지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
등록된 정보가 없습니다.
논문 유사도에 따라 DBpia 가 추천하는 논문입니다. 함께 보면 좋을 연관 논문을 확인해보세요!
Associations of GNAS Mutations with Surgical Outcomes in Patients with Growth Hormone-Secreting Pituitary Adenoma
Endocrinology and Metabolism
2021 .01
GNAS1 유전자 과오돌연변이가 관찰된 가성부갑상선기능저하증 Ia형 1예
Laboratory Medicine Online
2015 .01
A Case of Pseudohypoparathyroidism Type Ib Caused by Aberrant Methylation in the GNAS Complex Locus
Laboratory Medicine Online
2017 .01
Pseudohypoparathyroidism type 1b due to paternal uniparental disomy of chromosome 20q: A case report
Journal of genetic medicine
2017 .01
Neonatal transient pseudohypoparathyroidism: could it be included among inactivating parathyroid hormone (PTH)/PTH-related protein signalling disorders?
Annals of Pediatirc Endocrinology & Metabolism
2019 .01
Exploring the Key Genes and Pathways of Osteoarthritis in Knee Cartilage in a Rat Model Using Gene Expression Profiling
Yonsei Medical Journal
2018 .01
Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene
Annals of Pediatirc Endocrinology & Metabolism
2019 .01
Novel Mutation in PTHLH Related to Brachydactyly Type E2 Initially Confused with Unclassical Pseudopseudohypoparathyroidism
Endocrinology and Metabolism
2018 .01
The Association of Acquired T790M Mutation with Clinical Characteristics after Resistance to First-Line Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor in Lung Adenocarcinoma
Cancer Research and Treatment
2018 .01
Possible Protective Effects of Quercetin and Sodium Gluconate Against Colon Cancer Induction by Dimethylhydrazine in Mice
Asian Pacific journal of cancer prevention : APJCP
2015 .01
A family with X-linked Cornelia de Lange syndrome due to a novel SMC1A missense mutation identified by multi-gene panel sequencing
Journal of genetic medicine
2018 .01
Novel Germline Mutations of BRCA1 and BRCA2 in Korean Familial Breast Cancer Patients
전남의대학술지
2019 .01
A case of motor and sensory polyneuropathy induced by primary hyperparathyroidism
Annals of Clinical Neurophysiology
2021 .10
A novel mutation in the DNMT1 gene in a patient presenting with pure cerebellar ataxia
Journal of genetic medicine
2017 .01
Genetic Characterization of Molecular Targets in Korean Patients with Gastrointestinal Stromal Tumors
Journal of Gastric Cancer
2020 .01
Successful Treatment of Tolosa-Hunt Syndrome after a Single Infusion of Infliximab
Journal of Clinical Neurology
2018 .01
A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
Journal of genetic medicine
2018 .01
Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct
Clinical and Experimental Otorhinolaryngology
2019 .01
흡연, 음주, 식이행태에 따른 PHP index 비교
한국임상보건과학회지
2017 .01
외국인 근로자의 구강건강관리실태에 따른 구강건강영향지수(OHIP)
한국치위생학회지
2015 .01
0