Literature DB >> 984047

The physicochemical properties of hair in the BIDS syndrome.

H P Baden, C E Jackson, L Weiss, K Jimbow, L Lee, J Kubilus, R J Gold.   

Abstract

The physicochemical properties of hair from a new recessive syndrome associated with brittle hair, intellectual impairment, decreased fertility, and short stature have been studied. Electrophoresis of the SCM-structural proteins showed that the alpha polypeptides appeared normal, but the matrix component was markedly reduced. This was confirmed by finding a normal alpha X-ray diffraction pattern but a reduced 1/2 cystine content of hair and an abnormal stress-strain curve. Electron-microscopic studies revealed extreme disorganization of the filaments which most likely resulted from the absence of normal cross-linking. Nails, which contain structural proteins similar to hair, also showed the abnormality. Since the matrix component seen by electrophoresis consists of more than one component the defect cannot be explained as a single structural gene abnormality.

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Year:  1976        PMID: 984047      PMCID: PMC1685097     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  9 in total

1.  THE MARINESCO-SJOEGREN SYNDROME.

Authors:  W F NORWOOD
Journal:  J Pediatr       Date:  1964-09       Impact factor: 4.406

2.  A STRUCTURAL BASIC PROTEIN AS A COUNTERPART OF DEOXYRIBONUCLEIC ACID IN MAMMALIAN SPERMATOZOA.

Authors:  E BRIL-PETERSEN; H G WESTENBRINIK
Journal:  Biochim Biophys Acta       Date:  1963-09-17

3.  DISC ELECTROPHORESIS. II. METHOD AND APPLICATION TO HUMAN SERUM PROTEINS.

Authors:  B J DAVIS
Journal:  Ann N Y Acad Sci       Date:  1964-12-28       Impact factor: 5.691

4.  "Brittle" hair with short stature, intellectual impairment and decreased fertility: an autosomal recessive syndrome in an Amish kindred.

Authors:  C E Jackson; L Weiss; J H Watson
Journal:  Pediatrics       Date:  1974-08       Impact factor: 7.124

5.  A comparative study of the physicochemical properties of human keratinized tissues.

Authors:  H P Baden; L A Goldsmith; B Fleming
Journal:  Biochim Biophys Acta       Date:  1973-10-18

6.  Sibs with mental and physical retardation and trichorrhexis nodosa with abnormal amino acid composition of the hair.

Authors:  R J Pollitt; F A Jenner; M Davies
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

7.  A congenital hair defect: trichoschisis with alternating birefringence and low sulfur content.

Authors:  A C Brown; R B Belser; R G Crounse; R F Wehr
Journal:  J Invest Dermatol       Date:  1970-06       Impact factor: 8.551

8.  The genetics of human hair growth.

Authors:  P S Porter
Journal:  Birth Defects Orig Artic Ser       Date:  1971-06

9.  Isolation and characterization of a basic keratin-like protein from mammalian spermatozoa.

Authors:  D M Henricks; D T Mayer
Journal:  Exp Cell Res       Date:  1965-11       Impact factor: 3.905

  9 in total
  12 in total

1.  Viscoelastic response of human hair cortex.

Authors:  G Nikiforidis; C Balas; D Tsambaos
Journal:  Med Biol Eng Comput       Date:  1992-01       Impact factor: 2.602

Review 2.  Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations.

Authors:  S Faghri; D Tamura; K H Kraemer; J J Digiovanna
Journal:  J Med Genet       Date:  2008-06-25       Impact factor: 6.318

3.  Mental retardation, short stature and brittle hair (BIDS syndrome; hair brain syndrome).

Authors:  R K Hora; V S Murthy
Journal:  Indian J Pediatr       Date:  1996 Jan-Feb       Impact factor: 1.967

4.  Intraspecies heterogeneity of epidermal keratins isolated from bovine hoof and snout.

Authors:  L D Lee; J Kubilus; H P Baden
Journal:  Biochem J       Date:  1979-01-01       Impact factor: 3.857

5.  A novel locus for alopecia with mental retardation syndrome (APMR2) maps to chromosome 3q26.2-q26.31.

Authors:  A Wali; P John; A Gul; K Lee; M S Chishti; G Ali; M J Hassan; S M Leal; W Ahmad
Journal:  Clin Genet       Date:  2006-09       Impact factor: 4.438

6.  Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy.

Authors:  Kazuhiko Nakabayashi; Daniela Amann; Yan Ren; Ulpu Saarialho-Kere; Nili Avidan; Simone Gentles; Jeffrey R MacDonald; Erik G Puffenberger; Angela M Christiano; Amalia Martinez-Mir; Julio C Salas-Alanis; Renata Rizzo; Esther Vamos; Anja Raams; Clifford Les; Eric Seboun; Nicolaas G J Jaspers; Jacques S Beckmann; Charles E Jackson; Stephen W Scherer
Journal:  Am J Hum Genet       Date:  2005-01-11       Impact factor: 11.025

7.  The Tay syndrome (congenital ichthyosis with trichothiodystrophy).

Authors:  R Happle; H Traupe; H Gröbe; G Bonsmann
Journal:  Eur J Pediatr       Date:  1984-01       Impact factor: 3.183

8.  Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity.

Authors:  M Stefanini; P Lagomarsini; C F Arlett; S Marinoni; C Borrone; F Crovato; G Trevisan; G Cordone; F Nuzzo
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

9.  Unexplained diarrhoea and failure to thrive in 2 siblings with unusual facies and abnormal scalp hair shafts: a new syndrome.

Authors:  L Stankler; D Lloyd; R J Pollitt; E S Gray; H Thom; G Russell
Journal:  Arch Dis Child       Date:  1982-03       Impact factor: 3.791

10.  Trichothiodystrophy without photosensitivity. Biochemical, ultrastructural and DNA repair studies.

Authors:  A Fois; P Balestri; S Calvieri; M Zampetti; S Giustini; M Stefanini; P Lagomarsini
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

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