Found: 39
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Mcl-1, an anti-apoptotic Bcl-2 family member, essentially overlaps with insulin-producing cells in neonatal nesidioblastosis.
- Published in:
- 2008
- By:
- Publication type:
- Case Study
Bilateral Intralobar Sequestration of the Lung with a Bridging Isthmus: Pathologic and Radiologic Findings.
- Published in:
- 2014
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- Publication type:
- Case Study
Histology of a Paraumbilical Band in a Neonate with Gastroschisis.
- Published in:
- Pediatric & Developmental Pathology, 2011, v. 14, n. 6, p. 493, doi. 10.2350/11-06-1053-CR.1
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- Publication type:
- Article
PAX3 Is Expressed in the Stromal Compartment of the Developing Kidney and in Wilms Tumors with Myogenic Phenotype.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 5, p. 347, doi. 10.2350/08-05-0466.1
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- Publication type:
- Article
Reply to Dr. Sredni and Colleagues.
- Published in:
- Pediatric & Developmental Pathology, 2004, v. 7, n. 6, p. 670, doi. 10.1007/s10024-004-8093-8
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- Publication type:
- Article
Myogenesis in Wilms' Tumors Is Associated with Mutations of the WT1 Gene and Activation of Bcl-2 and the Wnt Signaling Pathway.
- Published in:
- Pediatric & Developmental Pathology, 2004, v. 7, n. 2, p. 125, doi. 10.1007/s10024-003-3023-8
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- Publication type:
- Article
Beckwith-Wiedemann Syndrome-associated Hepatoblastoma: Wnt Signal Activation Occurs Later in Tumorigenesis in Patients with 11p15.5 Uniparental Disomy.
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- Pediatric & Developmental Pathology, 2003, v. 6, n. 4, p. 299, doi. 10.1007/s10024-003-1009-1
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- Publication type:
- Article
Nesidioblastosis and Mixed Hamartoma of the Liver in Beckwith-Wiedemann Syndrome: Case Study Including Analysis of H19 Methylation and Insulin-like Growth Factor 2 Genotyping and Imprinting.
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- Pediatric & Developmental Pathology, 2001, v. 4, n. 4, p. 381, doi. 10.1007/s10024001-0003-8
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- Publication type:
- Article
Neonatal necrotizing fasciitis of the scrotum caused by Streptococcus agalactiae.
- Published in:
- Pediatrics International, 2015, v. 57, n. 2, p. e56, doi. 10.1111/ped.12563
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- Publication type:
- Article
Selective Ablation of Tumorigenic Cells Following Human Induced Pluripotent Stem Cell‐Derived Neural Stem/Progenitor Cell Transplantation in Spinal Cord Injury.
- Published in:
- Stem Cells Translational Medicine, 2019, v. 8, n. 3, p. 260, doi. 10.1002/sctm.18-0096
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- Publication type:
- Article
Radiological findings of perivascular epithelioid cell tumour (PEComa) of the falciform ligament.
- Published in:
- 2016
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- Publication type:
- journal article
A novel de novo germline mutation Glu40Lys in AKT3 causes megalencephaly with growth hormone deficiency.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 4, p. 1071, doi. 10.1002/ajmg.a.38099
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- Publication type:
- Article
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 95, doi. 10.1038/ng.270
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- Publication type:
- Article
PAX8 Mutation Disturbing Thyroid Follicular Growth: A Case Report.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 12, p. E2039, doi. 10.1210/jc.2011-1114
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- Publication type:
- Article
Germline mutations and somatic inactivation of TRIM28 in Wilms tumour.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 6, p. 1, doi. 10.1371/journal.pgen.1007399
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- Publication type:
- Article
A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta.
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- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0036809
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- Publication type:
- Article
Use of the Naphthoquinone YM155 (Sepantronium Bromide) in the Treatment of Cancer: A Systematic Review and Meta-Synthesis.
- Published in:
- Oncologie (Tech Science Press), 2022, v. 24, n. 2, p. 195, doi. 10.32604/oncologie.2022.022299
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- Publication type:
- Article
A Novel Mutation in NKX2-1 Shows Dominant-Negative Effects Only in the Presence of PAX8.
- Published in:
- Thyroid, 2018, v. 24, n. 8, p. 1071, doi. 10.1089/thy.2017.0481
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- Publication type:
- Article
The Mosaicism Ratio of 45,X May Explain the Phenotype in a Case of Mixed Gonadal Dysgenesis.
- Published in:
- Sexual Development, 2018, v. 12, n. 4, p. 175, doi. 10.1159/000489451
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- Publication type:
- Article
The Distribution and Cellular Lineages of XX and XY Cells in Gonads Associated with Ovotesticular Disorder of Sexual Development.
