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Items: 1 to 50 of 77

1.

Did Our Species Evolve in Subdivided Populations across Africa, and Why Does It Matter?

Scerri EML, Thomas MG, Manica A, Gunz P, Stock JT, Stringer C, Grove M, Groucutt HS, Timmermann A, Rightmire GP, d'Errico F, Tryon CA, Drake NA, Brooks AS, Dennell RW, Durbin R, Henn BM, Lee-Thorp J, deMenocal P, Petraglia MD, Thompson JC, Scally A, Chikhi L.

Trends Ecol Evol. 2018 Jun 14. pii: S0169-5347(18)30117-4. doi: 10.1016/j.tree.2018.05.005. [Epub ahead of print] Review.

PMID:
30007846
2.

Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients.

Deden AC, van Slegtenhorst MA, Ruijter GJG, Schoonderwoerd GC, Huidekoper HH, Oussoren E, Brooks AS, Demirdas S.

Clin Chim Acta. 2018 Jun 2;484:231. doi: 10.1016/j.cca.2018.06.003. [Epub ahead of print] No abstract available.

PMID:
29870682
3.

Identification of Variants in RET and IHH Pathway Members in a Large Family With History of Hirschsprung Disease.

Sribudiani Y, Chauhan RK, Alves MM, Petrova L, Brosens E, Harrison C, Wabbersen T, de Graaf BM, Rügenbrink T, Burzynski G, Brouwer RWW, van IJcken WFJ, Maas SM, de Klein A, Osinga J, Eggen BJL, Burns AJ, Brooks AS, Shepherd IT, Hofstra RMW.

Gastroenterology. 2018 Jul;155(1):118-129.e6. doi: 10.1053/j.gastro.2018.03.034. Epub 2018 Mar 28.

4.

Chronology of the Acheulean to Middle Stone Age transition in eastern Africa.

Deino AL, Behrensmeyer AK, Brooks AS, Yellen JE, Sharp WD, Potts R.

Science. 2018 Apr 6;360(6384):95-98. doi: 10.1126/science.aao2216. Epub 2018 Mar 15.

PMID:
29545510
5.

Long-distance stone transport and pigment use in the earliest Middle Stone Age.

Brooks AS, Yellen JE, Potts R, Behrensmeyer AK, Deino AL, Leslie DE, Ambrose SH, Ferguson JR, d'Errico F, Zipkin AM, Whittaker S, Post J, Veatch EG, Foecke K, Clark JB.

Science. 2018 Apr 6;360(6384):90-94. doi: 10.1126/science.aao2646. Epub 2018 Mar 15.

PMID:
29545508
6.

Environmental dynamics during the onset of the Middle Stone Age in eastern Africa.

Potts R, Behrensmeyer AK, Faith JT, Tryon CA, Brooks AS, Yellen JE, Deino AL, Kinyanjui R, Clark JB, Haradon CM, Levin NE, Meijer HJM, Veatch EG, Owen RB, Renaut RW.

Science. 2018 Apr 6;360(6384):86-90. doi: 10.1126/science.aao2200. Epub 2018 Mar 15.

PMID:
29545506
7.

A Missense Mutation in the Extracellular Domain of αENaC Causes Liddle Syndrome.

Salih M, Gautschi I, van Bemmelen MX, Di Benedetto M, Brooks AS, Lugtenberg D, Schild L, Hoorn EJ.

J Am Soc Nephrol. 2017 Nov;28(11):3291-3299. doi: 10.1681/ASN.2016111163. Epub 2017 Jul 14.

PMID:
28710092
8.

Postzygotic telomere capture causes segmental UPD, duplication and deletion of chromosome 8p in a patient with intellectual disability and obesity.

Knijnenburg J, Uytdewilligen MEW, van Hassel DACM, Oostenbrink R, Eussen BHJ, de Klein A, Brooks AS, van Zutven LJCM.

Eur J Med Genet. 2017 Sep;60(9):445-450. doi: 10.1016/j.ejmg.2017.06.003. Epub 2017 Jun 8.

PMID:
28602932
9.

Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.

