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Progressive metastatic pheochromocytoma induced by multiple endocrine neoplasia type 2A with a lethal outcome.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Fertilization, embryonic development, and offspring from mouse eggs injected with round spermatids combined with Ca2+ oscillation-inducing sperm factor.
- Published in:
- Molecular Human Reproduction, 1999, v. 5, n. 2, p. 132, doi. 10.1093/molehr/5.2.132
- By:
- Publication type:
- Article
Clinical characterization of patients with gBRCA1/2 mutation-positive unresectable pancreatic cancer: a multicenter prospective study.
- Published in:
- Japanese Journal of Clinical Oncology, 2024, v. 54, n. 1, p. 47, doi. 10.1093/jjco/hyad131
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- Publication type:
- Article
Clinical significance of comprehensive genomic profiling tests covered by public insurance in patients with advanced solid cancers in Hokkaido, Japan.
- Published in:
- Japanese Journal of Clinical Oncology, 2021, v. 51, n. 5, p. 753, doi. 10.1093/jjco/hyaa277
- By:
- Publication type:
- Article
Novel deletional mutation of the MEN1 gene in a kindred with multiple endocrine neoplasia type 1.
- Published in:
- Clinical Genetics, 2000, v. 58, n. 1, p. 61, doi. 10.1034/j.1399-0004.2000.580110.x
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- Publication type:
- Article
Identification of two novel mutations in the OCRLI gene in Japanese families with Lowe syndrome.
- Published in:
- Clinical Genetics, 1998, v. 54, n. 3, p. 199, doi. 10.1111/j.1399-0004.1998.tb04284.x
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- Publication type:
- Article
Parasitic myomas after laparoscopic-assisted myomectomy in multiple endocrine neoplasia type 1.
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2013, v. 39, n. 5, p. 1098, doi. 10.1111/jog.12009
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- Publication type:
- Article
Germline BRCA1‐Mutated Synchronous and Metachronous Pancreatic Acinar Cell Carcinoma With Long‐Term Survival.
- Published in:
- Cancer Reports, 2024, v. 7, n. 8, p. 1, doi. 10.1002/cnr2.70007
- By:
- Publication type:
- Article
Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan.
- Published in:
- Journal of Human Genetics, 2013, v. 58, n. 8, p. 560, doi. 10.1038/jhg.2013.34
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- Publication type:
- Article
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan.
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- Journal of Human Genetics, 2007, v. 52, n. 8, p. 675, doi. 10.1007/s10038-007-0170-1
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- Publication type:
- Article
LMNA::NTRK1 Fusion-positive Leiomyosarcoma: Discrepancy between DNA-based Comprehensive Genomic Profiling and RNA Sequencing.
- Published in:
- Internal Medicine, 2024, v. 63, n. 15, p. 2215, doi. 10.2169/internalmedicine.2879-23
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- Publication type:
- Article
Interval between the First Cancer and the Genetic Diagnosis in Lynch Syndrome Probands.
- Published in:
- Internal Medicine, 2021, v. 60, n. 17, p. 2719, doi. 10.2169/internalmedicine.6603-20
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- Publication type:
- Article
Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).
- Published in:
- 2012
- By:
- Publication type:
- journal article
Nationwide registry for patients with neuroendocrine neoplasm of pancreas, gastrointestinal tract, lungs, bronchi, or thymus in Japan.
- Published in:
- International Journal of Clinical Oncology, 2022, v. 27, n. 5, p. 840, doi. 10.1007/s10147-022-02130-y
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- Publication type:
- Article
Comprehensive genetics clinic for familial tumors: proposal for a suitable system in Japan.
- Published in:
- International Journal of Clinical Oncology, 2004, v. 9, n. 4, p. 304, doi. 10.1007/s10147-004-0405-5
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- Publication type:
- Article
Familial neuroendocrine tumor syndromes: From genetics to clinical practice.
- Published in:
- Pituitary, 2006, v. 9, n. 3, p. 231, doi. 10.1007/s11102-006-0268-z
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- Publication type:
- Article
Characterization of a novel mutant human thyroid hormone receptor β in a family with hereditary thyroid hormone resistance.
