References analysis of the Wikipedia article "Iminoglycinuria" in the English version

doi.org

Rosenberg LE, Durant JL, Elsas LJ (June 1968). "Familial iminoglycinuria. An inborn error of renal tubular transport". New England Journal of Medicine. 278 (26): 1407–13. doi:10.1056/NEJM196806272782601. PMID 5652624.

Bröer S, Bailey CG, Kowalczuk S, Ng C, Vanslambrouck JM, Rodgers H, Auray-Blais C, Cavanaugh, JA, Bröer A, Rasko JE (November 2008). "Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters" (Free full text). The Journal of Clinical Investigation. 118 (12): 3881–92. doi:10.1172/JCI36625. PMC 2579706. PMID 19033659.

Miyauchi S, Abbot EL, Zhuang L, Subramanian R, Ganapathy V, Thwaites DT (November 2005). "Isolation and function of the amino acid transporter PAT1 (slc36a1) from rabbit and discrimination between transport via PAT1 and system IMINO in renal brush-border membrane vesicles". Molecular Membrane Biology. 22 (6): 549–559. doi:10.1080/09687860500421779. PMID 16373326. S2CID 40085087.

Camargo SM, Bockenhauer D, Kleta R (April 2008). "Aminoacidurias: Clinical and molecular aspects". Kidney International. 73 (8): 918–925. doi:10.1038/sj.ki.5002790. ISSN 0085-2538. PMID 18200002.

Lasley L, Scriver CR (January 1979). "Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systems". Pediatric Research. 13 (1): 65–70. doi:10.1203/00006450-197901000-00014. ISSN 0031-3998. PMID 432003.

Weinberger B, Hanna N, Laskin JD, Heck DE, Gardner CR, Gerecke DR, Laskin DL (February 2005). "Mechanisms mediating the biologic activity of synthetic proline, glycine, and hydroxyproline polypeptides in human neutrophils" (Free full text). Mediators of Inflammation. 2005 (1): 31–38. doi:10.1155/MI.2005.31. PMC 1513057. PMID 15770064.

Procopis PG, Turner B (September 1971). "Iminoaciduria: a benign renal tubular defect". The Journal of Pediatrics. 79 (3): 419–422. doi:10.1016/S0022-3476(71)80150-6. ISSN 0022-3476. PMID 5567964.

Tancredi F, Guazzi G, Auricchio S (March 1970). "Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids". The Journal of Pediatrics. 76 (3): 386–392. doi:10.1016/S0022-3476(70)80477-2. ISSN 0022-3476. PMID 5308714.

Greene ML, Lietman PS, Rosenberg LE, Seegmiller JE (February 1973). "Familial hyperglycinuria. New defect in renal tubular transport of glycine and imino acids". The American Journal of Medicine. 54 (2): 265–271. doi:10.1016/0002-9343(73)90232-5. ISSN 0002-9343. PMID 4685850.

Kaser H, Cottier P, Antener I (September 1962). "Glucoglycinuria, a new familial syndrome". The Journal of Pediatrics. 61 (3): 386–394. doi:10.1016/S0022-3476(62)80369-2. ISSN 0022-3476. PMID 14454131.

Saito T, Hayasaka S, Yabata K, Omura K, Mizuno K, Tada K (November 1981). "Atypical gyrate atrophy of the choroid and retina and iminoglycinuria". The Tohoku Journal of Experimental Medicine. 135 (3): 331–332. doi:10.1620/tjem.135.331. ISSN 0040-8727. PMID 7314117.

Weleber RG, Kennaway NG, Buist NR (August 1981). "Gyrate atrophy of the choroid and retina. Approaches to therapy". International Ophthalmology. 4 (1–2): 23–32. doi:10.1007/BF00139577. ISSN 0165-5701. PMID 7028650. S2CID 26071922.

Rinaldi E, Stoppoloni GP, Savastano S, Russo S, Cotticelli L (March 1979). "Gyrate atrophy of choroid associated with hyperornithinaemia: report of the first case in Italy". Journal of Pediatric Ophthalmology and Strabismus. 16 (2): 133–5. doi:10.3928/0191-3913-19790301-12. ISSN 0191-3913. PMID 458520.

Saito T, Omura K, Hayasaka S, Nakajima H, Mizuno K, Tada K (December 1981). "Hyperornithinemia with gyrate atrophy of the choroid and retina: a disturbance in de novo formation of proline". The Tohoku Journal of Experimental Medicine. 135 (4): 395–402. doi:10.1620/tjem.135.395. ISSN 0040-8727. PMID 7336429.

De Vries A, Kochwa S, Lazebnik J, Frank M, Djaldetti M (September 1957). "Glycinuria, a hereditary disorder associated with nephrolithiasis". The American Journal of Medicine. 23 (3): 408–415. doi:10.1016/0002-9343(57)90320-0. ISSN 0002-9343. PMID 13458205.

Oberiter V, Puretić Z, Fabecić-Sabadi V (April 1978). "Hyperglycinuria with nephrolithiasis". European Journal of Pediatrics. 127 (4): 279–285. doi:10.1007/BF00493544. ISSN 0340-6199. PMID 668712. S2CID 32224980.

