178 related articles for article (PubMed ID: 28735299)
1. Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrix.
Sampaolo S; Napolitano F; Tirozzi A; Reccia MG; Lombardi L; Farina O; Barra A; Cirillo F; Melone MAB; Gianfrancesco F; Iorio GD; Esposito T
J Med Genet; 2017 Oct; 54(10):710-720. PubMed ID: 28735299
[TBL] [Abstract][Full Text] [Related]
2. Early posterior vitreous detachment is associated with LAMA5 dominant mutation.
Napolitano F; Di Iorio V; Di Iorio G; Melone MAB; Gianfrancesco F; Simonelli F; Esposito T; Testa F; Sampaolo S
Ophthalmic Genet; 2019 Feb; 40(1):39-42. PubMed ID: 30589377
[TBL] [Abstract][Full Text] [Related]
3. Laminin-10 is crucial for hair morphogenesis.
Li J; Tzu J; Chen Y; Zhang YP; Nguyen NT; Gao J; Bradley M; Keene DR; Oro AE; Miner JH; Marinkovich MP
EMBO J; 2003 May; 22(10):2400-10. PubMed ID: 12743034
[TBL] [Abstract][Full Text] [Related]
4. Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia.
Barad M; Csukasi F; Bosakova M; Martin JH; Zhang W; Paige Taylor S; Lachman RS; Zieba J; Bamshad M; Nickerson D; Chong JX; Cohn DH; Krejci P; Krakow D; Duran I
EBioMedicine; 2020 Dec; 62():103075. PubMed ID: 33242826
[TBL] [Abstract][Full Text] [Related]
5. Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis.
Gao J; DeRouen MC; Chen CH; Nguyen M; Nguyen NT; Ido H; Harada K; Sekiguchi K; Morgan BA; Miner JH; Oro AE; Marinkovich MP
Genes Dev; 2008 Aug; 22(15):2111-24. PubMed ID: 18676816
[TBL] [Abstract][Full Text] [Related]
6. Rare Variants in LAMA5 Gene associated with FLT4 and FOXC2 Mutations in Primary Lymphedema May Contribute to Severity.
Liu NF; Yu ZY; Sun D; Lou Y
Lymphology; 2016 Dec; 49(4):192-204. PubMed ID: 29908552
[TBL] [Abstract][Full Text] [Related]
7. Diagnostic Exome Sequencing Identifies a Novel Gene, EMILIN1, Associated with Autosomal-Dominant Hereditary Connective Tissue Disease.
Capuano A; Bucciotti F; Farwell KD; Tippin Davis B; Mroske C; Hulick PJ; Weissman SM; Gao Q; Spessotto P; Colombatti A; Doliana R
Hum Mutat; 2016 Jan; 37(1):84-97. PubMed ID: 26462740
[TBL] [Abstract][Full Text] [Related]
8. A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defects.
Kaimori JY; Kikkawa Y; Motooka D; Namba-Hamano T; Takuwa A; Okazaki A; Kobayashi K; Tanigawa A; Kotani Y; Uno Y; Yoshimi K; Hattori K; Asahina Y; Kajimoto S; Doi Y; Oka T; Sakaguchi Y; Mashimo T; Sekiguchi K; Nakaya A; Nomizu M; Isaka Y
JCI Insight; 2022 Dec; 7(23):. PubMed ID: 36173685
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of Lama5 as a candidate for the mouse ragged (Ra) mutation.
Durkin ME; Albrechtsen R; Chambers DM; Abbott CM; Wewer UM
Biochem Biophys Res Commun; 1998 Sep; 250(1):125-30. PubMed ID: 9735344
[TBL] [Abstract][Full Text] [Related]
10. A mutation affecting laminin alpha 5 polymerisation gives rise to a syndromic developmental disorder.
Jones LK; Lam R; McKee KK; Aleksandrova M; Dowling J; Alexander SI; Mallawaarachchi A; Cottle DL; Short KM; Pais L; Miner JH; Mallett AJ; Simons C; McCarthy H; Yurchenco PD; Smyth IM
Development; 2020 Jun; 147(21):. PubMed ID: 32439764
[TBL] [Abstract][Full Text] [Related]
11. Identification of the novel SDR42E1 gene that affects steroid biosynthesis associated with the oculocutaneous genital syndrome.
