197 related articles for article (PubMed ID: 36125728)
21. Newborn screening and single nucleotide variation profiling of TSHR, TPO, TG and DUOX2 candidate genes for congenital hypothyroidism.
Kollati Y; Akella RRD; Naushad SM; Borkar D; Thalla M; Nagalingam S; Lingappa L; Patel RK; Reddy GB; Dirisala VR
Mol Biol Rep; 2020 Oct; 47(10):7467-7475. PubMed ID: 32930933
[TBL] [Abstract][Full Text] [Related]
22. High frequency of DUOX2 mutations in transient or permanent congenital hypothyroidism with eutopic thyroid glands.
Jin HY; Heo SH; Kim YM; Kim GH; Choi JH; Lee BH; Yoo HW
Horm Res Paediatr; 2014; 82(4):252-60. PubMed ID: 25248169
[TBL] [Abstract][Full Text] [Related]
23. Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
Larrivée-Vanier S; Jean-Louis M; Magne F; Bui H; Rouleau GA; Spiegelman D; Samuels ME; Kibar Z; Van Vliet G; Deladoëy J
Thyroid; 2022 May; 32(5):486-495. PubMed ID: 35272499
[No Abstract] [Full Text] [Related]
24. Screening of 23 candidate genes by next-generation sequencing of patients with permanent congenital hypothyroidism: novel variants in TG, TSHR, DUOX2, FOXE1, and SLC26A7.
Acar S; Gürsoy S; Arslan G; Nalbantoğlu Ö; Hazan F; Köprülü Ö; Özkaya B; Özkan B
J Endocrinol Invest; 2022 Apr; 45(4):773-786. PubMed ID: 34780050
[TBL] [Abstract][Full Text] [Related]
25. Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population.
Huang M; Lu X; Dong G; Li J; Chen C; Yu Q; Li M; Su Y
Front Endocrinol (Lausanne); 2021; 12():695426. PubMed ID: 34276565
[TBL] [Abstract][Full Text] [Related]
26. Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis.
Molina MF; Papendieck P; Sobrero G; Balbi VA; Belforte FS; Martínez EB; Adrover E; Olcese MC; Chiesa A; Miras MB; González VG; Pio MG; González-Sarmiento R; Targovnik HM; Rivolta CM
Endocrine; 2022 Jun; 77(1):86-101. PubMed ID: 35507000
[TBL] [Abstract][Full Text] [Related]
27. Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients.
Fu C; Luo S; Zhang S; Wang J; Zheng H; Yang Q; Xie B; Hu X; Fan X; Luo J; Chen R; Su J; Shen Y; Gu X; Chen S
Clin Chim Acta; 2016 Jul; 458():30-4. PubMed ID: 27108200
[TBL] [Abstract][Full Text] [Related]
28. Identification and analyzes of DUOX2 mutations in two familial congenital hypothyroidism cases.
Li L; Liu W; Zhang L; Wang F; Wang F; Gu M; Wang X; Liu S
Endocrine; 2021 Apr; 72(1):147-156. PubMed ID: 32803677
[TBL] [Abstract][Full Text] [Related]
29. Next-generation sequencing analysis of TSHR in 384 Chinese subclinical congenital hypothyroidism (CH) and CH patients.
Fu C; Wang J; Luo S; Yang Q; Li Q; Zheng H; Hu X; Su J; Zhang S; Chen R; Luo J; Zhang Y; Shen Y; Wei H; Meng D; Gui B; Zeng Z; Fan X; Chen S
Clin Chim Acta; 2016 Nov; 462():127-132. PubMed ID: 27637299
[TBL] [Abstract][Full Text] [Related]