Acuna-Hidalgo R, Deriziotis P, Steehouwer M, Gilissen C, Graham SA, van Dam S, Hoover-Fong J, Telegrafi AB, Destree A, Smigiel R, Lambie LA, Kayserili H, Altunoglu U, Lapi E, Uzielli ML, Aracena M, Nur BG, Mihci E, Moreira LM, Borges Ferreira V, Horovitz DD, da Rocha KM, Jezela-Stanek A, Brooks AS, Reutter H, Cohen JS, Fatemi A, Smitka M, Grebe TA, Di Donato N, Deshpande C, Vandersteen A, Marques Lourenço C, Dufke A, Rossier E, Andre G, Baumer A, Spencer C, McGaughran J, Franke L, Veltman JA, De Vries BB, Schinzel A, Fisher SE, Hoischen A, van Bon BW.

PLoS Genet. 2017 Mar 27;13(3):e1006683. doi: 10.1371/journal.pgen.1006683. eCollection 2017 Mar.

10.

Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice.

Halim D, Wilson MP, Oliver D, Brosens E, Verheij JB, Han Y, Nanda V, Lyu Q, Doukas M, Stoop H, Brouwer RW, van IJcken WF, Slivano OJ, Burns AJ, Christie CK, de Mesy Bentley KL, Brooks AS, Tibboel D, Xu S, Jin ZG, Djuwantono T, Yan W, Alves MM, Hofstra RM, Miano JM.

Proc Natl Acad Sci U S A. 2017 Mar 28;114(13):E2739-E2747. doi: 10.1073/pnas.1620507114. Epub 2017 Mar 14.

11.

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes.

Gui H, Schriemer D, Cheng WW, Chauhan RK, Antiňolo G, Berrios C, Bleda M, Brooks AS, Brouwer RW, Burns AJ, Cherny SS, Dopazo J, Eggen BJ, Griseri P, Jalloh B, Le TL, Lui VC, Luzón-Toro B, Matera I, Ngan ES, Pelet A, Ruiz-Ferrer M, Sham PC, Shepherd IT, So MT, Sribudiani Y, Tang CS, van den Hout MC, van der Linde HC, van Ham TJ, van IJcken WF, Verheij JB, Amiel J, Borrego S, Ceccherini I, Chakravarti A, Lyonnet S, Tam PK, Garcia-Barceló MM, Hofstra RM.

Genome Biol. 2017 Mar 8;18(1):48. doi: 10.1186/s13059-017-1174-6.

12.

Previous miscarriages and GLI2 are associated with anorectal malformations in offspring.

van de Putte R, Wijers CH, de Blaauw I, Marcelis CL, Sloots CE, Brooks AS, Broens PM, Roeleveld N, van der Zanden LF, van Rooij IA.

Hum Reprod. 2017 Feb;32(2):299-306. doi: 10.1093/humrep/dew327. Epub 2017 Jan 5.

PMID:
28057877
13.

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula.

Brosens E, Marsch F, de Jong EM, Zaveri HP, Hilger AC, Choinitzki VG, Hölscher A, Hoffmann P, Herms S, Boemers TM, Ure BM, Lacher M, Ludwig M, Eussen BH, van der Helm RM, Douben H, Van Opstal D, Wijnen RM, Beverloo HB, van Bever Y, Brooks AS, IJsselstijn H, Scott DA, Schumacher J, Tibboel D, Reutter H, de Klein A.

Eur J Hum Genet. 2016 Dec;24(12):1715-1723. doi: 10.1038/ejhg.2016.86. Epub 2016 Jul 20.

14.

Genetics of enteric neuropathies.

Brosens E, Burns AJ, Brooks AS, Matera I, Borrego S, Ceccherini I, Tam PK, García-Barceló MM, Thapar N, Benninga MA, Hofstra RM, Alves MM.

Dev Biol. 2016 Sep 15;417(2):198-208. doi: 10.1016/j.ydbio.2016.07.008. Epub 2016 Jul 15. Review.

15.

Hematopoietic Stem Cell Transplantation in a Patient With ICF2 Syndrome Presenting With EBV-Induced Hemophagocytic Lymphohystiocytosis.

Harnisch E, Buddingh EP, Thijssen PE, Brooks AS, Driessen GJ, Kersseboom R, Lankester AC.

Transplantation. 2016 Jul;100(7):e35-6. doi: 10.1097/TP.0000000000001210. No abstract available.

PMID:
27326813
16.

De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.