Scriver CR, Arthus MF, Bergeron M (August 1982). "Neonatal iminoglycinuria: evidence that the prolinuria originates in selective deficiency of transport activity in the proximal nephron". Pediatric Research. 16 (8): 684–7. doi:10.1203/00006450-198208000-00022. ISSN 0031-3998. PMID 7110792.

Takanaga H, Mackenzie B, Suzuki Y, Hediger MA (March 2005). "Identification of mammalian proline transporter SIT1 (SLC6A20) with characteristics of classical system imino". The Journal of Biological Chemistry. 280 (10): 8974–84. doi:10.1074/jbc.M413027200. ISSN 0021-9258. PMID 15632147.

Kowalczuk S, Bröer A, Munzinger M, Tietzel N, Klingel K, Bröer S (March 2005). "Molecular cloning of the mouse IMINO system: an Na+- and Cl--dependent proline transporter". The Biochemical Journal. 386 (Pt 3): 417–422. doi:10.1042/BJ20050100. PMC 1134859. PMID 15689184.

Castagna M, Shayakul C, Trotti D, Sacchi VF, Harvey WR, Hediger MA (January 1997). "Molecular characteristics of mammalian and insect amino acid transporters: implications for amino acid homeostasis". The Journal of Experimental Biology. 200 (Pt 2): 269–286. doi:10.1242/jeb.200.2.269. ISSN 0022-0949. PMID 9050235.

Anderson CM, Grenade DS, Boll M, Foltz M, Wake KA, Kennedy DJ, Munck LK, Miyauchi S, Taylor PM, Campbell FC, Munck BG, Daniel H, Ganapathy V, Thwaites DT (November 2004). "H+/amino acid transporter 1 (PAT1) is the imino acid carrier: An intestinal nutrient/drug transporter in human and rat". Gastroenterology. 127 (5): 1410–22. doi:10.1053/j.gastro.2004.08.017. ISSN 0016-5085. PMID 15521011.

Thwaites DT, Anderson CM (February 2007). "Deciphering the mechanisms of intestinal imino (and amino) acid transport: the redemption of SLC36A1". Biochimica et Biophysica Acta (BBA) - Biomembranes. 1768 (2): 179–197. doi:10.1016/j.bbamem.2006.10.001. ISSN 0006-3002. PMID 17123464.

Bröer A, Cavanaugh JA, Rasko JE, Bröer S (January 2006). "The molecular basis of neutral aminoacidurias". Pflügers Archiv: European Journal of Physiology. 451 (4): 511–7. doi:10.1007/s00424-005-1481-8. ISSN 0031-6768. PMID 16052352. S2CID 43517786.

Ristic Z, Camargo SM, Romeo E, Bodoy S, Bertran J, Palacin M, Makrides V, Furrer EM, Verrey F (April 2006). "Neutral amino acid transport mediated by ortholog of imino acid transporter SIT1/SLC6A20 in opossum kidney cells". American Journal of Physiology. Renal Physiology. 290 (4): F880–7. doi:10.1152/ajprenal.00319.2005. PMID 16234310.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ohura T (1998). "Familial iminoglycinuria". Ryoikibetsu Shokogun Shirizu (19 Pt 2): 569–571. PMID 9645136.

Statter M, Ben-Zvi A, Shina A, Schein R, Russell A (August 1976). "Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype"". Helvetica Paediatrica Acta. 31 (2): 173–182. ISSN 0018-022X. PMID 955941.

Coşkun T, Ozalp I, Tokatli A (April 1993). "Iminoglycinuria: a benign type of inherited aminoaciduria". The Turkish Journal of Pediatrics. 35 (2): 121–125. ISSN 0041-4301. PMID 7504361.

Camargo SM, Bockenhauer D, Kleta R (April 2008). "Aminoacidurias: Clinical and molecular aspects". Kidney International. 73 (8): 918–925. doi:10.1038/sj.ki.5002790. ISSN 0085-2538. PMID 18200002.

ncbi.nlm.nih.gov

meshb.nlm.nih.gov

Proline at the U.S. National Library of Medicine Medical Subject Headings (MeSH)

semanticscholar.org

api.semanticscholar.org

worldcat.org

search.worldcat.org

Coşkun T, Ozalp I, Tokatli A (April 1993). "Iminoglycinuria: a benign type of inherited aminoaciduria". The Turkish Journal of Pediatrics. 35 (2): 121–125. ISSN 0041-4301. PMID 7504361.

Camargo SM, Bockenhauer D, Kleta R (April 2008). "Aminoacidurias: Clinical and molecular aspects". Kidney International. 73 (8): 918–925. doi:10.1038/sj.ki.5002790. ISSN 0085-2538. PMID 18200002.

Iminoglycinuria (English Wikipedia)

arizona.edu

biology.arizona.edu

doi.org

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

meshb.nlm.nih.gov

omim.org

semanticscholar.org

api.semanticscholar.org

uni-hamburg.de

www1.biologie.uni-hamburg.de

worldcat.org

search.worldcat.org