subcortical and cerebellar volumetric deficits in paediatric sickle cell anaemia.
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- British Journal of Haematology, 2013, v. 163, n. 3, p. 373, doi. 10.1111/bjh.12496
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- Publication type:
- Article
Is there a role for magnetic resonance imaging in the evaluation of non-traumatic intraparenchymal haemorrhage in children?
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- 2006
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- Publication type:
- journal article
Complication rates of diagnostic cerebral arteriography in children.
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- 2005
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- Publication type:
- journal article
Rare Variants in LRP4 Are Associated with Mesiodens, Root Maldevelopment, and Oral Exostoses in Humans.
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- Biology (2079-7737), 2023, v. 12, n. 2, p. 220, doi. 10.3390/biology12020220
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- Article
Transcriptomic analysis reveals the role of SIX1 in mouse cranial neural crest patterning and bone development.
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- Developmental Dynamics, 2023, v. 252, n. 10, p. 1303, doi. 10.1002/dvdy.597
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- Publication type:
- Article
Effects of Multi-Generational Soft Diet Consumption on Mouse Craniofacial Morphology.
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- Frontiers in Physiology, 2020, v. 11, p. 1, doi. 10.3389/fphys.2020.00783
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- Article
Leigh's Disease Associated With a Dorsal Midbrain Syndrome.
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- Journal of Pediatric Ophthalmology & Strabismus, 2009, v. 46, n. 5, p. 304, doi. 10.3928/01913913-20090903-09
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- Article
Microtia: Epidemiology and genetics.
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- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 124, doi. 10.1002/ajmg.a.34352
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- Article
SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway-Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification.
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- Brain Pathology, 2017, v. 27, n. 1, p. 64, doi. 10.1111/bpa.12362
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- Article
Expression of three spalt (sal) gene homologues in zebrafish embryos.
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- Development Genes & Evolution, 2003, v. 213, n. 1, p. 35, doi. 10.1007/s00427-002-0284-6
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- Article
Sonic Hedgehog upregulation does not enhance the survival and engraftment of stem cell-derived cardiomyocytes in infarcted hearts.
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- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0227780
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- Article
Impaired myocardial development resulting in neonatal cardiac hypoplasia alters postnatal growth and stress response in the heart.
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- Cardiovascular Research, 2015, v. 106, n. 1, p. 43, doi. 10.1093/cvr/cvv028
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- Article
A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 8, p. 2506, doi. 10.1093/brain/aws172
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- Article
Front Cover, Volume 40, Issue 10.
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- Human Mutation, 2019, v. 40, n. 10, p. i, doi. 10.1002/humu.23923
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- Article
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans.
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- Human Mutation, 2019, v. 40, n. 10, p. 1813, doi. 10.1002/humu.23793
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- Publication type:
- Article