Reijnders MR, Zachariadis V, Latour B, Jolly L, Mancini GM, Pfundt R, Wu KM, van Ravenswaaij-Arts CM, Veenstra-Knol HE, Anderlid BM, Wood SA, Cheung SW, Barnicoat A, Probst F, Magoulas P, Brooks AS, Malmgren H, Harila-Saari A, Marcelis CM, Vreeburg M, Hobson E, Sutton VR, Stark Z, Vogt J, Cooper N, Lim JY, Price S, Lai AH, Domingo D, Reversade B; DDD Study, Gecz J, Gilissen C, Brunner HG, Kini U, Roepman R, Nordgren A, Kleefstra T.

Am J Hum Genet. 2016 Feb 4;98(2):373-81. doi: 10.1016/j.ajhg.2015.12.015. Epub 2016 Jan 28.

17.

ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome.

Halim D, Hofstra RM, Signorile L, Verdijk RM, van der Werf CS, Sribudiani Y, Brouwer RW, van IJcken WF, Dahl N, Verheij JB, Baumann C, Kerner J, van Bever Y, Galjart N, Wijnen RM, Tibboel D, Burns AJ, Muller F, Brooks AS, Alves MM.

Hum Mol Genet. 2016 Feb 1;25(3):571-83. doi: 10.1093/hmg/ddv497. Epub 2015 Dec 8.

PMID:
26647307
18.

The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant.

Koolen DA, Pfundt R, Linda K, Beunders G, Veenstra-Knol HE, Conta JH, Fortuna AM, Gillessen-Kaesbach G, Dugan S, Halbach S, Abdul-Rahman OA, Winesett HM, Chung WK, Dalton M, Dimova PS, Mattina T, Prescott K, Zhang HZ, Saal HM, Hehir-Kwa JY, Willemsen MH, Ockeloen CW, Jongmans MC, Van der Aa N, Failla P, Barone C, Avola E, Brooks AS, Kant SG, Gerkes EH, Firth HV, Õunap K, Bird LM, Masser-Frye D, Friedman JR, Sokunbi MA, Dixit A, Splitt M; DDD Study, Kukolich MK, McGaughran J, Coe BP, Flórez J, Nadif Kasri N, Brunner HG, Thompson EM, Gecz J, Romano C, Eichler EE, de Vries BB.

Eur J Hum Genet. 2016 May;24(5):652-9. doi: 10.1038/ejhg.2015.178. Epub 2015 Aug 26.

19.

JS-X syndrome: A multiple congenital malformation with vocal cord paralysis, ear deformity, hearing loss, shoulder musculature underdevelopment, and X-linked recessive inheritance.

Hoeve HL, Brooks AS, Smit LS.

Int J Pediatr Otorhinolaryngol. 2015 Jul;79(7):1164-70. doi: 10.1016/j.ijporl.2015.05.001. Epub 2015 May 12.

PMID:
25998214
20.

An experimental study of hafting adhesives and the implications for compound tool technology.

Zipkin AM, Wagner M, McGrath K, Brooks AS, Lucas PW.

PLoS One. 2014 Nov 10;9(11):e112560. doi: 10.1371/journal.pone.0112560. eCollection 2014.

21.

No major role for periconceptional folic acid use and its interaction with the MTHFR C677T polymorphism in the etiology of congenital anorectal malformations.

Wijers CH, de Blaauw I, Zwink N, Draaken M, van der Zanden LF, Brunner HG, Brooks AS, Hofstra RM, Sloots CE, Broens PM, Wijnen MH, Ludwig M, Jenetzky E, Reutter H, Marcelis CL, Roeleveld N, van Rooij IA.

Birth Defects Res A Clin Mol Teratol. 2014 Jun;100(6):483-92. doi: 10.1002/bdra.23256. Epub 2014 May 20.

PMID:
24841934
22.

Plant foods and the dietary ecology of Neanderthals and early modern humans.

Henry AG, Brooks AS, Piperno DR.

J Hum Evol. 2014 Apr;69:44-54. doi: 10.1016/j.jhevol.2013.12.014. Epub 2014 Mar 5.

PMID:
24612646
23.

First early hominin from central Africa (Ishango, Democratic Republic of Congo).