Bouhouche A; Albaroudi N; El Alaoui MA; Askander O; Habbadi Z; El Hassani A; Iraqi H; El Fahime E; Belmekki M
Exp Eye Res; 2021 Aug; 209():108671. PubMed ID: 34133966
[TBL] [Abstract][Full Text] [Related]
12. [Expression of Laminin gene family in porcine pluripotent stem cells].
Li H; Yu T; Ma Y; Wang H
Sheng Wu Gong Cheng Xue Bao; 2017 Aug; 33(8):1304-1314. PubMed ID: 28853258
[TBL] [Abstract][Full Text] [Related]
13. Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue.
Alazami AM; Al-Qattan SM; Faqeih E; Alhashem A; Alshammari M; Alzahrani F; Al-Dosari MS; Patel N; Alsagheir A; Binabbas B; Alzaidan H; Alsiddiky A; Alharbi N; Alfadhel M; Kentab A; Daza RM; Kircher M; Shendure J; Hashem M; Alshahrani S; Rahbeeni Z; Khalifa O; Shaheen R; Alkuraya FS
Hum Genet; 2016 May; 135(5):525-540. PubMed ID: 27023906
[TBL] [Abstract][Full Text] [Related]
14. Maintenance of glomerular filtration barrier integrity requires laminin alpha5.
Goldberg S; Adair-Kirk TL; Senior RM; Miner JH
J Am Soc Nephrol; 2010 Apr; 21(4):579-86. PubMed ID: 20150535
[TBL] [Abstract][Full Text] [Related]
15. Requirement for basement membrane laminin α5 during urethral and external genital development.
Lin C; Werner R; Ma L; Miner JH
Mech Dev; 2016 Aug; 141():62-69. PubMed ID: 27208857
[TBL] [Abstract][Full Text] [Related]
16. Tumour-Derived Laminin α5 (LAMA5) Promotes Colorectal Liver Metastasis Growth, Branching Angiogenesis and Notch Pathway Inhibition.
Gordon-Weeks A; Lim SY; Yuzhalin A; Lucotti S; Vermeer JAF; Jones K; Chen J; Muschel RJ
Cancers (Basel); 2019 May; 11(5):. PubMed ID: 31064120
[TBL] [Abstract][Full Text] [Related]
17. A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney disease.
Shannon MB; Patton BL; Harvey SJ; Miner JH
J Am Soc Nephrol; 2006 Jul; 17(7):1913-22. PubMed ID: 16790509
[TBL] [Abstract][Full Text] [Related]
18. Laminin α5 in the keratinocyte basement membrane is required for epidermal-dermal intercommunication.
Wegner J; Loser K; Apsite G; Nischt R; Eckes B; Krieg T; Werner S; Sorokin L
Matrix Biol; 2016 Dec; 56():24-41. PubMed ID: 27234307
[TBL] [Abstract][Full Text] [Related]
19. Recessive
Luo S; Liu ZG; Wang J; Luo JX; Ye XG; Li X; Zhai QX; Liu XR; Wang J; Gao LD; Liu FL; Ye ZL; Li H; Gao ZF; Guo QH; Li BM; Yi YH; Liao WP
Front Mol Neurosci; 2022; 15():825390. PubMed ID: 35663266
[TBL] [Abstract][Full Text] [Related]
20. Identification of curcumin-inhibited extracellular matrix receptors in non-small cell lung cancer A549 cells by RNA sequencing.
Li H; Wu H; Zhang H; Li Y; Li S; Hou Q; Wu S; Yang SY
Tumour Biol; 2017 Jun; 39(6):1010428317705334. PubMed ID: 28618934
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