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- Sexual Development, 2016, v. 10, n. 4, p. 185, doi. 10.1159/000448677
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- Publication type:
- Article
Homozygous deletion of DIS3L2 exon 9 due to non-allelic homologous recombination between LINE-1s in a Japanese patient with Perlman syndrome.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1316, doi. 10.1038/ejhg.2013.45
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- Publication type:
- Article
Gonadal macrophage infiltration in congenital lipoid adrenal hyperplasia.
- Published in:
- European Journal of Endocrinology, 2016, v. 175, n. 2, p. 127, doi. 10.1530/EJE-16-0194
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- Publication type:
- Article
Laparoscopic subtotal colectomy for a patient with chronic idiopathic colonic pseudo‐obstruction: Report of a case.
- Published in:
- Asian Journal of Endoscopic Surgery, 2019, v. 12, n. 4, p. 469, doi. 10.1111/ases.12682
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- Publication type:
- Article
Acinic cell carcinoma in an African pygmy hedgehog ( Atelerix albiventris).
- Published in:
- Veterinary Clinical Pathology, 2004, v. 33, n. 1, p. 39, doi. 10.1111/j.1939-165X.2004.tb00348.x
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- Publication type:
- Article
Human Papillomavirus E6/E7 Expression in Preeclampsia-Affected Placentae.
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- Pathogens, 2020, v. 9, n. 3, p. 239, doi. 10.3390/pathogens9030239
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- Publication type:
- Article
Membranoproliferative glomerulonephritis and C3 glomerulonephritis: Frequency, clinical features, and outcome in children.
- Published in:
- Nephrology, 2015, v. 20, n. 4, p. 286, doi. 10.1111/nep.12382
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- Publication type:
- Article
High frequency of inactivation of the imprinted H19 gene in 'sporadic' hepatoblastoma.
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- International Journal of Cancer, 1999, v. 82, n. 4, p. 490, doi. 10.1002/(SICI)1097-0215(19990812)82:4<490::AID-IJC4>3.0.CO;2-I
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- Publication type:
- Article
A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors1.
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- Journal of Biochemistry, 2000, v. 128, n. 5, p. 847, doi. 10.1093/oxfordjournals.jbchem.a022823
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- Publication type:
- Article
Embryonal hyperplasia of Bowman's capsular epithelium in patients with WT1 mutations.
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- Pediatric Nephrology, 2003, v. 18, n. 1, p. 9, doi. 10.1007/s00467-002-1019-7
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- Publication type:
- Article
Characteristic Testicular Histology Is Useful for the Identification of NR5A1 Gene Mutations in Prepubertal 46,XY Patients.
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- Hormone Research in Paediatrics, 2013, v. 80, n. 2, p. 119, doi. 10.1159/000353763
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- Publication type:
- Article
Pathological classification of human iPSC-derived neural stem/progenitor cells towards safety assessment of transplantation therapy for CNS diseases.
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- Molecular Brain, 2016, v. 9, p. 1, doi. 10.1186/s13041-016-0265-8
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- Publication type:
- Article
Global demethylation in loss of imprinting subtype of wilms tumor.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 2, p. 174, doi. 10.1002/gcc.22017
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- Publication type:
- Article
Heterozygous C-propeptide mutations in COL1A1: Osteogenesis imperfecta type IIC and dense bone variant.
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- American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 9, p. 2269, doi. 10.1002/ajmg.a.34152
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- Publication type:
- Article
A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.
- Published in:
- Endocrine Journal, 2017, v. 64, n. 2, p. 229, doi. 10.1507/endocrj.ej16-0361
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- Publication type:
- Article
A case of transient neonatal diabetes due to a novel mutation in ABCC8.
- Published in:
- 2016
- By:
- Publication type:
- Case Study
MIRAGE syndrome is a rare cause of 46,XY DSD born SGA without adrenal insufficiency.
- Published in:
- PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0206184
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- Publication type:
- Article
A report of two novel NR5A1 mutation families: possible clinical phenotype of psychiatric symptoms of anxiety and/or depression.
- Published in:
- Clinical Endocrinology, 2013, v. 78, n. 6, p. 957, doi. 10.1111/cen.12054
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- Publication type:
- Article
The developmental programme for genesis of the entire kidney is recapitulated in Wilms tumour.
- Published in:
- PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0186333
- By:
- Publication type:
- Article
Expression of mitogen-activated protein kinases in human renal dysplasia.
- Published in:
- Kidney International, 2002, v. 61, n. 3, p. 899, doi. 10.1046/j.1523-1755.2002.00196.x
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- Publication type:
- Article