Crevecoeur I, Skinner MM, Bailey SE, Gunz P, Bortoluzzi S, Brooks AS, Burlet C, Cornelissen E, De Clerck N, Maureille B, Semal P, Vanbrabant Y, Wood B.

PLoS One. 2014 Jan 10;9(1):e84652. doi: 10.1371/journal.pone.0084652. eCollection 2014.

24.

Myhre and LAPS syndromes: clinical and molecular review of 32 patients.

Michot C, Le Goff C, Mahaut C, Afenjar A, Brooks AS, Campeau PM, Destree A, Di Rocco M, Donnai D, Hennekam R, Heron D, Jacquemont S, Kannu P, Lin AE, Manouvrier-Hanu S, Mansour S, Marlin S, McGowan R, Murphy H, Raas-Rothschild A, Rio M, Simon M, Stolte-Dijkstra I, Stone JR, Sznajer Y, Tolmie J, Touraine R, van den Ende J, Van der Aa N, van Essen T, Verloes A, Munnich A, Cormier-Daire V.

Eur J Hum Genet. 2014 Nov;22(11):1272-7. doi: 10.1038/ejhg.2013.288. Epub 2014 Jan 15. Erratum in: Eur J Hum Genet. 2014 Nov;22(11):1340.

25.

Structural and numerical changes of chromosome X in patients with esophageal atresia.

Brosens E, de Jong EM, Barakat TS, Eussen BH, D'haene B, De Baere E, Verdin H, Poddighe PJ, Galjaard RJ, Gribnau J, Brooks AS, Tibboel D, de Klein A.

Eur J Hum Genet. 2014 Sep;22(9):1077-84. doi: 10.1038/ejhg.2013.295. Epub 2014 Jan 8.

26.

Novel no-stop FLNA mutation causes multi-organ involvement in males.

Oegema R, Hulst JM, Theuns-Valks SD, van Unen LM, Schot R, Mancini GM, Schipper ME, de Wit MC, Sibbles BJ, de Coo IF, Nanninga V, Hofstra RM, Halley DJ, Brooks AS.

Am J Med Genet A. 2013 Sep;161A(9):2376-84. doi: 10.1002/ajmg.a.36109. Epub 2013 Jul 19.

PMID:
23873601
27.

Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.

Sen P, Yang Y, Navarro C, Silva I, Szafranski P, Kolodziejska KE, Dharmadhikari AV, Mostafa H, Kozakewich H, Kearney D, Cahill JB, Whitt M, Bilic M, Margraf L, Charles A, Goldblatt J, Gibson K, Lantz PE, Garvin AJ, Petty J, Kiblawi Z, Zuppan C, McConkie-Rosell A, McDonald MT, Peterson-Carmichael SL, Gaede JT, Shivanna B, Schady D, Friedlich PS, Hays SR, Palafoll IV, Siebers-Renelt U, Bohring A, Finn LS, Siebert JR, Galambos C, Nguyen L, Riley M, Chassaing N, Vigouroux A, Rocha G, Fernandes S, Brumbaugh J, Roberts K, Ho-Ming L, Lo IF, Lam S, Gerychova R, Jezova M, Valaskova I, Fellmann F, Afshar K, Giannoni E, Muhlethaler V, Liang J, Beckmann JS, Lioy J, Deshmukh H, Srinivasan L, Swarr DT, Sloman M, Shaw-Smith C, van Loon RL, Hagman C, Sznajer Y, Barrea C, Galant C, Detaille T, Wambach JA, Cole FS, Hamvas A, Prince LS, Diderich KE, Brooks AS, Verdijk RM, Ravindranathan H, Sugo E, Mowat D, Baker ML, Langston C, Welty S, Stankiewicz P.

Hum Mutat. 2013 Jun;34(6):801-11. doi: 10.1002/humu.22313. Epub 2013 Apr 12.

28.

Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutations.

van der Werf CS, Sribudiani Y, Verheij JB, Carroll M, O'Loughlin E, Chen CH, Brooks AS, Liszewski MK, Atkinson JP, Hofstra RM.

Genet Med. 2013 Apr;15(4):310-3. doi: 10.1038/gim.2012.123. Epub 2012 Oct 4.

PMID:
23037936
29.

Incidental finding of alpha-methylacyl-CoA racemase deficiency in a patient with oculocutaneous albinism type 4.