- Published in:
- Clinical Endocrinology, 1993, v. 38, n. 1, p. 29, doi. 10.1111/j.1365-2265.1993.tb00969.x
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- Publication type:
- Article
Prevalence of Germline Variants in a Large Cohort of Japanese Patients with Pheochromocytoma and/or Paraganglioma.
- Published in:
- Cancers, 2021, v. 13, n. 16, p. 4014, doi. 10.3390/cancers13164014
- By:
- Publication type:
- Article
High penetrance of pheochromocytoma in multiple endocrine neoplasia 2 caused by germ line RET codon 634 mutation in Japanese patients.
- Published in:
- European Journal of Endocrinology, 2013, v. 168, n. 5, p. 683, doi. 10.1530/EJE-12-1106
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- Publication type:
- Article
Surgery for a gastroenteropancreatic neuroendocrine tumor (GEPNET) in multiple endocrine neoplasia type 1.
- Published in:
- Surgery Today, 2013, v. 43, n. 3, p. 229, doi. 10.1007/s00595-012-0376-5
- By:
- Publication type:
- Article
Characterization of the MEN1 Gene Product, Menin, by Site-specific Polyclonal Antibodies.
- Published in:
- Cancer Science, 1999, v. 90, n. 10, p. 1088, doi. 10.1111/j.1349-7006.1999.tb00682.x
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- Publication type:
- Article
Genetic Screening in Hereditary Multiple Endocrine Neoplasia Type 1: Absence of a Founder Effect among Japanese Families.
- Published in:
- Cancer Science, 1996, v. 87, n. 9, p. 985, doi. 10.1111/j.1349-7006.1996.tb02130.x
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- Publication type:
- Article
Suppression of insulin-induced AP-1 transactivation by menin accompanies inhibition of c-Fos induction.
- Published in:
- International Journal of Cancer, 2003, v. 103, n. 6, p. 738, doi. 10.1002/ijc.10885
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- Publication type:
- Article
Electromagnetic Field Analysis by Boundary Element Method Using Spatial Eigenmodes.
- Published in:
- Electrical Engineering in Japan, 1992, v. 112, n. 2, p. 38, doi. 10.1002/eej.4391120205
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- Publication type:
- Article
Novel 14 Base-Pair Deletion of the MEN1 Gene in a Patient with Recurrent Primary Hyperparathyroidism.
- Published in:
- Japanese Journal of Clinical Oncology, 2006, v. 36, n. 6, p. 395, doi. 10.1093/jjco/hyl023
- By:
- Publication type:
- Article
Genetic basis of inter-individual variability in the effects of exercise on the alleviation of lifestyle-related diseases.
- Published in:
- Journal of Physiology, 2009, v. 587, n. 23, p. 5577, doi. 10.1113/jphysiol.2009.179283
- By:
- Publication type:
- Article
JNETS clinical practice guidelines for gastroenteropancreatic neuroendocrine neoplasms: diagnosis, treatment, and follow-up: a synopsis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Autosomally Transmitted Low Concentration of Thyroxine-Binding Globulin.
- Published in:
- Thyroid, 1999, v. 9, n. 2, p. 159, doi. 10.1089/thy.1999.9.159
- By:
- Publication type:
- Article
Ligand- and Nuclear Factor-Dependent Change in Hydrophobicity of Thyroid Hormone β<sub>1</sub> Receptor.
- Published in:
- Thyroid, 1998, v. 8, n. 4, p. 343, doi. 10.1089/thy.1998.8.343
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- Publication type:
- Article
A Novel Point Mutation of Thyroid Hormone Receptor β Gene in a Family with Resistance to Thyroid Hormone.
- Published in:
- Thyroid, 1997, v. 7, n. 5, p. 771, doi. 10.1089/thy.1997.7.771
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- Publication type:
- Article
A Novel Point Mutation (R243Q) in Exon 7 of the c-erbAβ Thyroid Hormone Receptor Gene in a Family with Resistance to Thyroid Hormone.
- Published in:
- Thyroid, 1995, v. 5, n. 5, p. 355, doi. 10.1089/thy.1995.5.355
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- Publication type:
- Article
Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutation.
- Published in:
- Endocrine Journal, 2015, v. 62, n. 7, p. 627, doi. 10.1507/endocrj.ej15-0057
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- Publication type:
- Article
A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma.
