220 related articles for article (PubMed ID: 35805171)
1. Whole Exome Sequencing Points towards a Multi-Gene Synergistic Action in the Pathogenesis of Congenital Combined Pituitary Hormone Deficiency.
Sertedaki A; Tatsi EB; Vasilakis IA; Fylaktou I; Nikaina E; Iacovidou N; Siahanidou T; Kanaka-Gantenbein C
Cells; 2022 Jun; 11(13):. PubMed ID: 35805171
[TBL] [Abstract][Full Text] [Related]
2. SEMA3A and IGSF10 Are Novel Contributors to Combined Pituitary Hormone Deficiency (CPHD).
Budny B; Zemojtel T; Kaluzna M; Gut P; Niedziela M; Obara-Moszynska M; Rabska-Pietrzak B; Karmelita-Katulska K; Stajgis M; Ambroziak U; Bednarczuk T; Wrotkowska E; Bukowska-Olech E; Jamsheer A; Ruchala M; Ziemnicka K
Front Endocrinol (Lausanne); 2020; 11():368. PubMed ID: 32612575
[No Abstract] [Full Text] [Related]
3. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
Madeira JL; Nishi MY; Nakaguma M; Benedetti AF; Biscotto IP; Fernandes T; Pequeno T; Figueiredo T; Franca MM; Correa FA; Otto AP; Abrão M; Miras MB; Santos S; Jorge AA; Costalonga EF; Mendonca BB; Arnhold IJ; Carvalho LR
Clin Endocrinol (Oxf); 2017 Dec; 87(6):725-732. PubMed ID: 28734020
[TBL] [Abstract][Full Text] [Related]
4. Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.
Vieira TC; Boldarine VT; Abucham J
Arq Bras Endocrinol Metabol; 2007 Oct; 51(7):1097-103. PubMed ID: 18157385
[TBL] [Abstract][Full Text] [Related]
5. Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion.
Dateki S; Fukami M; Uematsu A; Kaji M; Iso M; Ono M; Mizota M; Yokoya S; Motomura K; Kinoshita E; Moriuchi H; Ogata T
J Clin Endocrinol Metab; 2010 Aug; 95(8):4043-7. PubMed ID: 20534763
[TBL] [Abstract][Full Text] [Related]
6. Genetic screening of regulatory regions of pituitary transcription factors in patients with idiopathic pituitary hormone deficiencies.
Elizabeth M; Hokken-Koelega ACS; Schuilwerve J; Peeters RP; Visser TJ; de Graaff LCG
Pituitary; 2018 Feb; 21(1):76-83. PubMed ID: 29255988
[TBL] [Abstract][Full Text] [Related]
7. HESX1 mutations in patients with congenital hypopituitarism: variable phenotypes with the same genotype.
Fang Q; Benedetti AF; Ma Q; Gregory L; Li JZ; Dattani M; Sadeghi-Nejad A; Arnhold IJ; Mendonca BB; Camper SA; Carvalho LR
Clin Endocrinol (Oxf); 2016 Sep; 85(3):408-14. PubMed ID: 27000987
[TBL] [Abstract][Full Text] [Related]
8. Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins.
Zygmunt-Górska A; Wójcik M; Gilis-Januszewska A; Starmach A; Bik-Multanowski M; Starzyk JB
Hormones (Athens); 2024 Mar; 23(1):69-79. PubMed ID: 38147295
[TBL] [Abstract][Full Text] [Related]
9. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.
de Graaff LC; Argente J; Veenma DC; Drent ML; Uitterlinden AG; Hokken-Koelega AC
Horm Res Paediatr; 2010; 73(5):363-71. PubMed ID: 20389107
[TBL] [Abstract][Full Text] [Related]
10. Copy Number Variants Contributing to Combined Pituitary Hormone Deficiency.
Budny B; Karmelita-Katulska K; Stajgis M; Żemojtel T; Ruchała M; Ziemnicka K
Int J Mol Sci; 2020 Aug; 21(16):. PubMed ID: 32796691
[TBL] [Abstract][Full Text] [Related]
11. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
Avbelj Stefanija M; Kotnik P; Bratanič N; Žerjav Tanšek M; Bertok S; Bratina N; Battelino T; Trebušak Podkrajšek K
Horm Res Paediatr; 2015; 84(3):153-8. PubMed ID: 26111865
[TBL] [Abstract][Full Text] [Related]
12. Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.
Choi JH; Jung CW; Kang E; Kim YM; Heo SH; Lee BH; Kim GH; Yoo HW
Yonsei Med J; 2017 May; 58(3):527-532. PubMed ID: 28332357
[TBL] [Abstract][Full Text] [Related]
13. Mutations Within the Transcription Factor
Bulut FD; Özdemir Dilek S; Kotan D; Mengen E; Gürbüz F; Yüksel B
J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):261-268. PubMed ID: 31948187
[TBL] [Abstract][Full Text] [Related]
14. Association of Homozygous
Almatrafi AM; Hibshi AM; Basit S
Medicina (Kaunas); 2023 Feb; 59(3):. PubMed ID: 36984475
[No Abstract] [Full Text] [Related]
15. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
Baş F; Uyguner ZO; Darendeliler F; Aycan Z; Çetinkaya E; Berberoğlu M; Şiklar Z; Öcal G; Darcan Ş; Gökşen D; Topaloğlu AK; Yüksel B; Özbek MN; Ercan O; Evliyaoğlu O; Çetinkaya S; Şen Y; Atabek E; Toksoy G; Aydin BK; Bundak R
Endocrine; 2015 Jun; 49(2):479-91. PubMed ID: 25500790
[TBL] [Abstract][Full Text] [Related]
16. Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.
Ziemnicka K; Budny B; Drobnik K; Baszko-Błaszyk D; Stajgis M; Katulska K; Waśko R; Wrotkowska E; Słomski R; Ruchała M
J Appl Genet; 2016 Aug; 57(3):373-81. PubMed ID: 26608600
[TBL] [Abstract][Full Text] [Related]
17. A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.
Diaczok D; Romero C; Zunich J; Marshall I; Radovick S
J Clin Endocrinol Metab; 2008 Nov; 93(11):4351-9. PubMed ID: 18728160
[TBL] [Abstract][Full Text] [Related]
18. Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiency.
Bajuk Studen K; Stefanija MA; Saveanu A; Barlier A; Brue T; Pfeifer M
Endocrine; 2019 Aug; 65(2):379-385. PubMed ID: 31093944
[TBL] [Abstract][Full Text] [Related]
19. Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary.
Penta L; Bizzarri C; Panichi M; Novelli A; Lepri FR; Cappa M; Esposito S
Int J Mol Sci; 2019 Apr; 20(8):. PubMed ID: 30988269
[TBL] [Abstract][Full Text] [Related]
20. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
Turton JP; Mehta A; Raza J; Woods KS; Tiulpakov A; Cassar J; Chong K; Thomas PQ; Eunice M; Ammini AC; Bouloux PM; Starzyk J; Hindmarsh PC; Dattani MT
Clin Endocrinol (Oxf); 2005 Jul; 63(1):10-8. PubMed ID: 15963055
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