Verhagen JM, Huijmans JG, Williams M, van Ruyven RL, Bergen AA, Wouters CH, Brooks AS.

Am J Med Genet A. 2012 Nov;158A(11):2931-4. doi: 10.1002/ajmg.a.35611. Epub 2012 Sep 17.

PMID:
22987308
30.

The environmental context for the origins of modern human diversity: a synthesis of regional variability in African climate 150,000-30,000 years ago.

Blome MW, Cohen AS, Tryon CA, Brooks AS, Russell J.

J Hum Evol. 2012 May;62(5):563-92. doi: 10.1016/j.jhevol.2012.01.011. Epub 2012 Apr 17.

PMID:
22513381
31.

Sizing and phenotyping of cellular vesicles using Nanoparticle Tracking Analysis.

Dragovic RA, Gardiner C, Brooks AS, Tannetta DS, Ferguson DJ, Hole P, Carr B, Redman CW, Harris AL, Dobson PJ, Harrison P, Sargent IL.

Nanomedicine. 2011 Dec;7(6):780-8. doi: 10.1016/j.nano.2011.04.003. Epub 2011 May 4.

32.

Single nucleotide polymorphisms in collagenous lectins and other innate immune genes in pigs with common infectious diseases.

Keirstead ND, Hayes MA, Vandervoort GE, Brooks AS, Squires EJ, Lillie BN.

Vet Immunol Immunopathol. 2011 Jul 15;142(1-2):1-13. doi: 10.1016/j.vetimm.2011.02.011. Epub 2011 Feb 25.

PMID:
21570129
33.

Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalities.

Barge-Schaapveld DQ, Brooks AS, Lequin MH, van Spaendonk R, Vermeulen RJ, Cobben JM.

Pediatr Neurol. 2011 Apr;44(4):303-7. doi: 10.1016/j.pediatrneurol.2010.11.015.

PMID:
21397175
34.

Delayed complications of tooth extraction in patients taking warfarin, antibiotics, and other medications.

Brooks AS.

J Oral Maxillofac Surg. 2011 Apr;69(4):977-9. doi: 10.1016/j.joms.2010.05.012. Epub 2011 Jan 26. No abstract available.

PMID:
21272971
35.

Microfossils in calculus demonstrate consumption of plants and cooked foods in Neanderthal diets (Shanidar III, Iraq; Spy I and II, Belgium).

Henry AG, Brooks AS, Piperno DR.

Proc Natl Acad Sci U S A. 2011 Jan 11;108(2):486-91. doi: 10.1073/pnas.1016868108. Epub 2010 Dec 27.

36.

Bactericidal activity of porcine neutrophil secretions.

Scapinello S, Brooks AS, MacInnes JI, Hammermueller J, Clark ME, Caswell JL.

Vet Immunol Immunopathol. 2011 Feb 15;139(2-4):113-8. doi: 10.1016/j.vetimm.2010.09.004. Epub 2010 Sep 17.

PMID:
20932586
37.

KBP interacts with SCG10, linking Goldberg-Shprintzen syndrome to microtubule dynamics and neuronal differentiation.

Alves MM, Burzynski G, Delalande JM, Osinga J, van der Goot A, Dolga AM, de Graaff E, Brooks AS, Metzger M, Eisel UL, Shepherd I, Eggen BJ, Hofstra RM.

Hum Mol Genet. 2010 Sep 15;19(18):3642-51. doi: 10.1093/hmg/ddq280. Epub 2010 Jul 9.

PMID:
20621975
38.

The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.

Paulussen AD, Schrander-Stumpel CT, Tserpelis DC, Spee MK, Stegmann AP, Mancini GM, Brooks AS, Collée M, Maat-Kievit A, Simon ME, van Bever Y, Stolte-Dijkstra I, Kerstjens-Frederikse WS, Herkert JC, van Essen AJ, Lichtenbelt KD, van Haeringen A, Kwee ML, Lachmeijer AM, Tan-Sindhunata GM, van Maarle MC, Arens YH, Smeets EE, de Die-Smulders CE, Engelen JJ, Smeets HJ, Herbergs J.

Eur J Hum Genet. 2010 Sep;18(9):999-1005. doi: 10.1038/ejhg.2010.70. Epub 2010 Jun 9.

39.

Hirschsprung disease, associated syndromes and genetics: a review.

Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, Brooks AS, Antinolo G, de Pontual L, Clement-Ziza M, Munnich A, Kashuk C, West K, Wong KK, Lyonnet S, Chakravarti A, Tam PK, Ceccherini I, Hofstra RM, Fernandez R; Hirschsprung Disease Consortium.

J Med Genet. 2008 Jan;45(1):1-14. Epub 2007 Oct 26. Review.

PMID:
17965226
40.

Porcine plasma ficolin binds and reduces infectivity of porcine reproductive and respiratory syndrome virus (PRRSV) in vitro.

Keirstead ND, Lee C, Yoo D, Brooks AS, Hayes MA.

Antiviral Res. 2008 Jan;77(1):28-38. Epub 2007 Aug 27.

PMID:
17850894
41.

Bacterial-binding activity and plasma concentration of ladderlectin in rainbow trout (Oncorhynchus mykiss).

Young KM, Russell S, Smith M, Huber P, Ostland VE, Brooks AS, Anthony Hayes M, Lumsden JS.

Fish Shellfish Immunol. 2007 Aug;23(2):305-15. Epub 2006 Nov 22.

PMID:
17383895
42.

A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3.

Brooks AS, Leegwater PA, Burzynski GM, Willems PJ, de Graaf B, van Langen I, Heutink P, Oostra BA, Hofstra RM, Bertoli-Avella AM.

J Med Genet. 2006 Jul;43(7):e35.

43.

Two brothers with Goldberg-Shprintzen syndrome.

Murphy HR, Carver MJ, Brooks AS, Kenny SE, Ellis IH.

Clin Dysmorphol. 2006 Jul;15(3):165-9.

PMID:
16760737
44.

BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.

Stoetzel C, Laurier V, Davis EE, Muller J, Rix S, Badano JL, Leitch CC, Salem N, Chouery E, Corbani S, Jalk N, Vicaire S, Sarda P, Hamel C, Lacombe D, Holder M, Odent S, Holder S, Brooks AS, Elcioglu NH, Silva ED, Rossillion B, Sigaudy S, de Ravel TJ, Lewis RA, Leheup B, Verloes A, Amati-Bonneau P, Mégarbané A, Poch O, Bonneau D, Beales PL, Mandel JL, Katsanis N, Dollfus H.

Nat Genet. 2006 May;38(5):521-4. Epub 2006 Apr 2. Erratum in: Nat Genet. 2006 Jun;38(6):727. Da Silva, Eduardo [corrected to Silva, Eduardo D].

PMID:
16582908
45.

A 54-year-old woman with menorrhagia. Mixed mucinous and endometrioid carcinoma with small nonvillous papillae.

Fadare O, Brooks AS, Martel M.

Arch Pathol Lab Med. 2006 Mar;130(3):400-2. No abstract available.

PMID:
16519574
46.

The use of an alternative food source (red clover) as a means of reducing slug pest damage to winter wheat: towards field implementation.

Brooks AS, Wilcox A, Cook RT, James KL, Crook MJ.

Pest Manag Sci. 2006 Mar;62(3):252-62.

PMID:
16475236
47.

Comparative genetics and innate immune functions of collagenous lectins in animals.

Lillie BN, Brooks AS, Keirstead ND, Hayes MA.

Vet Immunol Immunopathol. 2005 Oct 18;108(1-2):97-110. Review.

PMID:
16098608
48.

Homozygous nonsense mutations in KIAA1279 are associated with malformations of the central and enteric nervous systems.

Brooks AS, Bertoli-Avella AM, Burzynski GM, Breedveld GJ, Osinga J, Boven LG, Hurst JA, Mancini GM, Lequin MH, de Coo RF, Matera I, de Graaff E, Meijers C, Willems PJ, Tibboel D, Oostra BA, Hofstra RM.

Am J Hum Genet. 2005 Jul;77(1):120-6. Epub 2005 May 9.

49.
50.

Identifying candidate Hirschsprung disease-associated RET variants.

Burzynski GM, Nolte IM, Bronda A, Bos KK, Osinga J, Plaza Menacho I, Twigt B, Maas S, Brooks AS, Verheij JB, Buys CH, Hofstra RM.

Am J Hum Genet. 2005 May;76(5):850-8. Epub 2005 Mar 9.

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