- Published in:
- Endocrine Journal, 2014, v. 61, n. 11, p. 1141, doi. 10.1507/endocrj.ej14-0334
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- Publication type:
- Article
Plasma free metanephrines in the diagnosis of pheochromocytoma: diagnostic accuracy and strategies for Japanese patients.
- Published in:
- Endocrine Journal, 2014, v. 61, n. 7, p. 667, doi. 10.1507/endocrj.ej13-0277
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- Publication type:
- Article
Application of an intracellular stability test of a novel missense menin mutant to the diagnosis of multiple endocrine neoplasia type 1.
- Published in:
- Endocrine Journal, 2012, v. 59, n. 12, p. 1093, doi. 10.1507/endocrj.ej12-0145
- By:
- Publication type:
- Article
Clinical features of insulinoma in patients with multiple endocrine neoplasia type 1: analysis of the database of the MEN Consortium of Japan.
- Published in:
- Endocrine Journal, 2012, v. 59, n. 10, p. 859, doi. 10.1507/endocrj.ej12-0173
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- Publication type:
- Article
Delay in the diagnosis of multiple endocrine neoplasia type 1: typical symptoms are frequently overlooked.
- Published in:
- Endocrine Journal, 2012, v. 59, n. 9, p. 797, doi. 10.1507/endocrj.ej12-0071
- By:
- Publication type:
- Article
A novel splice site mutation of the MEN1 gene identified in a patient with primary hyperparathyroidism.
- Published in:
- Endocrine Journal, 2012, v. 59, n. 6, p. 523, doi. 10.1507/endocrj.ej12-0037
- By:
- Publication type:
- Article
A synonymous VHL variant in exon 2 confers susceptibility to familial pheochromocytoma and von Hippel-Lindau disease.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Extra-endocrine phenotypes at infancy in multiple endocrine neoplasia type 2B: A case series of six Japanese patients.
- Published in:
- Clinical Pediatric Endocrinology, 2021, v. 30, n. 4, p. 195, doi. 10.1297/cpe.30.195
- By:
- Publication type:
- Article
An adolescent case of familial hyperparathyroidism with a germline frameshift mutation of the CDC73 gene.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Clinical application of long‐read nanopore sequencing in a preimplantation genetic testing pre‐clinical workup to identify the junction for complex Xq chromosome rearrangement‐related disease.
- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 3, p. 304, doi. 10.1002/pd.6334
- By:
- Publication type:
- Article
Effect of comprehensive cancer genomic profiling on therapeutic strategies and clinical outcomes in patients with advanced biliary tract cancer: A prospective multicenter study.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.988527
- By:
- Publication type:
- Article
Assessment for the timing of comprehensive genomic profiling tests in patients with advanced solid cancers.
- Published in:
- Cancer Science, 2023, v. 114, n. 8, p. 3385, doi. 10.1111/cas.15837
- By:
- Publication type:
- Article
Propagation characteristics of Omega signals and their triggered emissions observed by EXOS-D satellite.
- Published in:
- Geophysical Research Letters, 1991, v. 18, n. 2, p. 321, doi. 10.1029/91GL00038
- By:
- Publication type:
- Article
Thymic neuroendocrine tumour in multiple endocrine neoplasia type 1: female patients are not rare exceptions.
- Published in:
- Clinical Endocrinology, 2013, v. 78, n. 2, p. 248, doi. 10.1111/j.1365-2265.2012.04467.x
- By:
- Publication type:
- Article
Multiple endocrine neoplasia type 1 in Japan: establishment and analysis of a multicentre database.
- Published in:
- Clinical Endocrinology, 2012, v. 76, n. 4, p. 533, doi. 10.1111/j.1365-2265.2011.04227.x
- By:
- Publication type:
- Article
Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism–jaw tumour syndrome.
- Published in:
- Clinical Endocrinology, 2006, v. 65, n. 1, p. 9, doi. 10.1111/j.1365-2265.2006.02534.x
- By:
- Publication type:
- Article
Significance of prostate/pancreatic/skin cancer family history for detecting BRCA2 pathogenic variant careers among patients with breast cancer.
- Published in:
- Breast Cancer (13406868), 2022, v. 29, n. 5, p. 808, doi. 10.1007/s12282-022-01360-2
- By:
- Publication type:
- Article