30. The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism.
Zhang RJ; Sun F; Chen F; Fang Y; Yan CY; Zhang CR; Ying YX; Wang Z; Zhang CX; Wu FY; Han B; Liang J; Zhao SX; Song HD
Mol Cell Endocrinol; 2020 Apr; 506():110761. PubMed ID: 32088313
[TBL] [Abstract][Full Text] [Related]
31. Detection of Novel Gene Variants Associated with Congenital Hypothyroidism in a Finnish Patient Cohort.
Löf C; Patyra K; Kuulasmaa T; Vangipurapu J; Undeutsch H; Jaeschke H; Pajunen T; Kero A; Krude H; Biebermann H; Kleinau G; Kühnen P; Rantakari K; Miettinen P; Kirjavainen T; Pursiheimo JP; Mustila T; Jääskeläinen J; Ojaniemi M; Toppari J; Ignatius J; Laakso M; Kero J
Thyroid; 2016 Sep; 26(9):1215-24. PubMed ID: 27373559
[TBL] [Abstract][Full Text] [Related]
32. Mutation screening of the TPO gene in a cohort of 192 Chinese patients with congenital hypothyroidism.
Fu C; Xie B; Zhang S; Wang J; Luo S; Zheng H; Su J; Hu X; Chen R; Fan X; Luo J; Gu X; Chen S
BMJ Open; 2016 May; 6(5):e010719. PubMed ID: 27173810
[TBL] [Abstract][Full Text] [Related]
33. Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis.
Zou M; Alzahrani AS; Al-Odaib A; Alqahtani MA; Babiker O; Al-Rijjal RA; BinEssa HA; Kattan WE; Al-Enezi AF; Al Qarni A; Al-Faham MSA; Baitei EY; Alsagheir A; Meyer BF; Shi Y
J Clin Endocrinol Metab; 2018 May; 103(5):1889-1898. PubMed ID: 29546359
[TBL] [Abstract][Full Text] [Related]
34. New genetics in congenital hypothyroidism.
Stoupa A; Kariyawasam D; Muzza M; de Filippis T; Fugazzola L; Polak M; Persani L; Carré A
Endocrine; 2021 Mar; 71(3):696-705. PubMed ID: 33650047
[TBL] [Abstract][Full Text] [Related]
35. Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling.
Zhang HY; Wu FY; Zhang CX; Wu CY; Cui RJ; Liu XY; Yang L; Zhang Y; Sun F; Cheng F; Yang RM; Song HD; Zhao SX
Thyroid; 2024 Mar; 34(3):324-335. PubMed ID: 38183624
[No Abstract] [Full Text] [Related]
36. Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing.
Watanabe D; Yagasaki H; Narusawa H; Saito T; Mitsui Y; Miyake K; Ohta M; Inukai T
Endocr J; 2021 Dec; 68(12):1411-1419. PubMed ID: 34234053
[TBL] [Abstract][Full Text] [Related]
37. [Genetic of congenital hypothyroidism].
Stoupa A; Kariyawasam D; Polak M; Carré A
Med Sci (Paris); 2022 Mar; 38(3):263-273. PubMed ID: 35333163
[TBL] [Abstract][Full Text] [Related]
38. Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families.
Watanabe Y; Bruellman RJ; Ebrhim RS; Abdullah MA; Dumitrescu AM; Refetoff S; Weiss RE
Thyroid; 2019 Feb; 29(2):302-304. PubMed ID: 30375286
[TBL] [Abstract][Full Text] [Related]
39. [Genetic analysis of TPO, DUOX2 and DUOXA2 genes in children with permanent congenital hypothyroidism suspected dyshormonogenesis].
Huang YL; Tan MY; Jiang X; Li B; Chen QY; Jia XF; Tang CF; Liu JL; Liu L
Zhonghua Er Ke Za Zhi; 2017 Mar; 55(3):210-214. PubMed ID: 28273705
[No Abstract] [Full Text] [Related]
40. A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect.
Baş VN; Aycan Z; Cangul H; Kendall M; Ağladıoğlu SY; Çetinkaya S; Maher ER
J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):383-7. PubMed ID: 24158420
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
